Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
NCT06801236 · ClinicalTrials.gov registry record · Phase 1
Phase 1 Study of ACE-232 to Treat Patients With Metastatic Castration-Resistant Prostate Cancer
A Phase 1 study of Prostate Cancer (Adenocarcinoma) and mCRPC (Metastatic Castration-resistant Prostate Cancer), sponsored by Acerand Therapeutics (Hong Kong) Limited.
- Recruiting
- Registry status
- Phase 1
- Development phase
- 67
- Enrollment target
- 8
- Study locations
NCT06801236 is a Phase 1 study of Prostate Cancer (Adenocarcinoma) and mCRPC (Metastatic Castration-resistant Prostate Cancer) that is actively recruiting participants, run by Acerand Therapeutics (Hong Kong) Limited. The registered enrollment target is 67 participants, below the 125-participant average among 13 other Prostate Cancer (Adenocarcinoma) trials with a reported enrollment target (46% lower). The trial reports 8 study locations across 8 states.
The verdict
NCT06801236, a Phase 1 study of Prostate Cancer (Adenocarcinoma) and mCRPC (Metastatic Castration-resistant Prostate Cancer), is actively recruiting participants, sponsored by Acerand Therapeutics (Hong Kong) Limited.
- RECRUITING
- Registry status
- Phase 1
- Development phase
- 67 participants
- Enrollment target
- 8
- Study locations
Study Summary
This is an open label, phase I, multi-center study aiming to assess the safety and tolerability in patients with metastatic castration resistant prostate cancer (mCRPC).
Conditions Studied
Interventions
- DRUG ACE-232 tablets
Study Locations (8)
California
- University of California San Diego, Moores Cancer Center - La Jolla
Florida
- Moffitt Cancer Center, Tampa - Tampa
Maryland
- University of Maryland, Greenebaum Comprehensive Cancer Center - Baltimore
Massachusetts
- Harvard Medical School-Massachusetts General Hospital - Boston
Minnesota
- M Health Fairview Clinics and Surgery Center - Minneapolis
Nebraska
- Xcancer (Urology Cancer Center) - Omaha
South Carolina
- Carolina Urologic Research Center - Myrtle Beach
Washington
- Fred Hutchinson Cancer Research Center - Seattle
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 67 participants |
| Start Date | 2025-05-12 |
| Est. Completion | 2028-08-01 |
| Phase | Phase 1 |
Interested in This Trial?
Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT06801236
The ClinicalTrials.gov registry entry for NCT06801236 describes a study currently listed as recruiting, categorized as Phase 1. The registered enrollment target is 67 participants, a figure that helps gauge the scale of data the investigators plan to collect, below the 125-participant average among 13 other Prostate Cancer (Adenocarcinoma) trials with a reported enrollment target (46% lower). The listed sponsor is Acerand Therapeutics (Hong Kong) Limited, which has 1 total studies on file at ClinicalTrials.gov.
The record links to 2 conditions, with Prostate Cancer (Adenocarcinoma) appearing as the primary indexed condition, and to 1 intervention - of which ACE-232 tablets is the first listed.
NCT06801236 reports 8 study locations spanning 8 distinct geographic areas - top geographies include California, Florida, Maryland.
Frequently Asked Questions
What is clinical trial NCT06801236 about?
NCT06801236 is a clinical study titled "Phase 1 Study of ACE-232 to Treat Patients With Metastatic Castration-Resistant Prostate Cancer". This is an open label, phase I, multi-center study aiming to assess the safety and tolerability in patients with metastatic castration resistant prostate cancer (mCRPC).
What is the current status of trial NCT06801236?
This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 67 participants. The study started on 2025-05-12. Estimated completion is 2028-08-01.
What conditions does trial NCT06801236 study?
This clinical trial studies the following conditions: Prostate Cancer (Adenocarcinoma), mCRPC (Metastatic Castration-resistant Prostate Cancer).
What interventions are being tested in trial NCT06801236?
The interventions under investigation include: ACE-232 tablets (DRUG).
Who is sponsoring clinical trial NCT06801236?
This trial is sponsored by Acerand Therapeutics (Hong Kong) Limited, which has 1 total clinical trials registered on ClinicalTrials.gov.
Where is trial NCT06801236 being conducted?
This trial has 8 study locations across California, Florida, Maryland, Massachusetts, Minnesota. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
Learn More About Clinical Trials
Similar trials for Prostate Cancer (Adenocarcinoma)
Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.
-
Neoadjuvant Darolutamide and Relugolix Combination Preceding Radical Prostatectomy for Prostate Cancer
RECRUITING · Phase 1
-
A Study of HLD-0915 in Patients With Metastatic Castration Resistant Prostate Cancer (mCRPC)
RECRUITING · Phase 1
-
Neoadjuvant High Dose Rate Brachytherapy Prior to Radical Prostatectomy in Patients With Prostate Cancer
RECRUITING · Phase 1
-
PSMA PET for Surveillance After Focal Therapy
RECRUITING · NA
-
FK-PC101 as Adjuvant Therapy for Men With High-Risk Prostate Cancer
RECRUITING · Phase 2
-
Flotufolastat F 18 PET in Men With Very Low PSA Recurrence
RECRUITING
Explore more on PlainTrial
Prostate Cancer (Adenocarcinoma)
All registered trials for this condition
mCRPC (Metastatic Castration-resistant Prostate Cancer)
All registered trials for this condition
California
All trials with a study site in California
Recruiting now
Find trials open to new participants near you
Rankings
Top sponsors, conditions, and phases
Read our methodology - how this data is sourced, computed, and verified.
Related
Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.