Multiple Myeloma
Conditions
Keywords
Myeloma, Multiple Myeloma, Relapsed Multiple Myeloma, Refractory Multiple Myeloma, Relapsed or Refractory Multiple Myeloma
Brief summary
The purpose of this study is to determine the safety and the maximum tolerated dose (MTD) of GRN163L 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.
Interventions
25% dose escalation infused over 2 hours weekly
Sponsors
Geron Corporation
Study design
Allocation
NON_RANDOMIZED
Intervention model
SINGLE_GROUP
Primary purpose
TREATMENT
Masking
NONE
Eligibility
Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No
Inclusion criteria
* Confirmed diagnosis of multiple myeloma (either secretory or nonsecretory disease) * Relapsed or refractory disease * At least two prior treatment regimens * ECOG performance status 0-2 * Adequate hepatic/renal function and platelet count * If previously treated with an anthracycline, anthracenedione, or trastuzumab, must have left ventricular ejection fraction \> 50%
Exclusion criteria
* Prior allogeneic bone marrow transplant, including syngeneic transplant * Known intracranial disease or epidural disease * Prior malignancy (within the last 3 years) * Clinically significant cardiovascular disease or condition * Active or chronically recurrent bleeding (eg, active peptic ulcer disease * Prolongation of PT or aPTT \> the ULN or fibrinogen \< the LLN * Clinically relevant active infection * Serious co-morbid medical conditions, including cirrhosis and chronic obstructive or chronic restrictive pulmonary disease * Symptomatic hyperviscosity syndrome * Any other cancer therapy within 3 weeks prior to study, except for mitomycin C, nitrosoureas, or high-dose chemotherapy with stem cell support within 6 weeks prior to study * Investigational therapy within 4 weeks prior to study * Anti-platelet therapy within 2 weeks prior to study, other than low dose aspirin prophylaxis therapy and low dose heparin administration for management of IV access devices * Radiation therapy within 4 weeks prior to study * Major surgery within 4 weeks prior to study * Active autoimmune disease requiring immunosuppressive therapy * Known positive serology for HIV
Design outcomes
Primary
| Measure | Time frame |
|---|---|
| Safety and MTD | First 3 weeks |
Secondary
| Measure | Time frame |
|---|---|
| PK, PD, and efficacy | Baseline to end of treatment |
Countries
United States
Outcome results
None listed