CM518D1
/ Keymed Biosciences
- LARVOL DELTA
Home
Next
Prev
1 to 4
Of
4
Go to page
1
November 18, 2025
Study of CM518D1 in Patients With Advanced Solid Tumors
(clinicaltrials.gov)
- P1/2 | N=434 | Recruiting | Sponsor: Keymed Biosciences Co.Ltd | Not yet recruiting ➔ Recruiting
Enrollment open • Solid Tumor
June 13, 2025
Study of CM518D1 in Patients With Advanced Solid Tumors
(clinicaltrials.gov)
- P1/2 | N=434 | Not yet recruiting | Sponsor: Keymed Biosciences Co.Ltd
New P1/2 trial • Solid Tumor
April 24, 2025
Keymed Biosciences Announces Approval of IND for CM518D1 by the National Medical Products Administration of China for the Treatment of Gastrointestinal Cancers
(PRNewswire)
- "Keymed Biosciences Inc....received Investigational New Drug (IND) approval from the Center for Drug Evaluation (CDE) of the National Medical Products Administration (NMPA), and is currently undergoing Phase I/II clinical trials in China for the treatment of solid tumors....Future studies aim to provide a more precise, effective, and safe therapeutic option for patients worldwide with gastrointestinal cancers."
New P1/2 trial • Gastrointestinal Cancer • Solid Tumor
March 26, 2025
Keymed Biosciences Announces Annual Results of 2024
(GlobeNewswire)
- "CM518D1 (CDH17 ADC): We submitted IND application to CDE, and planned to conduct a multi-center, open-label Phase I/II clinical trial for evaluation of CM518D1 in treatment of patients with advanced solid tumors."
New P1/2 trial • Solid Tumor
1 to 4
Of
4
Go to page
1