drugset / Trial / NCT04379596

Ph1b/2 Study of the Safety and Efficacy of T-DXd Combinations in Advanced HER2-expressing Gastric Cancer (DESTINY-Gastric03)

NCT04379596 ↗

Phase 2 Recruiting 450 enrolled AstraZeneca Daiichi Sankyo · collab
RandomizedParallel-groupOpen-labelTreatment

Summary

DESTINY-Gastric03 will investigate the safety, tolerability, pharmacokinetics, immunogenicity, and preliminary antitumor activity of trastuzumab deruxtecan (T-DXd) alone or in combination with chemotherapy and/or immunotherapy in HER2-expressing advanced/metastatic gastric/gastroesophageal junction (GEJ) and esophageal adenocarcinoma patients. Study hypotheses: Combination of T-DXd with cytotoxic chemotherapy and/or immunotherapy administered to subjects at the recommended phase 2 dose will show manageable safety and tolerability and preliminary anti-tumor efficacy so as to permit further clinical testing. T-DXd in combination with cytotoxic chemotherapy or immune checkpoint inhibitor administered to HER2-expressing gastric, GEJ and esophageal cancer patients who have not received prior treatment for advanced/metastatic disease will show preliminary evidence of anti-tumour activity and the potential to become a therapeutic option for this patient population.

Timeline

Start
2020-06-03
Primary completion
2027-06-01
Completion
2027-06-01

Drugs

EvaluationDrugModalityDoseRoute
Subject Capecitabine Small molecule — Oral
Comparator Cisplatin Other / unclassified — Intravenous
Subject Durvalumab Monoclonal antibody — Intravenous
Subject Oxaliplatin Small molecule — Intravenous
Subject Pembrolizumab Monoclonal antibody — Intravenous
Subject Rilvegostomig Other / unclassified — Intravenous
Comparator Trastuzumab Monoclonal antibody — Intravenous
Subject Trastuzumab deruxtecan Monoclonal antibody — Intravenous
Subject Volrustomig Monoclonal antibody — Intravenous
Subject fluorouracil Small molecule — Intravenous

Indications