Corporate presentation
Logotype for Jade Biosciences Inc

Jade Biosciences (JBIO) Corporate presentation summary

Event summary combining transcript, slides, and related documents.

Logotype for Jade Biosciences Inc

Corporate presentation summary

13 Nov, 2026

Portfolio and funding

  • Three Paragon-licensed candidates target autoimmune diseases: JADE101, an anti-APRIL antibody for IgAN; JADE201, an anti-BAFF-R antibody for systemic autoimmune diseases; and JADE301, an anti-IFN-β antibody for dermatomyositis.

  • Cash runway extends into Q4 2028; planned milestones include JADE101 Phase 3 initiation in 4Q 2026 and interim Phase 2 data in 2Q 2027, JADE201 interim Phase 1 data in 2027, and JADE301 Phase 1 initiation in 4Q 2026 with interim data in 2H 2027.

JADE101 for IgAN

  • The presentation estimates a $20B+ potential U.S. market and 169K+ U.S. patients; 60–75% are estimated to require treatment under international guidelines.

  • Phase 1 data showed ~70% IgA reduction sustained for 12 weeks at 700 mg, rapid and sustained free APRIL suppression, and a 24.2-day half-life at the 700 mg induction dose.

  • JADE101 was well tolerated across tested doses in 32 healthy volunteers; no severe adverse events, serious adverse events, deaths, or discontinuations due to adverse events were reported.

  • A 700 mg induction dose followed by 350 mg maintenance is planned for Q12W or Q8W dosing; the ongoing Phase 2 trial is evaluating both schedules, with interim data anticipated in 2Q 2027.

  • The planned Phase 3 trial is expected to start in 4Q 2026, with ~420 participants randomized 2:1 to JADE101 or placebo for Year 1, followed by JADE101 for all participants in Year 2.

JADE201 for autoimmune diseases

  • JADE201 combines BAFF-R blockade and enhanced antibody-dependent cellular cytotoxicity; its dual mechanism is designed to deplete B cells and limit BAFF-mediated repopulation.

  • In non-human primates, JADE201 showed dose-dependent pharmacokinetics, complete receptor occupancy at doses above 1 mg/kg, and a 5.4-day half-life versus 2.7 days for ianalumab.

  • A first-in-human, randomized, placebo-controlled, single-ascending-dose Phase 1 study is underway in adults with rheumatoid arthritis; interim data are expected in 2027.

  • Potential indications include lupus nephritis, immune thrombocytopenia, Sjögren's disease, primary membranous nephropathy, ANCA-associated vasculitis, and rheumatoid arthritis.

Partial view of Summaries dataset, powered by Quartr API
AI can get things wrong. Verify important information.
All investor relations material. One API.
Learn more

Latest events from Jade Biosciences