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Spots Global Cancer Trial Database for Safety and Dose Study of GRN163L and Velcade to Treat Patients With Refractory or Relapsed Myeloma

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Trial Identification

Brief Title: Safety and Dose Study of GRN163L and Velcade to Treat Patients With Refractory or Relapsed Myeloma

Official Title: A Phase I Study of GRN163L in Combination With Bortezomib and Dexamethasone in Patients With Relapsed or Refractory Multiple Myeloma

Study ID: NCT00718601

Study Description

Brief Summary: The purpose of this study is to determine safety and the maximum tolerated dose (MTD) of GRN163L and Velcade with and without Decadron when administered to patients with refractory or relapsed multiple myeloma.

Detailed Description: GRN163L is a telomerase template antagonist with in vitro and in vivo activity in a variety of tumor model systems. Telomerase is an enzyme that is active primarily in tumor cells and is crucial for the indefinite growth of tumor cells. Inhibition of telomerase may result in antineoplastic effects.

Eligibility

Minimum Age: 18 Years

Eligible Ages: ADULT, OLDER_ADULT

Sex: ALL

Healthy Volunteers: No

Locations

Karmanos Cancer Center, Detroit, Michigan, United States

St. Vincent's Comprehensive Cancer Center, New York City, New York, United States

Fred Hutchinson Cancer Research Center, Seattle, Washington, United States

Contact Details

Name: Stephen Kelsey, MD

Affiliation: Geron Corporation

Role: STUDY_DIRECTOR

Useful links and downloads for this trial

Clinicaltrials.gov

Google Search Results

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