Clinical trial

A Phase 1b, Protocol Evaluating the Safety, Tolerability, Pharmacokinetics, and Efficacy of Sotorasib Monotherapy and in Combination With Other Anti-cancer Therapies in Subjects With Advanced Solid Tumors With KRAS p.G12C Mutation (CodeBreak 101)

Name
20190135
Description
To evaluate the safety and tolerability of sotorasib administered in investigational regimens in adult participants with KRAS p.G12C mutant advanced solid tumors.
Trial arms
Trial start
2019-12-17
Estimated PCD
2026-12-20
Trial end
2027-12-31
Status
Recruiting
Phase
Early phase I
Treatment
Sotorasib
Sotorasib administered orally as a tablet.
Arms:
Sotorasib + AMG 404, Sotorasib + BI 1701963, Sotorasib + MVASI® (bevacizumab-awwb)+ Chemotherapy, Sotorasib + RMC-4630, Sotorasib + TNO155, Sotorasib + afatinib, Sotorasib + atezolizumab, Sotorasib + carboplatin, pemetrexed, docetaxel, paclitaxel, pembrolizumab, Sotorasib + everolimus, Sotorasib + palbociclib, Sotorasib + panitumumab +/- chemotherapy, Sotorasib + pembrolizumab, Sotorasib + trametinib + panitumumab, Sotorasib Monotherapy
Trametinib
Trametinib administered orally as a tablet.
Arms:
Sotorasib + trametinib + panitumumab
RMC-4630
RMC-4630 administered orally as a capsule.
Arms:
Sotorasib + RMC-4630
Afatinib
afatinib administered orally as a tablet.
Arms:
Sotorasib + afatinib
Pembrolizumab
pembrolizumab administered as an intravenous (IV) infusion.
Arms:
Sotorasib + carboplatin, pemetrexed, docetaxel, paclitaxel, pembrolizumab, Sotorasib + pembrolizumab
Panitumumab
Panitumumab administered as an IV infusion.
Arms:
Sotorasib + panitumumab +/- chemotherapy, Sotorasib + trametinib + panitumumab
Carboplatin, pemetrexed, docetaxel, paclitaxel
Carboplatin, pemetrexed, docetaxel administered as an IV infusion.
Arms:
Sotorasib + carboplatin, pemetrexed, docetaxel, paclitaxel, pembrolizumab
Atezolizumab
Atezolizumab administered as an IV injection.
Arms:
Sotorasib + atezolizumab
Palbociclib
Palbociclib administered orally as a tablet.
Arms:
Sotorasib + palbociclib
MVASI® (bevacizumab-awwb)
MVASI® (bevacizumab-awwb) administered as an IV infusion.
Arms:
Sotorasib + MVASI® (bevacizumab-awwb)+ Chemotherapy
TNO155
TNO155 administered orally as a capsule.
Arms:
Sotorasib + TNO155
IV Chemotherapy (Regimen 1)
Chemotherapy combination of leucovorin administered as an IV injection, 5-fluorouracil (5-FU) administered as IV bolus injection or IV continuous infusion (depending on dose), and irinotecan administered as IV injection.
Arms:
Sotorasib + MVASI® (bevacizumab-awwb)+ Chemotherapy, Sotorasib + panitumumab +/- chemotherapy
IV Chemotherapy (Regimen 2)
IV chemotherapy combination of leucovorin administered as an IV injection, 5-FU administered as IV bolus injection or IV continuous infusion (depending on dose), and oxaliplatin administered as IV injection.
Arms:
Sotorasib + MVASI® (bevacizumab-awwb)+ Chemotherapy
BI 1701963
BI 1701963 administered orally
Arms:
Sotorasib + BI 1701963
AMG 404
AMG 404 administered as an IV infusion.
Arms:
Sotorasib + AMG 404
Everolimus
Everolimus administered orally.
Arms:
Sotorasib + everolimus
Size
1200
Primary endpoint
Number of Participants with Dose Limiting Toxicities (DLTs)
12 Months
Number of Participants with Treatment-emergent Adverse Events (TEAEs)
12 Months
Number of Participants with Treatment-related Adverse Events
12 Months
Number of Participants with Clinically Significant Changes in Vital Signs
12 Months
Number of Participants with Clinically Significant Changes in ECG Measurements
12 Months
Number of Participants with Clinically Significant Changes in Laboratory Test Values
12 Months
Eligibility criteria
Inclusion Criteria: * Men or women greater than or equal to 18 years old. * Pathologically documented, locally-advanced or metastatic malignancy with, KRAS p.G12C mutation identified through molecular testing performed according to in-country requirements. In the United States, this test must be performed in a Clinical Laboratory Improvement Amendments (CLIA)-certified laboratory. Exclusion Criteria: * Primary brain tumor. * Spinal cord compression, or untreated, or symptomatic, or active brain metastases, or leptomeningeal disease from non-brain tumors. * Myocardial infarction within 6 months of study day 1. * Gastrointestinal (GI) tract disease causing the inability to take oral medication.
Protocol
{'studyType': 'INTERVENTIONAL', 'phases': ['PHASE1'], 'designInfo': {'allocation': 'NON_RANDOMIZED', 'interventionModel': 'SEQUENTIAL', 'primaryPurpose': 'TREATMENT', 'maskingInfo': {'masking': 'NONE'}}, 'enrollmentInfo': {'count': 1200, 'type': 'ESTIMATED'}}
Updated at
2024-06-06

1 organization

14 products

1 drug

2 abstracts

2 indications

Organization
Amgen
Product
Sotorasib
Indication
Cancer
Product
Trametinib
Product
RMC-4630
Product
Afatinib
Product
MVASI
Product
TNO155
Product
BI 1701963
Product
AMG 404
Product
Everolimus
Abstract
Sotorasib plus panitumumab for pre-treated non-small cell lung cancer with KRAS G12C mutation: A phase 1b study.
Org: Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, University Hospital Saint-Luc, Brussels, Belgium, Hospital Clinic Barcelona, Barcelona, Spain, CHU de Québec-Université Laval, Québec, QC, Canada, University of Iowa Hospitals and Clinics, Iowa City, IA,
Abstract
Sotorasib (Soto) plus panitumumab (Pmab) and FOLFIRI for previously treated KRAS G12C-mutated metastatic colorectal cancer (mCRC): CodeBreaK 101 phase 1b safety and efficacy.
Org: University of Texas MD Anderson Cancer Center, National Cancer Center Hospital East, Kashiwa, Japan, Duke University Medical Center, City of Hope National Medical Center, Cliniques Universitaires Saint-Luc,