Phase 1b Study of Dato-DXd in Combination With Immunotherapy With or Without Carboplatin in Advanced or Metastatic Non-Small Cell Lung Cancer
NCT04612751 · Status: ACTIVE_NOT_RECRUITING · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 155
Last updated 2026-04-06
Summary
This study will assess safety, tolerability, and treatment activity of datopotamab deruxtecan (Dato-DXd) in combination with immunotherapy with or without carboplatin in participants with advanced or metastatic non-small cell lung cancer (NSCLC).
Conditions
- Advanced or Metastatic NSCLC
Interventions
- DRUG
-
Intravenous infusion every 3 weeks (Q3W) on Day 1 of each 21-day cycle
- DRUG
-
Intravenous infusion every 3 weeks (Q3W) on Day 1 of each 21-day cycle
- DRUG
-
Intravenous infusion Q3W on Day 1 or Day 2 of each 21-day cycle
- DRUG
-
AZD2936
Intravenous infusion prior to Dato-DXd every 3 weeks (Q3W) on Day 1 prior to Dato-Dxd of each 21-day cycle
- DRUG
-
MEDI5752
Intravenous infusion prior to Dato-DXd every 3 weeks (Q3W) on Day 1 prior to Dato-Dxd of each 21-day cycle
- DRUG
-
AZD7789
Intravenous infusion prior to Dato-DXd every 3 weeks (Q3W) on Day 1 prior to Dato-Dxd of each 21-day cycle
Sponsors & Collaborators
- collaborator INDUSTRY
- lead INDUSTRY
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- PARALLEL
Eligibility
- Min Age
- 18 Years
- Sex
- ALL
- Healthy Volunteers
- No
Timeline & Regulatory
- Start
- 2021-02-02
- Primary Completion
- 2026-05-04
- Completion
- 2026-05-04
- FDA Drug
- Yes
Countries
- United States
- Belgium
- Italy
- Japan
- Poland
- Spain
- Taiwan
- Turkey (Türkiye)
Study Locations
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