A Study of PARG Inhibitor IDE161 in Participants with Advanced Solid Tumors

Clinicaltrials.gov ID: NCT05787587
db-list-check Status RECRUITING
b-loader Phase PHASE1
b-people Age ≥ 18 Years
b-bullseye-arrow Enrollments 216

Conditions

Advanced or Metastatic Solid Tumors, Breast Cancer, Ovarian Cancer, Pancreas Cancer, Prostate Cancer, Endometrial Cancer, Colorectal Cancer, Head and Neck Cancers

Drugs

IDE-161, Pembrolizumab

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.

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

Study Director

  • Darrin Beaupre, MD,PhD

Status

  • RECRUITING

Contact Person

Study Director

  • Darrin Beaupre, MD,PhD

Status

  • RECRUITING

Contact Person

Study Director

  • Darrin Beaupre, MD,PhD

Status

  • RECRUITING

Contact Person

Study Director

  • Darrin Beaupre, MD,PhD

Status

  • RECRUITING

Contact Person

Study Director

  • Darrin Beaupre, MD,PhD

Status

  • RECRUITING

Contact Person

Study Director

  • Darrin Beaupre, MD,PhD

Status

  • RECRUITING

Contact Person

Study Director

  • Darrin Beaupre, MD,PhD

Status

  • RECRUITING

Contact Person

Study Director

  • Darrin Beaupre, MD,PhD

Status

  • RECRUITING

Contact Person

Study Director

  • Darrin Beaupre, MD,PhD

Status

  • RECRUITING

Contact Person

Study Director

  • Darrin Beaupre, MD,PhD

Status

  • RECRUITING

Contact Person

Study Director

  • Darrin Beaupre, MD,PhD

Status

  • RECRUITING

Contact Person

Study Director

  • Darrin Beaupre, MD,PhD

Status

  • RECRUITING

Contact Person

Study Director

  • Darrin Beaupre, MD,PhD

Status

  • RECRUITING

Contact Person

Study Director

  • Darrin Beaupre, MD,PhD

Status

  • RECRUITING

Contact Person

Study Director

  • Darrin Beaupre, MD,PhD

Status

  • RECRUITING

Contact Person

Study Director

  • Darrin Beaupre, MD,PhD

Status

  • RECRUITING

Contact Person

Study Director

  • Darrin Beaupre, MD,PhD

Status

  • RECRUITING

Contact Person

Study Director

  • Darrin Beaupre, MD,PhD

Status

  • RECRUITING

Contact Person

Study Director

  • Darrin Beaupre, MD,PhD

Status

  • RECRUITING

Contact Person

Study Director

  • Darrin Beaupre, MD,PhD

Status

  • RECRUITING

Contact Person

Study Director

  • Darrin Beaupre, MD,PhD

Status

  • RECRUITING

Contact Person

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-161

    Description:

    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-161

    Description:

    Oral Medication

Module 2 Part 1: Combination Dose Escalation with pembrolizumab

EXPERIMENTAL

Participants will be assigned to a dose level.

  • DRUG:

    IDE-161

    Description:

    Oral Medication
  • DRUG:

    Pembrolizumab

    Description:

    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-161

    Description:

    Oral Medication
  • DRUG:

    Pembrolizumab

    Description:

    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

Time Frame: Approximately 2 years

Part 2 (Dose Expansion): To further assess the safety and tolerability of IDE monotherapy and in combination with pembrolizumab at the RDE

Time Frame: Approximately 4 years

Part 2 (Dose Expansion): To evaluate preliminary anti-tumor activity of IDE161 monotherapy or in combination with pembrolizumab

Time Frame: Approximately 4 years

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

Time Frame: Approximately 4 years

To characterize the single dose PK Peak Plasma Concentration (Cmax) of IDE161 monotherapy and in combination with pembrolizumab.

Time Frame: Approximately 4 years

To characterize the multiple dose PK Peak Plasma Concentration (Cmax) of IDE161 monotherapy and in combination with pembrolizumab.

Time Frame: Approximately 4 years

To characterize the single dose PK Area under the plasma concentration versus time curve (AUC) of IDE161 monotherapy and in combination with pembrolizumab.

Time Frame: Approximately 4 years

To characterize the multiple dose PK Area under the plasma concentration versus time curve (AUC) of IDE161 monotherapy and in combination with pembrolizumab.

Time Frame: Approximately 4 years

To characterize the single dose PK Time to Peak drug Concentration (Tmax) of IDE161 monotherapy and in combination with pembrolizumab.

Time Frame: Approximately 4 years

To characterize the multiple dose PK Time to Peak drug Concentration (Tmax) of IDE161 monotherapy and in combination with pembrolizumab.

Time Frame: Approximately 4 years

Timeline

  • Last Updated
    October 28, 2024
  • Start Date
    March 28, 2023
  • Today
    February 5, 2025
  • Completion Date ( Estimated )
    May 1, 2027

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