Vera Therapeutics (VERA) Q3 2026 earnings summary
Event summary combining transcript, slides, and related documents.
Q3 2026 earnings summary
6 Nov, 2026Executive summary
TRUTAKNA launched in the U.S. after FDA accelerated approval on July 7; ~700 Patient Start Forms had been received by Nov. 5, and Q3 net product revenue was $10.277 million.
ORIGIN 3 met prespecified endpoints, showing 76% lower kidney disease progression risk through 104 weeks; an sBLA seeking full FDA approval was submitted Nov. 3, with a potential decision in mid-2027.
Priorities include expanding the U.S. launch, pursuing full U.S. and European approval, and advancing atacicept in antibody-mediated kidney diseases.
Financial highlights
Q3 net product revenue was $10.277 million and cost of sales was $3.3 million; Q3 2025 had no revenue or cost of sales.
Q3 operating expenses were $106.0 million, operating loss was $95.7 million and net loss was $93.711 million, versus $80.293 million net loss in Q3 2025.
Q3 R&D expense was $41.253 million versus $56.473 million YoY; SG&A was $61.430 million versus $27.459 million, reflecting launch investment.
Nine-month revenue was $10.3 million, operating expenses were $343.6 million and net loss was $324.216 million, versus $208.518 million net loss in 9M 2025.
9M cash used in operating activities was $305.9 million versus $171.1 million in 2025, primarily reflecting launch investment.
Outlook and guidance
Potential full FDA approval for adults with primary IgAN is expected in mid-2027, subject to sBLA review; an EMA Marketing Authorisation Application is planned for Q1 2027.
Payer coverage is progressing toward 50% of covered lives by year-end; management expects the demand share of sales to rise in coming quarters.
Atacicept monthly dose-ranging data from de novo cohorts are expected later in Q4 2026; switch-cohort results are expected in Q2 2027.
Expenses and capital expenditures are expected to increase as clinical programs advance and commercial manufacturing, sales, marketing and distribution scale; available resources are expected to fund planned operations for at least 12 months from the filing date.
Latest events from Vera Therapeutics
- ORIGIN 3 showed 76% lower kidney-progression risk with TRUTAKNA through week 104.VERA
Study update - TRUTAKNA's phase III data show strong efficacy and safety, driving rapid U.S. launch momentum.VERA
Morgan Stanley 24th Annual Global Healthcare Conference - Trutakna's launch redefines IgA nephropathy care with strong efficacy, safety, and commercial momentum.VERA
12th Annual Cantor Fitzgerald Global Healthcare Conference - TRUTAKNA launched after FDA accelerated approval; Q2 net loss $109.5M, cash $499.2M.VERA
Q2 2026 - Atacicept stabilized kidney function in IgA nephropathy; phase 3 data expected Q2 2025.VERA
7th Annual Evercore ISI HealthCONx Conference - FDA accelerated approval for TRUTAKNA introduces a novel therapy for adults with IgA nephropathy.VERA
FDA announcement - Atakicept shows strong efficacy and safety in IgAN, with launch and pipeline expansion imminent.VERA
Citi Annual Global Healthcare Conference 2025 - Atacicept nears pivotal data and broad expansion, targeting multiple autoimmune diseases.VERA
R&D Day 2024 - Atacicept achieved a 46% proteinuria reduction and strong safety in phase III IgAN trial.VERA
Study Result