Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Tanfanercept is a molecularly engineered recombinant fusion protein designed as a fragment of tumor necrosis factor receptor 1 (TNFR1) with high affinity for tumor necrosis factor alpha (TNF-α) and resistance to degradation by proteinases. It acts as a topical anti-inflammatory agent by selectively binding to and neutralizing TNF-α, a key cytokine mediating inflammation in dry eye disease (DED). Tanfanercept is being developed primarily for the treatment of moderate-to-severe DED and has shown statistically significant improvements in tear volume and other clinical endpoints in Phase III trials. The drug is co-developed by HanAll Biopharma and Daewoong Pharmaceutical, with additional development involvement from Harbour BioMed. Its small molecular size (~19 kDa) allows efficient ocular distribution when administered topically[1][3][4][5][6][8].
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 tanfanercept.