Main
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Note: This record shows only 22 elements of the WHO Trial Registration Data Set. To view changes that have been made to the source record, or for additional information about this trial, click on the URL below to go to the source record in the primary register. |
Register:
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EUCTR |
Last refreshed on:
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24 July 2017 |
Main ID: |
EUCTR2014-003239-21-SE |
Date of registration:
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29/05/2015 |
Prospective Registration:
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Yes |
Primary sponsor: |
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Public title:
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An expanded treatment protocol of panobinostat in combination therapy for relapsed and relapsed and refractory (RR) cancer of plasma cells.
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Scientific title:
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An open-label, multi-center, expanded treatment protocol of oral panobinostat in combination with bortezomib and dexamethasone in patients with relapsed and relapsed and refractory multiple myeloma |
Date of first enrolment:
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05/08/2015 |
Target sample size:
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200 |
Recruitment status: |
Not Recruiting |
URL:
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https://www.clinicaltrialsregister.eu/ctr-search/search?query=eudract_number:2014-003239-21 |
Study type:
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Interventional clinical trial of medicinal product |
Study design:
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Controlled: no
Randomised: no
Open: yes
Single blind: no
Double blind: no
Parallel group: no
Cross over: no
Other: no
If controlled, specify comparator, Other Medicinial Product: no
Placebo: no
Other: no
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Phase:
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Human pharmacology (Phase I): no
Therapeutic exploratory (Phase II): no
Therapeutic confirmatory - (Phase III): yes
Therapeutic use (Phase IV): no
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Countries of recruitment
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Austria
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Brazil
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Canada
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Colombia
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Denmark
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France
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Germany
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India
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Jordan
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Korea, Republic of
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Mexico
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Netherlands
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Norway
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Slovakia
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Sweden
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Taiwan
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Venezuela, Bolivarian Republic of
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Contacts
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Name:
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Clinical Trial Information Desk
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Address:
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Forum 1, Novartis Campus
4056
Basel
Switzerland |
Telephone:
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4161324 1111 |
Email:
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Affiliation:
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Novartis Pharma AG |
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Name:
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Clinical Trial Information Desk
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Address:
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Forum 1, Novartis Campus
4056
Basel
Switzerland |
Telephone:
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4161324 1111 |
Email:
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Affiliation:
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Novartis Pharma AG |
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Key inclusion & exclusion criteria
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Inclusion criteria: - Patient with diagnosis of multiple myeloma, based on IMWG definitions, that is relapsed or relapsed and refractory to at least two prior regimens including bortezomib and an immunomodulatory agent.
a. Relapsed, defined by disease that recurred in a patient that responded under at least two prior regimens including bortezomib and an immunomodulatory agent, by reaching a MR or better, and had not progressed under current therapy or up to 60 days of last dose of this therapy. Patients previously treated with bortezomib are eligible.
b. Relapsed-and-refractory to a therapy, provided that patient meets both conditions:
•patient has relapsed to at least two prior regimens including bortezomib and an immunomodulatory agent
•and patient was refractory to at least two prior regimens including bortezomib and an immunomodulatory agent by either not reaching a MR, or progressed while under this therapy, or within 60 days of its last dose. Patients previously treated with bortezomib are eligible even if they are deemed refractory.
- Patient has an Eastern Cooperative Oncology Group (ECOG) performance status of = 2
- Absolute neutrophil count (ANC) = 1.0 x 109 /L
- Platelet count = 100 x 109 /L
Are the trial subjects under 18? no Number of subjects for this age range: F.1.2 Adults (18-64 years) yes F.1.2.1 Number of subjects for this age range 75 F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range 125
Exclusion criteria: - Patient has shown intolerance or has any contraindications to bortezomib, dexamethasone or panobinostat
- Patient is refractory to panobinostat
- Patient has grade = 2 peripheral neuropathy
- Patient taking any anti-cancer therapy concomitantly (bisphosphonates are permitted)
- Patient requires medication with a risk of prolonging the QT interval or inducing Torsades de pointes
Age minimum:
Age maximum:
Gender:
Female: yes Male: yes
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Health Condition(s) or Problem(s) studied
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Therapeutic area: Diseases [C] - Cancer [C04]
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Multiple myeloma MedDRA version: 19.0
Level: LLT
Classification code 10028228
Term: Multiple myeloma
System Organ Class: 100000004864
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Intervention(s)
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Product Name: Farydak Product Code: LBH589 Pharmaceutical Form: Capsule, hard INN or Proposed INN: PANOBINOSTAT CAS Number: 404950-80-7 Current Sponsor code: LBH589 Concentration unit: mg milligram(s) Concentration type: equal Concentration number: 20-
Product Name: Bortezomib Pharmaceutical Form: Powder for solution for injection INN or Proposed INN: BORTEZOMIB CAS Number: 179324-69-7 Concentration unit: mg/m2 milligram(s)/square meter Concentration type: equal Concentration number: 1-
Product Name: Dexamethasone Pharmaceutical Form: Tablet INN or Proposed INN: DEXAMETHASONE Concentration unit: mg milligram(s) Concentration type: equal Concentration number: 2-
Product Name: Farydak Product Code: LBH589 Pharmaceutical Form: Capsule, hard INN or Proposed INN: PANOBINOSTAT CAS Number: 404950-80-7 Current Sponsor code: LBH589 Concentration unit: mg milligram(s) Concentration type: equal Concentration number: 10-
Product Name: Farydak Product Code: LBH589 Pharmaceutical Form: Capsule, hard INN or Proposed INN: PANOBINOSTAT CAS Number: 404950-80-7 Current Sponsor code: LBH589 Concentration unit: mg milligram(s) Concentration type: equal Concentration number: 15-
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Primary Outcome(s)
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Secondary Objective: Secondary: - To assess the efficacy of panobinostat when used in combination with BTZ/DEX by overall response rate (CR, nCR or PR) and progression-free survival per EBMT criteria
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Primary end point(s): AEs, Grade 3&4 AEs & SAEs, events of special interest, AEs leading to discontinuation, and deaths.
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Main Objective: - To provide multiple myeloma patients early access to treatment with panobinostat and to further evaluate safety of panobinostat when used in combination with BTZ/Dex in patients with multiple myeloma who have received at least two prior regimens including bortezomib and an immunomodulatory agent.
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Timepoint(s) of evaluation of this end point: discontinuation or deaths or after 16 cycles
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Secondary Outcome(s)
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Timepoint(s) of evaluation of this end point: discontinuation or deaths or after 16 cycles
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Secondary end point(s): Secondary:
- Overall response rate per modified EBMT criteria by investigator assessment
- Progression-free survival (PFS) based on investigator-assessed progression per modified EBMT criteria
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Secondary ID(s)
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CLBH589D2001X
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2014-003239-21-AT
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Source(s) of Monetary Support
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Novartis Pharma Services AG
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Results
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Results available:
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Date Posted:
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Date Completed:
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URL:
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