A Study of PARG Inhibitor IDE161 in Participants with Advanced Solid Tumors
Conditions
Advanced or Metastatic Solid Tumors, Breast Cancer, Ovarian Cancer, Pancreas Cancer, Prostate Cancer, Endometrial Cancer, Colorectal Cancer, Head and Neck CancersDrugs
IDE-161, PembrolizumabSummary
The purpose of this study is to characterize the safety, tolerability, and efficacy of IDE161 as a single agent and in combination with pembrolizumab.
Detailed Description
The purpose of this study is to characterize the safety, tolerability including determination of maximum tolerated dose (MTD), maximum accepted dose (MAD), recommended dose(s) for expansion (RDE) and/or recommended Phase 2 dose (RP2D), pharmacokinetics (PK), pharmacodynamics (PD) and preliminary anti-tumor activity of IDE161 as a single agent in participants with advanced or metastatic solid tumors harboring BRCA1/2 loss of function alterations and/or other defects in the homologous recombination (HR) pathway and in combination with pembrolizumab in participants with advanced/recurrent endometrial cancer.
Locations
22 locations Found with status Recruiting
Status
- RECRUITING
Contact Person
- Saba Mukarram
- 310-231-2181
- [email protected]
Study Director
- Darrin Beaupre, MD,PhD
Status
- RECRUITING
Contact Person
- Denise Fortun
- 415-600-1775
- [email protected]
Study Director
- Darrin Beaupre, MD,PhD
Status
- RECRUITING
Contact Person
- Carrie Wolff
- 720-754-2610
- [email protected]
Study Director
- Darrin Beaupre, MD,PhD
Status
- RECRUITING
Contact Person
- Ingrid Palma
- 203-833-1034
- [email protected]
Study Director
- Darrin Beaupre, MD,PhD
Status
- RECRUITING
Contact Person
- Kevin Kalinsky
- 404-778-1900
- [email protected]
Study Director
- Darrin Beaupre, MD,PhD
Status
- RECRUITING
Contact Person
- Kailene Sullivan
- 617-632-3482
- [email protected]
Study Director
- Darrin Beaupre, MD,PhD
Status
- RECRUITING
Contact Person
- Victoria LaBush
- 313-576-8411
- [email protected]
Study Director
- Darrin Beaupre, MD,PhD
Status
- RECRUITING
Contact Person
- AnaArlene SJ. Ramirez
- 702-952-3406
- [email protected]
Study Director
- Darrin Beaupre, MD,PhD
Status
- RECRUITING
Contact Person
- Roswell Park
- 1-800-767-9355
- [email protected]
Study Director
- Darrin Beaupre, MD,PhD
Status
- RECRUITING
Contact Person
- Cancer Clinical Trials Team
- 212-342-5162
- [email protected]
Study Director
- Darrin Beaupre, MD,PhD
Status
- RECRUITING
Contact Person
- Mahelia Bissassar
- (646) 962-7669
- [email protected]
Study Director
- Darrin Beaupre, MD,PhD
Status
- RECRUITING
Contact Person
- Sarah Cannon Research Institute
- 844-482-4812
- [email protected]
Study Director
- Darrin Beaupre, MD,PhD
Status
- RECRUITING
Contact Person
- Jennifer Louie
- 267-414-6179
- [email protected]
Study Director
- Darrin Beaupre, MD,PhD
Status
- RECRUITING
Contact Person
- Screening and Enrollment Team
- 215-586-0199
- [email protected]
Study Director
- Darrin Beaupre, MD,PhD
Status
- RECRUITING
Contact Person
- Tatiana Zabaleta
- 615-973-4926
- [email protected]
Study Director
- Darrin Beaupre, MD,PhD
Status
- RECRUITING
Contact Person
- Nicole Fabian-Aguirre
- 713-745-6332
- [email protected]
Study Director
- Darrin Beaupre, MD,PhD
Status
- RECRUITING
Contact Person
- Selena Morales
- 972-893-8820
- [email protected]
Study Director
- Darrin Beaupre, MD,PhD
Status
- RECRUITING
Contact Person
- Briana Flores
- 210-580-9521
- [email protected]
Study Director
- Darrin Beaupre, MD,PhD
Status
- RECRUITING
Contact Person
- Marie Asay
- 801-907-4770
- [email protected]
Study Director
- Darrin Beaupre, MD,PhD
Status
- RECRUITING
Contact Person
- Blake Patterson
- 703-783-4510
- [email protected]
Study Director
- Darrin Beaupre, MD,PhD
Status
- RECRUITING
Contact Person
- Swedish Cancer Center
- [email protected]
Study Director
- Darrin Beaupre, MD,PhD
Status
- RECRUITING
Contact Person
- UW Carbone Cancer Center - Cancer Connect
- 800-622-8922
- [email protected]
Study Director
- Darrin Beaupre, MD,PhD
Eligibility Criteria
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
Study Plan
Module 1 Part 1: Monotherapy Dose Escalation
EXPERIMENTAL
Participants will be assigned to a dose level.
DRUG:
IDE-161Description:
Oral Medication
Module 1 Part 2: Monotherapy Dose Expansion
EXPERIMENTAL
After a dose is decided in Part 1, participants entering part 2 will be assigned to a dose level.
DRUG:
IDE-161Description:
Oral Medication
Module 2 Part 1: Combination Dose Escalation with pembrolizumab
EXPERIMENTAL
Participants will be assigned to a dose level.
DRUG:
IDE-161Description:
Oral MedicationDRUG:
PembrolizumabDescription:
Intravenous Infusion
Module 2 Part 2: Combination Dose Expansion with pembrolizumab
EXPERIMENTAL
After a dose is decided in Part 1, participants entering part 2 will be assigned to a dose level.
DRUG:
IDE-161Description:
Oral MedicationDRUG:
PembrolizumabDescription:
Intravenous Infusion
Outcome Measures
Primary Outcome Measures
Part 1 (Dose Escalation): To characterize the safety and tolerability of IDE161 monotherapy or in combination with pembrolizumab to determine the MTD and/or RDE
Part 2 (Dose Expansion): To further assess the safety and tolerability of IDE monotherapy and in combination with pembrolizumab at the RDE
Part 2 (Dose Expansion): To evaluate preliminary anti-tumor activity of IDE161 monotherapy or in combination with pembrolizumab
Secondary Outcome Measures
Part 2 (Dose Expansion) Assess the risk/benefit at an IDE161 monotherapy dose and exposure alternative to the initial expansion dose; as well as an IDE161 dose in combination with a fixed dose of pembrolizumab and exposure alternative to the initial
To characterize the single dose PK Peak Plasma Concentration (Cmax) of IDE161 monotherapy and in combination with pembrolizumab.
To characterize the multiple dose PK Peak Plasma Concentration (Cmax) of IDE161 monotherapy and in combination with pembrolizumab.
To characterize the single dose PK Area under the plasma concentration versus time curve (AUC) of IDE161 monotherapy and in combination with pembrolizumab.
To characterize the multiple dose PK Area under the plasma concentration versus time curve (AUC) of IDE161 monotherapy and in combination with pembrolizumab.
To characterize the single dose PK Time to Peak drug Concentration (Tmax) of IDE161 monotherapy and in combination with pembrolizumab.
To characterize the multiple dose PK Time to Peak drug Concentration (Tmax) of IDE161 monotherapy and in combination with pembrolizumab.
Timeline
Last Updated
October 28, 2024Start Date
March 28, 2023Today
January 16, 2025Completion Date ( Estimated )
May 1, 2027
Sponsors of this trial
Lead Sponsor
IDEAYA BiosciencesCollaborating Sponsors
Merck Sharp & Dohme LLC