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Active, not recruiting Phase 3 Interventional

A Global Study to Assess the Effects of Durvalumab With Oleclumab or Durvalumab With Monalizumab Following Concurrent Chemoradiation in Patients With Stage III Unresectable Non-Small Cell Lung Cancer

ClinicalTrials.gov ID: NCT05221840

Public ClinicalTrials.gov record NCT05221840. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 19, 2026, 2:24 AM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Phase III, Double-blind, Placebo-controlled, Randomised, Multicentre, International Study of Durvalumab Plus Oleclumab and Durvalumab Plus Monalizumab in Patients With Locally Advanced (Stage III), Unresectable Non-small Cell Lung Cancer (NSCLC) Who Have Not Progressed Following Definitive, Platinum-Based Concurrent Chemoradiation Therapy

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

This is a Phase III, randomised, double-blind, multicentre, international study assessing the efficacy and safety of durvalumab (MEDI4736) in combination with oleclumab (MEDI9447) or durvalumab (MEDI4736) with monalizumab (IPH2201) in adults with locally advanced (Stage III), unresectable NSCLC, who have not progressed following platinum-based cCRT.

Study identification

NCT ID
NCT05221840
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
AstraZeneca
Industry
Enrollment
1,051 participants

Conditions and interventions

Interventions

Drug · Other

Eligibility (public fields only)

Age range
18 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Feb 7, 2022 (Actual)
Primary completion
Sep 30, 2026 (Estimated)
Completion
Jul 2, 2030 (Estimated)
Last update posted
Jun 18, 2026

2022 – 2030

United States locations

U.S. sites
33
U.S. states
21
U.S. cities
31
Facility City State ZIP Site status
Research Site San Diego California 92123 —
Research Site New Haven Connecticut 06510 —
Research Site Stuart Florida 34994 —
Research Site Urbana Illinois 61801 —
Research Site New Albany Indiana 47150 —
Research Site Lexington Kentucky 40503 —
Research Site Louisville Kentucky 40241 —
Research Site Annapolis Maryland 21401 —
Research Site Baltimore Maryland 21201 —
Research Site Baltimore Maryland 21229 —
Research Site Bethesda Maryland 20817 —
Research Site Grand Rapids Michigan 49503 —
Research Site Duluth Minnesota 55805 —
Research Site Billings Montana 59101 —
Research Site Ridgewood New Jersey 07450 —
Research Site Ithaca New York 14850 —
Research Site Greensboro North Carolina 27403 —
Research Site Cleveland Ohio 44124 —
Research Site Cleveland Ohio 44195 —
Research Site Maumee Ohio 43537 —
Research Site Portland Oregon 97239 —
Research Site Philadelphia Pennsylvania 19104 —
Research Site York Pennsylvania 17403 —
Research Site Sioux Falls South Dakota 57105 —
Research Site Houston Texas 77030 —
Research Site Charlottesville Virginia 22908 —
Research Site Fairfax Virginia 22031 —
Research Site Fredericksburg Virginia 22408 —
Research Site Richmond Virginia 23235 —
Research Site Richland Washington 99352 —
Research Site Spokane Washington 99204 —
Research Site Tacoma Washington 98405 —
Research Site Milwaukee Wisconsin 53226 —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 169 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05221840, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jun 18, 2026 · Synced Oct 19, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05221840 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →