Protagonist Therapeutics (PTGX) Corporate presentation summary
Event summary combining transcript, slides, and related documents.
Corporate presentation summary
10 Nov, 2026Business model and financial position
$834.6M in cash, equivalents and marketable securities as of Sept. 30, 2026; $275M received in October following MIMRYLO approval, including a $200M opt-out payment and $75M FDA milestone.
Partnerships offer ~ $1.5B in potential future milestones, plus tiered worldwide royalties of 6–10% on ICOTYDE and 14–29% on MIMRYLO.
$300M share buyback announced in September 2026; presentation cited no expected equity raise in the foreseeable future.
Partnered commercial assets and wholly owned programs target combined addressable markets exceeding $100B.
ICOTYDE
FDA-approved in March 2026 for moderate-to-severe plaque psoriasis; China approval followed in August and EC approval/marketing authorization in September 2026.
More than 20,000 U.S. patients initiated treatment through nearly 9,000 prescribers; ~60% were systemic-naïve, and coverage extended across all national plans.
Four Phase 3 studies supported approval, meeting all primary endpoints and showing a favorable safety profile in 2,500+ patients.
J&J partnership economics include $387.5M in payments earned, $580M in potential future milestones, 6–10% tiered royalties and >$10B peak-sales potential.
Phase 3 studies are ongoing in psoriatic arthritis and ulcerative colitis; Crohn’s disease is in Phase 2/3, with listed primary completion dates from 2027 to 2028.
MIMRYLO
FDA-approved in August 2026 for erythrocytosis in adults with polycythemia vera; the VERIFY Phase 3 study met its primary and all four key secondary endpoints.
76.9% of patients achieved response between Weeks 20–32; treatment maintains hematocrit control, reduces phlebotomy burden and improves fatigue.
Takeda partnership includes $800M in payments earned to date, $875M in potential future milestones and 14–29% tiered worldwide royalties; Takeda-guided peak sales are $1–2B.
Takeda reported rapid incorporation into NCCN guidelines in September 2026 as the only Category 1 option for both low- and high-risk PV.
Latest events from Protagonist Therapeutics
- Icotrokinra momentum and a broader oral pipeline anchor the development outlook.PTGX
8th Annual Wolfe Research Healthcare Conference - MIMRYLO approval payments helped drive Q3 revenue of $274.4M and net income of $220.0M.PTGX
Q3 2026 - FDA-approved assets and a strong pipeline drive growth in inflammation, hematology, and obesity.PTGX
Corporate presentation - Recent drug approvals and robust cash enable R&D expansion and a $300M share buyback.PTGX
12th Annual Cantor Fitzgerald Global Healthcare Conference - Strong drug approvals, innovative oral peptide pipeline, and strategic partnerships drive growth.PTGX
Citigroup’s Biopharma Back to School Summit 2026 - FDA approved MIMRYLO for PV, offering a novel, effective, and safe treatment with strong clinical results.PTGX
FDA announcement - Strong partnered revenues and a diversified pipeline position the company for major value creation.PTGX
Corporate presentation - Q2 2026 net income hit $162.8M, fueled by ICOTYDE sales and milestone payments; cash at $849.5M.PTGX
Q2 2026 - Rusfertide achieved rapid, sustained Hct control and symptom relief in PV; phase 3 results due 2025.PTGX
Study Update