LABELS · 29f2a48e-b9af-486e-bc0c-eab3a1ce0b3c
CLIGAVYX
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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
- 2026-06-24
- Captured
- 2026-09-09T23:37:42.544548+00:00
- Current indication reconciliation
- Not reconciled
Indications and usage: exact source text
- 1 INDICATIONS AND USAGE Monotherapy CLIGAVYX is indicated for the treatment of: Hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced breast cancer in postmenopausal women not previously treated with endocrine therapy, or HR-positive advanced breast cancer in postmenopausal women with disease progression following endocrine therapy. Combination Therapy CLIGAVYX is indicated for the treatment of: HR-positive, HER2-negative advanced or metastatic breast cancer in postmenopausal women in combination with ribociclib as initial endocrine based therapy or following disease progression on endocrine therapy. HR-positive, HER2-negative advanced or metastatic breast cancer in combination with palbociclib or abemaciclib in women with disease progression after endocrine therapy. CLIGAVYX is an estrogen receptor antagonist indicated for the treatment of: Hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced breast cancer in postmenopausal women not previously treated with endocrine therapy. ( 1 ) HR-positive advanced breast cancer in postmenopausal women with disease progression following endocrine therapy. ( 1 ) HR-positive, HER2-negative advanced or metastatic breast cancer in postmenopausal women in combination with ribociclib, as initial endocrine based therapy or following disease progression on endocrine therapy. ( 1 ) HR-positive, HER2-negative advanced or metastatic breast cancer in combination with palbociclib or abemaciclib in women with disease progression after endocrine therapy. ( 1 )
Full extracted label fields
- application numbers
- NDA210063
- boxed warning exact
- brand names
- CLIGAVYX
- current indication status
- not_reconciled
- dailymed set url
- https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=e20d8ca3-8837-4003-8b01-1ebec342062a
- generic names
- FULVESTRANT
- id
- 29f2a48e-b9af-486e-bc0c-eab3a1ce0b3c
- indications and usage exact
- 1 INDICATIONS AND USAGE Monotherapy CLIGAVYX is indicated for the treatment of: Hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced breast cancer in postmenopausal women not previously treated with endocrine therapy, or HR-positive advanced breast cancer in postmenopausal women with disease progression following endocrine therapy. Combination Therapy CLIGAVYX is indicated for the treatment of: HR-positive, HER2-negative advanced or metastatic breast cancer in postmenopausal women in combination with ribociclib as initial endocrine based therapy or following disease progression on endocrine therapy. HR-positive, HER2-negative advanced or metastatic breast cancer in combination with palbociclib or abemaciclib in women with disease progression after endocrine therapy. CLIGAVYX is an estrogen receptor antagonist indicated for the treatment of: Hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced breast cancer in postmenopausal women not previously treated with endocrine therapy. ( 1 ) HR-positive advanced breast cancer in postmenopausal women with disease progression following endocrine therapy. ( 1 ) HR-positive, HER2-negative advanced or metastatic breast cancer in postmenopausal women in combination with ribociclib, as initial endocrine based therapy or following disease progression on endocrine therapy. ( 1 ) HR-positive, HER2-negative advanced or metastatic breast cancer in combination with palbociclib or abemaciclib in women with disease progression after endocrine therapy. ( 1 )
- indications and usage tables exact
- is original packager
- true
- manufacturer names
- Avyxa Pharma, LLC
- matched search terms
- cancer
- package ndcs
- 83831-159-02
- product ndcs
- 83831-159
- product types
- HUMAN PRESCRIPTION DRUG
- recent major changes exact
- record type
- complete_spl_indications_section_candidate
- routes
- INTRAMUSCULAR
- rxcuis
- 727762
- 2745138
- source batch
- file
- /private/tmp/cancer-full-research/indications/raw/labels-00100.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
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- skip
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- total
- 830
- sha256
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Drugs@FDA application source records
- application number
- NDA210063
- payload
- all indexed label documents
- Appl No
- 210063
- Application Docs Date
- 2019-08-20 00:00:00
- Application Docs ID
- 59749
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
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- Submission No
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- Submission Type
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- Appl No
- 210063
- Application Docs Date
- 2021-04-12 00:00:00
- Application Docs ID
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- Application Docs Title
- 0
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- 2
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- Submission No
- 2
- Submission Type
- SUPPL
- Appl No
- 210063
- Application Docs Date
- 2021-11-15 00:00:00
- Application Docs ID
- 69311
- Application Docs Title
- 0
- Application Docs Type ID
- 2
- Application Docs URL
- http://www.accessdata.fda.gov/drugsatfda_docs/label/2021/210063s003lbl.pdf
- Submission No
- 3
- Submission Type
- SUPPL
- Appl No
- 210063
- Application Docs Date
- 2025-11-28 00:00:00
- Application Docs ID
- 84331
- Application Docs Title
- 0
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- Submission No
- 10
- Submission Type
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- all submission records
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- STANDARD
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- 15
- Submission No
- 1
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- AP
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- 2019-08-19 00:00:00
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- 210063
- Review Priority
- STANDARD
- Submission Class Code ID
- 3
- Submission No
- 2
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- Submission Status Date
- 2021-04-06 00:00:00
- Submission Type
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- Submissions Public Notes
- Appl No
- 210063
- Review Priority
- STANDARD
- Submission Class Code ID
- 3
- Submission No
- 3
- Submission Status
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- Submission Status Date
- 2021-11-12 00:00:00
- Submission Type
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- Appl No
- 210063
- Review Priority
- STANDARD
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- 3
- Submission No
- 10
- Submission Status
- AP
- Submission Status Date
- 2025-11-21 00:00:00
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- approval interpretation
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- has approved submission record
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- Appl Public Notes
- Appl Type
- NDA
- Sponsor Name
- AVYXA HOLDINGS
- openfda application present
- true
- products
- Active Ingredient
- FULVESTRANT
- Appl No
- 210063
- Drug Name
- CLIGAVYX
- Form
- SOLUTION;INTRAMUSCULAR
- Product No
- 001
- Reference Drug
- 0
- Reference Standard
- 1
- Strength
- 250MG/5ML (50MG/ML)
- marketing status
- Prescription
Source passages and status connections
Passage 1 · positive indication candidate
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- 1 INDICATIONS AND USAGE Monotherapy CLIGAVYX is indicated for the treatment of: Hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced breast cancer in postmenopausal women not previously treated with endocrine therapy, or HR-positive advanced breast cancer in postmenopausal women with disease progression following endocrine therapy. Combination Therapy CLIGAVYX is indicated for the treatment of: HR-positive, HER2-negative advanced or metastatic breast cancer in postmenopausal women in combination with ribociclib as initial endoc
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- 1 INDICATIONS AND USAGE Monotherapy CLIGAVYX is indicated for the treatment of: Hormone receptor (HR)-positive, human epidermal growth factor receptor 2 (HER2)-negative advanced breast cancer in postmenopausal women not previously treated with endocrine therapy, or HR-positive advanced breast cancer in postmenopausal women with disease progression following endocrine therapy.
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- reast cancer in postmenopausal women not previously treated with endocrine therapy, or HR-positive advanced breast cancer in postmenopausal women with disease progression following endocrine therapy. Combination Therapy CLIGAVYX is indicated for the treatment of: HR-positive, HER2-negative advanced or metastatic breast cancer in postmenopausal women in combination with ribociclib as initial endocrine based therapy or following disease progression on endocrine therapy. HR-positive, HER2-negative advanced or metastatic breast cancer in combination with palbociclib or abemaciclib in women with disease progression after endocrine therapy. CLIGAVYX is an estrogen recep
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- 0
- source field
- indications_and_usage_exact
- source text sha256
- fde85291414a11e3dce9194ef5c92a78973c0961ad101c39c488087b0c5ed107
- start
- 1592
- source url
- https://api.fda.gov/drug/label.json?search=id%3A%2229f2a48e-b9af-486e-bc0c-eab3a1ce0b3c%22
- spl effective date
- 2026-06-24
- spl set id
- e20d8ca3-8837-4003-8b01-1ebec342062a
- spl version
- 6
- 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
- unclear
Preserved source evidence · Not medical advice
Triangle