Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
NW-101C is an autologous T-cell receptor engineered T-cell (TCR-T) therapy developed by Neowise Biotechnology for the treatment of advanced solid malignant tumors. The therapy targets the Preferentially Expressed Antigen in Melanoma (PRAME), a cancer/testis antigen that is highly expressed in various solid tumors—including melanoma, lung cancer, and ovarian cancer—while maintaining restricted expression in healthy tissues. NW-101C utilizes T-cells genetically modified to express a high-affinity, natural TCR discovered via Neowise's proprietary CAST® (antigen-TCR pairing) platform. This TCR specifically recognizes a PRAME-derived peptide presented by the HLA-A*02:01 major histocompatibility complex (MHC). The drug is currently undergoing Phase 1 dose-escalation clinical trials to evaluate its safety, tolerability, and preliminary efficacy in patients with metastatic or heavily pretreated solid tumors that are HLA-A*02:01 positive and express the PRAME antigen.
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 NW-101C.