LABELS · bf986b71-66e2-4883-9687-f340388abafe
Darzalex Faspro
Open original source → · Download preserved record
Preserved label snapshot, not confirmation of a current approved indication. Approval/withdrawal status must be checked for the exact disease, setting and regimen.
- Label effective date
- 2026-09-03
- Captured
- 2026-09-09T23:37:58.719708+00:00
- Current indication reconciliation
- Not reconciled
Indications and usage: exact source text
- 1 INDICATIONS AND USAGE DARZALEX FASPRO is a combination of daratumumab, a CD38-directed cytolytic antibody, and hyaluronidase, an endoglycosidase, indicated for the treatment of adult patients with: multiple myeloma in combination with bortezomib, lenalidomide, and dexamethasone for induction and consolidation in newly diagnosed patients who are eligible for autologous stem cell transplant multiple myeloma in combination with bortezomib, lenalidomide, and dexamethasone in newly diagnosed patients who are ineligible for autologous stem cell transplant multiple myeloma in combination with bortezomib, melphalan and prednisone in newly diagnosed patients who are ineligible for autologous stem cell transplant multiple myeloma in combination with lenalidomide and dexamethasone in newly diagnosed patients who are ineligible for autologous stem cell transplant and in patients with relapsed or refractory multiple myeloma who have received at least one prior therapy multiple myeloma in combination with bortezomib, thalidomide, and dexamethasone in newly diagnosed patients who are eligible for autologous stem cell transplant multiple myeloma in combination with bortezomib and dexamethasone in patients who have received at least one prior therapy multiple myeloma in combination with pomalidomide and dexamethasone in patients who have received at least one prior line of therapy including lenalidomide and a proteasome inhibitor multiple myeloma in combination with carfilzomib and dexamethasone in patients with relapsed or refractory multiple myeloma who have received one to three prior lines of therapy multiple myeloma as monotherapy, in patients who have received at least three prior lines of therapy including a proteasome inhibitor (PI) and an immunomodulatory agent or who are double-refractory to a PI and an immunomodulatory agent high-risk smoldering multiple myeloma as monotherapy light chain (AL) amyloidosis in combination with bortezomib, cyclophosphamide and dexamethasone in newly diagnosed patients. Limitations of Use: DARZALEX FASPRO is not indicated and is not recommended for the treatment of patients with light chain (AL) amyloidosis who have NYHA Class IIIB or Class IV cardiac disease or Mayo Stage IIIB outside of controlled clinical trials ( 1.3 ) 1.1 Multiple Myeloma DARZALEX FASPRO is indicated for the treatment of adult patients with [see Clinical Studies (14) ] : multiple myeloma in combination with bortezomib, lenalidomide, and dexamethasone for induction and consolidation in newly diagnosed patients who are eligible for autologous stem cell transplant. multiple myeloma in combination with bortezomib, lenalidomide, and dexamethasone in newly diagnosed patients who are ineligible for autologous stem cell transplant. multiple myeloma in combination with bortezomib, melphalan and prednisone in newly diagnosed patients who are ineligible for autologous stem cell transplant. multiple myeloma in combination with lenalidomide and dexamethasone in newly diagnosed patients who are ineligible for autologous stem cell transplant and in patients with relapsed or refractory multiple myeloma who have received at least one prior therapy. multiple myeloma in combination with bortezomib, thalidomide, and dexamethasone in newly diagnosed patients who are eligible for autologous stem cell transplant. multiple myeloma in combination with bortezomib and dexamethasone in patients who have received at least one prior therapy. multiple myeloma in combination with pomalidomide and dexamethasone in patients who have received at least one prior line of therapy including lenalidomide and a proteasome inhibitor. multiple myeloma in combination with carfilzomib and dexamethasone in patients with relapsed or refractory multiple myeloma who have received one to three prior lines of therapy. multiple myeloma as monotherapy, in patients who have received at least three prior lines of therapy including a proteasome inhibitor (PI) and an immunomodulatory agent or who are double-refractory to a PI and an immunomodulatory agent. 1.2 High-Risk Smoldering Multiple Myeloma DARZALEX FASPRO as monotherapy is indicated for the treatment of adult patients with high-risk smoldering multiple myeloma. 1.3 Light Chain Amyloidosis DARZALEX FASPRO in combination with bortezomib, cyclophosphamide and dexamethasone is indicated for the treatment of adult patients with newly diagnosed light chain (AL) amyloidosis. Limitations of Use DARZALEX FASPRO is not indicated and is not recommended for the treatment of patients with light chain (AL) amyloidosis who have NYHA Class IIIB or Class IV cardiac disease or Mayo Stage IIIB outside of controlled clinical trials [see Warnings and Precautions (5.2) ] .
Full extracted label fields
- application numbers
- BLA761145
- boxed warning exact
- brand names
- Darzalex Faspro
- current indication status
- not_reconciled
- dailymed set url
- https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=4bb241af-4299-4373-8762-2d6709515db0
- generic names
- DARATUMUMAB AND HYALURONIDASE-FIHJ (HUMAN RECOMBINANT)
- id
- bf986b71-66e2-4883-9687-f340388abafe
- indications and usage exact
- 1 INDICATIONS AND USAGE DARZALEX FASPRO is a combination of daratumumab, a CD38-directed cytolytic antibody, and hyaluronidase, an endoglycosidase, indicated for the treatment of adult patients with: multiple myeloma in combination with bortezomib, lenalidomide, and dexamethasone for induction and consolidation in newly diagnosed patients who are eligible for autologous stem cell transplant multiple myeloma in combination with bortezomib, lenalidomide, and dexamethasone in newly diagnosed patients who are ineligible for autologous stem cell transplant multiple myeloma in combination with bortezomib, melphalan and prednisone in newly diagnosed patients who are ineligible for autologous stem cell transplant multiple myeloma in combination with lenalidomide and dexamethasone in newly diagnosed patients who are ineligible for autologous stem cell transplant and in patients with relapsed or refractory multiple myeloma who have received at least one prior therapy multiple myeloma in combination with bortezomib, thalidomide, and dexamethasone in newly diagnosed patients who are eligible for autologous stem cell transplant multiple myeloma in combination with bortezomib and dexamethasone in patients who have received at least one prior therapy multiple myeloma in combination with pomalidomide and dexamethasone in patients who have received at least one prior line of therapy including lenalidomide and a proteasome inhibitor multiple myeloma in combination with carfilzomib and dexamethasone in patients with relapsed or refractory multiple myeloma who have received one to three prior lines of therapy multiple myeloma as monotherapy, in patients who have received at least three prior lines of therapy including a proteasome inhibitor (PI) and an immunomodulatory agent or who are double-refractory to a PI and an immunomodulatory agent high-risk smoldering multiple myeloma as monotherapy light chain (AL) amyloidosis in combination with bortezomib, cyclophosphamide and dexamethasone in newly diagnosed patients. Limitations of Use: DARZALEX FASPRO is not indicated and is not recommended for the treatment of patients with light chain (AL) amyloidosis who have NYHA Class IIIB or Class IV cardiac disease or Mayo Stage IIIB outside of controlled clinical trials ( 1.3 ) 1.1 Multiple Myeloma DARZALEX FASPRO is indicated for the treatment of adult patients with [see Clinical Studies (14) ] : multiple myeloma in combination with bortezomib, lenalidomide, and dexamethasone for induction and consolidation in newly diagnosed patients who are eligible for autologous stem cell transplant. multiple myeloma in combination with bortezomib, lenalidomide, and dexamethasone in newly diagnosed patients who are ineligible for autologous stem cell transplant. multiple myeloma in combination with bortezomib, melphalan and prednisone in newly diagnosed patients who are ineligible for autologous stem cell transplant. multiple myeloma in combination with lenalidomide and dexamethasone in newly diagnosed patients who are ineligible for autologous stem cell transplant and in patients with relapsed or refractory multiple myeloma who have received at least one prior therapy. multiple myeloma in combination with bortezomib, thalidomide, and dexamethasone in newly diagnosed patients who are eligible for autologous stem cell transplant. multiple myeloma in combination with bortezomib and dexamethasone in patients who have received at least one prior therapy. multiple myeloma in combination with pomalidomide and dexamethasone in patients who have received at least one prior line of therapy including lenalidomide and a proteasome inhibitor. multiple myeloma in combination with carfilzomib and dexamethasone in patients with relapsed or refractory multiple myeloma who have received one to three prior lines of therapy. multiple myeloma as monotherapy, in patients who have received at least three prior lines of therapy including a proteasome inhibitor (PI) and an immunomodulatory agent or who are double-refractory to a PI and an immunomodulatory agent. 1.2 High-Risk Smoldering Multiple Myeloma DARZALEX FASPRO as monotherapy is indicated for the treatment of adult patients with high-risk smoldering multiple myeloma. 1.3 Light Chain Amyloidosis DARZALEX FASPRO in combination with bortezomib, cyclophosphamide and dexamethasone is indicated for the treatment of adult patients with newly diagnosed light chain (AL) amyloidosis. Limitations of Use DARZALEX FASPRO is not indicated and is not recommended for the treatment of patients with light chain (AL) amyloidosis who have NYHA Class IIIB or Class IV cardiac disease or Mayo Stage IIIB outside of controlled clinical trials [see Warnings and Precautions (5.2) ] .
- indications and usage tables exact
- is original packager
- true
- manufacturer names
- Janssen Biotech, Inc.
- matched search terms
- myeloma
- package ndcs
- 57894-503-01
- product ndcs
- 57894-503
- product types
- HUMAN PRESCRIPTION DRUG
- recent major changes exact
- Indications and Usage ( 1 ) 1/2026 Dosage and Administration ( 2.2 ) 1/2026 Dosage and Administration ( 2.3 , 2.8 ) 11/2025 Warnings and Precautions ( 5.1 , 5.3 ) 11/2025
- record type
- complete_spl_indications_section_candidate
- routes
- SUBCUTANEOUS
- rxcuis
- source batch
- file
- /private/tmp/cancer-full-research/indications/raw/labels-00600.json
- meta
- disclaimer
- Do not rely on openFDA to make decisions regarding medical care. While we make every effort to ensure that data is accurate, you should assume all results are unvalidated. We may limit or otherwise restrict your access to the API in line with our Terms of Service.
- last updated
- 2026-09-09
- results
- limit
- 100
- skip
- 600
- total
- 830
- sha256
- a9df7a5786dc51557d38f2a0881b5b5e9ae02ae396a6798e39ac96f586bcc5e6
- source url
- https://api.fda.gov/drug/label.json?search=id%3A%22bf986b71-66e2-4883-9687-f340388abafe%22
- spl effective date
- 2026-09-03
- spl effective time
- 20260903
- spl set id
- 4bb241af-4299-4373-8762-2d6709515db0
- spl version
- 33
- substance names
- DARATUMUMAB
- HYALURONIDASE (HUMAN RECOMBINANT)
- uniis
- 4Z63YK6E0E
- 743QUY4VD8
- verification flags
- oncology_keyword_candidate_not_clinically_classified
- spl_text_not_verified_identical_to_latest_approved_label
- individual_indications_not_split_or_reconciled
Drugs@FDA application source records
- application number
- BLA761145
- payload
- all indexed label documents
- Appl No
- 761145
- Application Docs Date
- 2020-05-01 00:00:00
- Application Docs ID
- 62799
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2020/761145s000lbl.pdf
- Submission No
- 1
- Submission Type
- ORIG
- Appl No
- 761145
- Application Docs Date
- 2021-01-14 00:00:00
- Application Docs ID
- 65908
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2021/761145s001lbl.pdf
- Submission No
- 1
- Submission Type
- SUPPL
- Appl No
- 761145
- Application Docs Date
- 2021-01-15 00:00:00
- Application Docs ID
- 65918
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2021/761145s002lbl.pdf
- Submission No
- 2
- Submission Type
- SUPPL
- Appl No
- 761145
- Application Docs Date
- 2021-02-16 00:00:00
- Application Docs ID
- 66218
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2021/761145s008lbl.pdf
- Submission No
- 8
- Submission Type
- SUPPL
- Appl No
- 761145
- Application Docs Date
- 2021-03-15 00:00:00
- Application Docs ID
- 66782
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2021/761145s005lbl.pdf
- Submission No
- 5
- Submission Type
- SUPPL
- Appl No
- 761145
- Application Docs Date
- 2021-07-12 00:00:00
- Application Docs ID
- 68044
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2021/761145s007lbl.pdf
- Submission No
- 7
- Submission Type
- SUPPL
- Appl No
- 761145
- Application Docs Date
- 2021-12-01 00:00:00
- Application Docs ID
- 69429
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2021/761145s009lbl.pdf
- Submission No
- 9
- Submission Type
- SUPPL
- Appl No
- 761145
- Application Docs Date
- 2022-01-26 00:00:00
- Application Docs ID
- 69972
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2022/761145s012lbl.pdf
- Submission No
- 12
- Submission Type
- SUPPL
- Appl No
- 761145
- Application Docs Date
- 2022-11-04 00:00:00
- Application Docs ID
- 72560
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2022/761145s018lbl.pdf
- Submission No
- 18
- Submission Type
- SUPPL
- Appl No
- 761145
- Application Docs Date
- 2024-07-31 00:00:00
- Application Docs ID
- 79256
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- https://www.accessdata.fda.gov/drugsatfda_docs/label/2024/761145s025lbl.pdf
- Submission No
- 25
- Submission Type
- SUPPL
- Appl No
- 761145
- Application Docs Date
- 2025-11-07 00:00:00
- Application Docs ID
- 84127
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2025/761145s029lbl.pdf
- Submission No
- 29
- Submission Type
- SUPPL
- Appl No
- 761145
- Application Docs Date
- 2025-11-17 00:00:00
- Application Docs ID
- 84176
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2025/761145s035lbl.pdf
- Submission No
- 35
- Submission Type
- SUPPL
- all submission records
- Appl No
- 761145
- Review Priority
- STANDARD
- Submission Class Code ID
- 3
- Submission No
- 39
- Submission Status
- AP
- Submission Status Date
- 2026-02-12 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 761145
- Review Priority
- STANDARD
- Submission Class Code ID
- 3
- Submission No
- 35
- Submission Status
- AP
- Submission Status Date
- 2025-11-14 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 761145
- Review Priority
- STANDARD
- Submission Class Code ID
- 2
- Submission No
- 32
- Submission Status
- AP
- Submission Status Date
- 2025-11-19 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 761145
- Review Priority
- STANDARD
- Submission Class Code ID
- 2
- Submission No
- 29
- Submission Status
- AP
- Submission Status Date
- 2025-11-06 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 761145
- Review Priority
- STANDARD
- Submission Class Code ID
- 2
- Submission No
- 28
- Submission Status
- AP
- Submission Status Date
- 2026-01-27 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 761145
- Review Priority
- PRIORITY
- Submission Class Code ID
- 2
- Submission No
- 25
- Submission Status
- AP
- Submission Status Date
- 2024-07-30 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 761145
- Review Priority
- STANDARD
- Submission Class Code ID
- 3
- Submission No
- 18
- Submission Status
- AP
- Submission Status Date
- 2022-11-02 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 761145
- Review Priority
- STANDARD
- Submission Class Code ID
- 3
- Submission No
- 12
- Submission Status
- AP
- Submission Status Date
- 2022-01-21 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 761145
- Review Priority
- STANDARD
- Submission Class Code ID
- 2
- Submission No
- 9
- Submission Status
- AP
- Submission Status Date
- 2021-11-30 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 761145
- Review Priority
- STANDARD
- Submission Class Code ID
- 3
- Submission No
- 8
- Submission Status
- AP
- Submission Status Date
- 2021-02-08 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 761145
- Review Priority
- STANDARD
- Submission Class Code ID
- 2
- Submission No
- 7
- Submission Status
- AP
- Submission Status Date
- 2021-07-09 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- Appl No
- 761145
- Review Priority
- STANDARD
- Submission Class Code ID
- 3
- Submission No
- 5
- Submission Status
- AP
- Submission Status Date
- 2021-03-12 00:00:00
- Submission Type
- SUPPL
- Submissions Public Notes
- application number
- BLA761145
- approval interpretation
- Application linkage and approved submission are not indication-level current approval verification
- current indication status
- not_reconciled
- drugsfda url
- https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=761145
- has approved submission record
- true
- latest approved submission date
- 2026-02-12
- latest label selection rule
- max FDA ApplicationDocsDate, including all ties; posting date is not approval date and latest indexed document may be incomplete
- latest posted label documents
- Appl No
- 761145
- Application Docs Date
- 2026-02-24 00:00:00
- Application Docs ID
- 85140
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2026/761145s039lbl.pdf
- Submission No
- 39
- Submission Type
- SUPPL
- official application record
- Appl No
- 761145
- Appl Public Notes
- Appl Type
- BLA
- Sponsor Name
- JANSSEN BIOTECH
- openfda application present
- true
- products
- Active Ingredient
- DARATUMUMAB AND HYALURONIDASE-FIHJ
- Appl No
- 761145
- Drug Name
- DARZALEX FASPRO
- Form
- INJECTABLE;INJECTION
- Product No
- 001
- Reference Drug
- 0
- Reference Standard
- 0
- Strength
- 120MG;2000UNITS/ML
- marketing status
- Prescription
Source passages and status connections
Passage 1 · positive indication candidate
- application numbers
- BLA761145
- brand names
- Darzalex Faspro
- classification reasons
- explicit_positive_indication_predicate
- tumor_or_malignant_hematology_words_in_positive_statement
- clinical review status
- pending
- content role
- positive_indication_candidate
- context span
- end
- 2230
- end exclusive
- true
- exact text
- 1 INDICATIONS AND USAGE DARZALEX FASPRO is a combination of daratumumab, a CD38-directed cytolytic antibody, and hyaluronidase, an endoglycosidase, indicated for the treatment of adult patients with: multiple myeloma in combination with bortezomib, lenalidomide, and dexamethasone for induction and consolidation in newly diagnosed patients who are eligible for autologous stem cell transplant multiple myeloma in combination with bortezomib, lenalidomide, and dexamethasone in newly diagnosed patients who are ineligible for autologous stem cell transplant multiple myeloma in combination with bortezomib, melphalan and prednisone in newly diagnosed patients who are ineligible for autologous stem cell transplant multiple myeloma in combination with lenalidomide and dexamethasone in newly diagnosed patients who are ineligible for autologous stem cell transplant and in patients with relapsed or refractory multiple myeloma who have received at least one prior therapy multiple myeloma in combination with bortezomib, thalidomide, and dexamethasone in newly diagnosed patients who are eligible for autologous stem cell transplant multiple myeloma in combination with bortezomib and dexamethasone in patients who have received at least one prior therapy multiple myeloma in combination with pomalidomide and dexamethasone in patients who have received at least one prior line of therapy including lenalidomide and a proteasome inhibitor multiple myeloma in combination with carfilzomib and dexamethasone in patients with relapsed or refractory multiple myeloma who have received one to three prior lines of therapy multiple myeloma as monotherapy, in patients who have received at least three prior lines of therapy including a proteasome inhibitor (PI) and an immunomodulatory agent or who are double-refractory to a PI and an immunomodulatory agent high-risk smoldering multiple myeloma as monotherapy light chain (AL) amyloidosis in combination with bortezomib, cyclophosphamide and dexamethasone in newly diagnosed patients. Limitations of Use: DARZALEX FASPRO is not indicated and is not recommended for the treatment of patients with light chain (AL) amyloidosis who have NYHA Class IIIB or Class IV cardiac disease or May
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 0
- current approval status
- not_reconciled
- duplicate text group
- dup-734b8277c6b09e080e52
- extraction review status
- automated_candidate_pending_source_review
- generic names
- DARATUMUMAB AND HYALURONIDASE-FIHJ (HUMAN RECOMBINANT)
- id
- ind-span-83cf64ef6fd5ccabd24e
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- positive predicate support span
- end
- 157
- end exclusive
- true
- exact text
- is a combination of daratumumab, a CD38-directed cytolytic antibody, and hyaluronidase, an endoglycosidase, indicated
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 40
- qualifier mentions
- context exact
- onidase, an endoglycosidase, indicated for the treatment of adult patients with: multiple myeloma in combination with bortezomib, lena
- kind
- age
- polarity
- not_inferred
- span
- end
- 193
- end exclusive
- true
- exact text
- adult patients
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 179
- context exact
- ND USAGE DARZALEX FASPRO is a combination of daratumumab, a CD38-directed cytolytic antibody, and hyaluronidase, an endoglycosidase, indicated for the t
- kind
- biomarker
- polarity
- not_inferred
- span
- end
- 107
- end exclusive
- true
- exact text
- CD38-directed cytolytic antibody
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 75
- context exact
- le for autologous stem cell transplant and in patients with relapsed or refractory multiple myeloma who have received at least one prior therapy multiple myeloma i
- kind
- stage_or_setting
- polarity
- not_inferred
- span
- end
- 930
- end exclusive
- true
- exact text
- relapsed or refractory multiple myeloma who
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 887
- context exact
- ination with carfilzomib and dexamethasone in patients with relapsed or refractory multiple myeloma who have received one to three prior lines of therapy multiple
- kind
- stage_or_setting
- polarity
- not_inferred
- span
- end
- 1566
- end exclusive
- true
- exact text
- relapsed or refractory multiple myeloma who
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 1523
- context exact
- ibitor (PI) and an immunomodulatory agent or who are double-refractory to a PI and an immunomodulatory agent high-risk smoldering multiple myeloma as monotherapy lig
- kind
- stage_or_setting
- polarity
- not_inferred
- span
- end
- 1849
- end exclusive
- true
- exact text
- refractory to a PI and an immunomodulatory ag
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 1804
- context exact
- nd in patients with relapsed or refractory multiple myeloma who have received at least one prior therapy multiple myeloma in combination with bortezomib, thalidomide, and dexamethasone in newly diagnosed patients who are eligible for autologous stem cell transplant multiple myeloma in combination
- kind
- prior_therapy_or_line
- polarity
- not_inferred
- span
- end
- 1104
- end exclusive
- true
- exact text
- who have received at least one prior therapy multiple myeloma in combination with bortezomib, thalidomide, and dexamethasone in newly diagnosed patients who are eligible for aut
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 927
- context exact
- n combination with bortezomib and dexamethasone in patients who have received at least one prior therapy multiple myeloma in combination with pomalidomide and dexamethasone in patients who have received at least one prior line of therapy including lenalidomide and a proteasome inhibitor multiple
- kind
- prior_therapy_or_line
- polarity
- not_inferred
- span
- end
- 1388
- end exclusive
- true
- exact text
- who have received at least one prior therapy multiple myeloma in combination with pomalidomide and dexamethasone in patients who have received at least one prior line of therapy
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 1211
- context exact
- ne in patients with relapsed or refractory multiple myeloma who have received one to three prior lines of therapy multiple myeloma as monotherapy, in patients who have received at least three prior lines of therapy including a proteasome inhibitor (PI) and an immunomodulatory agent or who are dou
- kind
- prior_therapy_or_line
- polarity
- not_inferred
- span
- end
- 1740
- end exclusive
- true
- exact text
- who have received one to three prior lines of therapy multiple myeloma as monotherapy, in patients who have received at least three prior lines of therapy including a proteasome
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 1563
- context exact
- for the treatment of adult patients with: multiple myeloma in combination with bortezomib, lenalidomide, and dexamethasone for induction and consolidation in newly diagnosed patients who are eligible for autologous stem cell transplant multiple myeloma in combination with bortezomib, lenalidomide,
- kind
- regimen
- polarity
- not_inferred
- span
- end
- 396
- end exclusive
- true
- exact text
- in combination with bortezomib, lenalidomide, and dexamethasone for induction and consolidation in newly diagnosed patients who are eligible for autologous stem cell transplant mu
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 217
- context exact
- igible for autologous stem cell transplant multiple myeloma in combination with bortezomib, lenalidomide, and dexamethasone in newly diagnosed patients who are ineligible for autologous stem cell transplant multiple myeloma in combination with bortezomib, melphalan and prednisone in newly diagnosed
- kind
- regimen
- polarity
- not_inferred
- span
- end
- 590
- end exclusive
- true
- exact text
- in combination with bortezomib, lenalidomide, and dexamethasone in newly diagnosed patients who are ineligible for autologous stem cell transplant multiple myeloma in combination
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 411
- context exact
- igible for autologous stem cell transplant multiple myeloma in combination with lenalidomide and dexamethasone in newly diagnosed patients who are ineligible for autologous stem cell transplant and in patients with relapsed or refractory multiple myeloma who have received at least one prior therapy
- kind
- regimen
- polarity
- not_inferred
- span
- end
- 911
- end exclusive
- true
- exact text
- in combination with lenalidomide and dexamethasone in newly diagnosed patients who are ineligible for autologous stem cell transplant and in patients with relapsed or refractory m
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 732
- context exact
- o have received at least one prior therapy multiple myeloma in combination with bortezomib, thalidomide, and dexamethasone in newly diagnosed patients who are eligible for autologous stem cell transplant multiple myeloma in combination with bortezomib and dexamethasone in patients who have received
- kind
- regimen
- polarity
- not_inferred
- span
- end
- 1168
- end exclusive
- true
- exact text
- in combination with bortezomib, thalidomide, and dexamethasone in newly diagnosed patients who are eligible for autologous stem cell transplant multiple myeloma in combination wit
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 989
- regulatory links
- schema version
- 0.1.0
- source batch sha256
- a9df7a5786dc51557d38f2a0881b5b5e9ae02ae396a6798e39ac96f586bcc5e6
- source defined aliases
- source span
- end
- 2030
- end exclusive
- true
- exact text
- 1 INDICATIONS AND USAGE DARZALEX FASPRO is a combination of daratumumab, a CD38-directed cytolytic antibody, and hyaluronidase, an endoglycosidase, indicated for the treatment of adult patients with: multiple myeloma in combination with bortezomib, lenalidomide, and dexamethasone for induction and consolidation in newly diagnosed patients who are eligible for autologous stem cell transplant multiple myeloma in combination with bortezomib, lenalidomide, and dexamethasone in newly diagnosed patients who are ineligible for autologous stem cell transplant multiple myeloma in combination with bortezomib, melphalan and prednisone in newly diagnosed patients who are ineligible for autologous stem cell transplant multiple myeloma in combination with lenalidomide and dexamethasone in newly diagnosed patients who are ineligible for autologous stem cell transplant and in patients with relapsed or refractory multiple myeloma who have received at least one prior therapy multiple myeloma in combination with bortezomib, thalidomide, and dexamethasone in newly diagnosed patients who are eligible for autologous stem cell transplant multiple myeloma in combination with bortezomib and dexamethasone in patients who have received at least one prior therapy multiple myeloma in combination with pomalidomide and dexamethasone in patients who have received at least one prior line of therapy including lenalidomide and a proteasome inhibitor multiple myeloma in combination with carfilzomib and dexamethasone in patients with relapsed or refractory multiple myeloma who have received one to three prior lines of therapy multiple myeloma as monotherapy, in patients who have received at least three prior lines of therapy including a proteasome inhibitor (PI) and an immunomodulatory agent or who are double-refractory to a PI and an immunomodulatory agent high-risk smoldering multiple myeloma as monotherapy light chain (AL) amyloidosis in combination with bortezomib, cyclophosphamide and dexamethasone in newly diagnosed patients.
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 0
- source url
- https://api.fda.gov/drug/label.json?search=id%3A%22bf986b71-66e2-4883-9687-f340388abafe%22
- spl effective date
- 2026-09-03
- spl set id
- 4bb241af-4299-4373-8762-2d6709515db0
- spl version
- 33
- structured fields status
- not_extracted_no_values_inferred_from_mentions
- structured indication
- age
- Source null
- approval pathway
- Source null
- biomarker and test
- Source null
- disease stage
- Source null
- limitations
- Source null
- line
- Source null
- prior therapy
- Source null
- regimen
- Source null
- tumor histology
- Source null
- use intent
- tumor_directed_candidate
Passage 2 · limitation of use
- application numbers
- BLA761145
- brand names
- Darzalex Faspro
- classification reasons
- negative_or_not_established_clause
- clinical review status
- pending
- content role
- limitation_of_use
- context span
- end
- 2488
- end exclusive
- true
- exact text
- mmunomodulatory agent high-risk smoldering multiple myeloma as monotherapy light chain (AL) amyloidosis in combination with bortezomib, cyclophosphamide and dexamethasone in newly diagnosed patients. Limitations of Use: DARZALEX FASPRO is not indicated and is not recommended for the treatment of patients with light chain (AL) amyloidosis who have NYHA Class IIIB or Class IV cardiac disease or Mayo Stage IIIB outside of controlled clinical trials ( 1.3 ) 1.1 Multiple Myeloma DARZALEX FASPRO is indicated for the treatment of adult patients with [see Clinical Studies (14) ] : multiple myeloma in combination with bortezomib, lenalidomide, and dexamethas
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 1831
- current approval status
- not_reconciled
- duplicate text group
- dup-520e19126cf8e2a873fa
- extraction review status
- automated_candidate_pending_source_review
- generic names
- DARATUMUMAB AND HYALURONIDASE-FIHJ (HUMAN RECOMBINANT)
- id
- ind-span-d306c64928d8633ae7c2
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- positive predicate support span
- Source null
- qualifier mentions
- regulatory links
- schema version
- 0.1.0
- source batch sha256
- a9df7a5786dc51557d38f2a0881b5b5e9ae02ae396a6798e39ac96f586bcc5e6
- source defined aliases
- source span
- end
- 2288
- end exclusive
- true
- exact text
- Limitations of Use: DARZALEX FASPRO is not indicated and is not recommended for the treatment of patients with light chain (AL) amyloidosis who have NYHA Class IIIB or Class IV cardiac disease or Mayo Stage IIIB outside of controlled clinical trials ( 1.3 )
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 2031
- source url
- https://api.fda.gov/drug/label.json?search=id%3A%22bf986b71-66e2-4883-9687-f340388abafe%22
- spl effective date
- 2026-09-03
- spl set id
- 4bb241af-4299-4373-8762-2d6709515db0
- spl version
- 33
- structured fields status
- not_extracted_no_values_inferred_from_mentions
- structured indication
- age
- Source null
- approval pathway
- Source null
- biomarker and test
- Source null
- disease stage
- Source null
- limitations
- Source null
- line
- Source null
- prior therapy
- Source null
- regimen
- Source null
- tumor histology
- Source null
- use intent
- not_applicable
Passage 3 · positive indication candidate
- application numbers
- BLA761145
- brand names
- Darzalex Faspro
- classification reasons
- explicit_positive_indication_predicate
- tumor_or_malignant_hematology_words_in_positive_statement
- clinical review status
- pending
- content role
- positive_indication_candidate
- context span
- end
- 4272
- end exclusive
- true
- exact text
- s not recommended for the treatment of patients with light chain (AL) amyloidosis who have NYHA Class IIIB or Class IV cardiac disease or Mayo Stage IIIB outside of controlled clinical trials ( 1.3 ) 1.1 Multiple Myeloma DARZALEX FASPRO is indicated for the treatment of adult patients with [see Clinical Studies (14) ] : multiple myeloma in combination with bortezomib, lenalidomide, and dexamethasone for induction and consolidation in newly diagnosed patients who are eligible for autologous stem cell transplant. multiple myeloma in combination with bortezomib, lenalidomide, and dexamethasone in newly diagnosed patients who are ineligible for autologous stem cell transplant. multiple myeloma in combination with bortezomib, melphalan and prednisone in newly diagnosed patients who are ineligible for autologous stem cell transplant. multiple myeloma in combination with lenalidomide and dexamethasone in newly diagnosed patients who are ineligible for autologous stem cell transplant and in patients with relapsed or refractory multiple myeloma who have received at least one prior therapy. multiple myeloma in combination with bortezomib, thalidomide, and dexamethasone in newly diagnosed patients who are eligible for autologous stem cell transplant. multiple myeloma in combination with bortezomib and dexamethasone in patients who have received at least one prior therapy. multiple myeloma in combination with pomalidomide and dexamethasone in patients who have received at least one prior line of therapy including lenalidomide and a proteasome inhibitor. multiple myeloma in combination with carfilzomib and dexamethasone in patients with relapsed or refractory multiple myeloma who have received one to three prior lines of therapy. multiple myeloma as monotherapy, in patients who have received at least three prior lines of therapy including a proteasome inhibitor (PI) and an immunomodulatory agent or who are double-refractory to a PI and an immunomodulatory agent. 1.2 High-Risk Smoldering Multiple Myeloma DARZALEX FASPRO as monotherapy is indicated for the treatment of adult patients with high-risk smoldering multiple myeloma. 1.3 Light Chain Amyloidosis DARZA
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 2089
- current approval status
- not_reconciled
- duplicate text group
- dup-3ec7d49c49b291d5953b
- extraction review status
- automated_candidate_pending_source_review
- generic names
- DARATUMUMAB AND HYALURONIDASE-FIHJ (HUMAN RECOMBINANT)
- id
- ind-span-40119ff65dde003789d9
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- positive predicate support span
- end
- 2338
- end exclusive
- true
- exact text
- is indicated
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 2326
- qualifier mentions
- context exact
- e Myeloma DARZALEX FASPRO is indicated for the treatment of adult patients with [see Clinical Studies (14) ] : multiple myeloma in com
- kind
- age
- polarity
- not_inferred
- span
- end
- 2374
- end exclusive
- true
- exact text
- adult patients
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 2360
- context exact
- le for autologous stem cell transplant and in patients with relapsed or refractory multiple myeloma who have received at least one prior therapy. multiple myeloma
- kind
- stage_or_setting
- polarity
- not_inferred
- span
- end
- 3144
- end exclusive
- true
- exact text
- relapsed or refractory multiple myeloma who
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 3101
- context exact
- ination with carfilzomib and dexamethasone in patients with relapsed or refractory multiple myeloma who have received one to three prior lines of therapy. multiple
- kind
- stage_or_setting
- polarity
- not_inferred
- span
- end
- 3784
- end exclusive
- true
- exact text
- relapsed or refractory multiple myeloma who
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 3741
- context exact
- ibitor (PI) and an immunomodulatory agent or who are double-refractory to a PI and an immunomodulatory agent.
- kind
- stage_or_setting
- polarity
- not_inferred
- span
- end
- 4068
- end exclusive
- true
- exact text
- refractory to a PI and an immunomodulatory ag
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 4023
- context exact
- nd in patients with relapsed or refractory multiple myeloma who have received at least one prior therapy. multiple myeloma in combination with bortezomib, thalidomi
- kind
- prior_therapy_or_line
- polarity
- not_inferred
- span
- end
- 3185
- end exclusive
- true
- exact text
- who have received at least one prior therapy
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 3141
- context exact
- n combination with bortezomib and dexamethasone in patients who have received at least one prior therapy. multiple myeloma in combination with pomalidomide and dexa
- kind
- prior_therapy_or_line
- polarity
- not_inferred
- span
- end
- 3471
- end exclusive
- true
- exact text
- who have received at least one prior therapy
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 3427
- context exact
- combination with pomalidomide and dexamethasone in patients who have received at least one prior line of therapy including lenalidomide and a proteasome inhibitor. multiple myeloma in combination with carfilzomib and dexam
- kind
- prior_therapy_or_line
- polarity
- not_inferred
- span
- end
- 3655
- end exclusive
- true
- exact text
- who have received at least one prior line of therapy including lenalidomide and a proteasome inhibitor
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 3553
- context exact
- ne in patients with relapsed or refractory multiple myeloma who have received one to three prior lines of therapy. multiple myeloma as monotherapy, in patients who have rece
- kind
- prior_therapy_or_line
- polarity
- not_inferred
- span
- end
- 3834
- end exclusive
- true
- exact text
- who have received one to three prior lines of therapy
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 3781
- context exact
- es of therapy. multiple myeloma as monotherapy, in patients who have received at least three prior lines of therapy including a proteasome inhibitor (PI) and an immunomodulatory agent or who are double-refractory to a PI and an immunomodulatory agent.
- kind
- prior_therapy_or_line
- polarity
- not_inferred
- span
- end
- 4058
- end exclusive
- true
- exact text
- who have received at least three prior lines of therapy including a proteasome inhibitor (PI) and an immunomodulatory agent or who are double-refractory to a PI and an immunomod
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 3881
- context exact
- tients with [see Clinical Studies (14) ] : multiple myeloma in combination with bortezomib, lenalidomide, and dexamethasone for induction and consolidation in newly diagnosed patients who are eligible for autologous stem cell transplant. multiple myeloma in combination with bortezomib, lenalidom
- kind
- regimen
- polarity
- not_inferred
- span
- end
- 2604
- end exclusive
- true
- exact text
- in combination with bortezomib, lenalidomide, and dexamethasone for induction and consolidation in newly diagnosed patients who are eligible for autologous stem cell transplant
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 2428
- context exact
- gible for autologous stem cell transplant. multiple myeloma in combination with bortezomib, lenalidomide, and dexamethasone in newly diagnosed patients who are ineligible for autologous stem cell transplant. multiple myeloma in combination with bortezomib, melphalan
- kind
- regimen
- polarity
- not_inferred
- span
- end
- 2769
- end exclusive
- true
- exact text
- in combination with bortezomib, lenalidomide, and dexamethasone in newly diagnosed patients who are ineligible for autologous stem cell transplant
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 2623
- context exact
- gible for autologous stem cell transplant. multiple myeloma in combination with bortezomib, melphalan and prednisone in newly diagnosed patients who are ineligible for autologous stem cell transplant. multiple myeloma in combination with lenalidomide and dexa
- kind
- regimen
- polarity
- not_inferred
- span
- end
- 2927
- end exclusive
- true
- exact text
- in combination with bortezomib, melphalan and prednisone in newly diagnosed patients who are ineligible for autologous stem cell transplant
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 2788
- regulatory links
- schema version
- 0.1.0
- source batch sha256
- a9df7a5786dc51557d38f2a0881b5b5e9ae02ae396a6798e39ac96f586bcc5e6
- source defined aliases
- source span
- end
- 4072
- end exclusive
- true
- exact text
- 1.1 Multiple Myeloma DARZALEX FASPRO is indicated for the treatment of adult patients with [see Clinical Studies (14) ] : multiple myeloma in combination with bortezomib, lenalidomide, and dexamethasone for induction and consolidation in newly diagnosed patients who are eligible for autologous stem cell transplant. multiple myeloma in combination with bortezomib, lenalidomide, and dexamethasone in newly diagnosed patients who are ineligible for autologous stem cell transplant. multiple myeloma in combination with bortezomib, melphalan and prednisone in newly diagnosed patients who are ineligible for autologous stem cell transplant. multiple myeloma in combination with lenalidomide and dexamethasone in newly diagnosed patients who are ineligible for autologous stem cell transplant and in patients with relapsed or refractory multiple myeloma who have received at least one prior therapy. multiple myeloma in combination with bortezomib, thalidomide, and dexamethasone in newly diagnosed patients who are eligible for autologous stem cell transplant. multiple myeloma in combination with bortezomib and dexamethasone in patients who have received at least one prior therapy. multiple myeloma in combination with pomalidomide and dexamethasone in patients who have received at least one prior line of therapy including lenalidomide and a proteasome inhibitor. multiple myeloma in combination with carfilzomib and dexamethasone in patients with relapsed or refractory multiple myeloma who have received one to three prior lines of therapy. multiple myeloma as monotherapy, in patients who have received at least three prior lines of therapy including a proteasome inhibitor (PI) and an immunomodulatory agent or who are double-refractory to a PI and an immunomodulatory agent.
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 2289
- source url
- https://api.fda.gov/drug/label.json?search=id%3A%22bf986b71-66e2-4883-9687-f340388abafe%22
- spl effective date
- 2026-09-03
- spl set id
- 4bb241af-4299-4373-8762-2d6709515db0
- spl version
- 33
- structured fields status
- not_extracted_no_values_inferred_from_mentions
- structured indication
- age
- Source null
- approval pathway
- Source null
- biomarker and test
- Source null
- disease stage
- Source null
- limitations
- Source null
- line
- Source null
- prior therapy
- Source null
- regimen
- Source null
- tumor histology
- Source null
- use intent
- tumor_directed_candidate
Passage 4 · positive indication candidate
- application numbers
- BLA761145
- brand names
- Darzalex Faspro
- classification reasons
- explicit_positive_indication_predicate
- tumor_or_malignant_hematology_words_in_positive_statement
- clinical review status
- pending
- content role
- positive_indication_candidate
- context span
- end
- 4438
- end exclusive
- true
- exact text
- atients who have received at least three prior lines of therapy including a proteasome inhibitor (PI) and an immunomodulatory agent or who are double-refractory to a PI and an immunomodulatory agent. 1.2 High-Risk Smoldering Multiple Myeloma DARZALEX FASPRO as monotherapy is indicated for the treatment of adult patients with high-risk smoldering multiple myeloma. 1.3 Light Chain Amyloidosis DARZALEX FASPRO in combination with bortezomib, cyclophosphamide and dexamethasone is indicated for the treatment of adult patients with newly diagnosed light chain (AL) a
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 3873
- current approval status
- not_reconciled
- duplicate text group
- dup-ec45e971f160603b93e1
- extraction review status
- automated_candidate_pending_source_review
- generic names
- DARATUMUMAB AND HYALURONIDASE-FIHJ (HUMAN RECOMBINANT)
- id
- ind-span-e34ef28a815bbb568e33
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- positive predicate support span
- end
- 4158
- end exclusive
- true
- exact text
- is indicated
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 4146
- qualifier mentions
- context exact
- LEX FASPRO as monotherapy is indicated for the treatment of adult patients with high-risk smoldering multiple myeloma.
- kind
- age
- polarity
- not_inferred
- span
- end
- 4194
- end exclusive
- true
- exact text
- adult patients
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 4180
- context exact
- 1.2 High-Risk Smoldering Multiple Myeloma DARZALEX FASPRO as monotherapy is indicated for the treatment of adult patients with high-risk smoldering multiple myeloma.
- kind
- regimen
- polarity
- not_inferred
- span
- end
- 4237
- end exclusive
- true
- exact text
- as monotherapy is indicated for the treatment of adult patients with high-risk smoldering multiple myeloma
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 4131
- regulatory links
- schema version
- 0.1.0
- source batch sha256
- a9df7a5786dc51557d38f2a0881b5b5e9ae02ae396a6798e39ac96f586bcc5e6
- source defined aliases
- source span
- end
- 4238
- end exclusive
- true
- exact text
- 1.2 High-Risk Smoldering Multiple Myeloma DARZALEX FASPRO as monotherapy is indicated for the treatment of adult patients with high-risk smoldering multiple myeloma.
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 4073
- source url
- https://api.fda.gov/drug/label.json?search=id%3A%22bf986b71-66e2-4883-9687-f340388abafe%22
- spl effective date
- 2026-09-03
- spl set id
- 4bb241af-4299-4373-8762-2d6709515db0
- spl version
- 33
- structured fields status
- not_extracted_no_values_inferred_from_mentions
- structured indication
- age
- Source null
- approval pathway
- Source null
- biomarker and test
- Source null
- disease stage
- Source null
- limitations
- Source null
- line
- Source null
- prior therapy
- Source null
- regimen
- Source null
- tumor histology
- Source null
- use intent
- tumor_directed_candidate
Passage 5 · positive indication candidate
- application numbers
- BLA761145
- brand names
- Darzalex Faspro
- classification reasons
- explicit_positive_indication_predicate
- no_tumor_directed_keyword_in_positive_statement
- clinical review status
- pending
- content role
- positive_indication_candidate
- context span
- end
- 4649
- end exclusive
- true
- exact text
- PI and an immunomodulatory agent. 1.2 High-Risk Smoldering Multiple Myeloma DARZALEX FASPRO as monotherapy is indicated for the treatment of adult patients with high-risk smoldering multiple myeloma. 1.3 Light Chain Amyloidosis DARZALEX FASPRO in combination with bortezomib, cyclophosphamide and dexamethasone is indicated for the treatment of adult patients with newly diagnosed light chain (AL) amyloidosis. Limitations of Use DARZALEX FASPRO is not indicated and is not recommended for the treatment of patients with light chain (AL) amyloidosis who have NYHA Class IIIB or Class IV cardiac disease or Mayo
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 4039
- current approval status
- not_reconciled
- duplicate text group
- dup-20b183e0c0df52e2acec
- extraction review status
- automated_candidate_pending_source_review
- generic names
- DARATUMUMAB AND HYALURONIDASE-FIHJ (HUMAN RECOMBINANT)
- id
- ind-span-a919d7c639807df9e13c
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- positive predicate support span
- end
- 4362
- end exclusive
- true
- exact text
- is indicated
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 4350
- qualifier mentions
- context exact
- phamide and dexamethasone is indicated for the treatment of adult patients with newly diagnosed light chain (AL) amyloidosis.
- kind
- age
- polarity
- not_inferred
- span
- end
- 4398
- end exclusive
- true
- exact text
- adult patients
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 4384
- context exact
- 1.3 Light Chain Amyloidosis DARZALEX FASPRO in combination with bortezomib, cyclophosphamide and dexamethasone is indicated for the treatment of adult patients with newly diagnosed light chain (AL) amyloidosis.
- kind
- regimen
- polarity
- not_inferred
- span
- end
- 4448
- end exclusive
- true
- exact text
- in combination with bortezomib, cyclophosphamide and dexamethasone is indicated for the treatment of adult patients with newly diagnosed light chain (AL) amyloidosis
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 4283
- regulatory links
- schema version
- 0.1.0
- source batch sha256
- a9df7a5786dc51557d38f2a0881b5b5e9ae02ae396a6798e39ac96f586bcc5e6
- source defined aliases
- source span
- end
- 4449
- end exclusive
- true
- exact text
- 1.3 Light Chain Amyloidosis DARZALEX FASPRO in combination with bortezomib, cyclophosphamide and dexamethasone is indicated for the treatment of adult patients with newly diagnosed light chain (AL) amyloidosis.
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 4239
- source url
- https://api.fda.gov/drug/label.json?search=id%3A%22bf986b71-66e2-4883-9687-f340388abafe%22
- spl effective date
- 2026-09-03
- spl set id
- 4bb241af-4299-4373-8762-2d6709515db0
- spl version
- 33
- structured fields status
- not_extracted_no_values_inferred_from_mentions
- structured indication
- age
- Source null
- approval pathway
- Source null
- biomarker and test
- Source null
- disease stage
- Source null
- limitations
- Source null
- line
- Source null
- prior therapy
- Source null
- regimen
- Source null
- tumor histology
- Source null
- use intent
- non_oncology_or_unclear_candidate
Passage 6 · limitation of use
- application numbers
- BLA761145
- brand names
- Darzalex Faspro
- classification reasons
- negative_or_not_established_clause
- clinical review status
- pending
- content role
- limitation_of_use
- context span
- end
- 4738
- end exclusive
- true
- exact text
- hain Amyloidosis DARZALEX FASPRO in combination with bortezomib, cyclophosphamide and dexamethasone is indicated for the treatment of adult patients with newly diagnosed light chain (AL) amyloidosis. Limitations of Use DARZALEX FASPRO is not indicated and is not recommended for the treatment of patients with light chain (AL) amyloidosis who have NYHA Class IIIB or Class IV cardiac disease or Mayo Stage IIIB outside of controlled clinical trials [see Warnings and Precautions (5.2) ] .
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 4250
- current approval status
- not_reconciled
- duplicate text group
- dup-f343152b7e9ff407341f
- extraction review status
- automated_candidate_pending_source_review
- generic names
- DARATUMUMAB AND HYALURONIDASE-FIHJ (HUMAN RECOMBINANT)
- id
- ind-span-2ee24f8138ecf3917798
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- positive predicate support span
- Source null
- qualifier mentions
- regulatory links
- schema version
- 0.1.0
- source batch sha256
- a9df7a5786dc51557d38f2a0881b5b5e9ae02ae396a6798e39ac96f586bcc5e6
- source defined aliases
- source span
- end
- 4738
- end exclusive
- true
- exact text
- Limitations of Use DARZALEX FASPRO is not indicated and is not recommended for the treatment of patients with light chain (AL) amyloidosis who have NYHA Class IIIB or Class IV cardiac disease or Mayo Stage IIIB outside of controlled clinical trials [see Warnings and Precautions (5.2) ] .
- label id
- bf986b71-66e2-4883-9687-f340388abafe
- offset unit
- unicode_code_points
- source array index
- 0
- source field
- indications_and_usage_exact
- source text sha256
- 68a46f6f825422b9a48435a6407494bef5a3afd14e061c7053d2336550c95324
- start
- 4450
- source url
- https://api.fda.gov/drug/label.json?search=id%3A%22bf986b71-66e2-4883-9687-f340388abafe%22
- spl effective date
- 2026-09-03
- spl set id
- 4bb241af-4299-4373-8762-2d6709515db0
- spl version
- 33
- structured fields status
- not_extracted_no_values_inferred_from_mentions
- structured indication
- age
- Source null
- approval pathway
- Source null
- biomarker and test
- Source null
- disease stage
- Source null
- limitations
- Source null
- line
- Source null
- prior therapy
- Source null
- regimen
- Source null
- tumor histology
- Source null
- use intent
- not_applicable
Preserved source evidence · Not medical advice
Triangle