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RECRUITING
NCT06800313
PHASE1/PHASE2

A Study of HLD-0915 in Patients With Metastatic Castration Resistant Prostate Cancer (mCRPC)

Sponsor: Halda Therapeutics OpCo, Inc.

View on ClinicalTrials.gov

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

DRUG

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