NCT05787587Active, not recruitingPhase 1
A Study of PARG Inhibitor IDE161 in Participants With Advanced Solid Tumors
Source: ClinicalTrials.gov · Last updated 13 Jul 2026
Brief summary (registry, in English)
The purpose of this study is to characterize the safety, tolerability, and efficacy of IDE161 as a single agent and in combination with pembrolizumab.
- Status (registry)
- Active, not recruiting
- Phase (registry)
- Phase 1
- Study type
- Interventional
- Enrollment
- 216 (estimated)
- First submitted
- 17 Mar 2023
- Start date
- 18 Apr 2023
- Primary completion date
- Oct 2026
- Lead sponsor
- IDEAYA Biosciences
- NCT number
- NCT05787587
What you commit to
- Study type: Interventional · Phase 1
- Planned participants: 216
- From 18 Apr 2023 to the primary completion date, Oct 2026
- 27 sites in 1 country
- Visits and tests: ask the trial team, the registry does not list them
Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.
Who cannot take part
Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.
Prior treatment
- Major surgery within 4 weeks prior to enrollment
- Radiation therapy within 2 weeks prior to enrollment
- Systemic cytotoxic chemotherapy within 4 weeks prior to enrollment
- Treatment with a therapeutic antibody within 4 weeks prior to enrollment
- Treatment with an anti-cancer small molecule within 5 half-lives (t1/2), or 2 weeks, whichever is shorter
- For Module 2 only, History or allogeneic tissue/solid organ transplant
Other illness
- Known primary CNS malignancy
- Impairment of GI function or GI disease that may significantly alter the absorption of IDE161
- Have active, uncontrolled infection
- Clinically significant cardiac abnormalities
- Have current active liver or biliary disease
- For Module 2 only, Active autoimmune disease that has required systemic treatment in past 2 years
- For Module 2 only, History of (noninfectious) pneumonitis/interstitial lung disease that required steroids or has current pneumonitis/interstitial lung disease
Other
- Radioimmunotherapy within 6 weeks of enrollment
Who the study is looking for
- Adult participants must be 18 years of age or older
- Advanced or metastatic solid tumors excluding primary central nervous system (CNS) tumors
- For Module 1 only, Have documented evidence of BRCA1/2 and/or genetic alterations conferring homologous recombination deficiency (HRD) (ATM, BARD1, BRIP1, CDK12, CHEK1, CHEK2, FANCL, PALB2, PPP2R2A, RAD51B, RAD51C, RAD51D, RAD54L, NBN, FANCA)
- For Module 2 only, results of MSI and/or MMR testing required.
- For Module 2 only, results of BRCA1/2 and HRD gene testing required.
- Participant must have progressed on at least one prior line of therapy in the advanced or metastatic setting that is considered an appropriate standard of care, or for which the participant has documented intolerance
- For Module 2 only, advanced or metastatic Endometrial Cancer (uterine carcinosarcoma is excluded)
- For Module 2 only, Must have progressed on treatment with an anti-PD-1/L1 monoclonal antibody (MAB)
Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers
Sites (27)
Sites in registry order. Pick your city on the disease page to sort them by distance.
| Site | City | Country | Site status |
|---|---|---|---|
| Emory University Coordinator of this site? Confirm its status | Atlanta | United States | Unknown status |
| Dana Faber Cancer Institute Coordinator of this site? Confirm its status | Boston | United States | Unknown status |
| Roswell Park Comprehensive Cancer Center Coordinator of this site? Confirm its status | Buffalo | United States | Unknown status |
| Sarah Cannon Research Institute Coordinator of this site? Confirm its status | Denver | United States | Unknown status |
| Karmanos Cancer Institute Coordinator of this site? Confirm its status | Detroit | United States | Unknown status |
| NEXT Oncology Coordinator of this site? Confirm its status | Fairfax | United States | Unknown status |
| MD Anderson Coordinator of this site? Confirm its status | Houston | United States | Unknown status |
| Indiana University Coordinator of this site? Confirm its status | Indianapolis | United States | Unknown status |
| NEXT Oncology Coordinator of this site? Confirm its status | Irving | United States | Unknown status |
| Comprehensive Cancer Centers of Nevada Coordinator of this site? Confirm its status | Las Vegas | United States | Unknown status |
| The Angeles Clinic Coordinator of this site? Confirm its status | Los Angeles | United States | Unknown status |
| University of Wisconsin Coordinator of this site? Confirm its status | Madison | United States | Unknown status |
| Sarah Cannon Research Institute Coordinator of this site? Confirm its status | Nashville | United States | Unknown status |
| Yale University Coordinator of this site? Confirm its status | New Haven | United States | Unknown status |
| Hoag Memorial Hospital Coordinator of this site? Confirm its status | Newport Beach | United States | Unknown status |
| Weil Cornell University Coordinator of this site? Confirm its status | New York | United States | Unknown status |
| Columbia University Medical Center Coordinator of this site? Confirm its status | New York | United States | Unknown status |
| Sarah Cannon Research Institute - Oklahoma University Coordinator of this site? Confirm its status | Oklahoma City | United States | Unknown status |
| Orlando Health Coordinator of this site? Confirm its status | Orlando | United States | Unknown status |
| OSF St Francis Medical Center Coordinator of this site? Confirm its status | Peoria | United States | Unknown status |
| Sarah Cannon Research Institute - Thomas Jefferson University Coordinator of this site? Confirm its status | Philadelphia | United States | Unknown status |
| University of Pennsylvania Coordinator of this site? Confirm its status | Philadelphia | United States | Unknown status |
| HonorHealth Research Institute Coordinator of this site? Confirm its status | Phoenix | United States | Unknown status |
| NEXT Oncology Coordinator of this site? Confirm its status | San Antonio | United States | Unknown status |
| California Pacific Medical Center Coordinator of this site? Confirm its status | San Francisco | United States | Unknown status |
| Swedish Cancer Institute Coordinator of this site? Confirm its status | Seattle | United States | Unknown status |
| START Mountain Region Coordinator of this site? Confirm its status | West Valley City | United States | Unknown status |
This page is information, not medical advice. Discuss any trial with your doctor.