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ClinicalTrials.gov record
Active, not recruiting Phase 3 Interventional

Phase III, Open-label, First-line Study of Dato-DXd in Combination With Durvalumab and Carboplatin for Advanced NSCLC Without Actionable Genomic Alterations

ClinicalTrials.gov ID: NCT05687266

Public ClinicalTrials.gov record NCT05687266. 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 17, 2026, 6:48 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, Randomised, Open-label, Multicentre, Global Study of Datopotamab Deruxtecan (Dato-DXd) in Combination With Durvalumab and Carboplatin Versus Pembrolizumab in Combination With Platinum-based Chemotherapy for the First-line Treatment of Patients With Locally Advanced or Metastatic NSCLC Without Actionable Genomic Alterations (D926NC00001; AVANZAR)

Brief summary

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

This is a Phase III, randomized, open-label, multicenter, global study to compare the efficacy and safety of Datopotamab Deruxtecan (Dato-DXd) in combination with durvalumab and carboplatin compared with pembrolizumab in combination with histology-specific platinum-based chemotherapy as first-line treatment of adults with stage IIIB, IIIC, or IV NSCLC without actionable genomic alterations (including sensitizing EGFR mutations, and ALK and ROS1 rearrangements).

Study identification

NCT ID
NCT05687266
Recruitment status
Active, not recruiting
Study type
Interventional
Phase
Phase 3
Lead sponsor
AstraZeneca
Industry
Enrollment
1,350 participants

Conditions and interventions

Eligibility (public fields only)

Age range
18 Years to 130 Years
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
Dec 29, 2022 (Actual)
Primary completion
Nov 1, 2027 (Estimated)
Completion
Nov 1, 2027 (Estimated)
Last update posted
Oct 9, 2026

2022 – 2027

United States locations

U.S. sites
52
U.S. states
24
U.S. cities
48
Facility City State ZIP Site status
Research Site Phoenix Arizona 85054 —
Research Site Tucson Arizona 85704 —
Research Site Hot Springs Arkansas 71913 —
Research Site Little Rock Arkansas 72205 —
Research Site Springdale Arkansas 72762 —
Research Site Fountain Valley California 92708 —
Research Site Los Angeles California 90017 —
Research Site Orange California 92868 —
Research Site Boulder Colorado 80303 —
Research Site Fort Myers Florida 33901 —
Research Site Jacksonville Florida 32224 —
Research Site St. Petersburg Florida 33705 —
Research Site West Palm Beach Florida 33401 —
Research Site Hinsdale Illinois 60521 —
Research Site Fort Wayne Indiana 46845 —
Research Site Bettendorf Iowa 52722 —
Research Site Iowa City Iowa 52242 —
Research Site Waukee Iowa 50263 —
Research Site Baton Rouge Louisiana 70808 —
Research Site Covington Louisiana 70433 —
Research Site Duluth Minnesota 55805 —
Research Site Rochester Minnesota 55905 —
Research Site Hannibal Missouri 63401 —
Research Site Lincoln Nebraska 68506 —
Research Site Lincoln Nebraska 68516 —
Research Site Clifton Park New York 12065 —
Research Site Asheville North Carolina 28806 —
Research Site Canton Ohio 44710 —
Research Site Columbus Ohio 43219 —
Research Site Maumee Ohio 43537 —
Research Site Tulsa Oklahoma 74134 —
Research Site Portland Oregon 97239 —
Research Site Salem Oregon 97301 —
Research Site Philadelphia Pennsylvania 19104 —
Research Site Philadelphia Pennsylvania 19107 —
Research Site Philadelphia Pennsylvania 19111 —
Research Site York Pennsylvania 17403 —
Research Site Watertown South Dakota 57201 —
Research Site Memphis Tennessee 38120 —
Research Site Dallas Texas 75246 —
Research Site Fort Worth Texas 76104 —
Research Site Houston Texas 77030 —
Research Site Houston Texas 77090 —
Research Site Irving Texas 75063 —
Research Site Fairfax Virginia 22031 —
Research Site Henrico Virginia 23229 —
Research Site Norfolk Virginia 23502 —
Research Site Renton Washington 98055 —
Research Site Spokane Washington 99202 —
Research Site Tacoma Washington 98405 —
Research Site Appleton Wisconsin 54911 —
Research Site La Crosse Wisconsin 54601 —

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 202 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT05687266, 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 Oct 9, 2026 · Synced Oct 17, 2026

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Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT05687266 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →