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Spots Global Cancer Trial Database for Safety Study of Oral Vinorelbine in Subjects With Non-Hematologic Malignancies

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Trial Identification

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

Study Description

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:

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Texas Oncology PA; Sammons Cancer Center, Dallas, Texas, United States

Contact Details

Name: George Tidmarsh, MD, PhD

Affiliation: Metronome Therapeutics

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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