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A Study of HLD-0915 in Patients With Metastatic Castration Resistant Prostate Cancer (mCRPC)
Sponsor: Halda Therapeutics OpCo, Inc.
Summary
Assessment of the safety and efficacy of HLD-0915 as monotherapy in patients with metastatic castration resistant prostate cancer (mCRPC) that have progressed on prior systemic therapies, once a recommended dose for expansion (RDE) has been determined in Phase 1 of the trial.
Official title: Phase 1/2 Study of HLD-0915 in Patients With Metastatic Castration Resistant Prostate Cancer (mCRPC)
Key Details
Gender
MALE
Age Range
18 Years - Any
Study Type
INTERVENTIONAL
Enrollment
33
Start Date
2025-02-24
Completion Date
2027-03
Last Updated
2025-10-16
Healthy Volunteers
No
Interventions
HLD-0915
A treatment cycle consists of 21 days. Treatment may continue until disease progression or study discontinuation (withdrawal of consent, intercurrent illness, unacceptable adverse event or any other changes unacceptable for further treatment, etc.)
Locations (11)
Sarah Cannon Research Institute at HealthONE
Denver, Colorado, United States
Yale - New Haven Hospital - Yale Cancer Center
New Haven, Connecticut, United States
Florida Cancer Specialists
Sarasota, Florida, United States
Massachusetts General Hospital
Boston, Massachusetts, United States
START Midwest, LLC
Grand Rapids, Michigan, United States
Evelyn H. Lauder Breast and Imaging Center (BAIC)
New York, New York, United States
Carolina Urologic Research Center, LLC
Myrtle Beach, South Carolina, United States
SCRI Oncology Partners
Nashville, Tennessee, United States
NEXT Austin
Austin, Texas, United States
The University of Texas M.D. Anderson Cancer Center
Houston, Texas, United States
Royal Marsden Hospital
Sutton, Surrey, United Kingdom