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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. 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
  1. BLA761049
boxed warning exact
    brand names
    1. 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
    1. AVELUMAB
    id
    990c5dd1-5670-4e2f-af5d-6e87b73b12b5
    indications and usage exact
    1. 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
      1. true
      manufacturer names
      1. EMD Serono, Inc.
      matched search terms
      1. carcinoma
      package ndcs
      1. 44087-3535-1
      product ndcs
      1. 44087-3535
      product types
      1. HUMAN PRESCRIPTION DRUG
      recent major changes exact
      1. Warnings and Precautions ( 5.1 ) 07/2026
      record type
      complete_spl_indications_section_candidate
      routes
      1. INTRAVENOUS
      rxcuis
      1. 1875542
      2. 1875547
      source batch
      file
      /private/tmp/cancer-full-research/indications/raw/labels-00500.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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      url
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      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 effective time
      20260825
      spl set id
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      spl version
      24
      substance names
      1. AVELUMAB
      uniis
      1. KXG2PJ551I
      verification flags
      1. oncology_keyword_candidate_not_clinically_classified
      2. spl_text_not_verified_identical_to_latest_approved_label
      3. individual_indications_not_split_or_reconciled
      4. fda_label_posted_after_spl_effective_date_requires_version_review
      Drugs@FDA application source records
      1. application number
        BLA761049
        payload
        all indexed label documents
        1. 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
          Submission No
          1
          Submission Type
          ORIG
        2. 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
          Submission No
          2
          Submission Type
          SUPPL
        3. 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
          Submission No
          3
          Submission Type
          SUPPL
        4. 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
          Submission No
          6
          Submission Type
          SUPPL
        5. 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
          Submission No
          9
          Submission Type
          SUPPL
        6. 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
          Submission No
          5
          Submission Type
          SUPPL
        7. 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
          Submission No
          13
          Submission Type
          SUPPL
        8. 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
          Submission No
          15
          Submission Type
          SUPPL
        9. Appl No
          761049
          Application Docs Date
          2024-03-08 00:00:00
          Application Docs ID
          77763
          Application Docs Title
          0
          Application Docs Type ID
          2
          Submission No
          16
          Submission Type
          SUPPL
        10. 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
          Submission No
          19
          Submission Type
          SUPPL
        11. Appl No
          761049
          Application Docs Date
          2024-12-02 00:00:00
          Application Docs ID
          80461
          Application Docs Title
          0
          Application Docs Type ID
          2
          Submission No
          20
          Submission Type
          SUPPL
        12. Appl No
          761049
          Application Docs Date
          2025-06-05 00:00:00
          Application Docs ID
          82467
          Application Docs Title
          0
          Application Docs Type ID
          2
          Submission No
          21
          Submission Type
          SUPPL
        all submission records
        1. Appl No
          761049
          Review Priority
          STANDARD
          Submission Class Code ID
          3
          Submission No
          26
          Submission Status
          AP
          Submission Status Date
          2026-08-31 00:00:00
          Submission Type
          SUPPL
          Submissions Public Notes
        2. Appl No
          761049
          Review Priority
          STANDARD
          Submission Class Code ID
          3
          Submission No
          21
          Submission Status
          AP
          Submission Status Date
          2025-06-04 00:00:00
          Submission Type
          SUPPL
          Submissions Public Notes
        3. Appl No
          761049
          Review Priority
          STANDARD
          Submission Class Code ID
          3
          Submission No
          20
          Submission Status
          AP
          Submission Status Date
          2024-11-26 00:00:00
          Submission Type
          SUPPL
          Submissions Public Notes
        4. Appl No
          761049
          Review Priority
          STANDARD
          Submission Class Code ID
          2
          Submission No
          19
          Submission Status
          AP
          Submission Status Date
          2024-10-11 00:00:00
          Submission Type
          SUPPL
          Submissions Public Notes
        5. Appl No
          761049
          Review Priority
          STANDARD
          Submission Class Code ID
          3
          Submission No
          16
          Submission Status
          AP
          Submission Status Date
          2024-03-06 00:00:00
          Submission Type
          SUPPL
          Submissions Public Notes
        6. Appl No
          761049
          Review Priority
          STANDARD
          Submission Class Code ID
          2
          Submission No
          15
          Submission Status
          AP
          Submission Status Date
          2023-09-06 00:00:00
          Submission Type
          SUPPL
          Submissions Public Notes
        7. Appl No
          761049
          Review Priority
          STANDARD
          Submission Class Code ID
          2
          Submission No
          13
          Submission Status
          AP
          Submission Status Date
          2022-07-15 00:00:00
          Submission Type
          SUPPL
          Submissions Public Notes
        8. Appl No
          761049
          Review Priority
          PRIORITY
          Submission Class Code ID
          2
          Submission No
          9
          Submission Status
          AP
          Submission Status Date
          2020-06-30 00:00:00
          Submission Type
          SUPPL
          Submissions Public Notes
        9. Appl No
          761049
          Review Priority
          PRIORITY
          Submission Class Code ID
          2
          Submission No
          6
          Submission Status
          AP
          Submission Status Date
          2019-05-14 00:00:00
          Submission Type
          SUPPL
          Submissions Public Notes
        10. Appl No
          761049
          Review Priority
          STANDARD
          Submission Class Code ID
          3
          Submission No
          5
          Submission Status
          AP
          Submission Status Date
          2020-11-10 00:00:00
          Submission Type
          SUPPL
          Submissions Public Notes
        11. Appl No
          761049
          Review Priority
          STANDARD
          Submission Class Code ID
          2
          Submission No
          3
          Submission Status
          AP
          Submission Status Date
          2018-10-19 00:00:00
          Submission Type
          SUPPL
          Submissions Public Notes
        12. Appl No
          761049
          Review Priority
          STANDARD
          Submission Class Code ID
          3
          Submission No
          2
          Submission Status
          AP
          Submission Status Date
          2017-10-12 00:00:00
          Submission Type
          SUPPL
          Submissions Public Notes
        application number
        BLA761049
        approval interpretation
        Application linkage and approved submission are not indication-level current approval verification
        current indication status
        not_reconciled
        has approved submission record
        true
        latest approved submission date
        2026-08-31
        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
        1. Appl No
          761049
          Application Docs Date
          2026-09-01 00:00:00
          Application Docs ID
          87108
          Application Docs Title
          0
          Application Docs Type ID
          2
          Submission No
          26
          Submission Type
          SUPPL
        official application record
        Appl No
        761049
        Appl Public Notes
        Appl Type
        BLA
        Sponsor Name
        EMD SERONO INC
        openfda application present
        true
        products
        1. Active Ingredient
          AVELUMAB
          Appl No
          761049
          Drug Name
          BAVENCIO
          Form
          INJECTABLE;INJECTION
          Product No
          001
          Reference Drug
          0
          Reference Standard
          Strength
          20MG/ML
          marketing status
          1. Prescription

      Source passages and status connections

      Passage classifications are automated and are not treatment recommendations. Connections apply only to their recorded indication scope.

      Passage 1 · positive indication candidate
      application numbers
      1. BLA761049
      brand names
      1. BAVENCIO
      classification reasons
      1. explicit_positive_indication_predicate
      2. tumor_or_malignant_hematology_words_in_positive_statement
      clinical review status
      pending
      content role
      positive_indication_candidate
      context span
      end
      402
      end exclusive
      true
      exact 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.
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      duplicate text group
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      generic names
      1. AVELUMAB
      id
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      label id
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      true
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      is a programmed death ligand-1 (PD-L1) blocking antibody indicated
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      qualifier mentions
      1. context exact
        locking antibody indicated for: Merkel Cell Carcinoma (MCC) Adults and pediatric patients 12 years and older with metastatic M
        kind
        age
        polarity
        not_inferred
        span
        end
        139
        end exclusive
        true
        exact text
        Adults
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      2. context exact
        ibody indicated for: Merkel Cell Carcinoma (MCC) Adults and pediatric patients 12 years and older with metastatic MCC.
        kind
        age
        polarity
        not_inferred
        span
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        end exclusive
        true
        exact text
        pediatric patients
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      3. context exact
        : Merkel Cell Carcinoma (MCC) Adults and pediatric patients 12 years and older with metastatic MCC.
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        span
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        exact text
        12 years and older
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      4. context exact
        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
        kind
        biomarker
        polarity
        not_inferred
        span
        end
        110
        end exclusive
        true
        exact text
        PD-L1) blocking antibody indicated for: Merke
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      5. context exact
        (MCC) Adults and pediatric patients 12 years and older with metastatic MCC.
        kind
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        polarity
        not_inferred
        span
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        201
        end exclusive
        true
        exact text
        metastatic MCC
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      6. context exact
        (MCC) Adults and pediatric patients 12 years and older with metastatic MCC.
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        end exclusive
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        metastatic MCC
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      regulatory links
        schema version
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        source defined aliases
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          true
          exact 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.
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          spl effective date
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          spl set id
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          structured fields status
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          Source null
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          Source null
          biomarker and test
          Source null
          disease stage
          Source null
          limitations
          Source null
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          Source null
          prior therapy
          Source null
          regimen
          Source null
          tumor histology
          Source null
          use intent
          tumor_directed_candidate
          Passage 2 · positive indication candidate
          application numbers
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          brand names
          1. BAVENCIO
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          clinical review status
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          exact text
          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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                                                Preserved source evidence · Not medical advice