Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Corneal epithelial stem cell supernatant is a topical biologic therapy developed by researchers at the Texas Tech University Health Sciences Center (TTUHSC) for the treatment of severe dry eye disease (DED). The product is derived from the secretome of expanded human corneal epithelial stem cells (CESCs) harvested from donor limbal tissue. Unlike traditional stem cell therapies that require surgical transplantation, this approach uses a cell-free supernatant formulated as eye drops, which contains various growth factors and cytokines that promote the regeneration of damaged ocular surface tissues and reduce inflammation. A pilot clinical study published in 2021 demonstrated that the therapy significantly improved patient-reported outcomes, including SPEED and OSDI scores, in individuals with severe DED who were refractory to conventional treatments. The therapy is currently undergoing further validation in double-blinded clinical trials.
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 corneal epithelial stem cell supernatant.