๐๏ธ Verified NIH Record โข Updated 2026-07-09
A Study of PARG Inhibitor IDE161 in Participants With Advanced Solid Tumors (NCT05787587)
๐ต Active, Not Recruiting Phase1 ๐ Investigational Drug / Biologic Sponsor: IDEAYA Biosciences
๐ฉบ Plain-English Summary (8th-Grade Level)
The purpose of this study is to characterize the safety, tolerability, and efficacy of IDE161 as a single agent and in combination with pembrolizumab.
Who can join: Review the eligibility criteria below.
Location: HonorHealth Research Institute โ Phoenix, Arizona
Age range: 18 Years
๐งช Interventions in This Study
๐ "Do I Qualify?" โ 1-Minute Self Screener
Instant ChecklistFull eligibility criteria are available on the official NIH protocol. View the criteria โ
๐ All Participating Trial Locations (27 Sites)
Showing the first 25 of 27 sites.
- HonorHealth Research Institute โ Phoenix, Arizona
- The Angeles Clinic โ Los Angeles, California
- Hoag Memorial Hospital โ Newport Beach, California
- California Pacific Medical Center โ San Francisco, California
- Sarah Cannon Research Institute โ Denver, Colorado
- Yale University โ New Haven, Connecticut
- Orlando Health โ Orlando, Florida
- Emory University โ Atlanta, Georgia
- OSF St Francis Medical Center โ Peoria, Illinois
- Indiana University โ Indianapolis, Indiana
- Dana Faber Cancer Institute โ Boston, Massachusetts
- Karmanos Cancer Institute โ Detroit, Michigan
- Comprehensive Cancer Centers of Nevada โ Las Vegas, Nevada
- Roswell Park Comprehensive Cancer Center โ Buffalo, New York
- Columbia University Medical Center โ New York, New York
- Weil Cornell University โ New York, New York
- Sarah Cannon Research Institute - Oklahoma University โ Oklahoma City, Oklahoma
- University of Pennsylvania โ Philadelphia, Pennsylvania
- Sarah Cannon Research Institute - Thomas Jefferson University โ Philadelphia, Pennsylvania
- Sarah Cannon Research Institute โ Nashville, Tennessee
- MD Anderson โ Houston, Texas
- NEXT Oncology โ Irving, Texas
- NEXT Oncology โ San Antonio, Texas
- START Mountain Region โ West Valley City, Utah
- NEXT Oncology โ Fairfax, Virginia
๐ฐ Cost, Insurance & Patient Rights
- 100% Free Items: The investigational treatment and protocol-required procedures are supplied at zero cost by the sponsor.
- Routine Patient Care: Under federal law (ACA ยง 2709) and many state statutes, routine care costs are covered during participation.
- Voluntary Participation: You may withdraw at any time without affecting your standard medical care.
More studies in Advanced or Metastatic Solid Tumors
- A Study of MK-1484 as Monotherapy and in Combination With Pembrolizumab (MK-3475) In Advanced or Metastatic Solid Tumors (MK-1484-001) โ Sioux Falls, South Dakota
- A Study of ERAS-007 as Monotherapy or in Combination With ERAS-601 in Patients With Advanced or Metastatic Solid Tumors โ Denver, Colorado
- A Study to Assess Naporafenib (ERAS-254) Administered With Trametinib in Patients With RAS Q61X Mutations โ San Francisco, California
- Safety and Tolerability of IPH4502 in Patients With Advanced Solid Tumors โ Boston, Massachusetts
- A Dose Escalation/Expansion Study of ERAS-601 in Patients With Advanced or Metastatic Solid Tumors โ Birmingham, Alabama
- A Dose Escalation and Expansion Study of TAC-001 in Patients With Select Advanced or Metastatic Solid Tumors โ Los Angeles, California
Explore by condition: All Advanced or Metastatic Solid Tumors clinical trials
๐ก How to Participate
- Check the checklist above to see if you may qualify.
- Review the official NIH record below to find the coordinating site.
- Ask about the visit schedule, what is covered at no cost, and any travel support.
- Confirm with your own doctor before making a decision.