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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

Full criteria on ClinicalTrials.gov

Sites (27)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Emory University
Coordinator of this site? Confirm its status
AtlantaUnited StatesUnknown status
Dana Faber Cancer Institute
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BostonUnited StatesUnknown status
Roswell Park Comprehensive Cancer Center
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BuffaloUnited StatesUnknown status
Sarah Cannon Research Institute
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DenverUnited StatesUnknown status
Karmanos Cancer Institute
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DetroitUnited StatesUnknown status
NEXT Oncology
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FairfaxUnited StatesUnknown status
MD Anderson
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HoustonUnited StatesUnknown status
Indiana University
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IndianapolisUnited StatesUnknown status
NEXT Oncology
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IrvingUnited StatesUnknown status
Comprehensive Cancer Centers of Nevada
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Las VegasUnited StatesUnknown status
The Angeles Clinic
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Los AngelesUnited StatesUnknown status
University of Wisconsin
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MadisonUnited StatesUnknown status
Sarah Cannon Research Institute
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NashvilleUnited StatesUnknown status
Yale University
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New HavenUnited StatesUnknown status
Hoag Memorial Hospital
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Newport BeachUnited StatesUnknown status
Weil Cornell University
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New YorkUnited StatesUnknown status
Columbia University Medical Center
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New YorkUnited StatesUnknown status
Sarah Cannon Research Institute - Oklahoma University
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Oklahoma CityUnited StatesUnknown status
Orlando Health
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OrlandoUnited StatesUnknown status
OSF St Francis Medical Center
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PeoriaUnited StatesUnknown status
Sarah Cannon Research Institute - Thomas Jefferson University
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PhiladelphiaUnited StatesUnknown status
University of Pennsylvania
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PhiladelphiaUnited StatesUnknown status
HonorHealth Research Institute
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PhoenixUnited StatesUnknown status
NEXT Oncology
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San AntonioUnited StatesUnknown status
California Pacific Medical Center
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San FranciscoUnited StatesUnknown status
Swedish Cancer Institute
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SeattleUnited StatesUnknown status
START Mountain Region
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West Valley CityUnited StatesUnknown status

This page is information, not medical advice. Discuss any trial with your doctor.