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Source document· March 18, 2026

Protagonist Therapeutics Announces U.S. FDA Approval of ICOTYDE(TM) (icotrokinra) for the Treatment of Moderate to Severe Plaque Psoriasis

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Protagonist Therapeutics Announces U.S…
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  • Rates of adverse reactions for ICOTYDE treated patients were within 1.1% of placebo through Week 16 and no new safety signals were identified through Week 52

    60% confidence
  • This is the beginning of a multi-year product-driven growth cycle for Protagonist Therapeutics

    60% confidence
  • The FDA approval of ICOTYDE demonstrates the strength of Protagonist's peptide technology platform to generate innovative therapies

    60% confidence
  • ICOTYDE offers a novel plaque psoriasis treatment that combines the established efficacy and safety of IL-23 pathway blockade with the convenience of a once-daily oral pill

    60% confidence
  • ICOTYDE offers a novel plaque psoriasis treatment that combines the established efficacy and safety of IL-23 pathway blockade with the convenience of a once-daily oral pill

    60% confidence
  • Rates of adverse reactions for ICOTYDE treated patients were within 1.1% of placebo through Week 16 and no new safety signals were identified through Week 52

    60% confidence
  • Transition to systemic therapy is recommended if two cycles of topical medications applied for four weeks fail to bring meaningful improvement

    60% confidence
  • Transition to systemic therapy is recommended if two cycles of topical medications applied for four weeks fail to bring meaningful improvement

    60% confidence
  • More than 125 million people worldwide live with plaque psoriasis

    60% confidence
  • The FDA approval of ICOTYDE demonstrates the strength of Protagonist's peptide technology platform to generate innovative therapies

    60% confidence
  • Approximately 70% of patients achieved clear or almost clear skin (IGA 0/1) and 55% of patients achieved PASI90 response at Week 16 in head-to-head studies

    60% confidence
  • Psoriasis affects more than eight million Americans

    60% confidence
  • Psoriasis affects more than eight million Americans

    60% confidence
  • More than 125 million people worldwide live with plaque psoriasis

    60% confidence
  • With the pending FDA decision for rusfertide this year, and the financial resources for accelerating pipeline investment, this is the beginning of a multi-year product-driven growth cycle for Protagonist Therapeutics

    60% confidence
  • Approximately 70% of patients achieved clear or almost clear skin (IGA 0/1) and 55% of patients achieved a PASI90 response at Week 16 in head-to-head studies

    60% confidence
  • ICOTYDE is the first and only IL-23R targeted oral peptide that delivers complete skin clearance and a favorable safety profile in a once-daily pill

    60% confidence
  • ICOTYDE is the first and only IL-23R targeted oral peptide that delivers complete skin clearance

    60% confidence
  • Nearly one-quarter of all people with plaque psoriasis have cases that are considered moderate to severe

    60% confidence
  • Nearly one-quarter of all people with plaque psoriasis have cases that are considered moderate to severe

    60% confidence
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Morgan Stanley & Co. LLC
Two significantly different EPS values (10.21 vs 2.68 USD_per_share) are reported for Morgan Stanley on the same observation date (2025-12-31). Fact A specifies FY 2025, while Fact B's 'N/A' fiscal period is ambiguous. If both represent FY 2025 annual EPS, these values directly conflict. The magnitude of the difference (3.8x) is too large to attribute to rounding or minor calculation variations. The missing fiscal period in Fact B raises data quality concerns, but same-date observation + same attribute should reference the same period.
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Protagonist Therapeutics Announces U.S. FDA Approval of ICOTYDE(TM) (icotrokinra) for the Treatment of Moderate to Severe Plaque Psoriasis — Source | Via News | fr.VIA.NEWS