Study of Ribociclib With Everolimus + Exemestane in HR+ HER2- Locally Advanced/Metastatic Breast Cancer Post Progression on CDK 4/6 Inhibitor.
Part of paid clinical trials in Chandler, Arizona.
- Sponsor
- Novartis Pharmaceuticals
- Study ID
- NCT02732119
- Phase
- PHASE1/PHASE2
- Status
- Completed
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Ribociclib — DRUGsupplied in 50 mg, 200 mg capsules/tablets taken orally and dosed daily for 28 day cycle
- Everolimus — DRUGsupplied in 2.5 mg tablets taken orally, daily for 28 day cycle
- Exemestane — DRUGsupplied in 25 mg tablets taken orally, daily for 28 day cycle
Study Details
The purpose of this study is determine if the triplet combination of ribociclib, everolimus and exemastane is safe and effective in the treatment of locally advanced/metastatic breast cancer following treatment with a CDK 4/6 inhibitor
Key Dates
- Start date
- Jun 14, 2016
- Status verified
- Apr 2021
- Primary completion
- Feb 25, 2020
- Completion
- Feb 25, 2020
Study Design
- Enrollment
- 104 participants (actual)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SINGLE_GROUP
- Primary purpose
- TREATMENT
Arms
- Experimental: Cohort ARibociclib (250 mg daily), everolimus (2.5 mg daily) and exemestane (25 mg daily) taken orally for 28 days. If no DLTs occurred, progressed to Cohort B
- Experimental: Cohort BRibociclib (300 mg daily), everolimus (2.5 mg daily) and exemestane (25 mg daily) taken orally
- Experimental: Cohort CRibociclib (200 mg daily), everolimus (5 mg daily) and exemestane (25 mg daily) taken orally
- Experimental: Group 1Ribociclib (300 mg daily), everolimus (2.5 mg daily) and exemestane (25 mg daily) taken orally
- Experimental: Group 2Ribociclib (200 mg daily), everolimus (5 mg daily) and exemestane (25 mg daily) taken orally
Primary Outcome Measure
Participants With Dose Limiting Toxicities by Preferred Term in Cycle 1 (28 Days) - in Phase I [ Time Frame: Baseline up to 28 days ]
Locations (25)
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Ironwood Cancer and Research Centers Ironwood Cancer· Chandler, AZHighlands Oncology Group· Fayetteville, ARUCLA Department of Medicine UCLA Hematology/Oncology· Los Angeles, CAUniversity of California San Francisco Comprehensive Cancer Center· San Francisco, CACentral Coast Medical Oncology Corporation Onc Dept· Santa Maria, CAYale University School of Medicine Smilow Cancer Hospital· New Haven, CT
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