Immunotherapy plus chemo aims to fight bile duct cancer
NCT ID NCT04910386
First seen Jun 27, 2026 · Last updated Jun 27, 2026
Summary
This Phase 2 trial tests whether adding the immunotherapy drug envafolimab to standard chemotherapy (gemcitabine plus cisplatin) helps people with advanced biliary tract cancers live longer without their cancer growing. About 126 adults who have not had prior treatment for advanced disease will be randomly assigned to receive either the combo or chemo alone. The study is open-label, meaning both doctors and patients know which treatment is given.
What this could mean
Our plain-language read of the trial. This is informational only — not medical advice or a prediction.
Active substance
envafolimab (an immunotherapy drug) plus gemcitabine and cisplatin (chemotherapy)
What this could lead to
If it works, this could offer a more effective first-line treatment for advanced biliary tract cancers, potentially slowing disease progression.
What could go wrong
This is an early Phase 2 trial with only 126 participants, so results may not be conclusive. Immunotherapy can cause immune-related side effects, and the combination may not improve outcomes over standard chemo alone.
Disclaimer
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the original study
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Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
This is a summary of the original study . Summaries may miss details or leave out important information. Before applying or accepting participation, make sure you have read and understood the full study. Curemydisease.com takes no responsibility whatsoever for anything missed, misunderstood, or acted upon as a result of our summary — we know it does not capture everything.
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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.