Biopharma Transcript

Kamada Ltd KMDA

Nasdaq · Phase 3 · infectious disease · biologic-other · EDGAR · Updated Oct 24, 2026

Kamada Ltd (Nasdaq: KMDA) is an infectious disease drug developer. Its lead program, KEDRAB (rabies immune globulin), is in Phase 3 for rabies post-exposure prophylaxis. Its next catalyst on record is Normal source plasma: start of NSP sales (H2 2026).

Upcoming catalysts

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

Next further out: Normal source plasma — start of NSP sales (H2 2026). 1 catalyst on record beyond the next 30 days; subscribers see each with its filing sentence.

Pipeline

ProgramIndicationModalityStage
KEDRABrabiesbiologic-otherApproved
GLASSIAalpha-1 antitrypsin deficiencyprotein/peptideApproved
CYTOGAMCMV prophylaxisbiologic-otherApproved
WINRHO SDFITP / Rh isoimmunizationbiologic-otherApproved
VARIZIGvaricella zoster post-exposurebiologic-otherApproved
HEPAGAM Bhepatitis Bbiologic-otherApproved
Inhaled AATAATD (orphan designation US and EU)protein/peptidePhase 3

Recent results and decisions

  1. Dec 8, 2025
    negative Prespecified interim futility analysis found Phase 3 InnovAATe unlikely to show a significant benefit in FEV1; trial discontinued, no safety concerns.the Phase 3 InnovAATe trial of Inhaled AAT for the treatment of Alpha-1 Antitrypsin Deficiency (AATD) is unlikely to demonstrate a statistically significant benefit in its primary endpoint - lung function measured by FEV1. Filing

For subscribers

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