Open Label Study With Imetelstat to Determine Effect of Imetelstat in Patients w/ Previously Treated Multiple Myeloma
|Study Design:||Endpoint Classification: Safety/Efficacy Study
Intervention Model: Single Group Assignment
Masking: Open Label
Primary Purpose: Treatment
|Official Title:||A Phase II Trial to Determine the Effect of Imetelstat (GRN163L) on Patients With Previously Treated Multiple Myeloma|
- Rate of Improvement in Response [ Time Frame: From time of first dose (Cycle 1 day 1) through end of study period (12 mos. after last participant is enrolled) ] [ Designated as safety issue: No ]To determine the rate of improvement in response in patients with previously treated multiple myeloma following treatment with imetelstat alone or in combination wtih lenalidomide maintenance therapy. Response will be assessed using the International Uniform Response Criteria for Multiple Myeloma (IURCMM).
- Progression-free Survival (PFS) [ Time Frame: From time of first dose (Cycle 1 day 1) through end of study (12 mos. after last participant is enrolled) ] [ Designated as safety issue: No ]As assessed from Cycle 1 Day 1 to first evidence of PD as defined by IURCMM, or death, whichever occurs first.
- Safety and Tolerability [ Time Frame: From time of first dose (Cycle 1 day 1) through end of study (12 mos. after last participant is enrolled) ] [ Designated as safety issue: Yes ]
The safety and tolerability of imetelstat will be assessed by the incidence, nature, relatedness and severity of adverse events, laboratory abnormalities and vital signs.
Patients who develop Grade 3 or 4 cytopenias (other than lyphophenia and/or leukopenia alon) will receive addiontal safety monitoring for reversibility.
|Study Start Date:||November 2010|
|Study Completion Date:||November 2014|
|Primary Completion Date:||November 2014 (Final data collection date for primary outcome measure)|
Experimental: Imetelstat plus standard of care
9.4 mg/kg over a 2 hour IV Infusion on Day 1 and Day 8 of a 28-day cycle.
Drug: Standard of Care
Standard of Care
Please refer to this study by its ClinicalTrials.gov identifier: NCT01242930
|United States, Maryland|
|Sidney Kimmel Cancer Center Johns Hopkins Hospital|
|Baltimore, Maryland, United States, 21231|
|University of Maryland Medical Center - M & S Greenebaum Cancer Center|
|Baltimore, Maryland, United States, 21201|
|Study Director:||Ted Shih, PharmD||Geron Corporation|
|Principal Investigator:||Carol Ann Huff, M.D.||Sidney Kimmel Cancer Center at Johns Hopkins Hospital|