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AbbVieLaunch

AbbVie Announces European Commission Approval of RINVOQ® (upadacitinib) for the Treatment of Children with Active Polyarticular Juvenile Idiopathic Arthritis

What happened

AbbVie's drug RINVOQ (upadacitinib) received approval from the European Commission for treating active polyarticular juvenile idiopathic arthritis in patients aged two and older.

Source

Article excerpt

Highlighted: the sentence this signal was extracted from

NORTH CHICAGO, Ill., Sept. 22, 2026 /PRNewswire/ -- AbbVie (NYSE: ABBV ) today announced that the European Commission (EC) has approved RINVOQ ® (upadacitinib; 15 mg tablet and weight-based 1 mg/mL oral solution) for the treatment of active polyarticular juvenile idiopathic arthritis (polyarticular rheumatoid factor positive [RF+] or negative [RF-], extended oligoarticular), in patients two years of age and older who have responded inadequately to, or who are intolerant to, one or more disease-modifying anti-rheumatic drugs (DMARDs). RINVOQ may be used as monotherapy or in combination with methotrexate. 1 "The European Commission's approval of RINVOQ for pJIA expands the treatment options available to pediatric patients and their families, offering the potential for remission, improvements in pain and physical function," said Roopal Thakkar, M.D., executive vice president, research and development, chief scientific officer, AbbVie. "RINVOQ's new indication continues to build on our differentiated immunology portfolio with breadth and depth across therapeutic areas and patient populations." Juvenile idiopathic arthritis (JIA) is the most common rheumatic disease of childhood and is estimated to impact approximately 126,000 children in Europe. 3 pJIA is a subtype of JIA and is characterized by inflammation in five or more joints – including the small joints of the hands and...

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Extracted by Autobound

From the Signal API record
Event
Launch

What this signalsA launch often needs new go-to-market and support spend.

Product
RINVOQ
Takes effect
Sep 22, 2026
Location
Europe

The full record

From the Signal API record

Topics and mentions

Product tags

  • medical

Extraction

Confidence
100%
Detected
Sep 22, 2026
signal_type
news
signal_subtype
launches

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This page shows a preview. The full news record in the Signal API and MCP can also have these 8 fields. Some fields are empty for some signals.

Company

  • linkedin_urlValue in the API
  • industriesValue in the API
  • employee_count_lowValue in the API
  • employee_count_highValue in the API
  • revenueValue in the API
  • descriptionValue in the API

Signal

  • signal_nameValue in the API
  • associationValue in the API
Show the full JSONThe record on this page and the API request

GET /v1/signals/423d63f1-a5dc-8859-28ec-a4736325f999 returns this record as JSON. POST /v1/companies/enrich returns every signal for abbvie.com.

{
  "signal_id": "423d63f1-a5dc-8859-28ec-a4736325f999",
  "signal_type": "news",
  "signal_subtype": "launches",
  "detected_at": "2026-09-22T06:00:00+00:00",
  "company": {
    "name": "AbbVie",
    "domain": "abbvie.com"
  },
  "data": {
    "url": "https://www.prnewswire.com/news-releases/abbvie-announces-european-commission-approval-of-rinvoq-upadacitinib-for-the-treatment-of-children-with-active-polyarticular-juvenile-idiopathic-arthritis-302885190.html",
    "title": "AbbVie Announces European Commission Approval of RINVOQ® (upadacitinib) for the Treatment of Children with Active Polyarticular Juvenile Idiopathic Arthritis",
    "excerpt": "NORTH CHICAGO, Ill. , Sept. 22, 2026 /PRNewswire/ -- AbbVie (NYSE: ABBV ) today announced that the European Commission (EC) has approved RINVOQ ® (upadacitinib; 15 mg tablet and weight-based 1 mg/mL oral solution) for the treatment of active polyarticular juvenile idiopathic arthritis (polyarticular rheumatoid factor positive [RF+] or negative [RF-], extended oligoarticular), in patients two years of age and older who have responded inadequately to, or who are intolerant to, one or more disease-modifying anti-rheumatic drugs (DMARDs). RINVOQ may be used as monotherapy or in combination with methotrexate. 1 \"The European Commission's approval of RINVOQ for pJIA expands the treatment options available to pediatric patients and their families, offering the potential for remission, improvements in pain and physical function,\" said Roopal Thakkar, M.D., executive vice president, research and development, chief scientific officer, AbbVie. \"RINVOQ's new indication continues to build on our differentiated immunology portfolio with breadth and depth across therapeutic areas and patient populations.\" Juvenile idiopathic arthritis (JIA) is the most common rheumatic disease of childhood and is estimated to impact approximately 126,000 children in Europe. 3 pJIA is a subtype of JIA and is characterized by inflammation in five or more joints – including the small joints of the hands and...",
    "product": "RINVOQ",
    "summary": "AbbVie's drug RINVOQ (upadacitinib) received approval from the European Commission for treating active polyarticular juvenile idiopathic arthritis in patients aged two and older.",
    "location": "Europe",
    "planning": false,
    "confidence": 1,
    "product_data": {
      "name": "RINVOQ",
      "full_text": "RINVOQ ® (upadacitinib; 15 mg tablet and weight-based 1 mg/mL oral solution)",
      "fuzzy_match": false
    },
    "product_tags": [
      "medical"
    ],
    "published_at": "2026-09-22T06:00:00Z",
    "location_data": [
      {
        "continent": "Europe",
        "fuzzy_match": false
      }
    ],
    "effective_date": "2026-09-22",
    "article_sentence": "AbbVie (NYSE: ABBV ) today announced that the European Commission (EC) has approved RINVOQ ® (upadacitinib; 15 mg tablet and weight-based 1 mg/mL oral solution) for the treatment of active polyarticular juvenile idiopathic arthritis (polyarticular rheumatoid factor positive [RF+] or negative [RF-], extended oligoarticular), in patients two years of age and older who have responded inadequately to, or who are intolerant to, one or more disease-modifying anti-rheumatic drugs (DMARDs)."
  }
}

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