Protagonist Therapeutics, Inc.

United Statesprotagonist-inc.com

Protagonist Therapeutics, Inc. is a clinical-stage biopharmaceutical company focused on the discovery and development of peptide-based medicines for hematologic and inflammatory diseases. The company uses a proprietary platform to design constrained peptides that modulate validated biological targets.

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Its lead wholly owned program is rusfertide (PTG-300), a hepcidin mimetic in late-stage development for polycythemia vera and other disorders of iron regulation. Protagonist also collaborates with Janssen on oral interleukin-23 receptor antagonists, including JNJ-2113 (formerly PN-235) for immune-mediated conditions. Additional pipeline candidates target gastrointestinal and systemic inflammatory pathways.

Protagonist is headquartered in the United States and conducts research and development across the U.S. and Australia.

Projects Protagonist is involved in

None yet. When a new project in the record names Protagonist as owner, partner or investor, it shows here.

Protagonist in chemical industry news

9 October 2026
Johnson & Johnson ICOTYDE delivers durable 2‑year plaque psoriasis results

Phase 3 data show sustained PASI90/PASI100 and IGA 0/1 responses to Week 112, durable itch improvement, and no new safety signals.

2 October 2026
Johnson & Johnson: Two‑year ICONIC‑TOTAL data show durable ICOTYDE efficacy in high‑impact plaque psoriasis

Oral ICOTYDE maintains durable skin clearance through Week 112 and yields high site‑specific clearance rates for scalp, genital, hand/foot and nails.

28 March 2026
Johnson & Johnson: ICOTYDE (icotrokinra) 52‑week data show sustained skin clearance and favorable safety

ICONIC Phase 3: PASI100 rose to 49%/48% (ADVANCE 1/2) by Week52; placebo switchers matched. Adolescents: 57% PASI100, 86% PASI90 at 52w. No new safety signals; fewer AEs vs deucravacitinib.

18 March 2026
Johnson & Johnson FDA approves ICOTYDE (icotrokinra) for first‑line systemic treatment of plaque psoriasis

First targeted oral IL‑23 receptor peptide approved for moderate‑to‑severe plaque psoriasis in adults and ≥12 (≥40kg). Once‑daily pill; ~70% IGA0/1, 55% PASI90 at Week16; safety like placebo.

2 March 2026
Takeda's Rusfertide Receives FDA Priority Review

Rusfertide shows promise in controlling hematocrit and reducing symptoms in polycythemia vera, with FDA review based on positive Phase 3 and long-term study data.

5 January 2026
Takeda and Protagonist Submit NDA for Rusfertide in Polycythemia Vera Treatment

Rusfertide shows promise in controlling hematocrit and reducing phlebotomy in PV patients, meeting key endpoints in Phase 3 VERIFY study.

6 December 2025
Protagonist and Takeda: Rusfertide's Long-Term Efficacy in Polycythemia Vera

Rusfertide shows sustained hematocrit control and reduced phlebotomy need in polycythemia vera over 52 weeks, with a consistent safety profile.