Catalyst Wire Dossier Catalyst Wire Dossier
CLINICAL_TRIALS ClinicalTrials.gov record update

Camrelizumab Combined With Apatinib and Capecitabine for Patients With Advanced Biliary Tract Cancer: a Phase 2, Single-arm, Prospective Study.

This page presents selected fields from the linked source record. It does not add a medical interpretation.

Open original source record ↗

Record identity and dates

Source
ClinicalTrials.gov
Source record ID
NCT04720131
Title field or adapter rule
protocolSection.identificationModule.officialTitle
Ingested At
2026-04-28T10:40:00.079345+00:00
Published At
2024-01-30T00:00:00+00:00
Record Updated At
2024-01-30
Timestamp Basis
source retrieval time was not retained by the feed adapter
Date limitation
source retrieval time was not retained by the feed adapter

Fields recorded by this source

protocolSection.conditionsModule.conditions
["Biliary Tract Cancer", "Anti-PD-1 Therapy", "Targeted Molecular Therapy", "Capecitabine"]
protocolSection.statusModule.lastUpdatePostDateStruct.date
"2024-01-30"
protocolSection.identificationModule.nctId
"NCT04720131"
protocolSection.identificationModule.officialTitle
"Camrelizumab Combined With Apatinib and Capecitabine for Patients With Advanced Biliary Tract Cancer: a Phase 2, Single-arm, Prospective Study."
protocolSection.statusModule.overallStatus
"COMPLETED"
protocolSection.designModule.phases
["PHASE2"]
protocolSection.statusModule.resultsFirstPostDateStruct.date
""

Study condition terms

  • Biliary Tract Cancer (protocolSection.conditionsModule.conditions)
  • Anti-PD-1 Therapy (protocolSection.conditionsModule.conditions)
  • Targeted Molecular Therapy (protocolSection.conditionsModule.conditions)
  • Capecitabine (protocolSection.conditionsModule.conditions)

Intervention details are not present in the imported fields for this record. No drug-condition relationship is inferred from co-listing.

This index keeps the source fields it imported; it may not contain the complete original record. Verify wording and context in the linked source.