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Expanded Treatment Prot of Panobinostat in Combo w/ Bortez and Dex in Pts w/ Relapsed and/or Refractory Multiple Myeloma

Conditions
Multiple Myeloma
Registration Number
NCT02204553
Lead Sponsor
Novartis Pharmaceuticals
Brief Summary

This will be a multi-center, open label, expanded treatment protocol of panobinostat, bortezomib and dexamethasone in patients with relapsed and/or refractory multiple myeloma. Panobinostat will be administered at a starting dose of 20mg orally three times a week (every other day) for two weeks on and one week off, with dose adjustments permitted based on observed toxicity. Bortezomib will be administered either intravenously or sub-cutaneously, twice a week on days 1 and 4, two weeks on 1 week off. After 8 cycles of treatment, patients who have achieved stable disease or better by modified EBMT 1998 criteria may continue combination therapy with bortezomib dosing changed to days 1 and 8 of a 21 day cycle for up to 48 weeks of therapy. At the end of the treatment period, (48 weeks) patients with stable disease or better may continue on therapy at the discretion of their investigator until September 2015 or until drug is commercially available, whichever comes first. Patients who have not achieved at least stable disease by 8 cycles must discontinue from study treatment. Dexamethasone will be administered on the day of and the day immediately following bortezomib treatment. Patients will not receive any study treatment during the third week of each cycle. Cycles will be defined as 21 days of treatment. Investigators may not add any other anti-myeloma agents (with the exception of bisphosphonates) while patients remain on study treatment. Patients will remain on study until disease progression, unacceptable toxicity, or end of the study

Detailed Description

Not available

Recruitment & Eligibility

Status
NO_LONGER_AVAILABLE
Sex
All
Target Recruitment
Not specified
Inclusion Criteria
  • This study is intended for patients with relapsed and/or refractory multiple myeloma, who have received at least one prior line of therapy. Patients must require retreatment as per IMWG definitions (Kyle et al 2003). Approximately 50-100 patients are expected to be enrolled into this trial.
  • Patient has a previous diagnosis of multiple myeloma, based on IMWG 2003 definitions all three of the following criteria had been met:
  • Monoclonal immunoglobulin (M component) on electrophoresis, and on immunofixation on serum or on total 24 hour urine (or demonstration of M protein in cytoplasm of plasma cell for non secretory myeloma).
  • Bone marrow (clonal) plasma cells ≥ 10% or biopsy proven plasmacytoma
  • Related organ or tissue impairment (CRAB symptoms: anemia, hypercalcemia, lytic bone lesions, renal insufficiency, hyperviscosity, amyloidosis or recurrent infections)
  • Patients who have received allogeneic stem cell transplant and do not have active graft vs host disease requiring immunosuppressive therapy are eligible.
  • Patient with multiple myeloma (per IMWG 2003 definition) that is relapsed and/or refractory to at least one prior line of therapy and requires retreatment
  • Relapsed-and-refractory to a therapy, provided that the patient meets any of the following conditions:
  • Relapsed, defined by disease that recurred in a patient that responded under a prior therapy, by reaching a MR or better, and had not progressed under this therapy nor up to 60 days of last dose of this therapy. Patients who previously responded to treatment with BTZ are eligible.
  • Patient has relapsed to at least one prior line and patient was refractory to at least one prior line by either not reaching a MR, or progressed while under this therapy, or within 60 days of its last dose. Patients previously refractory to BTZ are also eligible.
  • Patients with primary refractory disease are eligible.
  • Patients who have previously received high dose therapy/autologous stem cell transplant are eligible
  • Patients who have received allogeneic stem cell transplant and do not have active graft vs host disease requiring immunosuppressive therapy are eligible
Exclusion Criteria
  • Patient has shown intolerance to bortezomib, dexamethasone or panobinostat or has any contraindications to any of these therapies. following available prescribing information
  • Allogeneic stem cell transplant recipient presenting with graft versus host disease either active or requiring immunosuppression
  • Patient has grade ≥ 2 peripheral neuropathy or grade 1 peripheral neuropathy with pain on clinical examination within 14 days of treatment
  • Patient taking any anti-cancer therapy concomitantly
  • Patient has second primary malignancy < 3 years of first dose of study treatment (except for treated basal or squamous cell carcinoma, or in situ cancer of the cervix)

Study & Design

Study Type
EXPANDED_ACCESS
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod

Trial Locations

Locations (27)

Los Angeles Hematology/Oncology Medical Group

🇺🇸

Los Angeles, California, United States

Sinai Hospital of Baltimore Sinai Hospital, Baltimore

🇺🇸

Baltimore, Maryland, United States

Northern Utah Cancer Associates SC

🇺🇸

Ogden, Utah, United States

Alta Bates Cancer Center

🇺🇸

Berkeley, California, United States

University Cancer Institute Univ. Cancer Institute

🇺🇸

Boyton Beach, Florida, United States

Stormont-Vail Cancer Center

🇺🇸

Topeka, Kansas, United States

Bronson Battle Creek Cancer Care Center

🇺🇸

Battle Creek, Michigan, United States

Texas Oncology Texas Oncology - Arlington

🇺🇸

Dallas, Texas, United States

Morton Coleman, MD M. Coleman, MD (2)

🇺🇸

New York, New York, United States

University of Mississippi Medical Center Cancer Institute

🇺🇸

Jackson, Mississippi, United States

Hematology Oncology of Central New Jersey

🇺🇸

Little Silver, New Jersey, United States

Wellmont Medical Associates

🇺🇸

Bristol, Tennessee, United States

Texas Oncology TX Oncology Baylor

🇺🇸

Dallas, Texas, United States

Virginia Oncology Associates Virginia Oncology Assoc. (2)

🇺🇸

Norfolk, Virginia, United States

Fox Valley Hematology and Oncology

🇺🇸

Appleton, Wisconsin, United States

Ironwood Cancer and Research Centers Ironwood Cancer

🇺🇸

Chandler, Arizona, United States

Highlands Oncology Group Dept of Highlands Oncology Grp

🇺🇸

Fayetteville, Arkansas, United States

George Washington U Medical Center Medical Faculty Associates

🇺🇸

Washington, District of Columbia, United States

Oncology Hematology West, PC Nebraska Cancer Specialists

🇺🇸

Omaha, Nebraska, United States

Hematology Oncology Clinic Hematology Oncology Clinic

🇺🇸

Baton Rouge, Louisiana, United States

Kaiser Permanente Medical Group Kaiser Permanente-Moanalua M.C

🇺🇸

Anaheim, California, United States

Emory University School of Medicine/Winship Cancer Institute Winship Cancer Institute (2)

🇺🇸

Atlanta, Georgia, United States

Stanford Cancer Center Stanford Cancer Institute (2)

🇺🇸

Stanford, California, United States

Memorial Cancer Institute Memorial Cancer Inst.

🇺🇸

Hollywod, Florida, United States

Lakes Research SC

🇺🇸

Miami Lakes, Florida, United States

Cancer Centers of the Carolinas GHS Cancer Institute

🇺🇸

Greenville, South Carolina, United States

Research Medical Center Research Med. Center

🇺🇸

Kansas City, Missouri, United States

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