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NCT04764227

Phase II Study of Postoperative Concurrent Chemoradiotherapy for Esophageal Squamous Cell Carcinoma (ESO- Shanghai 17)

Active, enrolled Phase 2 Last updated 3 August 2023
What this trial tests

Phase 2 trial testing Paclitaxel in Esophagus Cancer in 70 participants. Participants enrolled and being followed up; not accepting new ones.

Timeline
30 May 2020
Primary endpoint
30 March 2024
30 March 2027

Quick facts

Lead sponsorFudan University
PhasePhase 2
StatusActive, enrolled
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposetreatment
Enrollment70
Start date30 May 2020
Primary completion30 March 2024
Estimated completion30 March 2027
Sites1 location across China

Drugs / interventions tested

Conditions studied

Sponsor

Fudan University

Who can join

Adults 18 to 75, any sex, with Esophagus Cancer or Esophageal Squamous Cell Carcinoma. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to evaluate safety and 2-year local control rate for postoperative concurrent chemoradiotherapy for esophageal squamous cell carcinoma.

Publications & conference data

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

  1. Postoperative chemoradiotherapy for esophageal squamous cell Carcinoma: Results from ESO-Shanghai 17 and joint analyses for phase II clinical trials.
    Shen J, Ai D, Chen Y, Liu Q, et al · · 2026 · PMID 41531940 · DOI 10.1016/j.ctro.2025.101073

Verify or expand the search:

Other trials of Paclitaxel

Trials testing the same drug.

Other recruiting trials for Esophagus Cancer

Currently open trials in the same condition.

Other Fudan 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/NCT04764227.

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