Open Label Study With Imetelstat to Determine Effect of Imetelstat in Patients w/ Previously Treated Multiple Myeloma

PHASE2CompletedINTERVENTIONAL
Enrollment

13

Participants

Timeline

Start Date

November 30, 2010

Primary Completion Date

November 30, 2014

Study Completion Date

November 30, 2014

Conditions
Multiple Myeloma
Interventions
DRUG

Imetelstat (7.5 mg/kg)

Imetelstat 7.5 mg/kg as a 2-hour intravenous infusion (± 10 minutes) on Days 1 and 8 of a 28-day cycle; the Day 8 dose will be omitted in patients with a prior history of bone marrow or stem cell transplant.

DRUG

lenalidomide standard of care

Patients who are receiving lenalidomide as maintenance therapy upon enrollment as part of their treatment regimen may remain on this therapy during trial participation, provided that they have received this treatment for a minimum of 3 months and demonstrate evidence of stabilization of their response.

DRUG

Imetelstat (9.4 mg/kg)

Imetelstat 9.4 mg/kg as a 2-hour intravenous infusion (± 10 minutes) on Days 1 and 8 of a 28-day cycle; the Day 8 dose will be omitted in patients with a prior history of bone marrow or stem cell transplant.

Trial Locations (2)

21201

University of Maryland Medical Center - M & S Greenebaum Cancer Center, Baltimore

21231

Sidney Kimmel Cancer Center Johns Hopkins Hospital, Baltimore

Sponsors

Lead Sponsor

All Listed Sponsors
lead

Geron Corporation

INDUSTRY