Durvalumab: Participants will receive Durvalumab via intravenous route.
Oleclumab: Participants will receive Oleclumab via intravenous route.
Monalizumab: Participants will receive Monalizumab via intravenous route.
Dato-DXd: Participants will receive datopotamab deruxtecan (Dato-DXd) via intravenous route.
AZD0171: Participants will receive AZD0171 via intravenous route.
Carboplatin: Carboplatin as chemotherapy
Cisplatin: Cisplatin as chemotherapy
Pemetrexed/Cisplatin: Pemetrexed/Cisplatin as chemotherapy
Pemetrexed/Carboplatin: Pemetrexed/Carboplatin as chemotherapy
Carboplatin/Paclitaxel: Carboplatin/Paclitaxel, as chemotherapy
Volrustomig: Participants will receive Volrustomig via intravenous route.
Rilvegostomig: Participants will receive Rilvegostomig via intravenous route.
Study summary
The study is intended to assess the safety and efficacy of perioperative treatment with Durvalumab in combination with Oleclumab, Monalizumab, or AZD0171 and platinum doublet chemotherapy (CTX); or Volrustomig or Rilvegostomig in combination with CTX; or Datopotamab deruxtecan (Dato-DXd) in combination with Durvalumab or Rilvegostomig and single agent platinum chemotherapy in participants with resectable, early-stage non-small cell lung cancer.
Eligibility
Sex
ALL
Min age
18 Years
Max age
95 Years
Healthy volunteers
No
Inclusion Criteria:
* Newly diagnosed NSCLC patients with resectable disease (Stage IIA to Stage IIIB).
* WHO or Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1.
* Adequate organ and bone marrow function.
* Provision of tumour samples (newly acquired or archival tumour tissue \[≤ 6 months old\]) to confirm Programmed death-ligand 1 (PD-L1) status, epidermal growth factor receptor (EGFR), or anaplastic lymphoma kinase (ALK) status.
* Adequate pulmonary function.
Exclusion Criteria:
* Participants with sensitising EGFR mutations or ALK translocations.
* Participants with baseline PD-L1 expression status \<1% (Arms 6 and 7 only).
* Active or prior documented autoimmune or inflammatory disorders.
* Uncontrolled intercurrent illness, uncontrolled hypertension, unstable angina pectoris, uncontrolled cardiac arrhythmia, active bleeding diseases, serious chronic gastrointestinal conditions associated with diarrhoea, or psychiatric illness/social situations that would limit compliance with study requirement.
* History of another primary malignancy.
* Participants with small-cell lung cancer or mixed small-cell lung cancer.
* History of active primary immunodeficiency.
* History of non-infectious interstitial lung disease (ILD) ILD/pneumonitis that required steroids, has current ILD/pneumonitis, or has suspected ILD/pneumonitis that cannot be ruled out by imaging at screening.
* Participants who have preoperative radiotherapy treatment as part of their care plan.
* Participants who require or may require pneumonectomy, segmentectomies, or wedge resections, as assessed by their surgeon at baseline, to obtain potentially curative resection of primary tumour.
* QTcF (QT interval corrected by Fridericia's formula) interval ≥ 470 ms.
* Any medical contraindication to treatment with chemotherapy as listed in the local labelling.
* Participants with moderate or severe cardiovascular disease.
* Any concurrent chemotherapy, investigational product, biologic, or hormonal therapy for cancer treatment.
* Receipt of live attenuated vaccine within 30 days prior to the first dose of study interventions.
* Prior exposure to approved or investigational immune-mediated therapy including, but not limited to, other anti-CTLA-4, anti-TIGIT (T cell immunoreceptor with Ig and ITIM domains), anti-PD-1, anti-PD-L1, and anti-PD-L2 antibodies. Participants who received agents targeting the adenosine pathway, anti-NKG2A, anti-HLA-E agents, and anti-LIF agents are also excluded. Participants who have received previous treatment with a TROP2 targeting ADC or with another ADC containing a chemotherapy agent that inhibits TOP1 activity are also excluded.
* Current or prior use of immunosuppressive medication within 14 days before the first dose of study interventions.
* Active or uncontrolled infections including HBA, HBV, HCV, and HIV.
Primary outcome measure(s)
Number of participants with pathological complete response (pCR) — From randomization to approximately 15 weeks after the first dose of study interventions
Number of participants with adverse events (AEs) and serious adverse events (SAEs) — Until Day 90 after the last dose of study interventions (Up to approximately 3 years)
Trial sites (97)
Facility
City
Region
Status
Research Site
Little Rock
Arkansas
Recruiting
Research Site
Los Angeles
California
Recruiting
Research Site
Oakland
California
Withdrawn
Research Site
New Haven
Connecticut
Recruiting
Research Site
Stuart
Florida
Completed
Research Site
Gainesville
Georgia
Withdrawn
Research Site
Chicago
Illinois
Recruiting
Research Site
Baltimore
Maryland
Withdrawn
Research Site
Baltimore
Maryland
Recruiting
Research Site
Boston
Massachusetts
Recruiting
Research Site
Saint Louis Park
Minnesota
Completed
Research Site
Omaha
Nebraska
Recruiting
Research Site
Buffalo
New York
Recruiting
Research Site
Cleveland
Ohio
Recruiting
Research Site
Pittsburgh
Pennsylvania
Recruiting
Research Site
Chattanooga
Tennessee
Recruiting
Research Site
Memphis
Tennessee
Recruiting
Research Site
Nashville
Tennessee
Withdrawn
Research Site
Nashville
Tennessee
Recruiting
Research Site
Nashville
Tennessee
Recruiting
Research Site
Houston
Texas
Recruiting
Research Site
Houston
Texas
Terminated
Research Site
Fairfax
Virginia
Recruiting
Research Site
Edmonds
Washington
Recruiting
Research Site
Seattle
Washington
Recruiting
Research Site
Ghent
Belgium
Recruiting
Research Site
Ghent
Belgium
Completed
Research Site
Roeselare
Belgium
Recruiting
Research Site
Edmonton
Alberta
Completed
Research Site
Winnipeg
Manitoba
Recruiting
Research Site
Montreal
Quebec
Recruiting
Research Site
Montreal
Quebec
Recruiting
Research Site
Avignon
France
Recruiting
Research Site
Bobigny
France
Withdrawn
Research Site
Bordeaux
France
Recruiting
Research Site
Limoges
France
Recruiting
Research Site
Rennes
France
Recruiting
Research Site
Rouen
France
Recruiting
Research Site
Suresnes
France
Recruiting
Research Site
Toulon
France
Recruiting
+ 57 more sites — see the full list on the official registry below.
This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.
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