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RECRUITING
NCT07540572
PHASE1

A Study to Investigate the Safety, Pharmacokinetics, and Preliminary Efficacy of IDE574 Therapy in Adult Participants With Advanced Solid Tumors

Sponsor: IDEAYA Biosciences

View on ClinicalTrials.gov

Summary

IDE574 is a synthetically manufactured small molecule inhibitor that co-targets the lysine acetyltransferase enzymes KAT6 and KAT7. The purpose of this study is to evaluate the safety, preliminary efficacy, pharmacokinetics (PK), and pharmacodynamics (PD) of IDE574 as monotherapy in participants with locally advanced or metastatic solid tumors and as combination therapy with fulvestrant in participants with advanced or metastatic ER+, HER2- breast cancer.

Official title: An Open Label, Multicenter Study to Evaluate the Safety, Pharmacokinetics, Pharmacodynamics, and Preliminary Efficacy of IDE574 as Monotherapy in Locally Advanced or Metastatic Solid Tumors and as Combination Therapy With Fulvestrant in Locally Advanced or Metastatic ER+, HER2- Breast Cancer

Key Details

Gender

All

Age Range

18 Years - 99 Years

Study Type

INTERVENTIONAL

Enrollment

160

Start Date

2026-03-17

Completion Date

2030-06-30

Last Updated

2026-06-16

Healthy Volunteers

No

Interventions

DRUG

IDE574

IDE574

DRUG

Fulvestrant injection

Fulvestrant Injection

Locations (11)

Florida Clinical Trials Group

Plantation, Florida, United States

START Astera, LLC

East Brunswick, New Jersey, United States

START New York Long Island, LLC

Lake Success, New York, United States

NEXT Texas LLC - Austin

Austin, Texas, United States

NEXT Texas LLC - Dallas

Dallas, Texas, United States

START Dallas Fort Worth, LLC

Fort Worth, Texas, United States

NEXT Texas LLC - Houston

Houston, Texas, United States

NEXT Texas LLC - San Antonio

San Antonio, Texas, United States

Start San Antonio, LLC

San Antonio, Texas, United States

START Mountain Region, LLC

West Valley City, Utah, United States

NEXT Virginia

Fairfax, Virginia, United States