First-in-Human Trial of DS-2243a in Participants With Advanced Solid Tumors
This 2-part study will evaluate safety, tolerability, and clinical efficacy of DS-2243a as a treatment for participants with advanced solid tumors.
Trial Details
- NCT ID
- NCT06644755
- Phase
- PHASE1
- Sponsor
- Daiichi Sankyo
- Status
- RECRUITING
- Cancer Type
- Liposarcoma Sarcoma
- Interventions
- Locations (sample)
- Boston, Massachusetts, United States|42.35843,-71.05977
- New York, New York, United States|40.71427,-74.00597
- Nashville, Tennessee, United States|36.16589,-86.78444
- Leuven, Belgium|50.87959,4.70093
- Lyon, France|45.74906,4.84789
Key Eligibility Criteria
- Sign and date the main ICF.
- Adults ≥18 years at the time the biosample ICF or main ICF, whichever is signed first.
- Follow local regulatory requirements if the legal age of consent for trial participation is \>18 years old.
- One of the following histologically or cytologically documented cancers:
For full eligibility, visit ClinicalTrials.gov.