Overview

This trial is active, not recruiting.

Condition multiple myeloma
Treatment darinaparson
Phase phase 2
Sponsor Ziopharm
Start date January 2007
End date December 2013
Trial size 17 participants
Trial identifier NCT00423644, SGL2001b

Summary

The study of safety of a new organic arsenic compound in the treatment of advanced multiple myeloma

United States No locations recruiting
Other Countries No locations recruiting

Study Design

Allocation non-randomized
Endpoint classification safety/efficacy study
Intervention model single group assignment
Masking open label
Primary purpose treatment
Arm
(Experimental)
darinaparson ZIO-101
420 mg/m2 of Darinaparsin given twice weekly for three weeks, followed by one week of rest for up to six months

Primary Outcomes

Measure
Response Rate
time frame: 6 months

Secondary Outcomes

Measure
Survival (overall and progression free)
time frame: 6 months
toxicities
time frame: 6 months

Eligibility Criteria

Male or female participants at least 18 years old.

Inclusion Criteria 1. Subjects with a confirmed diagnosis of active multiple myeloma with measurable protein criteria present to evaluate response. Measurable disease is defined as having at least one of the following criteria within 28 days prior to registration: 1. Serum M-protein level > 0.5 gm/dl (10.0 g/L) measured by serum protein electrophoresis. 2. Urinary M-protein excretion > 0.2 g/24 hours by urine electrophoresis. 2. Subjects must have relapsed or resistant disease, defined as either relapsing or is resistant after > 2 lines of prior therapy for myeloma. A minimum of 42 days must have elapsed since prior autologous or allogeneic transplant; 3. Informed consent compliant with ZIOPHARM policies and approved by the Human Investigation Review Committee with jurisdiction over the site; 4. ECOG performance score ≤ 1; 5. No chemotherapy, bortezomib, lenalidomide, thalidomide, arsenic trioxide, radiation therapy or immune therapy for ≥ 3 w and recovered from all treatment associated toxicities prior to registration; 5a. Patients may not receive more than the equivalent of 10 mg of prednisone per day for 2 weeks prior to registration. 6. Age ≥ 18; 7. Granulocytes ≥ 1.0 x 109/L; platelets ≥ 50 x 109/L; 8. Bilirubin ≤ 2.0 mg/dL; AST and ALT ≤ 2 x ULN; 9. Creatinine ≤ 3 X ULN. 10. No investigational agents within 28 days of study entry. 11. Males who agree to use a double-barrier method of birth control, (Double barrier method is defined as: a condom and either a diaphragm/cervical cap or an IUD). Exclusion Criteria 1. NYHA functional class ≥ 3, myocardial infarction ≤ 6 mo or uncontrolled cardiac arrhythmia other than asymptomatic atrial fibrillation; QTc ≥ 450msec; AV-block ≥ grade-2 or LBBB; 2. Women of childbearing potential. (Non-childbearing potential is defined as: surgical sterilization or 2 years post-menopausal) 3. Active infection requiring antibiotics; 4. Allergy to ZIO-101 or its excipients; 5. Baseline confusion or dementia, defined as grade > 2 CTCAE Version 3.0; 6. Significant neurotoxicityneuropathology, defined as grade > 2 neurotoxicity neuropathology per CTCAE Version 3.0; 7. Prior seizures ≥ grade-3 in CTC v.3 criteria. 8. Prior history of neurological deficits (e.g., stroke, dementia, ischemia) that has the potential to confound a post-dose neurological assessment

Additional Information

Official title A Phase II Trial of ZIO-101 in Advanced Multiple Myeloma: Protocol SGL2001b
Trial information was received from ClinicalTrials.gov and was last updated in November 2013.
Information provided to ClinicalTrials.gov by Ziopharm.