Novel Combinations in Participants With Locally Advanced Unresectable or Metastatic Gastric or Gastroesophageal Junction Adenocarcinoma
Condition(s) studied
Investigational drug(s) / intervention(s)
Rilvegostomig: an anti PD-1 and anti-TIGIT bispecific antibody; IV infusion
Volrustomig: an anti PD-1 and anti CTLA-4 bispecific antibody; IV infusion
FOLFOX: 5-fluorouracil oxaliplatin, leucovorin (levoleucovorin when locally preferred and available)
XELOX: capecitabine and oxaliplatin
AZD0901: an anti Claudin18.2 ADC; IV infusion
5-Fluorouracil: 5-FU, IV infusion
Capecitabine: Oral take
Study summary
This is a Phase II, open-label, multi-drug, multi-centre study designed to assess the efficacy, safety, tolerability, pharmacokinetics, and immunogenicity of novel combination therapies in participants with locally advanced unresectable or metastatic gastric or GEJ adenocarcinoma.
Eligibility
Primary outcome measure(s)
- ORR (per RECIST 1.1 as assessed by Investigator) — Through substudy completion, an average of 2 years
the proportion of participants who have a confirmed complete response or confirmed partial response, as determined by the Investigator at local site per RECIST 1.1. - PFS6 (per RECIST 1.1 as assessed by Investigator) — Through substudy completion, an average of 2 years
the proportion of participants alive and progression-free at 6 months.
Trial sites (44)
| Facility | City | Region | Status |
|---|---|---|---|
| Research Site | Los Angeles | California | Recruiting |
| Research Site | Los Angeles | California | Withdrawn |
| Research Site | Baton Rouge | Louisiana | Recruiting |
| Research Site | Grand Rapids | Michigan | Recruiting |
| Research Site | New Hyde Park | New York | Withdrawn |
| Research Site | New York | New York | Withdrawn |
| Research Site | New York | New York | Recruiting |
| Research Site | New York | New York | Withdrawn |
| Research Site | Shirley | New York | Withdrawn |
| Research Site | The Bronx | New York | Withdrawn |
| Research Site | Pittsburgh | Pennsylvania | Withdrawn |
| Research Site | Beijing | China | Recruiting |
| Research Site | Hangzhou | China | Recruiting |
| Research Site | Hangzhou | China | Recruiting |
| Research Site | Harbin | China | Recruiting |
| Research Site | Hefei | China | Recruiting |
| Research Site | Kunming | China | Completed |
| Research Site | Wuhan | China | Recruiting |
| Research Site | Yinchuan | China | Recruiting |
| Research Site | Zhengzhou | China | Recruiting |
| Research Site | Chūōku | Japan | Recruiting |
| Research Site | Kashiwa | Japan | Recruiting |
| Research Site | Sunto-gun | Japan | Recruiting |
| Research Site | Seoul | South Korea | Recruiting |
| Research Site | Seoul | South Korea | Recruiting |
| Research Site | Seoul | South Korea | Recruiting |
| Research Site | Seoul | South Korea | Recruiting |
| Research Site | Barcelona | Spain | Recruiting |
| Research Site | Elche(Alicante) | Spain | Recruiting |
| Research Site | L'Hospitalet de Llobregat | Spain | Recruiting |
| Research Site | Madrid | Spain | Recruiting |
| Research Site | Madrid | Spain | Recruiting |
| Research Site | Santander | Spain | Recruiting |
| Research Site | Hsinchu | Taiwan | Recruiting |
| Research Site | Kaohsiung City | Taiwan | Recruiting |
| Research Site | Taichung | Taiwan | Recruiting |
| Research Site | Tainan | Taiwan | Recruiting |
| Research Site | Taipei | Taiwan | Recruiting |
| Research Site | Taipei | Taiwan | Recruiting |
| Research Site | Taoyuan | Taiwan | Recruiting |
+ 4 more sites — see the full list on the official registry below.
More AstraZeneca trials in Spain
Other trials for the same condition
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 NCT05702229 on ClinicalTrials.gov ↗ ← All trials in Spain