Surgical Pembro +/- Olaparib w TMZ for rGBM

Part of paid clinical trials in Boston, Massachusetts.

Sponsor
L. Nicolas Gonzalez Castro, MD, PhD
Study ID
NCT05463848
Phase
PHASE2
Status
Active Not Recruiting

Conditions

Eligibility Criteria

Sex
ALL
Age
18 Years - N/A
Healthy Volunteers
Not accepted

Interventions

  • Pembrolizumab — DRUG
    Intravenous infusion
  • Olaparib — DRUG
    Pill taken by mouth
  • Temozolomide — DRUG
    Pill taken by mouth

Study Details

This research study is studying a combination therapy as a possible treatment for recurrent glioblastoma (GBM), a brain tumor that is growing or progressing despite earlier treatment. The names of the study interventions involved in this study are/is: * Pembrolizumab * Olaparib * Temozolomide (Temodar)

Key Dates

First listed
Jul 19, 2022
Start date
Oct 21, 2022
Status verified
Aug 2026
Primary completion
May 19, 2026
Completion
Mar 1, 2027

Study Design

Enrollment
52 participants (actual)
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT

Arms

  • Experimental: Cohort 1 (Safety Lead In): pembrolizumab plus olaparib and temozolomide
    Following a 3 + 3 dose escalation design 6-18 participants will receive: * Olaparib 2x daily on Days 1-7 of each 21-day study cycle. * Temozolomide 1x daily on Days 1-7 of each 21-day study cycle. * Pembrolizumab on Day 1 of every other 21-day cycle (once every 6 weeks).
  • Experimental: Cohort 2 (Surgical Cohort): Arm A - Pembrolizumab plus olaparib and temozolomide
    Cohort 2 participants will be randomized into either group a or b (1:1): Group A participants will receive pembrolizumab, olaparib, and temozolomide before and after surgery. * Olaparib 2x daily on Days 1-7 of each 21-day study cycle. * Temozolomide 1x daily on Days 1-7 of each 21-day study cycle. * Pembrolizumab on Day 1 of every other 21-day cycle (once every 6 weeks).
  • Experimental: Cohort 2 (Surgical Cohort): Arm B - Pembrolizumab monotherapy
    Cohort 2 participants will be randomized into either group a or b (1:1): Group B participants will receive pembrolizumab monotherapy before and after surgery. * Pembrolizumab Before Surgery: Day 1 of the pre-surgical treatment cycle. * Pembrolizumab After Surgery: Day 1 of every other 21-day cycle (once every 6 weeks).

Primary Outcome Measure

6-month Progression-Free Survival (PFS6) [ Time Frame: 6 months after surgery. Surgery will occur 14 days +/- 5 days after initiation of treatment. ]

Locations (4)

FacilityCityStateZIPSite coordinators
Beth Israel Deaconess Medical CenterBostonMassachusetts02215-
Dana-Farber Cancer InstituteBostonMassachusetts02215-
Massachusetts General HospitalBostonMassachusetts02114-
Memorial Sloan Kettering Cancer CenterNew YorkNew York10065-

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