Recruiting
Phase 2

Durvalumab & Oleclumab

Sponsor:

University Health Network, Toronto

Code:

NCT06060405

Conditions

Pancreatic Ductal Adenocarcinoma

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Interventions

Durvalumab

Oleclumab

Study Details

Brief summary:

This is a multi-site Canadian, window of opportunity study to evaluate the immune activity of durvalumab and oleclumab in resectable pancreatic ductal adenocarcinoma (PDAC) when given prior to surgery.

Conditions

Pancreatic Ductal Adenocarcinoma

Study ID

NCT06060405

Start date

Nov 29, 2023

Status verified date

Jun, 2026

Completion date

Oct 30, 2026

Anticipated

Primary completion date

Oct 30, 2026

Anticipated

Eligibility Criteria

Eligibility Criteria

Sex: All

Age: 18+

Healthy Volunteers: Not accepted

Inclusion Criteria:

  • Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
  • Weight ≥ 35 kg
  • Have a life expectancy ≥ 12 weeks
  • Have histologically or cytologically confirmed pancreatic ductal adenocarcinoma (PDAC).
  • Upfront resectable PDAC
  • Have adequate organ and marrow function required for the study
  • Baseline images taken prior to treatment must undergo central review
  • Participants must agree to use study approved methods to prevent pregnancy for study required period

Exclusion Criteria:

  • Receipt of any conventional or investigational anticancer therapy within 21 days or palliative radiotherapy within 14 days prior to the scheduled first dose of study treatment
  • Prior receipt of any immune-mediated therapy including, but not limited to, other anti CTLA-4, anti-PD-1, anti-PD-L1 including durvalumab antibodies and agents targeting CD73, CD39, or adenosine receptors, excluding therapeutic anticancer vaccines.
  • Concurrent enrolment in another therapeutic clinical study. Enrolment in observational studies will be allowed.
  • Have a history of Grade 3 or greater thromboembolic events in the prior 3 months or thromboembolic event of any grade with ongoing symptoms.
  • Have prior history of myocardial infarction, transient ischemic attack, congestive heart failure ≥ Class 3 based on New York Heart Association Functional Classification or stroke within the past 3 months prior to the scheduled first dose of study treatment.
  • Active or prior documented autoimmune disorders within the past 3 years prior to the scheduled first dose of study treatment with the following exceptions

  • Vitiligo or alopecia
  • Hypothyroidism not requiring systemic treatment or stable on hormone replacement
  • Psoriasis not requiring systemic treatment
  • Any chronic skin condition that does not require systemic therapy
  • Have known active hepatitis infection. Participants with a past or resolved Hepatitis B (HBV) infection are eligible. Participants positive for Hepatitis C (HCV) antibody are eligible only if polymerase chain reaction is negative for HCV RNA.
  • Known to have tested positive for human immunodeficiency virus (HIV) (positive HIV 1/2 antibodies) or active tuberculosis infection
  • Other invasive malignancy within 5 years.
  • Known allergy or hypersensitivity to investigational product formulations.
  • Active grade 3 or greater edema
  • Uncontrolled intercurrent illness
  • Current or prior use of immunosuppressive medication within 14 days prior to the scheduled first dose of study treatment with the following exceptions:

  • Intranasal, topical, inhaled corticosteroids or local steroid injections
  • Systemic corticosteroids at physiologic doses not to exceed 10 mg/day of prednisone or equivalent
  • Steroids as premedication for hypersensitivity reaction
  • Receipt of live, attenuated vaccine within 30 days prior to the scheduled first dose of study treatment
  • Major surgery within 28 days prior to scheduled first dose of study treatment or still recovering from prior surgery. Local are allowed, without needing to wait for the 28 day recovery period.
  • Are pregnant, lactating, or intend to become pregnant during their participation in the study
  • Any condition that, in the opinion of the investigator, would interfere with safe administration or evaluation of the investigational products or interpretation of subject safety or study results

Study Design

Enrollment

22 participants

Anticipated

Intervention Model

Single group

Primary purpose

Treatment

Interventions and Outcome Measures

Arms

experimental: Durvalumab and Oleclumab

Durvalumab, 1500 mg x 1 dose and oleclumab 3000 mg x 2 doses every 2 weeks prior to surgical resection.

Interventions

Durvalumab

Durvalumab is a monoclonal antibody that blocks the interaction of PD-L1 with PD-1 on immune cells.

Oleclumab

Oleclumab is a monoclonal antibody that binds to and inhibits the activity of CD73.

Primary outcome measure

  • Percent change in CD8+ cell infiltration [ Time Frame: Baseline biopsy to surgical resection (35 days) ]

Central Contacts and Locations

Central contacts

Malcolm Moore, MD

416-946-2263malcolm.moore@uhn.ca

Locations

Princess Margaret Cancer Centre

Recruiting

Toronto, Ontario, Canada, M5G 2M9

Principal Investigator:

Malcolm Moore, MD

More Information

Sponsor

University Health Network, Toronto

Last update posted

Jun 23, 2026

Last verified

Jun, 2026

Trial information was received from ClinicalTrials.gov and was last updated on 2026-09-10. This information was provided to ClinicalTrials.gov by University Health Network, Toronto on 2026-06-23.