Liver cancer research aims to unlock secrets of immunotherapy response
NCT ID NCT04145141
First seen Jun 26, 2026 · Last updated Aug 27, 2026 · Updated 5 times
Summary
This study gathers blood, urine, stool, and tissue samples from 132 adults with primary liver cancer who are receiving or have received immunotherapy. Researchers will analyze these samples along with medical records to learn more about how liver cancer develops and responds to treatment. Participants are followed for life by phone or email, but no new treatments are given as part of this study.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- What this could lead to
- If successful, this research could help doctors design better, more personalized immunotherapies for liver cancer patients.
- What could go wrong
- This is an observational study, not a treatment trial. It collects data and samples but does not test a new therapy directly, so it may not lead to immediate changes in care.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Participants
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132 people
The number who actually took part.
- Started
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Jul 2021
- Finished
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Aug 2026
- Lead sponsor
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A government research agency
The lead sponsor is the US National Institutes of Health.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
primary clinical
- Ages
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18 to 120 years
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
* INCLUSION CRITERIA: * Participants with histologically/ultrasound/imaging confirmed or suspicious lesions of HCC or CCA. * Participants with planned or a history of at least 1 dose of immunotherapy for HCC or CCA. * Ability of individual to understand and the willingness to sign a written informed consent document. * Age greater than or equal to 18 years old at date of study consent. EXCLUSION CRITERIA: -Participants with known HIV infection (as these individuals may have abnormal test results which may confound the endpoints of this study)
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Memorial Sloan Kettering Cancer Center
New York, New York, 10065, United States
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National Institutes of Health Clinical Center
Bethesda, Maryland, 20892, United States
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Thomas Jefferson University
Philadelphia, Pennsylvania, 19107, United States
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University of Texas Southwestern Medical Center
Dallas, Texas, 75390, United States
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- New antibody drug conjugate tested against advanced cancers
- Sparing the liver: targeted chemoembolization meets lenvatinib in liver cancer
- AI-Enhanced ultrasound aims to catch liver cancer earlier
- Can turbocharged immune cells stop liver cancer from coming back?
- Two blood markers put to the test for early liver cancer detection
- New antibody pair takes aim at advanced liver cancer in major trial