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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30 June 2019 |
Main ID: |
EUCTR2012-003065-17-GB |
Date of registration:
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25/02/2013 |
Prospective Registration:
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Yes |
Primary sponsor: |
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Public title:
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Study of efficacy and safety of everolimus and letrozole in estrogen receptor positive HER2 negative metastatic or locally advanced breast cancer patients
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Scientific title:
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An open-label, phase II, single-arm study of everolimus in combination with letrozole in the treatment of postmenopausal women with estrogen receptor positive HER2 negative metastatic or locally advanced breast cancer |
Date of first enrolment:
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16/05/2013 |
Target sample size:
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200 |
Recruitment status: |
Authorised-recruitment may be ongoing or finished |
URL:
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https://www.clinicaltrialsregister.eu/ctr-search/search?query=eudract_number:2012-003065-17 |
Study type:
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Interventional clinical trial of medicinal product |
Study design:
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Controlled: no Randomised: Open: Single blind: Double blind: Parallel group: Cross over: Other: If controlled, specify comparator, Other Medicinial Product: Placebo: Other:
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Phase:
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Human pharmacology (Phase I): no
Therapeutic exploratory (Phase II): yes
Therapeutic confirmatory - (Phase III): no
Therapeutic use (Phase IV): no
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Countries of recruitment
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Argentina
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Austria
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Brazil
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France
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Hungary
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Japan
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Korea, Republic of
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Netherlands
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Portugal
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Spain
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Thailand
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Turkey
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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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Medical Collaboration Centre
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Address:
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Frimley Business Park
GU16 7SR
Frimely, Camberley, Surrey
United Kingdom |
Telephone:
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+4401276698 370 |
Email:
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medinfo.uk@novartis.com |
Affiliation:
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Novartis Pharmaceuticals UK Ltd |
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Name:
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Medical Collaboration Centre
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Address:
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Frimley Business Park
GU16 7SR
Frimely, Camberley, Surrey
United Kingdom |
Telephone:
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+4401276698 370 |
Email:
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medinfo.uk@novartis.com |
Affiliation:
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Novartis Pharmaceuticals UK Ltd |
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Key inclusion & exclusion criteria
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Inclusion criteria: •Patients 18 years old or greater
•Patients with metastatic or locally advanced, unresectable breast cancer not amenable to curative treatment by surgery or radiotherapy
•Histological or cytological confirmation of estrogen-receptor positive (ER+) human epidermal growth factor receptor 2 negative (HER2-) breast cancer
•Postmenopausal women
•No prior treatment for metastatic breast cancer
Other protocol based inclusion criteria may apply 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 108 F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range 94
Exclusion criteria: •Patients with only non-measurable lesions other than bone metastases (e.g., pleural effusion, ascites, etc)
•Patients who have received prior hormonal or any other systemic therapy for metastatic breast cancer.
•Patients may have received prior neoadjuvant or adjuvant endocrine therapy. In the case of neoadjuvant or adjuvant NSAI (letrozole/anastrozole) therapy patients must have completed therapy at least 1 year prior to study enrollment.
•Previous treatment with mTOR inhibitors.
•Known hypersensitivity to mTOR inhibitors, e.g., sirolimus (rapamycin).
•Other protocol-defined inclusion/exclusion criteria may apply
Other protocol based exclusion criteria may apply
Age minimum:
Age maximum:
Gender:
Female: yes Male: no
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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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Estrogen receptor positive metastatic breast cancer
MedDRA version: 20.0
Level: PT
Classification code 10070577
Term: Oestrogen receptor positive breast cancer
System Organ Class: 10029104 - Neoplasms benign, malignant and unspecified (incl cysts and polyps)
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Intervention(s)
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Trade Name: Afinitor Product Name: Everolimus Product Code: RAD001 Pharmaceutical Form: Tablet CAS Number: 159351-69-6 Current Sponsor code: RAD001 Other descriptive name: EVEROLIMUS Concentration unit: mg milligram(s) Concentration type: equal Concentration number: 5-
Trade Name: Afinitor Product Name: Everolimus Product Code: RAD001 Pharmaceutical Form: Tablet CAS Number: 159351-69-6 Current Sponsor code: RAD001 Other descriptive name: EVEROLIMUS Concentration unit: mg milligram(s) Concentration type: equal Concentration number: 10-
Product Name: exemestane Pharmaceutical Form: Coated tablet INN or Proposed INN: exemestane CAS Number: 107868-30-4 Other descriptive name: EXEMESTANE Concentration unit: mg milligram(s) Concentration type: equal Concentration number: 25-
Product Name: Femara Product Code: FEM345 Pharmaceutical Form: Tablet INN or Proposed INN: LETROZOLE CAS Number: 112809-51-5 Current Sponsor code: FEM345 Concentration unit: mg milligram(s) Concentration type: equal Concentration number: 2.5-
Trade Name: Afinitor Product Name: Everolimus Product Code: RAD001 Pharmaceutical Form: Tablet CAS Number: 159351-69-6 Current Sponsor code: RAD001 Other descriptive name: EVEROLIMUS Concentration unit: mg milligram(s) Concentration typ
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Primary Outcome(s)
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Main Objective: The primary objective is to estimate progression-free survival in patients treated with everolimus + letrozole in the first line metastatic setting.
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Secondary Objective: - Determine the overall response rate and clinical benefit rate of everolimus + letrozole in the first line metastatic setting - Determine the progression free survival and clinical benefit rate of everolimus + exemestane in second line population - Estimate the overall survival of patients treated with everolimus + letrozole in the first line setting - Evaluate a therapeutic intervention to reduce the severity and duration of stomatitis - Evaluate the safety of everolimus + letrozole in the first line setting - Evaluate the safety of everolimus + exemestane in the second line setting - Evaluate clinical benefit as assessed by the investigator during the Extension Phase - Evaluate long term safety data
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Primary end point(s): Percentage of patients progression-free after completion of 1st line treatment (everolimus + letrozole)
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Timepoint(s) of evaluation of this end point: 12 months after last patient recruited
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Secondary Outcome(s)
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Secondary end point(s): - Overall response rate and clinical benefit rate in patients receiving the first line study treatment (everolimus + letrozole)
- Progression-free survival in the second line is defined as the time interval between start of 2nd line treatment and documented disease progression or death due to any cause reported during or after second-line treatment
- Overall survival of patients receiving first line study treatment (everolimus + letrozole)
- Reduction in severity and duration of oral stomatitis
- Assessment of safety based on the frequency of adverse events that fall outside normal pre-specified ranges
- Overall response rate and clinical benefit rate in patients receiving the second line study treatment (everolimus + exemestane)
- Reduction in severity and duration of oral stomatitis
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Timepoint(s) of evaluation of this end point: - Baseline, every 8 weeks
- Baseline, every 8 weeks
- Baseline, every 8 weeks
- Continous during the study and every 12weeks after last treatment
- Upon onset of 1st stomatitis, patient will complete diary daily until resolution of stomatitis
- Continuous during the study, up to 28 days after last treatment
- Baseline every 8 weeks
- Upon onset of 1st stomatitis and in countries where the alcohol-free dexamethasone solution (0.5mg/5ml) is commercially available, patient will be randomised to dexamethasone oral solution rinse or standard of care.
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Secondary ID(s)
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CRAD001Y24135
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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:
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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