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Vera Therapeutics, Inc.

Pipeline3 assets

  • AtaciceptVT-001 / BAFF and APRIL / Recombinant Fusion Protein / Immunology / Nephrology
    IgA Nephropathy (IgAN)BLA SubmittedPriority Review (PDUFA July 2026)USGlobalLupus NephritisPhase 2OngoingGlobalFocal Segmental Glomerulosclerosis (FSGS)Phase 2OngoingGlobal
  • MAU868MAU868 / BK Virus / Monoclonal Antibody / Infectious Disease / Transplantation
    BK Viremia in Kidney Transplant RecipientsPhase 2Evaluating for future developmentGlobal
  • VT-109VT-109 / BAFF and APRIL / Fusion Protein / Immunology
    B Cell Mediated DiseasesPreclinicalActiveGlobal

Latest news15 items

All news

Vera Therapeutics Announces ORIGIN 3 Final Efficacy Analysis of TRUTAKNA™ (atacicept-vymj) in IgA Nephropathy Will be A Featured Late-breaking Oral Presentation at the Opening Plenary Session of ASN Kidney Week 2026

BRISBANE, Calif., Oct. 02, 2026 (GLOBE NEWSWIRE) -- Vera Therapeutics, Inc. (Nasdaq: VERA), a commercial-stage biotechnology company, today announced that there will be multiple presentations at the American Society of Nephrology (ASN) Kidney Week 2026 in Denver, Colorado, from October 22 to 25.

Presentation / AbstractASN Kidney Week late-breaking oral presentation Thu, Oct 22, 2026, 9:05 AM MDT

Vera Therapeutics Announces TRUTAKNA™ (atacicept-vymj) Stabilized eGFR and Prevented Kidney Disease Progression Through Two Years in ORIGIN 3 Final Efficacy Analysis in IgA Nephropathy

TRUTAKNA, the first and only FDA-approved BAFF and APRIL inhibitor, met all prespecified endpoints, including unprecedented placebo-adjusted estimated glomerular filtration rate (eGFR) and composite kidney disease progression benefits. Favorable safety profile, and generally comparable to placebo.

Trial Results • Phase 3ORIGIN 3 final efficacy analysis results Tue, Sep 15, 2026

Vera Therapeutics to Participate at Upcoming Investor Conferences

BRISBANE, Calif., Sept. 01, 2026 (GLOBE NEWSWIRE) -- Vera Therapeutics, Inc. (Nasdaq: VERA), a commercial-stage biotechnology company, today announced that the Company’s management team will present and participate in one-on-one meetings at upcoming investor conferences.

Vera Therapeutics Announces Alignment with U.S. FDA on Earlier ORIGIN Phase 3 Analysis to Support Potential Full Approval for Atacicept in Adults with IgA Nephropathy

Prescription Drug User Fee Act (PDUFA) date of July 7, 2026 for Biologics License Application (BLA) for accelerated approval of atacicept in patients with IgA Nephropathy (IgAN) Revised ORIGIN 3 eGFR analysis now planned for Q3 2026, pulled forward from 2027 Pending positive eGFR analysis, plans to

Interim Data • Phase 3ORIGIN 3 eGFR analysis Wed, Jul 1, 2026
Vera Therapeutics, Inc. • Endpoint Arena