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  • Organizations: Surrozen
FDA clears Surrozen's IND for DME therapy
Pipeline

FDA clears Surrozen's IND for DME therapy

First patient dosing in the DUET trial planned for later this year; study will be the first to evaluate humans treated with the bifunctional antibody.
Surrozen submits IND to FDA for DME therapeutic
Pipeline

Surrozen submits IND to FDA for DME therapeutic

Phase 1b/2a study to evaluate a bifunctional Wnt agonist and VEGF antagonist antibody that targets vascular leakage and promote retinal vascular integrity
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