Clinical Trials Directory

Trials / Recruiting

RecruitingNCT05608252

VS-6766+Abema+Fulv in Met HR+/HER- BC

A Single Arm Phase 1/2 Trial of Abemaciclib + VS-6766 + Fulvestrant in Metastatic HR+/HER2- Breast Cancer

Status
Recruiting
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
63 (estimated)
Sponsor
Adrienne G. Waks · Academic / Other
Sex
All
Age
18 Years
Healthy volunteers
Not accepted

Summary

This research is being done to evaluate the safety and effectiveness of a drug currently known as VS-6766 in combination with the drugs abemaciclib and fulvestrant in HR+/HER2-negative breast cancer. The names of the study drugs involved in this study are: * VS-6766 * Abemaciclib * Fulvestrant

Detailed description

This is single-arm open-label phase 1/2 trial assessing the safety and efficacy of the new drug, VS-6766, plus abemaciclib and fulvestrant in treating metastatic hormone receptor-positive and HER2-negative (HR+/HER2-) breast cancer. VS-6766 is a unique small molecule drug that targets and interrupts a pathway that allows cancer cells to grow.The U.S. Food and Drug Administration (FDA) has not approved VS-6766 as a treatment for any disease. The FDA has approved abemaciclib and fulvestrant as a treatment option for breast cancer. The study is divided into three study periods: a screening period; a treatment period; and a post-treatment follow-up period. Participants will receive study treatment for as long there are no serious side effects and the disease does not get worse. It is expected that about 63 people will take part in this research study. Verastem Oncology, a biopharmaceutical company, is supporting this research study by providing VS-6766 and funding to conduct this trial. Eli Lilly, a pharmaceutical company, is supporting this research study by providing the drug, abemaciclib.

Conditions

Interventions

TypeNameDescription
DRUGVS-6766Taken Orally
DRUGAbemaciclibTaken Orally
DRUGFulvestrantAdministered by intramuscular injection

Timeline

Start date
2023-02-23
Primary completion
2027-12-31
Completion
2028-12-31
First posted
2022-11-08
Last updated
2025-10-29

Locations

3 sites across 1 country: United States

Regulatory

Source: ClinicalTrials.gov record NCT05608252. Inclusion in this directory is not an endorsement.