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NCT06464601

A Real-World Study of Neoadjuvant/Conversion Therapy for Locally Advanced or Metastatic Gastric Cancer

Not yet recruiting Last updated 18 June 2024
What this trial tests

trial testing fruquintinib combined with immune checkpoint inhibitors and chemotherapy in Gastric Cancer in 70 participants. Not yet recruiting.

Timeline
1 April 2025
Primary endpoint
31 March 2026
31 March 2027

Quick facts

Lead sponsorWuhan University
StatusNot yet recruiting
Study typeOBSERVATIONAL
Enrollment70
Start date1 April 2025
Primary completion31 March 2026
Estimated completion31 March 2027
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Wuhan University

Who can join

Adults 18 to 75, any sex, with Gastric Cancer. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Chemotherapy, immune checkpoint inhibitors, and anti-angiogenic targeted therapies have been explored in combination for neoadjuvant and conversion therapies. However, the efficacy of the novel anti-angiogenic agent fruquintinib in combination with immune checkpoint inhibitors and chemotherapy in the neoadjuvant and conversion treatment of locally advanced or metastatic gastric cancer has not been reported. This study aims to observe the efficacy and safety of fruquintinib combined with immune checkpoint inhibitors and chemotherapy in real-world settings.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Gastric Cancer

Currently open trials in the same condition.

Other Wuhan University 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/NCT06464601.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing