Phase 1b Single Arm, Open Label, Multi-Center Study of Fluphenazine HCl Monotherapy in Relapsed or Relapsed-and-Refractory Multiple Myeloma
| City: |
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San Antonio |
| State: |
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Texas |
| Zip Code: |
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78229 |
| Conditions: |
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Multiple Myeloma |
| Purpose: |
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The purpose of this study is to evaluate the safety and tolerability of fluphenazine in
patients with advanced multiple myeloma. The study will also describe the efficacy of this
drug.
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| Study Summary: |
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This is a multicenter, dose-escalating, Phase 1b trial in patients with relapsed or
relapsed-and-refractory multiple myeloma. Patients will be dosed on Days 1 and 8 of each 21
day cycle.
This study will be conducted in two parts. In Part 1, the MTD determining portion of the
study, patients will be enrolled in cohorts of 3 patients at each dose level. At least 3
patients will complete 21 days at each dose level and will be evaluated for safety and
tolerability before additional patients are treated at higher doses. Doses will be
increased following a modified Fibonacci scheme.
In Part 2, twelve additional patients will be enrolled at the MTD determined in Part 1 (or
the dose for the highest dose cohort completed if the MTD has not been reached) to further
evaluate the safety, tolerability, and preliminary efficacy of this dose regimen.
Serum fluphenazine pharmacokinetic studies will be performed during the first cycle of the
therapy in all Part 1 and Part 2 consenting patients.
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| Criteria: |
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Inclusion Criteria:
- Histologically or cytologically confirmed diagnosis of multiple myeloma that is
relapsed or relapsed-and-refractory after at least 2 or more prior lines of therapy.
Patients must have achieved at least minor response (MR) to at least one prior line
of therapy
- Progressive disease must have occurred either during or subsequent to the patient's
last treatment for multiple myeloma prior to the current enrollment
- Measurable disease defined by serum M-protein ≥1 g/dL, or urine light chain ≥200
mg/24 hours, or abnormal serum FLC ratio with involved FLC > 10 mg/dL provided serum
FLC ratio is abnormal
- Age >18 years
- Eastern Cooperative Oncology Group (performance status of ≤20
- Life expectancy ≥12 weeks
- Signed written informed consent per institutional and federal regulatory requirements
- Did not receive chemotherapy (including systemic steroids), immunotherapy
(interferon), Imids (thalidomide/lenalidomide), proteasome inhibitors (bortezomib),
or radiotherapy for at least 21 days prior to Day 1 of Cycle 1
- Did not receive any investigational treatment for at least 28 days prior to study
entry
- Absolute granulocyte count of ≥1,000/μL, platelet count ≥50,000/μL, and hemoglobin
≥8.0 g/dL, with no transfusion within the preceding 7 days
- Adequate liver function defined by a bilirubin value ≤2 times the upper limit of
normal (ULN), and transaminases (AST and ALT) values ≤2.5 times ULN
- Adequate renal function defined by a creatinine clearance of ≥30 mL/min
- Adequate cardiac function defined by a left ventricular ejection fraction (LVEF)
≥40%, QTc <450 msec, and no evidence of clinically significant dysrhythmias on ECG
- Patient must have substantially recovered from clinically significant toxicities from
prior therapies for multiple myeloma
- Fertile men and women must agree to use a medically effective contraception method
throughout the treatment period. Premenopausal women of reproductive capacity and
women less than 24 months post menopause must have a negative serum pregnancy test
documented prior to study entry
Exclusion Criteria:
- Patients who never achieved at least minor response (MR) to at least one prior line
of therapy
- Clinical spinal cord compression syndromes (unless patient has undergone treatment,
for example, surgery or radiation therapy, and neurological findings are ≤ Grade 1
and patient is off corticosteroids for spinal cord edema or on a stable regimen of <
10 mg/day prednisone equivalent
- Clinical signs of brain involvement or leptomeningeal disease
- Plasma cell leukemia (plasma cells > 2000/cubic mm)
- Women who are pregnant or breast feeding
- Other serious illness or medical condition(s) (see protocol)
- Hypersensitivity to fluphenazine or other phenothiazines
- Currently being treated with hematopoietic growth factors other than erythropoietin
(EPO). Treatment with hematopoietic growth factors may be started during the study
with development, or worsening, of cytopenia
- Concurrent use of anticholinergics
- Concurrent use of phenothiazine and atypical antipsychotics
- Concurrent use of anti-seizure drugs, with the exception of gabapentin for treatment
of neuropathy
- Grade 2 or higher persisting prior treatment-related neuropathy
- Concurrent use of systemic steroids with the exception of chronically administered
steroids equivalent to ≤ 10 mg/day prednisone if patient has been on this therapy for
≥1month
- History of seizures or extrapyramidal symptoms
- History of other malignancies within the past 3 years, other than adequately treated
non-melanoma skin cancer, or in situ carcinoma of the cervix, unless the other
malignancy is quiescent and medical monitor approval is obtained
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| NCT ID: |
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NCT00821301 |
| Primary Contact: |
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Study Director
Bruce A Silver, M.D., FACP
Stephen Roth, Ph.D.
Phone: 610-941-2972
Email: sroth@immunecontrol.com
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| Backup Contact: |
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N/A |
| Location Contact: |
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San Antonio, Texas 78229
United States
Lyanna Smith, BSN, RN
Phone: 210-450-5816
Email: smithl6@uthscsa.edu
Site Status: Recruiting |
| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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June 18, 2013 |
| Modifications to this listing: |
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