Skyline Therapeutics Receives the US FDA’s IND Clearance of SKG0106 for Neovascular Age-related Macular Degeneration
Shots:
- The US FDA has cleared an IND application to initiate the P-I/IIa trial evaluating SKG0106, a novel intravitreally delivered AAV gene therapy for nAMD. The trial is expected to be initiated shortly
- SKG0106 showed a potent efficacy of inhibition of intraocular neovascularization in comprehensive preclinical studies with a favorable safety profile, and long-lasting durability, following a single IVT administration
- SKG0106 was a safe and effective anti-angiogenic therapy in preclinical proof-of-concept tests, with durable suppression of neovascular lesions with a low-dose single IVT injection. This prevented choroidal or retinal neovascularization and relieved retinal edoema and vascular leakage
Ref: Skyline | Image: Skyline
Related News:- BioMarin Collaborates with Skyline to Develop and Commercialize AAV Gene Therapies for Genetic Cardiovascular Diseases
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