Trastuzumab Deruxtecan for Subjects With HER2-Positive Gastric Cancer or Gastro-Esophageal Junction Adenocarcinoma After Progression on or After a Trastuzumab-Containing Regimen (DESTINY-Gastric04)
- Sponsor
- Daiichi Sankyo
- Study ID
- NCT04704934
- Phase
- PHASE3
- Status
- Active Not Recruiting
Conditions
- Gastric Cancer, Adenocarcinoma
- Gastroesophageal Junction Adenocarcinoma
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- Trastuzumab deruxtecan — DRUG6.4 mg/kg IV infusion every 3 weeks on Day 1 of each 21-day cycle
- Ramucirumab — DRUG8 mg/kg IV infusion on Days 1 and 15 of a 28-day cycle
- Paclitaxel — DRUG80 mg/m\^2 IV infusion on Days 1, 8, and 15 of a 28-day cycle
Study Details
This study will evaluate the efficacy and safety of trastuzumab deruxtecan (T-DXd) compared with ramucirumab and paclitaxel (Ram + PTX) in participants with HER2-positive gastric or gastro-esophageal junction (GEJ) adenocarcinoma who have progressed on or after a trastuzumab-containing regimen and have not received any additional systemic therapy.
Key Dates
- Start date
- May 21, 2021
- Status verified
- May 2026
- Primary completion
- Aug 31, 2026
- Completion
- Aug 31, 2026
Study Design
- Enrollment
- 490 participants (estimated)
- Allocation
- RANDOMIZED
- Intervention model
- PARALLEL
- Primary purpose
- TREATMENT
Arms
- Experimental: Trastuzumab deruxtecanParticipants who will be randomized to receive a 6.4 mg/kg intravenous (IV) dose of trastuzumab deruxtecan once every 3 weeks on Day 1 of each 21-day cycle.
- Active Comparator: Ramucirumab + paclitaxelParticipants who will be randomized to receive a 8 mg/kg IV dose of ramucirumab on Days 1 and 15 in combination with 80 mg/m\^2 IV dose of paclitaxel on Days 1, 8, and 15 of a 28-day cycle.
Primary Outcome Measure
Overall Survival in Participants Who Were Administered Trastuzumab Deruxtecan Compared With Ramucirumab in Combination With Paclitaxel [ Time Frame: Time from date of randomization until death (due to any cause), up to approximately 36 months ]
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