A Phase 2 interventional study of Pembrolizumab and Paclitaxel in Breast Cancer, sponsored by Queen Mary University of London. Withdrawn. Open to female participants aged 18 Years and older. Per ClinicalTrials.gov, last updated 2024-03-12.
Sponsored by Queen Mary University of London · Phase 2, Interventional, and Treatment
PELICAN is a randomised phase II trial that aims to evaluate the efficacy and safety of paclitaxel plus pembrolizumab relative to paclitaxel alone, in patients with locally advanced or metastatic ER-positive, HER2-negative, Luminal B breast cancer who have received no prior chemotherapy for advanced or metastatic disease.
Patients will be randomised (2:1) to one of the two treatment arms:
12,544 studies on the registry are indexed under Breast Neoplasms; 2,892 are open to participants now.
Browse Breast Neoplasms studies →Queen Mary University of London is the lead sponsor of 250 studies on the registry; 59 are open to participants now.
Counted across the registry records on this site, refreshed daily.
Exclusion Criteria:
200 mg Pembrolizumab IV Q3W plus 80 mg/m2 paclitaxel IV on Days 1,8, and 15 of each 28 day cycle.
Drug: Pembrolizumab · Drug: Paclitaxel
80 mg/m2 paclitaxel IV on Days 1,8, and 15 of each 28 day cycle.
Drug: Paclitaxel
200 mg Pembrolizumab IV Q3W.
Also known as: KEYTRUDA, lambrolizumab
80 mg/m2 paclitaxel IV on Days 1,8, and 15 of each 28 day cycle.
Also known as: Taxol
Progression-free survival
Progression-free survival, defined as the time from the date of randomisation to the date of first documented tumour progression (using RECIST 1.1) or death from any cause, whichever occurs first.
Time frame: At 12months
Overall Survival
Overall Survival is defined as the time from date of randomisation to the date of death due to any cause in all patients.
Time frame: At 24 months.
Objective Response Rates
Objective Response Rate is defined as the proportion of the patients in the analysis population who have a CR or PR (using RECIST 1.1).
Time frame: Date of first documentation of CR or PR or to the date of first documented tumour progression (using RECIST 1.1) or death from any cause, whichever occurs first, assessed up to 30 months.
Safety and tolerability of paclitaxel plus pembrolizumab versus paclitaxel through review of all AEs and SAEs assessed by CTCAE v4.03
Incidence, nature and severity of adverse events with severity determined according to CTCAE v4.03
Time frame: Date of randomisation to date of all adverse event resolution following discontinuation for any reason or death, assessed up to 30 months.
No study locations are listed for this record.
This study is withdrawn, as verified in Mar 2024. You cannot join it, but the record below documents what was studied.
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Queen Mary University of London