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Brief Title: A Phase 1-2 Dose-Escalation and Cohort-Expansion Study of Oral Tomivosertib (eFT-508) in Subjects With Hematological Malignancies
Official Title: A Phase 1-2 Dose-Escalation and Cohort-Expansion Study of Oral Tomivosertib (eFT-508) in Subjects With Hematological Malignancies
Study ID: NCT02937675
Brief Summary: This clinical trial is a Phase 1-2, open-label, sequential-group, dose-escalation and cohort-expansion study evaluating the safety, pharmacokinetics, pharmacodynamics, and antitumor activity of Tomivosertib (eFT-508). The study will evaluate oral daily administration of Tomivosertib (eFT-508). Treatment and study subject evaluation will be performed in 21-day cycles.
Detailed Description:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Samuel Oschin comprehensive Cancer Institute at Cedars-Sinai Medical Center, Los Angeles, California, United States
Florida Cancer Specialist, Sarasota, Florida, United States
Karmanos Cancer Institute, Detroit, Michigan, United States
Henry Ford Hospital, Detroit, Michigan, United States
Mayo Clinic, Rochester, Minnesota, United States
University of Rochester, Rochester, New York, United States
Gabrail Cancer Center Research, Canton, Ohio, United States
Baylor Scott & White Research Institute, Dallas, Texas, United States
Seattle Cancer Care Alliance, Seattle, Washington, United States
West Virginia University, Morgantown, West Virginia, United States
Name: Jeremy Barton, MD
Affiliation: CMO
Role: STUDY_DIRECTOR