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Endogena Therapeutics

Ownership: Private
Development stage: Phase 1

Overview

Endogena Therapeutics has advanced its lead program EA‑2353 into Phase 1/2 clinical trials for retinitis pigmentosa, with Fast Track designation from the FDA. Early data show preliminary evidence of efficacy. The company also received IND clearance from the FDA to begin clinical investigation of EA‑2351 in geographic atrophy secondary to AMD. Additional programs are in earlier stages targeting dry AMD, idiopathic pulmonary fibrosis, and hematopoietic recovery.

Therapeutic areas: OphthalmologyHematologyPulmonology
Modalities: Small molecules (selective regulation of endogenous adult stem and progenitor cells)
Industry: Biotech

Drug pipeline

3 assets

EA-2351

Unknown

2 more assets in the full pipeline.

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Partnerships

JLABS Toronto (Johnson & Johnson Innovation incubator site hosting R&D facility)

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