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Recruiting
NCT05061550
Neoadjuvant and Adjuvant Treatment in Resectable Non-small Cell Lung Cancer
Conditions: Non-small Cell Lung Cancer
Sex: All
Ages: 18 Years – 95 Years
Healthy volunteers: No
Phase: PHASE2
Enrollment: 630
Sponsor: AstraZeneca
Location: Research Site Little Rock Arkansas
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 Criteria
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 \
Source: ClinicalTrials.gov (NCT05061550). StuddyBuddy aggregates publicly available trial information.