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Alkylating agents
Dose Escalation for Breast Cancer
Phase 1
Waitlist Available
Led By Heather Han, M.D.
Research Sponsored by H. Lee Moffitt Cancer Center and Research Institute
Eligibility Criteria Checklist
Specific guidelines that determine who can or cannot participate in a clinical trial Must have
Be older than 18 years old
Timeline
Screening 3 weeks
Treatment Varies
Follow Up 30 months
Awards & highlights
Study Summary
This trial is testing if a combination of two chemotherapy drugs, eribulin and carboplatin, is safe and effective in treating advanced breast cancer.
Eligible Conditions
- Breast Cancer
Timeline
Screening ~ 3 weeks3 visits
Treatment ~ Varies
Follow Up ~ 30 months
Screening ~ 3 weeks
Treatment ~ Varies
Follow Up ~30 months
Treatment Details
Study Objectives
Outcome measures can provide a clearer picture of what you can expect from a treatment.Primary outcome measures
Maximum Tolerated Dose (MTD)
Secondary outcome measures
Response Rate (RR)
Trial Design
1Treatment groups
Experimental Treatment
Group I: Dose EscalationExperimental Treatment2 Interventions
Every patient will receive eribulin and carboplatin. Each cycle is 21 days (or 3 weeks). Eribulin and carboplatin will be given intravenously on days 1 and 8 of each cycle.
Treatment
First Studied
Drug Approval Stage
How many patients have taken this drug
Eribulin
2012
Completed Phase 3
~2700
Carboplatin
2014
Completed Phase 3
~6670
Find a Location
Who is running the clinical trial?
Eisai Inc.Industry Sponsor
515 Previous Clinical Trials
158,952 Total Patients Enrolled
16 Trials studying Breast Cancer
2,025 Patients Enrolled for Breast Cancer
H. Lee Moffitt Cancer Center and Research InstituteLead Sponsor
543 Previous Clinical Trials
135,463 Total Patients Enrolled
40 Trials studying Breast Cancer
5,761 Patients Enrolled for Breast Cancer
Heather Han, M.D.Principal InvestigatorH. Lee Moffitt Cancer Center and Research Institute
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