Status:

UNKNOWN

Real-world Data (RWD) of Ramucirumab Plus Paclitaxel

Lead Sponsor:

Hallym University Medical Center

Conditions:

Gastric Cancer

Gastroesophageal Junction Adenocarcinoma

Eligibility:

All Genders

19+ years

Brief Summary

Real World Data (RWD) obtained from real clinical sites is data obtained after administering a drug to patients with different characteristics in daily practice, and Real World Evidence (RWE) is estab...

Detailed Description

Most drugs are introduced into the medical market based on efficacy derived from randomized controlled trials (RCTs) in a subset of patient groups in which the age, presence of comorbidities, and gene...

Eligibility Criteria

Inclusion

  • Prospective population
  • Patients aged 19 years or older and histologically or cytologically confirmed gastric adenocarcinoma or gastroesophageal junction adenocarcinoma
  • Patients with locally advanced or metastatic disease for which curative resection is not possible.
  • Patients who have failed fluoropyrimidine and platinum (cisplatin or oxaliplatin)-based chemotherapy as palliative first-line therapy
  • Patients who is starting ramucirumab/paclitaxel combination therapy after the study initiation date

Exclusion

  • Patients receiving ramucirumab monotherapy
  • Patients receiving ramucirumab/paclitaxel in clinical trial or receiving without being covered by health insurance
  • Patients unable to communicate or incapable of understanding documents for patient report outcomes
  • Historical retrospective population
  • Inclusion Criteria:
  • Patients aged 19 years or older and histologically or cytologically confirmed gastric adenocarcinoma or gastroesophageal junction adenocarcinoma
  • Patients with locally advanced or metastatic disease for which curative resection is not possible
  • Patients who have failed platinum-based palliative first-line therapy, and who started the following second-line therapy: taxane, irinotecan , or fluoropyrimidine-based single or combined chemotherapy, before May 1, 2018

Key Trial Info

Start Date :

June 1 2021

Trial Type :

OBSERVATIONAL

Allocation :

ESTIMATED

End Date :

September 1 2023

Estimated Enrollment :

222 Patients enrolled

Trial Details

Trial ID

NCT04915807

Start Date

June 1 2021

End Date

September 1 2023

Last Update

June 7 2021

Active Locations (9)

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Page 1 of 3 (9 locations)

1

Hallym University Sacred Heart Hospital

Anyang, South Korea, 14068

2

Kyungpook National University Chilgok Hospital

Daegu, South Korea, 41404

3

Keimyung University Dongsan Medical Center

Daegu, South Korea, 42601

4

Seoul National University Bundang Hospital

Seongnam, South Korea, 13620