Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
EyeLief + EyeLief-SD is a combination therapy under development by Re-Vana Therapeutics, delivered via a biodegradable sustained-release intravitreal (IVT) implant. The therapy combines EyeLief, which contains the anti-VEGF agent aflibercept, with EyeLief-SD, a bispecific antibody. This combination is designed to provide long-term therapeutic effects for retinal diseases such as wet age-related macular degeneration (wet AMD) and diabetic macular edema (DME) by reducing the frequency of injections. The EyeLief platform uses pre-fabricated implants to ensure controlled drug release over several months. While aflibercept targets vascular endothelial growth factor (VEGF), the specific targets of the bispecific antibody in EyeLief-SD remain undisclosed.
Beyond the preview
Explore the evidence, development activity, and competitive landscape with Gosset’s full data platform.
Follow clinical development from study design and recruitment through results.
Explore development by indication, patient population, and geography.
Trace asset ownership, licensing agreements, and commercial partnerships.
Explore the patent landscape and regulatory exclusivity around an asset.
Compare development programs by target, modality, and indication.
Connect source evidence and development news to your research questions.
See how Gosset can support your research on EyeLief + EyeLief-SD.