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Spots Global Cancer Trial Database for A Study of AC682 for the Treatment of Locally Advanced or Metastatic ER+ Breast Cancer

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Trial Identification

Brief Title: A Study of AC682 for the Treatment of Locally Advanced or Metastatic ER+ Breast Cancer

Official Title: A Phase I Clinical Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Preliminary Anti-Tumor Activity of AC682 in Patients With Estrogen Receptor Positive/Human Epidermal Growth Factor Receptor 2 Negative (ER+/HER2-) Locally Advanced or Metastatic Breast Cancer

Study ID: NCT05080842

Conditions

Breast Cancer

Interventions

AC682

Study Description

Brief Summary: This clinical trial is evaluating a drug called AC682 in participants with estrogen receptor positive/human epidermal growth factor 2 negative (ER+/HER2-) locally advanced or metastatic breast cancer. The main goals of this study are to: * Identify the recommended dose of AC682 that can be given safely to participants * To evaluate the side effects of AC682 * To evaluate pharmacokinetics of AC682 * To evaluate the effectiveness of AC682

Detailed Description: This is a Phase I, first in human, open-label dose-escalation study of AC682, an orally available estrogen receptor degrader, given as a single agent.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Site 01, Denver, Colorado, United States

Site 04, Orlando, Florida, United States

Site 02, Sarasota, Florida, United States

Site 03, Nashville, Tennessee, United States

Site 05, Houston, Texas, United States

Contact Details

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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