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LABELS · a09d3635-1735-4ac9-884e-5c49897da6f5

Ilaris

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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
2026-06-08
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 ILARIS is an interleukin-1β blocker indicated for the treatment of: • Periodic Fever Syndromes ( 1.1 ): - Cryopyrin-Associated Periodic Syndromes (CAPS), in adults and children 4 years of age and older, including: ◾ Familial Cold Auto-inflammatory Syndrome (FCAS) ◾ Muckle-Wells Syndrome (MWS) - Tumor Necrosis Factor Receptor Associated Periodic Syndrome (TRAPS) in adult and pediatric patients - Hyperimmunoglobulin D Syndrome (HIDS)/ Mevalonate Kinase Deficiency (MKD) in adult and pediatric patients - Familial Mediterranean Fever (FMF) in adult and pediatric patients • Active Still’s Disease, including Adult-Onset Still’s Disease (AOSD) and Systemic Juvenile Idiopathic Arthritis (SJIA) in patients 2 years of age and older ( 1.2 ) • Gout flares in adults in whom non-steroidal anti-inflammatory drugs (NSAIDs) and colchicine are contraindicated, are not tolerated, or do not provide an adequate response, and in whom repeated courses of corticosteroids are not appropriate ( 1.3 ) 1.1 Periodic Fever Syndromes ILARIS ® (canakinumab) is an interleukin-1β (IL-1β) blocker indicated for the treatment of the following autoinflammatory Periodic Fever Syndromes: Cryopyrin-Associated Periodic Syndromes (CAPS) ILARIS is indicated for the treatment of Cryopyrin-Associated Periodic Syndromes (CAPS), in adults and pediatric patients 4 years of age and older, including: Familial Cold Autoinflammatory Syndrome (FCAS) Muckle-Wells Syndrome (MWS) Tumor Necrosis Factor Receptor (TNF) Associated Periodic Syndrome (TRAPS) ILARIS is indicated for the treatment of Tumor Necrosis Factor (TNF) Receptor Associated Periodic Syndrome (TRAPS) in adult and pediatric patients. Hyperimmunoglobulin D Syndrome (HIDS)/Mevalonate Kinase Deficiency (MKD) ILARIS is indicated for the treatment of Hyperimmunoglobulin D (Hyper-IgD) Syndrome (HIDS)/Mevalonate Kinase Deficiency (MKD) in adult and pediatric patients. Familial Mediterranean Fever (FMF) ILARIS is indicated for the treatment of Familial Mediterranean Fever (FMF) in adult and pediatric patients. 1.2 Still’s Disease (Adult-Onset Still’s Disease [AOSD] and Systemic Juvenile Idiopathic Arthritis [SJIA]) ILARIS is indicated for the treatment of active Still’s Disease, including Adult-Onset Still’s Disease (AOSD) and Systemic Juvenile Idiopathic Arthritis (SJIA) in patients 2 years of age and older. 1.3 Gout Flares ILARIS is indicated for the symptomatic treatment of adult patients with gout flares in whom non-steroidal anti-inflammatory drugs (NSAIDs) and colchicine are contraindicated, are not tolerated, or do not provide an adequate response, and in whom repeated courses of corticosteroids are not appropriate.
Full extracted label fields
application numbers
  1. BLA125319
boxed warning exact
    brand names
    1. Ilaris
    current indication status
    not_reconciled
    dailymed set url
    https://dailymed.nlm.nih.gov/dailymed/drugInfo.cfm?setid=7d271f3b-e4f9-4d80-8dcf-28d49123f80e
    generic names
    1. CANAKINUMAB
    id
    a09d3635-1735-4ac9-884e-5c49897da6f5
    indications and usage exact
    1. 1 INDICATIONS AND USAGE ILARIS is an interleukin-1β blocker indicated for the treatment of: • Periodic Fever Syndromes ( 1.1 ): - Cryopyrin-Associated Periodic Syndromes (CAPS), in adults and children 4 years of age and older, including: ◾ Familial Cold Auto-inflammatory Syndrome (FCAS) ◾ Muckle-Wells Syndrome (MWS) - Tumor Necrosis Factor Receptor Associated Periodic Syndrome (TRAPS) in adult and pediatric patients - Hyperimmunoglobulin D Syndrome (HIDS)/ Mevalonate Kinase Deficiency (MKD) in adult and pediatric patients - Familial Mediterranean Fever (FMF) in adult and pediatric patients • Active Still’s Disease, including Adult-Onset Still’s Disease (AOSD) and Systemic Juvenile Idiopathic Arthritis (SJIA) in patients 2 years of age and older ( 1.2 ) • Gout flares in adults in whom non-steroidal anti-inflammatory drugs (NSAIDs) and colchicine are contraindicated, are not tolerated, or do not provide an adequate response, and in whom repeated courses of corticosteroids are not appropriate ( 1.3 ) 1.1 Periodic Fever Syndromes ILARIS ® (canakinumab) is an interleukin-1β (IL-1β) blocker indicated for the treatment of the following autoinflammatory Periodic Fever Syndromes: Cryopyrin-Associated Periodic Syndromes (CAPS) ILARIS is indicated for the treatment of Cryopyrin-Associated Periodic Syndromes (CAPS), in adults and pediatric patients 4 years of age and older, including: Familial Cold Autoinflammatory Syndrome (FCAS) Muckle-Wells Syndrome (MWS) Tumor Necrosis Factor Receptor (TNF) Associated Periodic Syndrome (TRAPS) ILARIS is indicated for the treatment of Tumor Necrosis Factor (TNF) Receptor Associated Periodic Syndrome (TRAPS) in adult and pediatric patients. Hyperimmunoglobulin D Syndrome (HIDS)/Mevalonate Kinase Deficiency (MKD) ILARIS is indicated for the treatment of Hyperimmunoglobulin D (Hyper-IgD) Syndrome (HIDS)/Mevalonate Kinase Deficiency (MKD) in adult and pediatric patients. Familial Mediterranean Fever (FMF) ILARIS is indicated for the treatment of Familial Mediterranean Fever (FMF) in adult and pediatric patients. 1.2 Still’s Disease (Adult-Onset Still’s Disease [AOSD] and Systemic Juvenile Idiopathic Arthritis [SJIA]) ILARIS is indicated for the treatment of active Still’s Disease, including Adult-Onset Still’s Disease (AOSD) and Systemic Juvenile Idiopathic Arthritis (SJIA) in patients 2 years of age and older. 1.3 Gout Flares ILARIS is indicated for the symptomatic treatment of adult patients with gout flares in whom non-steroidal anti-inflammatory drugs (NSAIDs) and colchicine are contraindicated, are not tolerated, or do not provide an adequate response, and in whom repeated courses of corticosteroids are not appropriate.
    indications and usage tables exact
      is original packager
      1. true
      manufacturer names
      1. Novartis Pharmaceuticals Corporation
      matched search terms
      1. tumor
      package ndcs
      1. 0078-0734-61
      product ndcs
      1. 0078-0734
      product types
      1. HUMAN PRESCRIPTION DRUG
      recent major changes exact
      1. Warnings and Precautions, Hypersensitivity Reactions ( 5.3 ) 11/2024
      record type
      complete_spl_indications_section_candidate
      routes
      1. SUBCUTANEOUS
      rxcuis
      1. 1864324
      2. 1864326
      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
      100
      skip
      500
      total
      830
      sha256
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      url
      https://api.fda.gov/drug/label.json?search=%28indications_and_usage%3Acancer+OR+indications_and_usage%3Acarcinoma+OR+indications_and_usage%3Acarcinomas+OR+indications_and_usage%3Alymphoma+OR+indications_and_usage%3Alymphomas+OR+indications_and_usage%3Aleukemia+OR+indications_and_usage%3Aleukaemia+OR+indications_and_usage%3Asarcoma+OR+indications_and_usage%3Asarcomas+OR+indications_and_usage%3Amelanoma+OR+indications_and_usage%3Amyeloma+OR+indications_and_usage%3Atumor+OR+indications_and_usage%3Atumors+OR+indications_and_usage%3Atumour+OR+indications_and_usage%3Atumours+OR+indications_and_usage%3Aneoplasm+OR+indications_and_usage%3Aneoplasms+OR+indications_and_usage%3Amalignant+OR+indications_and_usage%3Amalignancy+OR+indications_and_usage%3Amyelodysplastic+OR+indications_and_usage%3Amyelofibrosis+OR+indications_and_usage%3Amastocytosis+OR+indications_and_usage%3Aglioma+OR+indications_and_usage%3Aglioblastoma+OR+indications_and_usage%3Aneuroblastoma+OR+indications_and_usage%3Aretinoblastoma+OR+indications_and_usage%3Apheochromocytoma+OR+indications_and_usage%3Aparaganglioma+OR+indications_and_usage%3Amyeloproliferative+OR+indications_and_usage%3Awaldenstrom+OR+indications_and_usage%3Apolycythemia+OR+indications_and_usage%3Athrombocythemia+OR+indications_and_usage%3Adesmoid+OR+indications_and_usage%3Aneurofibromatosis+OR+indications_and_usage%3Ahistiocytosis%29+AND+%28openfda.application_number%3ANDA%2A+OR+openfda.application_number%3ABLA%2A%29&limit=100&skip=500&sort=id%3Aasc
      source url
      https://api.fda.gov/drug/label.json?search=id%3A%22a09d3635-1735-4ac9-884e-5c49897da6f5%22
      spl effective date
      2026-06-08
      spl effective time
      20260608
      spl set id
      7d271f3b-e4f9-4d80-8dcf-28d49123f80e
      spl version
      31
      substance names
      1. CANAKINUMAB
      uniis
      1. 37CQ2C7X93
      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
      Drugs@FDA application source records
      1. application number
        BLA125319
        payload
        all indexed label documents
        1. Appl No
          125319
          Application Docs Date
          2009-06-29 00:00:00
          Application Docs ID
          18860
          Application Docs Title
          0
          Application Docs Type ID
          2
          Submission No
          1
          Submission Type
          ORIG
        2. Appl No
          125319
          Application Docs Date
          2012-04-02 00:00:00
          Application Docs ID
          18861
          Application Docs Title
          0
          Application Docs Type ID
          2
          Submission No
          47
          Submission Type
          SUPPL
        3. Appl No
          125319
          Application Docs Date
          2012-10-12 00:00:00
          Application Docs ID
          39915
          Application Docs Title
          0
          Application Docs Type ID
          2
          Submission No
          54
          Submission Type
          SUPPL
        4. Appl No
          125319
          Application Docs Date
          2013-05-13 00:00:00
          Application Docs ID
          39916
          Application Docs Title
          0
          Application Docs Type ID
          2
          Submission No
          62
          Submission Type
          SUPPL
        5. Appl No
          125319
          Application Docs Date
          2014-10-21 00:00:00
          Application Docs ID
          39917
          Application Docs Title
          0
          Application Docs Type ID
          2
          Submission No
          81
          Submission Type
          SUPPL
        6. Appl No
          125319
          Application Docs Date
          2016-07-22 00:00:00
          Application Docs ID
          39918
          Application Docs Title
          0
          Application Docs Type ID
          2
          Submission No
          84
          Submission Type
          SUPPL
        7. Appl No
          125319
          Application Docs Date
          2016-09-27 00:00:00
          Application Docs ID
          45391
          Application Docs Title
          0
          Application Docs Type ID
          2
          Submission No
          85
          Submission Type
          SUPPL
        8. Appl No
          125319
          Application Docs Date
          2016-09-27 00:00:00
          Application Docs ID
          45392
          Application Docs Title
          0
          Application Docs Type ID
          2
          Submission No
          86
          Submission Type
          SUPPL
        9. Appl No
          125319
          Application Docs Date
          2016-09-27 00:00:00
          Application Docs ID
          45393
          Application Docs Title
          0
          Application Docs Type ID
          2
          Submission No
          87
          Submission Type
          SUPPL
        10. Appl No
          125319
          Application Docs Date
          2016-12-22 00:00:00
          Application Docs ID
          46510
          Application Docs Title
          0
          Application Docs Type ID
          2
          Submission No
          88
          Submission Type
          SUPPL
        11. Appl No
          125319
          Application Docs Date
          2020-06-17 00:00:00
          Application Docs ID
          63604
          Application Docs Title
          0
          Application Docs Type ID
          2
          Submission No
          97
          Submission Type
          SUPPL
        12. Appl No
          125319
          Application Docs Date
          2020-09-22 00:00:00
          Application Docs ID
          64649
          Application Docs Title
          0
          Application Docs Type ID
          2
          Submission No
          100
          Submission Type
          SUPPL
        all submission records
        1. Appl No
          125319
          Review Priority
          STANDARD
          Submission Class Code ID
          3
          Submission No
          110
          Submission Status
          AP
          Submission Status Date
          2024-11-01 00:00:00
          Submission Type
          SUPPL
          Submissions Public Notes
        2. Appl No
          125319
          Review Priority
          STANDARD
          Submission Class Code ID
          2
          Submission No
          107
          Submission Status
          AP
          Submission Status Date
          2023-08-25 00:00:00
          Submission Type
          SUPPL
          Submissions Public Notes
        3. Appl No
          125319
          Review Priority
          STANDARD
          Submission Class Code ID
          3
          Submission No
          100
          Submission Status
          AP
          Submission Status Date
          2020-09-18 00:00:00
          Submission Type
          SUPPL
          Submissions Public Notes
        4. Appl No
          125319
          Review Priority
          PRIORITY
          Submission Class Code ID
          2
          Submission No
          97
          Submission Status
          AP
          Submission Status Date
          2020-06-16 00:00:00
          Submission Type
          SUPPL
          Submissions Public Notes
        5. Appl No
          125319
          Review Priority
          STANDARD
          Submission Class Code ID
          4
          Submission No
          88
          Submission Status
          AP
          Submission Status Date
          2016-12-22 00:00:00
          Submission Type
          SUPPL
          Submissions Public Notes
        6. Appl No
          125319
          Review Priority
          PRIORITY
          Submission Class Code ID
          2
          Submission No
          87
          Submission Status
          AP
          Submission Status Date
          2016-09-23 00:00:00
          Submission Type
          SUPPL
          Submissions Public Notes
        7. Appl No
          125319
          Review Priority
          PRIORITY
          Submission Class Code ID
          2
          Submission No
          86
          Submission Status
          AP
          Submission Status Date
          2016-09-23 00:00:00
          Submission Type
          SUPPL
          Submissions Public Notes
        8. Appl No
          125319
          Review Priority
          PRIORITY
          Submission Class Code ID
          2
          Submission No
          85
          Submission Status
          AP
          Submission Status Date
          2016-09-23 00:00:00
          Submission Type
          SUPPL
          Submissions Public Notes
        9. Appl No
          125319
          Review Priority
          STANDARD
          Submission Class Code ID
          2
          Submission No
          84
          Submission Status
          AP
          Submission Status Date
          2016-07-21 00:00:00
          Submission Type
          SUPPL
          Submissions Public Notes
        10. Appl No
          125319
          Review Priority
          STANDARD
          Submission Class Code ID
          3
          Submission No
          81
          Submission Status
          AP
          Submission Status Date
          2014-10-16 00:00:00
          Submission Type
          SUPPL
          Submissions Public Notes
        11. Appl No
          125319
          Review Priority
          PRIORITY
          Submission Class Code ID
          2
          Submission No
          62
          Submission Status
          AP
          Submission Status Date
          2013-05-09 00:00:00
          Submission Type
          SUPPL
          Submissions Public Notes
        12. Appl No
          125319
          Review Priority
          STANDARD
          Submission Class Code ID
          3
          Submission No
          54
          Submission Status
          AP
          Submission Status Date
          2012-10-11 00:00:00
          Submission Type
          SUPPL
          Submissions Public Notes
        application number
        BLA125319
        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
        2024-11-01
        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
          125319
          Application Docs Date
          2024-11-05 00:00:00
          Application Docs ID
          80144
          Application Docs Title
          0
          Application Docs Type ID
          2
          Submission No
          110
          Submission Type
          SUPPL
        official application record
        Appl No
        125319
        Appl Public Notes
        Appl Type
        BLA
        Sponsor Name
        NOVARTIS PHARMS
        openfda application present
        true
        products
        1. Active Ingredient
          CANAKINUMAB
          Appl No
          125319
          Drug Name
          ILARIS
          Form
          INJECTABLE; SUBCUTANEOUS
          Product No
          001
          Reference Drug
          0
          Reference Standard
          Strength
          180MG
          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. BLA125319
      brand names
      1. Ilaris
      classification reasons
      1. explicit_positive_indication_predicate
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      clinical review status
      pending
      content role
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      context span
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      291
      end exclusive
      true
      exact text
      1 INDICATIONS AND USAGE ILARIS is an interleukin-1β blocker indicated for the treatment of: • Periodic Fever Syndromes ( 1.1 ): - Cryopyrin-Associated Periodic Syndromes (CAPS), in adults and children 4 years of age and older, including: ◾ Familial Cold Auto-inflammatory Syndrome (FCAS) ◾ M
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      is an interleukin-1β blocker indicated
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            1 INDICATIONS AND USAGE ILARIS is an interleukin-1β blocker indicated for the treatment of:
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            structured fields status
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            Source null
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            Source null
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            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
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            1 INDICATIONS AND USAGE ILARIS is an interleukin-1β blocker indicated for the treatment of: • Periodic Fever Syndromes ( 1.1 ): - Cryopyrin-Associated Periodic Syndromes (CAPS), in adults and children 4 years of age and older, including: ◾ Familial Cold Auto-inflammatory Syndrome (FCAS) ◾ Muckle-Wells Syndrome (MWS) - Tumor Necrosis Factor Receptor Associated Periodic Syndrome (TRAPS) in adult and pediatric patients - Hyperimmunoglobulin D Syndrome (HIDS)/ Mevalonate Kinase Deficiency (MKD) in adult and pediatric patients - Familial Mediterranean Fever (FMF) in adult and pediatric patients • Active Still’s Disease, including Adult-Onset Still’s Disease (AOSD) and Systemic Juvenile Idiopathic Arthritis (SJIA) in patients 2 years of age and older ( 1.2 ) • Gout flares in adults in whom n
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              1.1 ): - Cryopyrin-Associated Periodic Syndromes (CAPS), in adults and children 4 years of age and older, including: ◾ Familia
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                                Hyperimmunoglobulin D Syndrome (HIDS)/Mevalonate Kinase Deficiency (MKD) ILARIS is indicated for the treatment of Hyperimmunoglobulin D (Hyper-IgD) Syndrome (HIDS)/Mevalonate Kinase Deficiency (MKD) in adult and pediatric patients.
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                                HIDS)/Mevalonate Kinase Deficiency (MKD) ILARIS is indicated for the treatment of Hyperimmunoglobulin D (Hyper-IgD) Syndrome (HIDS)/Mevalonate Kinase Deficiency (MKD) in adult and pediatric patients. Familial Mediterranean Fever (FMF) ILARIS is indicated for the treatment of Familial Mediterranean Fever (FMF) in adult and pediatric patients. 1.2 Still’s Disease (Adult-Onset Still’s Disease [AOSD] and Systemic Juvenile Idiopathic Arthritis [SJIA]) ILARIS is indicated for the treatment of active Still’s Disease, including Adult-Onset Still
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                                    Familial Mediterranean Fever (FMF) ILARIS is indicated for the treatment of Familial Mediterranean Fever (FMF) in adult and pediatric patients.
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                                    inase Deficiency (MKD) in adult and pediatric patients. Familial Mediterranean Fever (FMF) ILARIS is indicated for the treatment of Familial Mediterranean Fever (FMF) in adult and pediatric patients. 1.2 Still’s Disease (Adult-Onset Still’s Disease [AOSD] and Systemic Juvenile Idiopathic Arthritis [SJIA]) ILARIS is indicated for the treatment of active Still’s Disease, including Adult-Onset Still’s Disease (AOSD) and Systemic Juvenile Idiopathic Arthritis (SJIA) in patients 2 years of age and older. 1.3 Gout Flares ILARIS is indicated for the symptomatic treatment of adult patients with gout flares in whom non-steroidal anti-inflammatory drugs (NSAIDs) and colchicine are contraindicated, are not
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                                        1.2 Still’s Disease (Adult-Onset Still’s Disease [AOSD] and Systemic Juvenile Idiopathic Arthritis [SJIA]) ILARIS is indicated for the treatment of active Still’s Disease, including Adult-Onset Still’s Disease (AOSD) and Systemic Juvenile Idiopathic Arthritis (SJIA) in patients 2 years of age and older.
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                                        qualifier mentions
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                                            1.3 Gout Flares ILARIS is indicated for the symptomatic treatment of adult patients with gout flares in whom non-steroidal anti-inflammatory drugs (NSAIDs) and colchicine are contraindicated, are not tolerated, or do not provide an adequate response, and in whom repeated courses of corticosteroids are not appropriate.
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                                            Preserved source evidence · Not medical advice