Enhancing ICB Efficacy Through IL-1 Inhibition in TNBC

Trial statusNot yet recruiting
Trial phasePhase 1, Phase 2
Trial typeInterventional
Biological sexAll
Age18+
SponsorUniversity Health Network, Toronto

About this trial

This study is a phase I/II open-label randomized clinical trial to examine whether administration of isunakinra (EBI-005), a modified recombinant IL1 receptor antagonist, can sensitize human TNBC to the PD1 inhibitor-pembrolizumab-based neoadjuvant chemotherapy (NAC/P) by changing the tumor microenvironment (TME) via reducing the recruitment of immunosuppressive tumorassociated macrophages (TAMs) and increasing activated cytotoxic T-lymphocytes (CTLs).

Eligibility criteria

Qualifiers

Age > 18 years

Provides core needle biopsies consisting of at least 2 separate tumor cores from the primary tumor to the central laboratory

Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1

Demonstrates adequate organ function

Disqualifiers

Male Gender

Luminal A/B and HER2 positive breast cancer

Multifocal early breast cancer

History of invasive malignancy ≤5 years prior to signing informed consent, except for adequately treated basal cell or squamous cell skin cancer or in situ cervical cancer

Trial design

Treatments tested in this trial

  • Group 1-Isunakinra

Treatment groups

60 Participants
are divided into 2 treatment groups

Locations

This trial has no locations

Sponsors and collaborators

University Health Network, Toronto

Lead sponsor

Buzzard Pharmaceuticals

Collaborator