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Spots Global Cancer Trial Database for Study to Describe the Interaction Between Tazemetostat and Itraconazole and Between Tazemetostat and Rifampin in Participants With Advanced Cancer

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Trial Identification

Brief Title: Study to Describe the Interaction Between Tazemetostat and Itraconazole and Between Tazemetostat and Rifampin in Participants With Advanced Cancer

Official Title: A Phase I, Open-label Multi-dose Two-part Study to Characterize the Effects of a Strong CYP3A4 Inhibitor and a Strong CYP3A4 Inducer on the Steady-State Pharmacokinetics of Tazemetostat (EPZ-6438) in Subjects With Advanced Malignancies

Study ID: NCT04537715

Study Description

Brief Summary: The participants of this study will have advanced malignancies (also known as advanced cancer). The main aim of this trial will be to study the blood levels (known as pharmacokinetics) of the tazemtostat (the study drug) when administered in combination with another drug. Part 1 of the study will evaluate the interaction between the drugs tazemetostat and itraconazole. Part 2 of the study will evaluate the interaction between the drugs tazemetostat and rifampin For both Parts 1 and 2, safety and the level that effects of the study drug can be tolerated (known as tolerability) will be assessed throughout.

Detailed Description: This two-part study is designed to characterize the steady-state PK of oral tazemetostat and its metabolite EPZ 6930 when administered as a single and twice daily dose in subjects with advanced malignancies while taken alone or in combination with either itraconazole or rifampin. Part 1: tazemetostat and Itraconazole Drug Interaction Part 1 of the study will evaluate the drug-drug interaction between tazemetostat and itraconazole in an open-label, fixed sequential cross over design. Part 2: tazemetostat and Rifampin Drug Interaction Part 2 of the study will evaluate the drug-drug interaction between tazemetostat and rifampin in an open-label, fixed sequential cross over design. For both Parts 1 and 2, safety and tolerability will be assessed throughout the subject's participation. Subjects must have an end of study visit after 30 days of the last dose of tazemetostat for safety assessment.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

California Cancer Associates for Research and Excellence, Inc. (cCARE), Encinitas, California, United States

The Angeles Clinic and Research Institute, Los Angeles, California, United States

Northwestern University-Robert H. Lurie Comprehensive Cancer Center, Chicago, Illinois, United States

South Texas Accelerated Research Therapeutics (START) Midwest, Grand Rapids, Michigan, United States

Gabrail Cancer Center, Canton, Ohio, United States

University of Cincinnati Medical Center, Cincinnati, Ohio, United States

Mary Crowley Cancer Research, Dallas, Texas, United States

Onkologikoa, Donostia, Gipuzkoa, Spain

Hospital Universitario Vall d'Hebron, Barcelona, , Spain

Hospital Fundacion Jimenez Diaz, Madrid, , Spain

Contact Details

Name: Ipse Medical Director

Affiliation: Ipsen

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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