A Study of Ipatasertib in Combination With Atezolizumab and Paclitaxel as a Treatment for Participants With Locally Advanced or Metastatic Triple-Negative Breast Cancer
Part of paid clinical trials in Mobile, Alabama.
- Sponsor
- Hoffmann-La Roche
- Study ID
- NCT04177108
- Phase
- PHASE3
- Status
- Completed
Conditions
- Triple-Negative Breast Cancer
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Atezolizumab — DRUGAtezolizumab was administered as per the dosage regimen mentioned in arm descriptions.
- Ipatasertib — DRUGIpatasertib was administered as per the dosage regimen mentioned in arm descriptions.
- Paclitaxel — DRUGPaclitaxel was administered as per the dosage regimen mentioned in arm descriptions.
- Placebo for Atezolizumab — DRUGPlacebo was administered as per the dosage regimen mentioned in arm descriptions.
- Placebo for Ipatasertib — DRUGPlacebo was administered as per the dosage regimen mentioned in arm descriptions.
Study Details
This study evaluated the efficacy and safety of ipatasertib in combination with atezolizumab and paclitaxel in locally advanced or metastatic Triple-Negative Breast Cancer (TNBC) previously untreated in this setting.
Key Dates
- Start date
- Nov 25, 2019
- Status verified
- Feb 2024
- Primary completion
- Feb 28, 2023
- Completion
- Feb 28, 2023
Study Design
- Enrollment
- 242 participants (actual)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Cohort 1 Arm A: Ipatasertib + Atezolizumab + PaclitaxelTNBC participants with programmed death-ligand 1 (PD-L1) non-positive received a combination of paclitaxel, 80 milligrams per meter square (mg/m\^2), intravenous (IV) infusion on Days 1, 8, and 15 of each 28-day cycle and ipatasertib, 400 mg, orally (PO), once daily (QD), from Day 1 to Day 21 of each 28-day cycle and atezolizumab, 840 mg, IV infusion on Day 1 and 15 of each 28-day cycle until loss of clinical benefit, unacceptable toxicity, or withdrawal of consent, whichever occurred first.
- Experimental: Cohort 1 Arm B: Ipatasertib + Placebo + PaclitaxelTNBC participants with PD-L1 non-positive received a combination of paclitaxel, 80 mg/m\^2, IV infusion on Days 1, 8, and 15 of each 28-day cycle and ipatasertib, 400 mg, PO, QD, from Day 1 to Day 21 of each 28-day cycle and atezolizumab-matching placebo, IV infusion on Day 1 and 15 of each 28-day cycle until loss of clinical benefit, unacceptable toxicity, or withdrawal of consent, whichever occurred first.
- Experimental: Cohort 1 Arm C: Placebo + Placebo + PaclitaxelTNBC participants with PD-L1 non-positive received a combination of paclitaxel, 80 mg/m\^2, IV infusion on Days 1, 8, and 15 of each 28-day cycle and ipatasertib-matching placebo, PO, QD, from Day 1 to Day 21 of each 28-day cycle and atezolizumab-matching placebo, IV infusion on Day 1 and 15 of each 28-day cycle until loss of clinical benefit, unacceptable toxicity, or withdrawal of consent, whichever occurred first.
- Experimental: Cohort 2 Arm A: Ipatasertib + Atezolizumab + PaclitaxelTNBC participants with PD-L1 positive received a combination of paclitaxel, 80 mg/m\^2, IV infusion on Days 1, 8, and 15 of each 28-day cycle and ipatasertib, 400 mg, PO, QD, from Day 1 to Day 21 of each 28-day cycle and atezolizumab, 840 mg, IV infusion on Day 1 and 15 of each 28-day cycle until loss of clinical benefit, unacceptable toxicity, or withdrawal of consent, whichever occurred first.
- Experimental: Cohort 2 Arm B: Placebo+ Atezolizumab + PaclitaxelTNBC participants with PD-L1 positive received a combination of paclitaxel, 80 mg/m\^2, IV infusion on Days 1, 8, and 15 of each 28-day cycle and ipatasertib-matching placebo, PO, QD, from Day 1 to Day 21 of each 28-day cycle and atezolizumab, 840 mg, IV infusion on Day 1 and 15 of each 28-day cycle until loss of clinical benefit, unacceptable toxicity, or withdrawal of consent, whichever occurred first.
Primary Outcome Measure
Progression-Free Survival (PFS) According to Response Evaluation Criteria in Solid Tumors (RECIST) Version 1.1 [ Time Frame: From Randomization to disease progression, study completion, or death (up to 39 months) ]
Locations (31)
Find similar trials in Mobile, AL
Related Studies
- Phase 1a and Phase 2 Study for Safety, Preliminary Efficacy, PK and PD of ST-067PHASE1/PHASE2 · Recruiting · Simcha IL-18, Inc. · Scottsdale, Arizona
- Sacituzumab Tirumotecan (MK-2870) Plus Pembrolizumab Versus TPC in TNBC Who Did Not Achieve pCR (MK-2870-012)PHASE3 · Recruiting · Merck Sharp & Dohme LLC · Mobile, Alabama
- The Gut Microbiome and Immune Checkpoint Inhibitor Therapy in Solid TumorsRecruiting · VastBiome · Elizabethtown, Kentucky