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WithdrawnNCT03841747PELICANUpdated Mar 12, 2024

Paclitaxel Plus Pembrolizumab vs. Paclitaxel Weekly in ER+ Luminal B Metastatic Breast Cancer

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 Withdrawn.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

Why this study was withdrawn
Funding restrictions
Phase
Phase 2
Study type
Interventional
Enrollment
0
Allocation
Randomized
Ages
18 Years and older
Sex
Female
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Study summary

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:

  • Pembrolizumab plus Paclitaxel
  • Paclitaxel
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Conditions studied

  • Breast Cancer

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Keywords

  • ER-positive
  • Metastatic
  • Locally Advanced
  • Ki67
  • PAM50
  • Pembrolizumab
  • Paclitaxel
  • HER2-negative
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In context

Breast Neoplasms

12,544 studies on the registry are indexed under Breast Neoplasms; 2,892 are open to participants now.

Browse Breast Neoplasms studies →

Lead sponsor

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.

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Who can participate

Ages eligible
18 Years and older
Sexes eligible
Female
Accepts healthy volunteers
No

Inclusion criteria

  1. Willing and able to provide written informed consent
  2. Ability to comply with the protocol
  3. Female ≥ 18 years of age
  4. Histologically confirmed metastatic or locally advanced breast cancer that is Luminal B, ER+ve, HER2-ve.
  5. Patients must have measurable disease.
  6. Representative formalin-fixed paraffin embedded breast tumour samples from the primary or recurrent cancer.
  7. ECOG performance status 0-1
  8. Adequate haematologic and end-organ function within 28 days prior to the first study treatment
  9. Patients of childbearing potential are eligible provided they have a negative serum or urine pregnancy test on Day 1 Cycle 1 (within 72 hours) of study treatment, preferably as close to the first dose as possible.

Exclusion criteria

Exclusion Criteria:

  1. Luminal A breast cancer
  2. Prior chemotherapy for advanced or metastatic disease
  3. Prior treatment with paclitaxel in the (neo)adjuvant setting within 12 months from the end of paclitaxel treatment and randomisation into this study
  4. Patients with neuropathy ≥ Grade 2
  5. Previous systemic treatment for other neoplasms within 5 years prior to randomisation.
  6. Patients with prior allogeneic stem cell or solid organ transplantation.
  7. Prior treatment with CD137 agonists, AKT inhibitors, anti-CTLA-4, anti-OX-40, anti-programmed death-1 (PD-1), or anti-PD-L1 therapeutic antibody or pathway-targeting agents.
  8. Patients must not have a diagnosis of immunodeficiency or receiving chronic systemic steroid therapy.
  9. Received therapeutic oral or intravenous antibiotics within 14 days prior to randomisation.
  10. Administration of a live vaccine within 30 days prior to the first dose of study drug.
  11. Treatment with systemic immunostimulatory agents (including but not limited to interferons or interleukin [IL] -2) within 28days or five half-lives of the drug, whichever is shorter, prior to randomisation.
  12. History of autoimmune disease.
  13. History of idiopathic pulmonary fibrosis, drug-induced pneumonitis, organizing pneumonia requiring steroids, or evidence of active pneumonitis on screening chest CT scan.
  14. Active infection requiring systemic therapy.
  15. History of HIV infection
  16. Known active hepatitis infection.
  17. Known history of active tuberculosis
05

Study design

Phase
Phase 2
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Parallel assignment
Masking
None (open label)
Enrollment
0 participants (actual)

Study arms

  • Experimental
    Pembrolizumab + Paclitaxel

    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

  • Active comparator
    Paclitaxel

    80 mg/m2 paclitaxel IV on Days 1,8, and 15 of each 28 day cycle.

    Drug: Paclitaxel

Interventions

  • DrugPembrolizumab

    200 mg Pembrolizumab IV Q3W.

    Also known as: KEYTRUDA, lambrolizumab

  • DrugPaclitaxel

    80 mg/m2 paclitaxel IV on Days 1,8, and 15 of each 28 day cycle.

    Also known as: Taxol

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What researchers measure

Primary outcomes

  1. 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

  2. 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.

Secondary outcomes

  1. 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.

  2. 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.

07

Study locations

No study locations are listed for this record.

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Updates

Tracking since Sep 25, 2026
No changes since tracking began. The registry record was last updated on Mar 12, 2024, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT03841747
Lead sponsor
Queen Mary University of London
Collaborators
Merck Sharp & Dohme LLC, European Institute of Oncology
Responsible party
Sponsor
First posted
Feb 15, 2019
Start date
Dec 2020 (estimated)
Primary completion
Jun 2023 (estimated)
Completion
Jun 2025 (estimated)
Last update
Mar 12, 2024

Study contacts

Peter Schmid, MD PhD FRCP
principal investigator · Queen Mary University of London

Oversight

Data monitoring committee
Yes
FDA-regulated drug
No
FDA-regulated device
No
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

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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