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

Phase 2
18 Years
Open (Enrolling)
Multiple Myeloma

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Trial Information

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

Inclusion 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

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

Type of Study:


Study Design:

Allocation: Non-Randomized, Endpoint Classification: Safety/Efficacy Study, Intervention Model: Single Group Assignment, Masking: Open Label, Primary Purpose: Treatment

Outcome Measure:

Response Rate

Outcome Time Frame:

6 months

Safety Issue:



United States: Food and Drug Administration

Study ID:




Start Date:

January 2007

Completion Date:

June 2013

Related Keywords:

  • Multiple Myeloma
  • Multiple Myeloma
  • arsenic
  • cancer study
  • failed treatment
  • Multiple Myeloma
  • Neoplasms, Plasma Cell



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