M6620 and Irinotecan Hydrochloride in Treating Patients With Solid Tumors That Are Metastatic or Cannot Be Removed by Surgery
Part of paid clinical trials in Los Angeles, California.
- Sponsor
- National Cancer Institute (NCI)
- Study ID
- NCT02595931
- Phase
- PHASE1
- Status
- Active Not Recruiting
Conditions
- Metastatic Colorectal Carcinoma
- Metastatic Lung Small Cell Carcinoma
- Metastatic Malignant Solid Neoplasm
- Metastatic Pancreatic Carcinoma
- Refractory Colorectal Carcinoma
- Refractory Lung Small Cell Carcinoma
- Refractory Malignant Solid Neoplasm
- Refractory Pancreatic Carcinoma
- Stage III Colorectal Cancer AJCC v8
- Stage III Lung Cancer AJCC v8
- Stage III Pancreatic Cancer AJCC v8
- Stage IV Colorectal Cancer AJCC v8
- Stage IV Lung Cancer AJCC v8
- Stage IV Pancreatic Cancer AJCC v8
- Unresectable Colorectal Carcinoma
- Unresectable Lung Small Cell Carcinoma
- Unresectable Malignant Solid Neoplasm
- Unresectable Pancreatic Carcinoma
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Berzosertib — DRUGGiven IV
- Biopsy Specimen — PROCEDUREUndergo biopsy
- Biospecimen Collection — PROCEDURECorrelative studies
- Computed Tomography — PROCEDUREUndergo CT
- Irinotecan Hydrochloride — DRUGGiven IV
Study Details
This phase I trial studies the side effects and best dose of M6620 and irinotecan hydrochloride in treating patients with solid tumors that have spread to other places in the body (metastatic) or cannot be removed by surgery (unresectable). M6620 and irinotecan hydrochloride may stop the growth of tumor cells by blocking some of the enzymes needed for cell growth.
Key Dates
- Start date
- Jul 22, 2016
- Status verified
- Mar 2026
- Primary completion
- Mar 7, 2023
- Completion
- Mar 6, 2027
Study Design
- Enrollment
- 66 participants (actual)
- Allocation
- NA
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Treatment (irinotecan, M6620)Patients receive irinotecan hydrochloride IV over 90 minutes and M6620 IV over 60 minutes on days 1 and 15. Treatment repeats every 28 days for 12 cycles in the absence of disease progression or unacceptable toxicity. Patients also undergo biopsy and collection of blood samples throughout the study and undergo CT at screening, throughout the study, and during follow up.
Primary Outcome Measure
Maximum tolerated dose (MTD) [ Time Frame: Up to 28 days ]
Locations (23)
Find similar trials in Los Angeles, CA
By research site
Los Angeles General Medical Center· Los Angeles, CAUSC / Norris Comprehensive Cancer Center· Los Angeles, CAStanford Cancer Institute Palo Alto· Palo Alto, CAKeck Medical Center of USC Pasadena· Pasadena, CAUniversity of California Davis Comprehensive Cancer Center· Sacramento, CAUCSF Medical Center-Mount Zion· San Francisco, CA
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