Protagonist Therapeutics (PTGX) Q2 2026 earnings summary
Event summary combining transcript, slides, and related documents.
Q2 2026 earnings summary
5 Aug, 2026Executive summary
Achieved net income of $162.8 million for Q2 2026, reversing a net loss of $34.8 million in Q2 2025, driven by major milestone and opt-out payments from collaboration agreements.
ICOTYDE received FDA approval in March 2026 for moderate-to-severe plaque psoriasis, with first full quarter of commercial sales and strong early adoption.
Exercised opt-out right under Takeda Collaboration Agreement, resulting in a $200 million payment and eligibility for further milestone and royalty payments.
Rusfertide NDA for polycythemia vera under FDA Priority Review, with PDUFA date in August 2026.
Advanced R&D pipeline with PN-881 moving to Phase 2b for psoriasis and PN-477sc entering Phase 1 for obesity.
Financial highlights
Q2 2026 license and collaboration revenue was $213.5 million, up from $5.5 million in Q2 2025, mainly due to Takeda opt-out and JNJ milestone payments.
Net income for Q2 2026 was $162.8 million ($2.47 per basic share, $2.29 per diluted share), compared to a net loss of $34.8 million ($0.55 per share) in Q2 2025.
Operating expenses increased 15% year-over-year to $54.7 million, reflecting higher R&D and G&A costs.
Cash, cash equivalents, and marketable securities totaled $849.5 million as of June 30, 2026, up from $646.0 million at year-end 2025.
Working capital as of June 30, 2026: $770.0 million.
Outlook and guidance
Existing cash and investments expected to fund operations for at least the next twelve months.
Anticipates significant increases in R&D expenses in the second half of 2026 due to advancement of clinical programs and new trials.
PN-881 Phase 2b psoriasis program to initiate in early Q1 2027; Phase 1 for oral PN-477 anticipated in H1 2027.
IND-enabling studies ongoing for PN-4580 and PN-8047, with Phase 1 starts expected in late 2027 and Q1 2027, respectively.
Eligible for substantial future milestone and royalty payments from JNJ and Takeda, contingent on regulatory approvals and commercial launches.
Latest events from Protagonist Therapeutics
- Strong partnered revenues and a diversified pipeline position the company for major value creation.PTGX
Corporate presentation - Two first-in-class therapies near launch, backed by strong partnerships and financial strength.PTGX
TD Cowen 46th Annual Health Care Conference - All proposals, including director elections and equity plan, were approved at the AGM.PTGX
AGM 2026 - Icotyde's strong launch and a robust pipeline drive growth, with Rusfertide approval expected soon.PTGX
Goldman Sachs 47th Annual Global Healthcare Conference 2026 - Major partnerships, strong pipeline, and financial strength drive growth and shareholder returns.PTGX
Jefferies Global Healthcare Conference 2026 - FDA approved the first oral IL-23R antagonist for moderate-to-severe plaque psoriasis.PTGX
FDA announcement - Rusfertide achieved rapid, sustained Hct control and symptom relief in PV; phase 3 results due 2025.PTGX
Study Update - PN-477, a potent triple agonist, advances toward Phase 1 trials with dual oral and injectable options.PTGX
Status Update - Rusfertide met all efficacy and safety endpoints in phase 3 PV trial; NDA filings planned for 2025.PTGX
Investor Update