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Completed Phase 2 Interventional Results available

A Trial of Tisotumab Vedotin in Cervical Cancer

ClinicalTrials.gov ID: NCT03438396

Public ClinicalTrials.gov record NCT03438396. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Sep 2, 2026, 11:31 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Single Arm, Multicenter, International Trial of Tisotumab Vedotin (HuMax®-TF-ADC) in Previously Treated, Recurrent or Metastatic Cervical Cancer

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

A Single arm, Multicenter, International Trial of Tisotumab Vedotin (HuMax®-TF-ADC) in Previously Treated, Recurrent or Metastatic Cervical Cancer.

Study identification

NCT ID
NCT03438396
Recruitment status
Completed
Study type
Interventional
Phase
Phase 2
Lead sponsor
Seagen Inc.
Industry
Enrollment
102 participants

Conditions and interventions

Interventions

Drug

Eligibility (public fields only)

Age range
18 Years and older
Sex
Female
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Jun 11, 2018
Primary completion
Feb 5, 2020
Completion
Aug 1, 2022
Last update posted
Jul 24, 2023

2018 – 2022

United States locations

U.S. sites
20
U.S. states
17
U.S. cities
20
Facility City State ZIP Site status
University of Alabama Birmingham Alabama 35294
Arizona Oncology Associate - Biltmore Cancer Center Phoenix Arizona 85016
UCLA Dept. of OBGYN Los Angeles California 90095
Southern Baptist Hospital of Florida, Inc Jacksonville Florida 32258
University of Miami Miller School of Medicine Miami Florida 33136
University of Gynecologic Oncology Atlanta Georgia 30342
Community Hospital East Indianapolis Indiana 46219
Louisville Oncology Louisville Kentucky 40207
Baystate Medical Center Springfield Massachusetts 01105
Women's Cancer Center of Nevada Las Vegas Nevada 89169
MD Anderson Cancer Center at Cooper University Hospital Camden New Jersey 08103
University of New Mexico Comprehensive Cancer Center (UNMCCC) Albuquerque New Mexico 87102
University of Cincinnati Cincinnati Ohio 45267
The Ohio State University Wexner Medical Center Hilliard Ohio 43210
Stephenson Cancer Center Oklahoma City Oklahoma 73104
Oklahoma Cancer Specialists and Research Institute, LLC Tulsa Oklahoma 74146
Abington Memorial Hospital Willow Grove Pennsylvania 19090
Bon Secours Saint Francis Cancer Center Greenville South Carolina 29607
UT Health McGovern Medical School Houston Texas 77030
Froedtert & Medical College Clinics Milwaukee Wisconsin 53226

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

Non-U.S. locations

This page focuses on the U.S. directory. The official record also lists 33 non-U.S. sites.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT03438396, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Jul 24, 2023 · Synced Sep 2, 2026

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Open the official record

The complete protocol, eligibility criteria, and contact information for NCT03438396 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →