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Clinical Trials List

Protocol NumberV503-001

2007-09-17 - 2012-05-31

Phase II

Terminated8

ICD-10C53.9

Malignant neoplasm of cervix uteri, unspecified

ICD-10Z51.12

Encounter for antineoplastic immunotherapy

ICD-9180.9

Malignant neoplasm of cervix uteri, unspecified

  • Trial Applicant

    Merck Sharp & Dohme (I.A.) LLC

  • Sponsor

  • Trial scale

    Multi-Regional Multi-Center

  • Update

    2025/08/20

Investigators and Locations

Principal Investigator 周宏學 Division of Obstetrics & Gynecology

Co-Principal Investigator

  • 周宏學 Division of Obstetrics & Gynecology

The Actual Total Number of Participants Enrolled

0 Terminated

Principal Investigator 陳祈安 Division of Obstetrics & Gynecology

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Terminated

Principal Investigator 楊育正 Division of Obstetrics & Gynecology

Co-Principal Investigator

  • 王功亮 Division of Obstetrics & Gynecology
  • 陳子健 Division of Obstetrics & Gynecology

The Actual Total Number of Participants Enrolled

0 Terminated

Principal Investigator 楊育正 Division of Obstetrics & Gynecology

Co-Principal Investigator

  • 王功亮 Division of Obstetrics & Gynecology
  • 陳子健 Division of Obstetrics & Gynecology

The Actual Total Number of Participants Enrolled

0 Terminated

Principal Investigator

Co-Principal Investigator

  • 李中遠 Division of Obstetrics & Gynecology
  • 曾敬程 Division of Obstetrics & Gynecology
  • 林于翔 Division of Obstetrics & Gynecology
  • 曾志仁 Division of Obstetrics & Gynecology

The Actual Total Number of Participants Enrolled

0 Terminated

Principal Investigator 朱堂元 Division of Obstetrics & Gynecology

Co-Principal Investigator

  • 陳寶珠 Division of Obstetrics & Gynecology

The Actual Total Number of Participants Enrolled

0 Terminated

Principal Investigator Nae-Fang Twu Division of Obstetrics & Gynecology

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Terminated

Principal Investigator 余慕賢 Division of Obstetrics & Gynecology

Co-Principal Investigator

The Actual Total Number of Participants Enrolled

0 Terminated

Condition/Disease

Objectives

Test Drug

Active Ingredient

Dosage Form

Dosage

Endpoints

Inclution Criteria

The Estimated Number of Participants

  • Taiwan

    100 participants

  • Global

    3720 participants