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Articles GetSignal writes with AI from a company's own 8-K filing or press release, newest first. Each one links to the filing or release it was written from.Articles GetSignal writes with AI from a company's own 8-K filing or press release, newest first.

9 articles on ABBV

  1. ABBVCompany release
    U.S. FDA approves subcutaneous induction for AbbVie's SKYRIZI in Crohn's disease

    The induction doses are given by on-body injector at weeks 0, 2, 4 and 8, followed by maintenance doses every eight weeks starting at week 12.

  2. ABBVCompany release
    AbbVie to present new and updated data at 2026 ESMO Congress in Madrid

    The presentations cover seven assets across lung, colorectal, ovarian, prostate and gastric cancers.

  3. ABBVCompany release
    AbbVie presents 20 IBD abstracts with long-term Skyrizi and Rinvoq data at UEGW 2026

    The company said the meeting runs October 17 to 20 in Barcelona, Spain, and includes new endoscopic remission data for investigational ABBV-466 in Crohn's disease.

  4. ABBVCompany release
    AbbVie to present 22 inflammatory bowel disease abstracts at ACG 2026 meeting

    AbbVie said new Phase 3 AFFIRM data showed higher clinical and endoscopic response rates for subcutaneous SKYRIZI than placebo in Crohn's disease patients.

  5. ABBVCompany release
    AbbVie's Temab-A receives two FDA Breakthrough Therapy Designations

    The designations cover colorectal cancer and non-small cell lung cancer, and are the first for the drug.

  6. ABBVCompany release
    AbbVie presents continued repigmentation data for RINVOQ in non-segmental vitiligo

    The late-breaking data from the Phase 3 Viti-Up-1 and Viti-Up-2 studies were presented at the 2026 EADV Congress in Vienna, Austria.

  7. ABBVCompany release
    AbbVie presents Phase 1 data for obesity candidate ABBV-295 at EASD 2026

    AbbVie said the findings support advancing ABBV-295 into Phase 2 development for chronic weight management.

  8. ABBVCompany release
    AbbVie zumilokibart Phase 2 study meets primary endpoint in atopic dermatitis

    The mid-dose regimen was selected for Phase 3 development, the company said.

  9. ABBVCompany release
    U.S. FDA approves AbbVie's JUVMO (tavapadon) for Parkinson's disease

    The tablets are taken once daily, with or without levodopa therapy, the company said.

How these are written

  • The source: the company's own 8-K filing or press release, linked from every article. What the company says is attributed to the company.
  • The checks: each article is written by GetSignal with AI and checked against its source before it is shown.
  • The date: the day the company filed the 8-K or published the release.
  • Not investment advice. An article reports what the company disclosed; it is not a view on the stock.

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