PD-1 +/- IL-4 Inhibition in ER+ Breast Cancer
- Sponsor
- Ottawa Hospital Research Institute
- Study ID
- NCT05967884
- Phase
- PHASE2
- Status
- Unknown
Conditions
Eligibility Criteria
- Sex
- FEMALE
- Age
- 18 Years - 90 Years
- Healthy Volunteers
- Not accepted
Interventions
- Arm A: Cemiplimab, Arm B: Cemiplimab + Dupilumab — DRUGArm A: Cemiplimab: 350mg IV x 1 dose administered prior to surgery Arm B: Cemiplimab + Dupilumab: Cemiplimab 350mg IV x 1 dose + Dupilumab 600 mg SC x 1 dose administered prior to surgery
Study Details
This proposal is for a Window of Opportunity (WOO) clinical trial using a novel combination of two Health Canada approved agents, cemiplimab (Libtayo) and dupilumab (Dupixent), for off label use in early-stage estrogen receptor positive (ER+) breast cancer.
Key Dates
- Start date
- Aug 4, 2023
- Status verified
- Jul 2023
- Primary completion
- Aug 1, 2024
- Completion
- Aug 1, 2024
Study Design
- Enrollment
- 20 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Active Comparator: Arm A: CemiplimabArm A: Cemiplimab (n=10), 350mg IV x 1 dose administered prior to surgery.
- Experimental: Arm B: Cemiplimab + DupilumabArm B: Cemiplimab + Dupilumab (n=10), Cemiplimab 350mg IV x 1 dose + Dupilumab 600 mg SC x 1 dose administered prior to surgery.
Primary Outcome Measure
Immune Cell Population Analysis [ Time Frame: up to 6 months ]
Central Contacts
- Angel Arnaout, MD613-798-5555
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