A Study Evaluating the Safety and Efficacy of Targeted Therapies in Subpopulations of Patients With Metastatic Colorectal Cancer (INTRINSIC)

Launched by HOFFMANN-LA ROCHE · Jun 11, 2021

Keywords

ClinConnect Summary

The INTRINSIC trial is studying how safe and effective certain targeted therapies or immunotherapies are for patients with metastatic colorectal cancer (mCRC). This means they are looking at treatments specifically designed to target cancer cells in patients whose tumors have certain biological markers. The study will include adult participants aged 18 and older, who have been diagnosed with mCRC and have specific test results showing they are eligible for the treatment being tested.

Participants in this trial can expect to receive either a targeted therapy or immunotherapy, either alone or in combination with other treatments, based on their individual tumor characteristics. Before starting the treatment, participants will need to provide consent and undergo certain tests to confirm their eligibility. They will also be asked to provide tumor samples for further research. Since this is an exploratory study, the focus is on gathering information about the safety and effectiveness of these therapies, which may help improve treatment options for future patients. It's important to note that participants cannot be involved in other clinical trials or have certain health conditions that might interfere with the study.

Gender

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Eligibility criteria

• • Inclusion Criteria
• • Signed cohort-specific Informed Consent Form
• • Age \>= 18 years at time of signing Informed Consent Form
• * Biomarker eligibility as determined by:
• • A validated test approved by local health authorities for detection of the specified biomarkers/mutations.
• • A validated test performed at a College of American Pathologists/clinical laboratory improvement amendments (CAP/CLIA) -certified or equivalently accredited diagnostic laboratory using a validated test for detection of the specified biomarkers.
• • Prior test results completed before signing cohort-specific Informed Consent Form or local test results generated prior to or during screening, and availability of a full report of the testing results OR
• • Blood-based FoundationOne Liquid CDx biomarker eligibility test result generated prior to or during screening or, in case of re-enrollment after treatment discontinuation, prior to starting a new anti-cancer therapy.
• • Eastern Cooperative Oncology Group (ECOG) Performance Status of \<= 1
• • Life expectancy \>= 3 months, as determined by the investigator
• • Histologically confirmed adenocarcinoma originating from the colon or rectum
• • Metastatic disease
• • Prior therapies for metastatic disease
• • Ability to comply with the study protocol, in the investigators judgment
• • Measurable disease (at least one target lesion) according to Response Evaluation Criteria in Solid Tumors, Version 1.1 (RECIST v1.1)
• • Baseline tumor tissue samples will be collected from all participants for exploratory biomarker research
• • Adequate hematologic and organ function within 14 days prior to initiation of study treatment
• • For women of childbearing potential: agreement to remain abstinent (refrain from heterosexual intercourse) or use contraceptive measures
• • For men: agreement to remain abstinent or use contraceptive measures, and agreement to refrain from donating sperm
• • Exclusion Criteria
• • Current participation or enrollment in another interventional clinical trial. Participants who are participating in the follow-up period of an interventional clinical trial are eligible for the study.
• • Any systemic anti-cancer treatment within 2 weeks or 5 half-lives (whichever is shorter) prior to start of study treatment
• • Treatment with investigational therapy within 28 days prior to initiation of study treatment
• • Pregnant or breastfeeding, or intending to become pregnant during the study
• • History of or concurrent serious medical condition or abnormality in clinical laboratory tests that, in the investigator's judgment, precludes the patient's safe participation in and completion of the study or confounds the ability to interpret data from the study
• • Severe infection within 4 weeks prior to initiation of study treatment or any active infection that, in the opinion of the investigator, could impact patient safety
• • Incomplete recovery from any surgery prior to the start of study treatment that would interfere with the determination of safety or efficacy of study treatment
• • Uncontrolled pleural effusion, pericardial effusion, or ascites requiring recurrent drainage procedures (once monthly or more frequently)
• • Uncontrolled tumor-related pain
• • Uncontrolled or symptomatic hypercalcemia
• • Clinically significant and active liver disease
• • Negative HIV test at screening, with the following exception: Participants with a positive HIV test at screening are eligible provided they are stable on anti-retroviral therapy for at least 4 weeks, have a CD4 count greater than or equal to 200/uL, have an undetectable viral load, and have not had a history of opportunistic infection attributable to AIDS within the last 12 months.
• • Symptomatic, untreated, or actively progressing CNS metastases
• • History of leptomeningeal disease or carcinomatous meningitis
• • History of malignancy other than CRC within 2 years prior to screening, with the exception of malignancies with a negligible risk of metastasis or death
• • Any other disease, unresolved toxicity from prior therapy, metabolic dysfunction, physical examination finding, or clinical laboratory finding that contraindicates the use of an investigational drug, may affect the interpretation of the results, or may render the participant at high risk from treatment complications
• • Requirement for treatment with any medicinal product that contraindicates the use of any of the study treatments, may interfere with the planned treatment, affects participant compliance, or puts the patient at higher risk for treatment-related complications