A Phase II Trial of ZIO-101 in Advanced Multiple Myeloma: Protocol SGL2001b

NCT ID: NCT00423644

Last Updated: 2013-11-14

Basic Information

• Recruitment Status: UNKNOWN
• Clinical Phase: PHASE2
• Total Enrollment: 17 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2007-01-31
• Study Completion Date: 2013-12-31

Brief Summary

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

Conditions

Multiple Myeloma

Keywords

Multiple Myeloma; arsenic; cancer study; failed treatment

Study Design

• Allocation Method: NON_RANDOMIZED
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

Single Arm

Group Type: EXPERIMENTAL

Darinaparson

Intervention Type: DRUG

420 mg/m2 of Darinaparsin given twice weekly for three weeks, followed by one week of rest for up to six months

Interventions

Darinaparson

420 mg/m2 of Darinaparsin given twice weekly for three weeks, followed by one week of rest for up to six months

Intervention Type: DRUG

Other Intervention Names

ZIO-101

Eligibility Criteria

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

• Minimum Eligible Age: 18 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Alaunos Therapeutics

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Locations

Glendale, Arizona, United States

Santa Barbara, California, United States

Santa Rosa, California, United States

West Hollywood, California, United States

Bethesda, Maryland, United States

Buffalo, New York, United States

Charlotte, North Carolina, United States

Sioux Falls, South Dakota, United States

Countries

United States

Other Identifiers

SGL2001b

Identifier Type: -

Identifier Source: org_study_id