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進行HER2発現胃癌におけるT-DXd併用療法の安全性と有効性に関するPh1b/2試験(DESTINY-Gastric03)

基本情報

NCT ID
NCT04379596
ステータス
募集中
試験のフェーズ
第2相
試験タイプ
介入
目標被験者数
413
治験依頼者名
AstraZeneca

概要

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.

対象疾患

Gastric Cancer

介入

Fluorouracil (5-FU)(DRUG)
Capecitabine(DRUG)
Durvalumab(BIOLOGICAL)
Oxaliplatin(DRUG)
Trastuzumab(BIOLOGICAL)
Trastuzumab deruxtecan(DRUG)
Cisplatin(DRUG)
Pembrolizumab(BIOLOGICAL)
Volrustomig(BIOLOGICAL)
Rilvegostomig(BIOLOGICAL)

依頼者(Sponsor)