A Study of DS9051b in Participants With Advanced or Metastatic Adrenocortical Carcinoma and Metastatic Castration-resistant Prostate Cancer
This FIH study is designed to assess the safety, tolerability, and preliminary efficacy signals of DS9051b in participants with ACC and mCRPC.
Trial Details
- NCT ID
- NCT07189403
- Phase
- PHASE1
- Sponsor
- Daiichi Sankyo
- Status
- RECRUITING
- Cancer Type
- Castration-Resistant (CRPC) Prostate Cancer
- Interventions
- Locations (sample)
- Sarasota, Florida, United States|27.33643,-82.53065
- New York, New York, United States|40.71427,-74.00597
- Providence, Rhode Island, United States|41.82399,-71.41283
- Toulouse, France|43.60426,1.44367
- Villejuif, France|48.7939,2.35992
Key Eligibility Criteria
- Sign and date the main ICF, prior to the start of any trial-specific procedures.
- Adults ≥18 years of age at the time the ICF is signed (Follow local regulatory requirements if the legal age of consent for trial participation is …
- Histologically confirmed diagnosis of ACC or adenocarcinoma of the prostate
- ECOG PS of 0 or 1 assessed no more than 14 days prior to C1D1. (ECOG PS of 2 due to cancer pain is acceptable)
For full eligibility, visit ClinicalTrials.gov.