A Longitudinal Observational Study of the Natural History and Management of Patients With HCC

Description

TARGET-HCC is a longitudinal, observational study of patients being managed for HCC in usual clinical practice. TARGET-HCC will create a research registry of participants with HCC within academic and community real-world practices in order to assess the safety and effectiveness of the entire spectrum of current and future therapies across diverse populations.

Conditions

Hepatocellular Cancer

Study Overview

Study Details

Study overview

TARGET-HCC is a longitudinal, observational study of patients being managed for HCC in usual clinical practice. TARGET-HCC will create a research registry of participants with HCC within academic and community real-world practices in order to assess the safety and effectiveness of the entire spectrum of current and future therapies across diverse populations.

A Longitudinal Observational Study of the Natural History and Management of Patients With Hepatocellular Carcinoma

A Longitudinal Observational Study of the Natural History and Management of Patients With HCC

Condition
Hepatocellular Cancer
Intervention / Treatment

-

Contacts and Locations

Phoenix

Banner University Medical Center, Phoenix, Arizona, United States, 85006

Little Rock

University of Arkansas, Little Rock, Arkansas, United States, 72205

Los Angeles

University of Southern California/Norris Comprehensive Cancer Center, Los Angeles, California, United States, 90033

Palo Alto

Stanford University, Palo Alto, California, United States, 94304

Pasadena

California Liver Research Institute, Pasadena, California, United States, 91105

Sacramento

University of California-Davis, Sacramento, California, United States, 95817

San Francisco

University of California, San Francisco, California, United States, 94158

Washington

Georgetown University, Washington, District of Columbia, United States, 20007

Clearwater

Gastro Florida, Clearwater, Florida, United States, 33762

Gainesville

University of Florida Hepatology Research at CTRB, Gainesville, Florida, United States, 32610-0272

Participation Criteria

Researchers look for people who fit a certain description, called eligibility criteria. Some examples of these criteria are a person's general health condition or prior treatments.

For general information about clinical research, read Learn About Studies.

Eligibility Criteria

  • 1. Male or female patients, age ≥18 years
  • 2. Patients with a histological/cytological or radiological diagnosis of HCC (mixed HCC cholangiocarcinoma may be included; patients who are candidates for surgical and non-surgical treatment, as well as those being followed without specific HCC therapy may be included)
  • 1. Inability to provide written informed consent

Ages Eligible for Study

18 Years to

Sexes Eligible for Study

ALL

Accepts Healthy Volunteers

No

Collaborators and Investigators

Target PharmaSolutions, Inc.,

Study Record Dates

2024-10