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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1 February 2020 |
Main ID: |
EUCTR2012-002540-25-FR |
Date of registration:
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12/06/2013 |
Prospective Registration:
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No |
Primary sponsor: |
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Public title:
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Study to allow access to imatinib for patients who are on imatinib treatment in a Novartis-sponsored study and are benefiting from the treatment as judged by the investigator.
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Scientific title:
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An open label, multi-center imatinib roll-over protocol for patients who have completed a previous Novartis sponsored imatinib study and are judged by the investigator to benefit from continued imatinib treatment |
Date of first enrolment:
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23/01/2013 |
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:2012-002540-25 |
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: yes Other trial design description: roll-over protocol 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): no
Therapeutic use (Phase IV): yes
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Countries of recruitment
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Finland
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France
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Switzerland
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United Kingdom
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United States
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Contacts
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Name:
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Information&communication médicales
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Address:
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2 et 4 rue Lionel Terray
92500
Rueil-Malmaison
France |
Telephone:
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+33155476600 |
Email:
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icm.phfr@novartis.com |
Affiliation:
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Novartis Pharma S.A.S |
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Name:
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Information&communication médicales
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Address:
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2 et 4 rue Lionel Terray
92500
Rueil-Malmaison
France |
Telephone:
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+33155476600 |
Email:
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icm.phfr@novartis.com |
Affiliation:
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Novartis Pharma S.A.S |
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Key inclusion & exclusion criteria
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Inclusion criteria: Patient is currently enrolled in a Novartis- sponsored, Oncology Clinical Development & Medical Affairs study receiving imatinib and has fulfilled all their requirements in the parent study.
Patient is currently benefiting from the treatment with imatinib, as determined by the investigator.
Patient has demonstrated compliance, as assessed by the investigator, with the parent study protocol requirements. Are the trial subjects under 18? 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 F.1.3 Elderly (>=65 years) F.1.3.1 Number of subjects for this age range
Exclusion criteria: Patient has been permanently discontinued from imatinib study treatment in the
parent study due to unacceptable toxicity, non-compliance to study procedures,
withdrawal of consent or any other reason.
Patient has participated in a Novartis sponsored combination trial where imatinib
was dispensed in combination with another study medication and is still receiving
combination therapy.
Age minimum:
Age maximum:
Gender:
Female: yes Male: yes
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Health Condition(s) or Problem(s) studied
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Male and female patients who are currently enrolled in a Novartis-sponsored,
Oncology CD&MA imatinib study, are benefiting from treatment with imatinib and
have fulfilled all their requirements in the parent study.
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Therapeutic area: Diseases [C] - Cancer [C04]
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Intervention(s)
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Trade Name: Glivec Product Name: Glivec Product Code: STI571 Pharmaceutical Form: Tablet INN or Proposed INN: imatinib CAS Number: 152459-95-5 Current Sponsor code: STI571 Other descriptive name: IMATINIB Concentration unit: mg milligram(s) Concentration type: equal Concentration number: 100-
Trade Name: Glivec Product Name: Glivec Product Code: STI571 Pharmaceutical Form: Tablet INN or Proposed INN: imatinib CAS Number: 152459-95-5 Current Sponsor code: STI571 Other descriptive name: IMATINIB Concentration unit: mg milligram(s) Concentration type: equal Concentration number: 400-
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Primary Outcome(s)
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Primary end point(s): Number of patients receiving imatinib.
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Main Objective: To allow continued use of imatinib to patients receiving imatinib in a Novartis-sponsored Oncology CD&MA study which has reached its objectives and who are benefiting from treatment with imatinib.
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Secondary Objective: To collect long term data on serious adverse events.
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Secondary Outcome(s)
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Secondary end point(s): Frequency and nature of serious adverse events.
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Secondary ID(s)
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2012-002540-25-FI
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CSTI571A2406
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Source(s) of Monetary Support
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Novartis Pharma Services AG
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Ethics review
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Status: Approved
Approval date: 23/01/2013
Contact:
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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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