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NCT03869294

GS Regimen as the First-line Chemotherapy in Chinese Advanced PC Patients

Completed Last updated 4 March 2020
What this trial tests

trial testing GS in Pancreatic Cancer in 96 participants. Completed in 31 December 2017.

Timeline
1 January 2014
Primary endpoint
31 December 2017
31 December 2017

Quick facts

Lead sponsorZhejiang University
StatusCompleted
Study typeOBSERVATIONAL
Enrollment96
Start date1 January 2014
Primary completion31 December 2017
Estimated completion31 December 2017
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Zhejiang University

Who can join

Adults 18 to 80, any sex, with Pancreatic Cancer or Chemotherapy Effect. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

Gemcitabine plus S-1 (GS) prolonged progression-free survival (PFS) and greatly improved objective response rate (ORR) as well as disease control rate (DCR) of Asian patients with locally advanced and metastatic pancreatic cancer (PC). However, limited data of GS regimen exist on the efficacy and safety in the treatment of Chinese patients with advanced PC. To assess the efficacy and safety of gemcitabine plus S-1 (GS regimen) as the first-line chemotherapy in Chinese patients with advanced PC, we designed this prospective study.

Publications & conference data

No peer-reviewed publications indexed yet for this trial. Completed trials usually publish results within 12-18 months.

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Other trials of GS

Trials testing the same drug.

Other recruiting trials for Pancreatic Cancer

Currently open trials in the same condition.

Other Zhejiang University trials

Trials by the same sponsor.

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Data sources for this page

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