LABELS · 990c5dd1-5670-4e2f-af5d-6e87b73b12b5
BAVENCIO
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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
- 2026-08-25
- Captured
- 2026-09-09T23:37:54.830918+00:00
- Current indication reconciliation
- Not reconciled
Indications and usage: exact source text
- 1 INDICATIONS AND USAGE BAVENCIO is a programmed death ligand-1 (PD-L1) blocking antibody indicated for: Merkel Cell Carcinoma (MCC) Adults and pediatric patients 12 years and older with metastatic MCC. ( 1.1 , 14.1 ) Urothelial Carcinoma (UC) Maintenance treatment of patients with locally advanced or metastatic UC that has not progressed with first-line platinum-containing chemotherapy. ( 1.2 , 14.2 ) Patients with locally advanced or metastatic UC who: Have disease progression during or following platinum-containing chemotherapy. ( 1.2 , 14.2 ) Have disease progression within 12 months of neoadjuvant or adjuvant treatment with platinum-containing chemotherapy. ( 1.2 , 14.2 ) Renal Cell Carcinoma (RCC) First-line treatment, in combination with axitinib, of patients with advanced RCC. ( 1.3 , 14.3 ) 1.1 Metastatic Merkel Cell Carcinoma BAVENCIO (avelumab) is indicated for the treatment of adults and pediatric patients 12 years and older with metastatic Merkel cell carcinoma (MCC) [see Clinical Studies (14.1) ] . 1.2 Locally Advanced or Metastatic Urothelial Carcinoma First-Line Maintenance Treatment of Urothelial Carcinoma BAVENCIO is indicated for the maintenance treatment of patients with locally advanced or metastatic urothelial carcinoma (UC) that has not progressed with first-line platinum-containing chemotherapy [see Clinical Studies (14.2) ] . Previously-treated Urothelial Carcinoma BAVENCIO is indicated for the treatment of patients with locally advanced or metastatic urothelial carcinoma (UC) who: Have disease progression during or following platinum-containing chemotherapy Have disease progression within 12 months of neoadjuvant or adjuvant treatment with platinum-containing chemotherapy [see Clinical Studies (14.2) ]. 1.3 Advanced Renal Cell Carcinoma BAVENCIO in combination with axitinib is indicated for the first-line treatment of patients with advanced renal cell carcinoma (RCC) [see Clinical Studies (14.3) ] .
Full extracted label fields
- application numbers
- BLA761049
- boxed warning exact
- brand names
- BAVENCIO
- current indication status
- not_reconciled
- dailymed set url
- https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=5cd725a1-2fa4-408a-a651-57a7b84b2118
- generic names
- AVELUMAB
- id
- 990c5dd1-5670-4e2f-af5d-6e87b73b12b5
- indications and usage exact
- 1 INDICATIONS AND USAGE BAVENCIO is a programmed death ligand-1 (PD-L1) blocking antibody indicated for: Merkel Cell Carcinoma (MCC) Adults and pediatric patients 12 years and older with metastatic MCC. ( 1.1 , 14.1 ) Urothelial Carcinoma (UC) Maintenance treatment of patients with locally advanced or metastatic UC that has not progressed with first-line platinum-containing chemotherapy. ( 1.2 , 14.2 ) Patients with locally advanced or metastatic UC who: Have disease progression during or following platinum-containing chemotherapy. ( 1.2 , 14.2 ) Have disease progression within 12 months of neoadjuvant or adjuvant treatment with platinum-containing chemotherapy. ( 1.2 , 14.2 ) Renal Cell Carcinoma (RCC) First-line treatment, in combination with axitinib, of patients with advanced RCC. ( 1.3 , 14.3 ) 1.1 Metastatic Merkel Cell Carcinoma BAVENCIO (avelumab) is indicated for the treatment of adults and pediatric patients 12 years and older with metastatic Merkel cell carcinoma (MCC) [see Clinical Studies (14.1) ] . 1.2 Locally Advanced or Metastatic Urothelial Carcinoma First-Line Maintenance Treatment of Urothelial Carcinoma BAVENCIO is indicated for the maintenance treatment of patients with locally advanced or metastatic urothelial carcinoma (UC) that has not progressed with first-line platinum-containing chemotherapy [see Clinical Studies (14.2) ] . Previously-treated Urothelial Carcinoma BAVENCIO is indicated for the treatment of patients with locally advanced or metastatic urothelial carcinoma (UC) who: Have disease progression during or following platinum-containing chemotherapy Have disease progression within 12 months of neoadjuvant or adjuvant treatment with platinum-containing chemotherapy [see Clinical Studies (14.2) ]. 1.3 Advanced Renal Cell Carcinoma BAVENCIO in combination with axitinib is indicated for the first-line treatment of patients with advanced renal cell carcinoma (RCC) [see Clinical Studies (14.3) ] .
- indications and usage tables exact
- is original packager
- true
- manufacturer names
- EMD Serono, Inc.
- matched search terms
- carcinoma
- package ndcs
- 44087-3535-1
- product ndcs
- 44087-3535
- product types
- HUMAN PRESCRIPTION DRUG
- recent major changes exact
- Warnings and Precautions ( 5.1 ) 07/2026
- record type
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- routes
- INTRAVENOUS
- rxcuis
- 1875542
- 1875547
- source batch
- file
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- 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
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Drugs@FDA application source records
- application number
- BLA761049
- payload
- all indexed label documents
- Appl No
- 761049
- Application Docs Date
- 2017-03-23 00:00:00
- Application Docs ID
- 47651
- Application Docs Title
- 0
- Application Docs Type ID
- 2
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- Submission No
- 1
- Submission Type
- ORIG
- Appl No
- 761049
- Application Docs Date
- 2017-10-25 00:00:00
- Application Docs ID
- 50178
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2017/761049s002lbl.pdf
- Submission No
- 2
- Submission Type
- SUPPL
- Appl No
- 761049
- Application Docs Date
- 2018-10-26 00:00:00
- Application Docs ID
- 56125
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2018/761049s003lbl.pdf
- Submission No
- 3
- Submission Type
- SUPPL
- Appl No
- 761049
- Application Docs Date
- 2019-05-15 00:00:00
- Application Docs ID
- 58712
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2019/761049s006lbl.pdf
- Submission No
- 6
- Submission Type
- SUPPL
- Appl No
- 761049
- Application Docs Date
- 2020-07-01 00:00:00
- Application Docs ID
- 63762
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2020/761049s009lbl.pdf
- Submission No
- 9
- Submission Type
- SUPPL
- Appl No
- 761049
- Application Docs Date
- 2020-11-13 00:00:00
- Application Docs ID
- 65208
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2020/761049s005lbl.pdf
- Submission No
- 5
- Submission Type
- SUPPL
- Appl No
- 761049
- Application Docs Date
- 2022-07-19 00:00:00
- Application Docs ID
- 71597
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2022/761049s013lbl.pdf
- Submission No
- 13
- Submission Type
- SUPPL
- Appl No
- 761049
- Application Docs Date
- 2023-09-07 00:00:00
- Application Docs ID
- 75368
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2023/761049s015lbl.pdf
- Submission No
- 15
- Submission Type
- SUPPL
- Appl No
- 761049
- Application Docs Date
- 2024-03-08 00:00:00
- Application Docs ID
- 77763
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- 0
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- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2024/761049s016lbl.pdf
- Submission No
- 16
- Submission Type
- SUPPL
- Appl No
- 761049
- Application Docs Date
- 2024-10-14 00:00:00
- Application Docs ID
- 79877
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2024/761049s019lbl.pdf
- Submission No
- 19
- Submission Type
- SUPPL
- Appl No
- 761049
- Application Docs Date
- 2024-12-02 00:00:00
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- 80461
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- 0
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- 2
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- Submission No
- 20
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- Appl No
- 761049
- Application Docs Date
- 2025-06-05 00:00:00
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- application number
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- approval interpretation
- Application linkage and approved submission are not indication-level current approval verification
- current indication status
- not_reconciled
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- 761049
- Application Docs Date
- 2026-09-01 00:00:00
- Application Docs ID
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- Submission No
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- Sponsor Name
- EMD SERONO INC
- openfda application present
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- Active Ingredient
- AVELUMAB
- Appl No
- 761049
- Drug Name
- BAVENCIO
- Form
- INJECTABLE;INJECTION
- Product No
- 001
- Reference Drug
- 0
- Reference Standard
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- 20MG/ML
- marketing status
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Source passages and status connections
Passage 1 · positive indication candidate
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- 1 INDICATIONS AND USAGE BAVENCIO is a programmed death ligand-1 (PD-L1) blocking antibody indicated for: Merkel Cell Carcinoma (MCC) Adults and pediatric patients 12 years and older with metastatic MCC. ( 1.1 , 14.1 ) Urothelial Carcinoma (UC) Maintenance treatment of patients with locally advanced or metastatic UC that has not progressed with first-line platinum-containing chemotherapy. ( 1.2 , 14.
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- ICATIONS AND USAGE BAVENCIO is a programmed death ligand-1 (PD-L1) blocking antibody indicated for: Merkel Cell Carcinoma (MCC) Adults and pediatric patients 12 year
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- 1 INDICATIONS AND USAGE BAVENCIO is a programmed death ligand-1 (PD-L1) blocking antibody indicated for: Merkel Cell Carcinoma (MCC) Adults and pediatric patients 12 years and older with metastatic MCC.
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- NDICATIONS AND USAGE BAVENCIO is a programmed death ligand-1 (PD-L1) blocking antibody indicated for: Merkel Cell Carcinoma (MCC) Adults and pediatric patients 12 years and older with metastatic MCC. ( 1.1 , 14.1 ) Urothelial Carcinoma (UC) Maintenance treatment of patients with locally advanced or metastatic UC that has not progressed with first-line platinum-containing chemotherapy. ( 1.2 , 14.2 ) Patients with locally advanced or metastatic UC who: Have disease progression during or following platinum-containing chemotherapy. ( 1.2 , 14.2 ) Have disease progression within 12 mo
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- indications_and_usage_exact
- source text sha256
- ee94c4359d9d68823f2c72071b40190fc0b529fd149cee1822f57991d54267de
- start
- 1759
- source url
- https://api.fda.gov/drug/label.json?search=id%3A%22990c5dd1-5670-4e2f-af5d-6e87b73b12b5%22
- spl effective date
- 2026-08-25
- spl set id
- 5cd725a1-2fa4-408a-a651-57a7b84b2118
- spl version
- 24
- 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
Preserved source evidence · Not medical advice
Triangle