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NCT06277024

A Study on the Safety and Efficacy of the Combination of Candenizumab, Lenvatinib, and SOX Regimen in the Treatment of HER2 Negative Advanced Gastric or Gastroesophageal Junction Adenocarcinoma Patients

Recruiting now NA Last updated 26 February 2024
What this trial tests

NA trial testing Combination of Cardonizumab with Lenvatinib and SOX regimen in Overall Response Rate in 50 participants. Currently enrolling.

Timeline
1 January 2023
Primary endpoint
31 December 2024
31 December 2027

Quick facts

Lead sponsorFujian Medical University
PhaseNA
StatusRecruiting now
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment50
Start date1 January 2023
Primary completion31 December 2024
Estimated completion31 December 2027
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Fujian Medical University

Who can join

Adults 18 to 75, any sex, with Overall Response Rate. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Evaluate the objective response rate (ORR) of the combination of candenizumab, lenvatinib, and SOX regimen for the treatment of HER2 negative advanced gastric or gastroesophageal junction adenocarcinoma patients

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Other recruiting trials for Overall Response Rate

Currently open trials in the same condition.

Other Fujian Medical 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/NCT06277024.

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