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A Study of PARG Inhibitor IDE161 in Participants With Advanced Solid Tumors
RECRUITINGPhase 1Sponsored by IDEAYA Biosciences
Actively Recruiting
PhasePhase 1
SponsorIDEAYA Biosciences
Started2023-04-18
Est. completion2026-10
Eligibility
Age18 Years+
Healthy vol.Accepted
Locations27 sites
View on ClinicalTrials.gov →
NCT05787587
Summary
The purpose of this study is to characterize the safety, tolerability, and efficacy of IDE161 as a single agent and in combination with pembrolizumab.
Eligibility
Age: 18 Years+Healthy volunteers accepted
Inclusion Criteria: 1. Adult participants must be 18 years of age or older 2. Advanced or metastatic solid tumors excluding primary central nervous system (CNS) tumors 3. 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. 4. 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 5. For Module 2 only, advanced or metastatic Endometrial Cancer (uterine carcinosarcoma is excluded) 6. For Module 2 only, Must have progressed on treatment with an anti-PD-1/L1 monoclonal antibody (MAB) Exclusion Criteria: 1. Known primary CNS malignancy 2. Impairment of GI function or GI disease that may significantly alter the absorption of IDE161 3. Have active, uncontrolled infection 4. Clinically significant cardiac abnormalities 5. Major surgery within 4 weeks prior to enrollment 6. Radiation therapy within 2 weeks prior to enrollment 7. Systemic cytotoxic chemotherapy within 4 weeks prior to enrollment 8. Radioimmunotherapy within 6 weeks of enrollment 9. Treatment with a therapeutic antibody within 4 weeks prior to enrollment 10. Treatment with an anti-cancer small molecule within 5 half-lives (t1/2), or 2 weeks, whichever is shorter 11. Have current active liver or biliary disease 12. For Module 2 only, History or allogeneic tissue/solid organ transplant 13. For Module 2 only, Active autoimmune disease that has required systemic treatment in past 2 years 14. For Module 2 only, History of (noninfectious) pneumonitis/interstitial lung disease that required steroids or has current pneumonitis/interstitial lung disease
Conditions11
Advanced or Metastatic Solid TumorsBreast CancerCancerColorectal CancerEndometrial CancerExtensive Stage Small Cell Lung Cancer (ES-SCLC)Head and Neck CancersLung CancerNSCLCOvarian Cancer
Locations27 sites
HonorHealth Research Institute
Phoenix, Arizona, 85027
The Angeles Clinic
Los Angeles, California, 90025
Hoag Memorial Hospital
Newport Beach, California, 92663
California Pacific Medical Center
San Francisco, California, 94115
Sarah Cannon Research Institute
Denver, Colorado, 80218
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Trial data from ClinicalTrials.gov. Trial status and eligibility can change — verify directly with the study contact or on ClinicalTrials.gov.
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Actively Recruiting
PhasePhase 1
SponsorIDEAYA Biosciences
Started2023-04-18
Est. completion2026-10
Eligibility
Age18 Years+
Healthy vol.Accepted
Locations27 sites
View on ClinicalTrials.gov →
NCT05787587