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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27 February 2017 |
Main ID: |
EUCTR2011-001112-53-ES |
Date of registration:
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24/11/2011 |
Prospective Registration:
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Yes |
Primary sponsor: |
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Public title:
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A study of AMG 386 or placebo in combination with paclitaxel and carboplatin to treat ovarian cancer
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Scientific title:
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A Phase 3 Randomized, Double-blind, Placebo-controlled, Multicenter Study of AMG 386 With Paclitaxel and Carboplatin as First-line Treatment of Subjects With FIGO Stage III-IV Epithelial Ovarian, Primary Peritoneal or Fallopian Tube Cancers |
Date of first enrolment:
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24/01/2012 |
Target sample size:
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2000 |
Recruitment status: |
Not Recruiting |
URL:
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https://www.clinicaltrialsregister.eu/ctr-search/search?query=eudract_number:2011-001112-53 |
Study type:
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Interventional clinical trial of medicinal product |
Study design:
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Controlled: yes
Randomised: yes
Open: no
Single blind: no
Double blind: yes
Parallel group: yes
Cross over: no
Other: no
If controlled, specify comparator, Other Medicinial Product: no
Placebo: yes
Other: no
Number of treatment arms in the trial: 2
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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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Belgium
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Canada
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Denmark
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European Union
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Germany
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Greece
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Hong Kong
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Italy
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Japan
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Korea, Republic of
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Netherlands
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Russian Federation
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Spain
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United States
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Contacts
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Name:
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IHQ Medical Info - Clinical trials
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Address:
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Dammstrasse 23
CH-6300 Zug
P.O. Box 1557
Switzerland |
Telephone:
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N/A |
Email:
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MedinfoInternational@amgen.com |
Affiliation:
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Amgen (EUROPE) GmbH |
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Name:
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IHQ Medical Info - Clinical trials
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Address:
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Dammstrasse 23
CH-6300 Zug
P.O. Box 1557
Switzerland |
Telephone:
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N/A |
Email:
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MedinfoInternational@amgen.com |
Affiliation:
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Amgen (EUROPE) GmbH |
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Key inclusion & exclusion criteria
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Inclusion criteria: Female subjects 18 years of age or older with FIGO Stages III-IV epithelial ovarian, primary peritoneal or fallopian tube cancer with an indication for first-line treatment with paclitaxel and carboplatin x 6 cycles (subjects with pseudomyxoma, mesothelioma, adenocarcinoma with unknown primary tumour, carcinosarcoma, sarcoma, mucinous or neuroendocrine histology are excluded)
Subjects with FIGO Stage IIIA or IIIB disease must have undergone PDS for ovarian, primary peritoneal or fallopian tube cancer within 12 weeks prior to randomization
Subjects with FIGO Stage IIIc or IV disease must either: - undergo PDS for epithelial ovarian, primary peritoneal or fallopian tube cancer within 12 weeks prior to randomization or - plan to have IDS following 3 cycles of paclitaxel and carboplatin plus AMG 386 or AMG 386 placebo for biopsy proven epithelial ovarian, primary peritoneal or fallopian tube cancer
ECOG performance status os 0 or 1
Adequate bone marrow, renal and hepatic funtion 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 1400 F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range 600
Exclusion criteria: Prior use of any anticancer therapy or experimental therapy for epithelial ovarian, primary peritoneal or fallopian tube cancers
Previous abdonimal and/or pelvic external beam radiotherapy
History of central nervous metastasis
History of arterial or venous thromboembolism within 12 months prior to randomization
Clinically significant cardiovascular disease within 12 months prior to randomization
Age minimum:
Age maximum:
Gender:
Female: yes Male: no
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Health Condition(s) or Problem(s) studied
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FIGO Stage III-IV Epithelial Ovarian, Primary Peritoneal or Fallopian Tube Cancers MedDRA version: 14.0
Level: PT
Classification code 10033128
Term: Ovarian cancer
System Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
MedDRA version: 14.0
Level: PT
Classification code 10061269
Term: Malignant peritoneal neoplasm
System Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
MedDRA version: 14.0
Level: PT
Classification code 10016180
Term: Fallopian tube cancer
System Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
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Therapeutic area: Diseases [C] - Cancer [C04]
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Intervention(s)
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Product Name: AMG 386 Product Code: AMG 386 Pharmaceutical Form: Powder for solution for infusion INN or Proposed INN: AMG 386 CAS Number: N/A Current Sponsor code: AMG 386 Other descriptive name: AMG 386 Concentration unit: mg milligram(s) Concentration type: range Concentration number: 150-600 Pharmaceutical form of the placebo: Powder for solution for infusion Route of administration of the placebo: Intravenous use
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Primary Outcome(s)
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Main Objective: To determine if 6 cycles of paclitaxel and carboplatin plus AMG 386 followed by 18 months of AMG 386 maintenance improves progression-free survival (PFS) compared to 6 cycles of paclitaxel and carboplatin plus AMG 386 placebo followed by 18 months of AMG 386 placebo maintenance in the first-line treatment of subjects with FIGO Stage III-IV epithelial ovarian, primary peritoneal or fallopian tube cancers
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Primary end point(s): Pogression Free Survival (PFS) PFS is defined as the time from the randomization date to the earlier of the dates of (1) the first objective disease progression per RECIST 1.1 with modifications (see protocol for details) or (2) death from any cause.
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Secondary Objective: To determine if 6 cycles of paclitaxel and carboplatin plus AMG 386 followed by 18 months of AMG 386 maintenance improves overall survival (OS) compared to 6 cycles of paclitaxel and carboplatin plus AMG 386 placebo followed by 18 months of AMG 386 placebo maintenance.
To evaluate the safety and tolerability of AMG 386 plus paclitaxel and carboplatin.
To evaluate the pharmacokinetics (PK) of AMG 386 (Cmax and Cmin).
To estimate the incidence of anti-AMG 386 antibody formation.
To estimate the effect of AMG 386 on patient reported ovarian cancer-specific symptoms and overall health status as measured by the EuroQOL (EQ-5D) questionnaire.
To evaluate AMG 386 exposure-response relationships for PFS and OS.
To investigate potential biomarker development based on assessment of blood samples and tumor samples, genetic analysis of tumor samples, the proposed mechanism of action of AMG 386 and response.
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Timepoint(s) of evaluation of this end point: Interim analysis ? 438 PFS events (21 months post FSE) Primary analysis ? 719 PFS events (3 months post completion of accrual)
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Secondary Outcome(s)
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Timepoint(s) of evaluation of this end point: Interim analysis ? 477 OS events (33 months post FSE) Primary analysis ? 900 OS events (54 months post FSE)
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Secondary end point(s): - Overall Survival (OS) OS is defined as the time from the randomization date to the date of death from any cause. Subjects who have been lost to follow-up before the analysis data cutoff date or otherwise have not died by the analysis data cutoff date will be censored at their last contact date (last known to be alive) - Incidence of adverse events and significant laboratory abnormalities - Pharmacokinetics of AMG 386 (Cmax and Cmin) - Incidence of anti-AMG 386 antibody formation - Patient reported ovarian cancer-specific symptoms and health related quality of life - Patient reported health status as measured by the EQ-5D - AMG 386 exposure-response relationships for PFS and OS - Correlation of serum biomarkers with measures of response
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Secondary ID(s)
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2011-001112-53-GR
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20101129
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Source(s) of Monetary Support
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Amgen Inc.
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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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