Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
BS01 is a recombinant adeno-associated virus (AAV)-based gene therapy developed for the treatment of retinitis pigmentosa. It expresses an enhanced light-sensitive channelrhodopsin gene, which encodes optogenetic proteins that activate the optic nerve directly, bypassing damaged retinal photoreceptors. The therapy aims to restore vision by enabling light perception and object recognition in patients with advanced retinal degeneration. Delivered as a one-time intravitreal injection, BS01 has shown promising results in early clinical trials, including significant improvements in light sensitivity and visual acuity without serious safety concerns. The therapy is paired with a device that sends signals to the treated ganglion cells to further enhance visual function[1][2][3][5][6].
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 BS01.