Biopharma Transcript

Edesa Biotech, Inc. EDSA

Nasdaq · Phase 3 · respiratory · antibody · EDGAR · Updated Oct 24, 2026

Edesa Biotech, Inc. (Nasdaq: EDSA) is a respiratory drug developer. Its lead program, EB05 (paridiprubart), is in Phase 3 for Acute Respiratory Distress Syndrome (ARDS). Its next catalyst on record is EB06: Start of Phase 2 proof-of-concept enrollment in vitiligo (Health Canada approved; FDA IND CMC information being provided) (date not stated).

Upcoming catalysts

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

Next further out: EB06 — Start of Phase 2 proof-of-concept enrollment in vitiligo (Health Canada approved; FDA IND CMC information being provided) (date not stated). 1 catalyst on record beyond the next 30 days; subscribers see each with its filing sentence.

Pipeline

ProgramIndicationModalityStage
EB05 (paridiprubart)ARDS (truncated Phase 3 reported Oct 2025; ongoing US government-funded platform study)antibodyPhase 3
EB01 (daniluromer 1.0% cream)chronic Allergic Contact Dermatitis (Phase 3-ready, at partnering stage)small moleculePhase 2
EB06moderate-to-severe nonsegmental vitiligoantibodyPhase 1

Recent results and decisions

  1. Feb 24, 2026
    met Additional Phase 3 data in the full 278-patient population: adjusted 28-day mortality 24% vs 33% on placebo (27% relative reduction, p<0.001).Paridiprubart reduced adjusted 28-day mortality to 24% from 33%, a 27% relative reduction in the risk of death (p<0.001). Filing

For subscribers

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