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 October 2014 |
Main ID: |
EUCTR2012-000073-23-SE |
Date of registration:
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28/03/2012 |
Prospective Registration:
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Yes |
Primary sponsor: |
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Public title:
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An expanded access study for postmenopausal women with estrogen receptor positive locally advanced or metastatic breast cancer who have progressed following prior endocrine therapy, investigating the treatment of everolimus (RAD001) in combination with exemestane
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Scientific title:
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An open-label, multi-center, expanded access study for postmenopausal women with estrogen receptor positive locally advanced or metastatic breast cancer who have progressed following prior endocrine therapy, investigating the treatment of everolimus (RAD001) in combination with exemestane |
Date of first enrolment:
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16/05/2012 |
Target sample size:
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2500 |
Recruitment status: |
Not Recruiting |
URL:
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https://www.clinicaltrialsregister.eu/ctr-search/search?query=eudract_number:2012-000073-23 |
Study type:
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Interventional clinical trial of medicinal product |
Study design:
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Controlled: no
Randomised: no
Open: no
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
Number of treatment arms in the trial: 1
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Phase:
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Countries of recruitment
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Austria
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Belgium
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Bulgaria
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Denmark
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Finland
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Hungary
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Ireland
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Italy
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Netherlands
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Norway
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Slovakia
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Spain
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Sweden
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Contacts
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Name:
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Medical Information
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Address:
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Box 1150
183 11
Täby
Sweden |
Telephone:
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4687323200 |
Email:
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medinfo.se@novartis.com |
Affiliation:
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Novartis Sverige AB |
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Name:
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Medical Information
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Address:
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Box 1150
183 11
Täby
Sweden |
Telephone:
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4687323200 |
Email:
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medinfo.se@novartis.com |
Affiliation:
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Novartis Sverige AB |
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Key inclusion & exclusion criteria
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Inclusion criteria: 1.Adult women (= 18 years of age) with metastatic or locally advanced breast cancer not amenable to curative treatment by surgery or radiotherapy, whose disease recurred or progressed following a NSAI
treatment.
Letrozole or anastrozole do not have to be last treatment prior to study
enrollment.
2.Histological or cytological confirmation of estrogen-receptor positive (ER+) breast cancer and/or progesterone receptor-positive (PgR+)
3. Postmenopausal women. Postmenopausal status is defined either by:
• Age = 55 years and one year or more of amenorrhea
• Age < 55 years and one year or more of amenorrhea, with an
estradiol assay < 20 pg/ml
• Surgical menopause with bilateral oophorectomy
4. Radiological or clinical evidence of recurrence or progression on last therapy prior to enrollment.
5. Adequate bone marrow and coagulation function as shown by:
• Absolute neutrophil count (ANC) = 1.5 109/L
• Platelets = 100 ×109/L
• Hemoglobin (Hgb) = 9.0 g/dL
• INR = 2
6. Adequate liver function as shown by:
• Serum aspartate aminotransferase (AST) and alanine
aminotransferase (ALT) = 2.5 ULN (or = 5 if hepatic metastases are
present)
• Total serum bilirubin = 1.5 × ULN (= 3 × ULN for patients known to
have Gilbert Syndrome)
7. Adequate renal function as shown by:
• Serum creatinine = 1.5 × ULN
8. Fasting serum cholesterol = 300 mg/dl or 7.75 mmol/L and fasting
triglycerides = 2.5 × ULN. In case one or both of these thresholds are
exceeded, the patient can only be included after initiation of statin
therapy or other lipid lowering drugs (eg fibrates), and when the above
mentioned values have been achieved
9. Written informed consent obtained before any screening procedure
and according to local guidelines
Other protocol defined 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 1250 F.1.3 Elderly (>=65 years) yes F.1.3.1 Number of subjects for this age range 1250
Exclusion criteria: 1.HER2-overexpressing patients by local laboratory testing (IHC 3+ staining or in situ hybridization positive).
2. Pre-menopausal, pregnant, lactating women
3. Known hypersensitivity to mTOR inhibitors, e.g. sirolimus (rapamycin)
or to their excipients.
4. Known hypersensitivity to exemestane, to the active substance or to
any of the excipients.
5. Patients with rare hereditary problems of galactose intolerance, Lapp
lactase deficiency or glucose galactose malabsorption.
6. Radiotherapy within four weeks prior to enrollment (baseline/treatment
start) except in case of localized radiotherapy for analgesic purpose or for lytic lesions at risk of fracture which can then be completed within two weeks prior to enrollment (baseline/treatment
start). Patients must have recovered from radiotherapy toxicities
prior to enrollment.
7. Currently receiving hormone replacement therapy, unless
discontinued prior to enrollment.
8. Patients receiving concomitant immunosuppressive agents or chronic
corticosteroids use, at the time of study entry except in cases outlined
below:
Prolonged systemic corticosteroid treatment during study, except for
topical applications (e.g. rash),inhaled sprays (e.g. obstructive airways
diseases), eye drops or local injections (e.g. intraarticular) should not be
given. However, during the study:
• short duration (<2 weeks) of systemic corticosteroids is allowed (e.g.
chronic obstructive pulmonary disease, anti-emetic) ;
• low doses of corticosteroids for brain metastasis treatment is allowed
9. Patients with symptomatic visceral disease in need of urgent disease
control
10. Symptomatic brain or other CNS metastases.
Previously treated symptomatic brain metastases are allowed provided
the patient is free of symptoms, prior radiotherapy for brain metastasis
was more than four weeks before enrollment and the dose of
corticosteroids is low and stable for at least two weeks prior to
enrollment
Other protocol defined 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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Estrogen receptor positive locally advanced or metastatic breast cancer in postmenopausal women MedDRA version: 17.0
Level: LLT
Classification code 10070575
Term: Estrogen receptor positive breast cancer
System Organ Class: 100000004864
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Therapeutic area: Diseases [C] - Cancer [C04]
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Intervention(s)
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Trade Name: Afinitor Product Name: Everolimus Product Code: RAD001 Pharmaceutical Form: Tablet INN or Proposed INN: everolimus 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 INN or Proposed INN: everolimus 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-
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Primary Outcome(s)
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Secondary Objective: - to evaluate adverse events grade 3 and 4 in the routine practice - to explore the tolerability of the concomitant treatment of zoledronic acid RTU (Ready To Use) formulation in patients who will receive this treatment according to the clinical practice
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Main Objective: to evaluate safety of everolimus (RAD001) in postmenopausal women with estrogen receptor positive locally advanced or metastatic breast cancer that is refractory to NSAIs
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Primary end point(s): frequency of adverse events and number of laboratory values that are new or worsening
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Timepoint(s) of evaluation of this end point: Adverse events: continuously, up to 28 days after last treatment Laboratory values: continuously or as frequently as clinically indicated
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Secondary Outcome(s)
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Timepoint(s) of evaluation of this end point: Continuously, up to 28 days after the last treatment
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Secondary end point(s): - frequency of adverse events that is recorded as Grade 3 or 4 or as Serious Adverse Event
- frequency of adverse events of any grade in the group of patients who have received concomitant treatment with zoledronic acid RTU formulation, administered according to clinical practice
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Secondary ID(s)
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CRAD001YIC04
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2012-000073-23-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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