Clinical trials
Full profile accessFollow clinical development from study design and recruitment through results.
- Trial phase
- Status
- Readouts
Drug intelligence / Profile preview
Ecubectedin (PM14) is a novel small molecule antitumor agent under clinical investigation for the treatment of advanced solid tumors. It is structurally related to the ecteinascidin family (which includes trabectedin and lurbinectedin). Ecubectedin acts as a transcriptional inhibitor by forming DNA adducts that specifically inhibit RNA synthesis and block active transcription of protein-coding genes. This mechanism leads to potent antiproliferative activity in various human solid cancer models both in vitro and in vivo. The drug has demonstrated antitumor effects across multiple tumor types, including soft tissue sarcoma, ovarian, pancreatic, prostate, lung, kidney, gastric, breast, and renal cancers. Clinical trials are ongoing to determine its safety profile and optimal dosing when administered intravenously[3][4][5][7].
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 ecubectedin.