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

Status unconfirmed · Phase 2

Conditions studied: Multiple Myeloma

In brief

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

Key facts

Study ID

NCT00423644

Run by

Alaunos Therapeutics

People needed

17

Starts

2007-01-01

Expected to finish

2013-12-01

Last updated by the study team

2013-11-14

Who can join

Age: 18 and older. Sex: any. Healthy volunteers: not accepted.

You may qualify if…

• 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:
• Serum M-protein level > 0.5 gm/dl (10.0 g/L) measured by serum protein electrophoresis.
• Urinary M-protein excretion > 0.2 g/24 hours by urine electrophoresis.
• 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;
• Informed consent compliant with ZIOPHARM policies and approved by the Human Investigation Review Committee with jurisdiction over the site;
• ECOG performance score ≤ 1;
• 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.
• Age ≥ 18;
• Granulocytes ≥ 1.0 x 109/L; platelets ≥ 50 x 109/L;
• Bilirubin ≤ 2.0 mg/dL; AST and ALT ≤ 2 x ULN;
• Creatinine ≤ 3 X ULN.
• No investigational agents within 28 days of study entry.
• 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).

You may not qualify if…

• 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;
• Women of childbearing potential. (Non-childbearing potential is defined as: surgical sterilization or 2 years post-menopausal)
• Active infection requiring antibiotics;
• Allergy to ZIO-101 or its excipients;
• Baseline confusion or dementia, defined as grade > 2 CTCAE Version 3.0;
• Significant neurotoxicityneuropathology, defined as grade > 2 neurotoxicity neuropathology per CTCAE Version 3.0;
• Prior seizures ≥ grade-3 in CTC v.3 criteria.
• Prior history of neurological deficits (e.g., stroke, dementia, ischemia) that has the potential to confound a post-dose neurological assessment

Where it is running

• Study site — Glendale, Arizona, United States
• Study site — Santa Barbara, California, United States
• Study site — Santa Rosa, California, United States
• Study site — West Hollywood, California, United States
• Study site — Bethesda, Maryland, United States
• Study site — Buffalo, New York, United States
• Study site — Charlotte, North Carolina, United States
• Study site — Sioux Falls, South Dakota, United States

Full record on ClinicalTrials.gov

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