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NCT06610799

Study of IBI363 in Patients with Advanced First-line Gastric Cancer

Recruiting now Phase 1 Last updated 20 November 2024
What this trial tests

Phase 1 trial testing IBI363 in IBI363 + Chemotherapy in 40 participants. Currently enrolling.

Timeline
15 October 2024
Primary endpoint
30 June 2025
31 December 2026

Quick facts

Lead sponsorXiangdong Cheng
PhasePhase 1
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment40
Start date15 October 2024
Primary completion30 June 2025
Estimated completion31 December 2026
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Xiangdong Cheng — full company profile →

Who can join

Adults 18 to 75, any sex, with IBI363 + Chemotherapy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

This is a phase 1b study designed to evaluate the safety, tolerability and efficacy of IBI363 in combination with oxaliplatin and capecitabine (XELOX) in first-line treatment of unresectable advanced or metastatic gastric and gastroesophageal junction adenocarcinoma.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Bispecific Antibodies in Solid Tumors: Advances and Challenges.
    Shan KS, Musleh Ud Din S, Dalal S, Gonzalez T, et al · · 2025 · cited 12× · PMID 40565299 · DOI 10.3390/ijms26125838

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Other trials of IBI363

Trials testing the same drug.

Other recruiting trials for IBI363 + Chemotherapy

Currently open trials in the same condition.

Other Xiangdong Cheng trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT06610799.

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