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A Randomized Trial of Ridaforolimus in Combination with Dalotuzumab Compared to Exemestane in Estrogen Receptor Positive Breast Cancer Patients

Conditions
Estrogen receptor positive breast cancer
Registration Number
EUCTR2010-019867-13-DE
Lead Sponsor
Merck Sharp & Dohme Corp., a subsidiary of Merck & Co., Inc.
Brief Summary

Not available

Detailed Description

Not available

Recruitment & Eligibility

Status
ot Recruiting
Sex
Female
Target Recruitment
350
Inclusion Criteria

•Patient has diagnosis of breast cancer that is metastatic or locally advanced and is estrogen receptor positive and HER-2 negative
•Patient is post-menopausal
•Patient's cancer has recurred or progressed after prior treatment with a non-steroidal aromatase inhibitor (anastrozole or letrozole) in the adjuvant or metastatic setting and patient has received at least one line of endocrine therapy for metastatic disease OR the patient's cancer has recurred within 6 months of the last dose of anastrozole or letrozole
•An archival tumor specimen is available
•Patient has a performance status of 1 or less on the ECOG (Eastern Cooperative Oncology Group) performance scale

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
F.1.3 Elderly (>=65 years) yes
F.1.3.1 Number of subjects for this age range

Exclusion Criteria

•Patient is receiving any other systemic tumor therapy
•Patient has previously received rapamycin or rapamycin analogs
•Patient has received prior treatment with IGF-1R inhibitors, PI3K inhibitors, or other experimental agents that target the PI3K, AKT, or mTOR pathways
•Patient has an active infection that requires antibiotics
•Patient has significant or uncontrolled cardiovascular disease
•Patient has poorly controlled Type 1 or 2 diabetes mellitus

Study & Design

Study Type
Interventional clinical trial of medicinal product
Study Design
Not specified
Primary Outcome Measures
NameTimeMethod
Secondary Outcome Measures
NameTimeMethod
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