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Completed Phase 1Phase 2 Interventional

A Study of HSP90 Inhibitor AT13387 Alone or in Combination With Abiraterone Acetate

ClinicalTrials.gov ID: NCT01685268

Public ClinicalTrials.gov record NCT01685268. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 22, 2026, 11:04 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Study of HSP90 Inhibitor AT13387 Alone or in Combination With Abiraterone Acetate in the Treatment of Castration-Resistant Prostate Cancer (CRPC) no Longer Responding to Abiraterone

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

A 2-part, Phase 1-2, open-label, parallel group, randomized study in patients with Castration-Resistant Prostate Cancer (CRPC) who are no longer responding to treatment with abiraterone and steroids. In Part A (Phase 1), patients will continue to receive the same doses of abiraterone and steroids they were receiving prior to study entry and will be randomized to receive 1 of 2 different treatment regimens of AT13387 in combination with abiraterone. Once the best regimen is established in Part A, based on safety and antitumor activity, patients will be randomized to the selected treatment regimen and dose of AT13387 in combination with abiraterone or AT13387 alone in Part B (Phase 2).

Study identification

NCT ID
NCT01685268
Recruitment status
Completed
Study type
Interventional
Phase
Phase 1, Phase 2
Lead sponsor
Astex Pharmaceuticals, Inc.
Industry
Enrollment
49 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
Male
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 2012 (Type not available)
Primary completion
Jul 2014 (Actual)
Completion
Dec 2014 (Actual)
Last update posted
Aug 2, 2024

2012 – 2014

United States locations

U.S. sites
20
U.S. states
12
U.S. cities
19
Facility City State ZIP Site status
University of California, Los Angeles Institute of Urologic Oncology Los Angeles California 90024 —
Stanford Cancer Center Stanford California 94305 —
Holy Cross Hospital Fort Lauderdale Florida 33308 —
Florida Cancer Specialists-Fort Myers Fort Myers Florida 33916 —
Lakeland Regional Cancer Center Lakeland Florida 33805 —
Southern Illinois University School of Medicine Springfield Illinois 62702 —
University of Maryland, Greenebaum Cancer Center Baltimore Maryland 21201 —
Center for Cancer & Blood Disorders Bethesda Maryland 20817 —
Washington University School of Medicine St Louis Missouri 63110 —
University of Nebraska Medical Center Omaha Nebraska 68198 —
Comprehensive Cancer Centers of Nevada Las Vegas Nevada 89169 —
Roswell Park Cancer Institute Buffalo New York 14263 —
Clinical Research Alliance, Inc. Lake Success New York 11042 —
Columbia University Medical Center New York New York 10032 —
Memorial Sloan Kettering Cancer Center New York New York 10065 —
SUNY Upstate Medical University Syracuse New York 13210 —
Cleveland Clinic Cleveland Ohio 44195 —
University of Pittsburgh Medical Center Pittsburgh Pennsylvania 15232 —
The West Clinic Memphis Tennessee 38120 —
Northwest Medical Specialists, PLLC Tacoma Washington 98405 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 12 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01685268, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Aug 2, 2024 · Synced Oct 22, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01685268 live on ClinicalTrials.gov.

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