CI

At a glance

ClinicalIndex Comparison Record
Phase 2Completed· 79 enrolled
Drug / intervention
Trastuzumab deruxtecandrug
Likely dose
Not stated in record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT04014075
NCT04014075Phase 2Completed

A Phase 2, Open-label, Single-arm Trial of Trastuzumab Deruxtecan (DS 8201a) in HER2-positive, Unresectable or Metastatic Gastric or Gastro-esophageal Junction (GEJ) Adenocarcinoma Subjects Who Have Progressed on or After a Trastuzumab-containing Regimen (DESTINY-Gastric02)

Daiichi Sankyo·interventional·Posted Jul 10, 2019·Updated Apr 3, 2025

In Brief

A Phase 2 clinical trial evaluating Trastuzumab deruxtecan for Adenocarcinoma Gastric Stage IV With Metastases and Adenocarcinoma - GEJ. Completed, enrolled 79 participants across 37 sites in 5 countries.

Detailed Summary

This study will find out if trastuzumab deruxtecan is safe and works for participants with gastric or gastroesophageal junction cancer. They must have human epidermal growth factor receptor 2 (HER2)-positive gastric or gastro-esophageal junction (GEJ) cancer: * that cannot be removed surgically * that has moved to other parts of the body * that got worse during or after treatment that included trastuzumab The study will enroll about 80 participants. Sites will be in North America and the European Union.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
CountriesBelgium, Italy, Spain, United Kingdom, United States
CollaboratorsAstraZeneca

Timeline

Phase 2CompletedFinished
2020202120222023202420252026
First PostedJul 10, 2019
Enrollment StartNov 26, 2019
Primary CompletionNov 8, 2021
Study CompletionFeb 13, 2024
TodayJul 2, 2026
Enrollment to primary: 1.9 yearsPosted 7.0 years ago

Interventions

Trastuzumab deruxtecandrug

Antibody component covalently conjugated to a drug component, prepared by dilution based on body weight for intravenous (IV) infusion