Biopharma Transcript

First Tracks Biotherapeutics, Inc. TRAX

Nasdaq · Phase 2 · immunology/inflammation · antibody · EDGAR · Updated Oct 24, 2026

First Tracks Biotherapeutics, Inc. (Nasdaq: TRAX) is an immunology/inflammation drug developer. Its lead program, Rosnilimab, is in Phase 2 for rheumatoid arthritis. Its next catalyst on record is ANB033: Cohort 2 enrollment completing imminently; topline Q1 2027. (Q1 2027).

Upcoming catalysts

No catalyst is dated to the next 30 days or to an FDA action date.

Next further out: ANB033 — Cohort 2 enrollment completing imminently; topline Q1 2027. (Q1 2027). 1 catalyst on record beyond the next 30 days; subscribers see each with its filing sentence.

Pipeline

ProgramIndicationModalityStage
Rosnilimabrheumatoid arthritis (Phase 2b completed; EOP2 meeting held Q1 2026)antibodyPhase 2
Rosnilimabulcerative colitis (Phase 2, not positive)antibodyPhase 2
ANB033celiac disease (Phase 1b, ~70 pts, Fast Track)antibodyPhase 1
ANB033eosinophilic esophagitis (Phase 1b, 50 pts)antibodyPhase 1
ANB101BDCA2 modulator, autoimmune (healthy-volunteer Phase 1 completed Aug 2026)antibodyPhase 1

Recent results and decisions

  1. Oct 19, 2026
    n/a First Tracks Biotherapeutics closed private placement of 6,106,870 shares of common stock on October 19, 2026.On October 19, 2026 (the 'Closing Date'), First Tracks Biotherapeutics, Inc. (the 'Company') closed its previously announced private placement (the 'Private Placement') of an aggregate 6,106,870 shares (the 'Shares') of the Company's common stock, par value $0.001 per share. Filing
  2. Oct 12, 2026
    met Cohort 1 met key endpoints: Vh:Cd change -0.17 vs -0.66 placebo (+0.49, p=0.009); IEL density -20.03 vs placebo (p<0.001); symptoms prevented; no SAEs.ANB033 achieved a statistically significant and clinically meaningful protective effect on both gluten-induced intestinal damage and symptoms Filing
  3. Aug 12, 2026
    n/a FDA granted Fast Track designation to ANB033 for celiac disease.U.S. FDA granted Fast Track designation for ANB033 for the treatment of CeD Filing

For subscribers

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