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Brief Title: Safety Study of Oral Vinorelbine in Subjects With Non-Hematologic Malignancies
Official Title: A Phase 1 Study of the Safety, Pharmacokinetics, and Biological Activity of Metronomic Dosing With Orally Administered Vinorelbine Tablets in Subjects With Non-Hematologic Malignancies For Which There Are No Currently Accepted Therapies
Study ID: NCT00641160
Brief Summary: The purpose of this study is to determine the safety of oral administration of vinorelbine once daily for at least 7 days. The study will be conducted in subjects with a non-hematologic malignancy for which there are no currently accepted therapies.
Detailed Description:
Minimum Age: 18 Years
Eligible Ages: ADULT, OLDER_ADULT
Sex: ALL
Healthy Volunteers: No
Texas Oncology PA; Sammons Cancer Center, Dallas, Texas, United States
Name: George Tidmarsh, MD, PhD
Affiliation: Metronome Therapeutics
Role: STUDY_DIRECTOR