CU06 (Rivasterat) – DME

An oral drug candidate designed to normalize endothelial dysfunction

Therapeutic Function of CU06 in Diabetic Macular Edema

Therapeutic Function of CU06 in Diabetic Macular Edema

Ph2a results of Rivasterat

Dose- & treatment duration-dependent BCVA improvement in patients with poor vision

Ph2a results of Rivasterat

Modality

Oral small molecule

Mechanism of Action

Vascular normalization and functional restoration through improvement of endothelial dysfunction
(Active ingredient: Rivasterat)

Indication

Diabetic macular edema (DME)

Development Status

U.S. Phase 2a clinical study report (CSR) received (2024.04)
U.S. IND submission for Phase 2b planned in 2026

Key Differentiators

A differentiated therapeutic approach focused on endothelial dysfunctionVisual acuity improvement and safety observed in a Phase 2a trialOral administration designed to offer greater treatment convenience than intravitreal injections

Market Opportunity

As an oral candidate, CU06 has the potential to reduce the treatment burden associated with intravitreal anti-VEGF therapy, the current standard of care. Subject to further clinical validation, it aims to expand treatment options for patients and clinicians as a standalone therapy or as a complementary treatment alongside existing therapies.

Development & Partnerships

Pursuing global out-licensing opportunities