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Clinical Trials in China / NCT05048797
Active, not recruiting Phase 3

A Study to Investigate the Efficacy and Safety of Trastuzumab Deruxtecan as the First Treatment Option for Unresectable, Locally Advanced/Metastatic Non-Small Cell Lung Cancer With HER2 Mutations

NCT05048797 · tracked via the Priya Life Science China tracker
Sponsor
AstraZeneca
Phase
Phase 3
Started
2021-10-28
Last updated
2026-07-10

Condition(s) studied

Locally Advanced or Metastatic Non-Small Cell Lung Cancer

Investigational drug(s) / intervention(s)

Trastuzumab DeruxtecanCisplatinCarboplatinPembrolizumabPemetrexed

Trastuzumab Deruxtecan: Trastuzumab Deruxtecan administered by intravenous infusion

Cisplatin: Investigator's choice of platinum chemotherapy (cisplatin) administered by intravenous infusion

Carboplatin: Investigator's choice of platinum chemotherapy (carboplatin) administered by intravenous infusion

Pembrolizumab: Pembrolizumab administered by intravenous infusion

Pemetrexed: Pemetrexed administered by intravenous infusion

Study summary

DESTINY-Lung04 will investigate the efficacy and safety of Trastuzumab Deruxtecan (T-DXd) versus Standard of Care (SoC) as first-line treatment of Non-Small Cell Lung Cancer (NSCLC) with HER2 Exon 19 or 20 mutations

Eligibility

Sex
ALL
Min age
18 Years
Max age
123 Years
Healthy volunteers
No
Inclusion Criteria: * Participants at least 18 years of age * Locally advanced and unresectable NSCLC, not amenable to curative therapy, or metastatic disease * Histologically documented non-squamous NSCLC with HER2 mutation in exons 19 or 20 by tissue NGS or ctDNA * Treatment-naïve for palliative intent systemic therapy for locally advanced or metastatic disease * Left ventricular ejection fraction (LVEF) ≥ 50% * Measurable disease assessed by Investigator based on RECIST 1.1 * Protocol-defined adequate organ function including cardiac, renal, hepatic function * ECOG 0-1 * Having tumour tissue available for central testing Exclusion Criteria: * Tumors with targetable alterations to EGFR (or other targetable mutations including but not limited to ALK, if routinely tested as a targetable alteration with approved available therapy) * Any untreated brain metastases, including asymptomatic or clinically inactive brain metastases * Active autoimmune or inflammatory disorders * Medical history of myocardial infarction within 6 months prior to randomization * History of non-infectious pneumonitis/ILD, current or suspected ILD * Lung-specific intercurrent clinical significant severe illness * Contraindication to platinum-based doublet chemotherapy or pembrolizumab

Primary outcome measure(s)

Trial sites (130)

FacilityCityRegionStatus
Research Site Anchorage Alaska
Research Site Los Alamitos California
Research Site Los Angeles California
Research Site Orange California
Research Site San Francisco California
Research Site Santa Monica California
Research Site Silver Spring Maryland
Research Site Boston Massachusetts
Research Site Ann Arbor Michigan
Research Site Basking Ridge New Jersey
Research Site Middletown New Jersey
Research Site Montvale New Jersey
Research Site New Brunswick New Jersey
Research Site Commack New York
Research Site Harrison New York
Research Site New York New York
Research Site Uniondale New York
Research Site Pittsburgh Pennsylvania
Research Site Dallas Texas
Research Site Linz Austria
Research Site Vienna Austria
Research Site Ghent Belgium
Research Site Leuven Belgium
Research Site Barretos Brazil
Research Site Blumenau Brazil
Research Site Brasília Brazil
Research Site Natal Brazil
Research Site Salvador Brazil
Research Site São Paulo Brazil
Research Site São Paulo Brazil
Research Site Uberlândia Brazil
Research Site Vancouver British Columbia
Research Site Brampton Ontario
Research Site Toronto Ontario
Research Site Montreal Quebec
Research Site Beijing China
Research Site Beijing China
Research Site Changchun China
Research Site Changsha China
Research Site Changsha China

+ 90 more sites — see the full list on the official registry below.

On this site

📄 Enhertu (trastuzumab deruxtecan) drug profile → 📄 Keytruda (pembrolizumab) drug profile →

More AstraZeneca trials in China

Other trials for the same condition

Official registry record

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.

View NCT05048797 on ClinicalTrials.gov ↗ ← All trials in China