Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
TAEST16001 is an autologous, affinity-enhanced, NY‑ESO‑1 antigen-specific, transduced T-cell receptor (TCR) therapy. Patient-derived (autologous) lymphocytes are genetically modified using a lentiviral vector to express a high-affinity engineered NY‑ESO‑1–specific TCR. The product is designed to target and kill tumor cells expressing the cancer-testis antigen NY‑ESO‑1 in HLA-A*02:01 positive patients. It is being developed primarily for advanced soft tissue sarcoma and has shown promising clinical activity with an overall response rate of approximately 41.7% in early-phase trials, with acceptable safety and no dose-limiting toxicities observed[2][3][4][5]. The developers include several Chinese academic and industry partners.
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 TAEST16001.