Pulmonary Hypertension Trial, Recruiting
Who may be able to join
AI generated eligibility summary. Written by an AI model from the official source data and checked on a sample basis. It can contain mistakes, so confirm anything important against the original source. How we use AI
Who might be able to join this trial:
- You have been diagnosed with a type of bile duct cancer called intrahepatic cholangiocarcinoma (ICC), confirmed by a tissue biopsy, and had surgery to remove it within the past 12 weeks with the goal of curing the disease.
- Your cancer has not spread to distant parts of the body (no distant metastasis), regardless of the original tumor size or whether nearby lymph nodes were affected.
- You have at least one feature that puts you at higher risk of the cancer returning — such as: the tumor had grown through the surface of the liver or into nearby structures before surgery; scans showed multiple tumors or a single tumor larger than 5 cm; there was evidence of cancer in blood or lymph vessels; or cancer was found in nearby lymph nodes.
- You have not had any previous systemic (whole-body) treatment for this cancer.
- You are reasonably active and able to carry out daily activities (your doctor will assess this using a standard scale called ECOG, scoring 0–2).
- Your doctor expects you to live for at least 3 more months.
- Your heart, liver, kidneys, and other organs are working well enough to handle treatment.
- You are willing to use reliable contraception (or have had surgical sterilisation) during the study and for 120 days after your last dose of treatment.
- You are willing to sign a consent form and are expected to be able to follow the study requirements.
Who may not be able to join:
- You have taken medication that suppresses the immune system in the 28 days before joining (not including low-dose steroid creams, inhalers, or very low-dose oral steroids).
- You have taken certain herbal or immune-boosting treatments (such as thymosin or interferons) in the past 4 weeks.
- You have serious heart problems that are not well controlled, such as recent heart attack, unstable chest pain, certain irregular heartbeats, severe heart failure, or poor heart pumping function.
- You have had a serious active infection recently requiring intravenous antibiotics or antivirals, a fever above 38.5°C in the past 4 weeks, or major surgery in the past 3 weeks.
- You have an active autoimmune condition (where your immune system attacks your own body) or immune deficiency disease — for example, active hepatitis, lung inflammation, or rheumatoid arthritis — with some exceptions such as well-controlled thyroid disease or well-controlled Type 1 diabetes (confirm with trial site).
- You have HIV/AIDS, or active hepatitis B (with virus levels above a certain threshold) or active hepatitis C, unless your hepatitis B is well controlled on antiviral treatment for at least 14 days.
- You have had, or are planned to have, an organ transplant (corneal eye grafts are an exception).
- You are currently taking part in another clinical trial involving an experimental treatment, or have done so recently without fully recovering from any side effects.
- You are known to be allergic to any of the ingredients in the study drug.
- You have had, or are planned to have, a bone marrow or stem cell transplant from another person.
- You have a mental health condition or substance use problem that is not well controlled.
- You have high blood pressure that remains at 140/90 mmHg or above even with treatment.
- You have had significant bleeding in your digestive system in the past 3 months, or a blood clot event (such as a stroke, deep vein thrombosis, or pulmonary embolism) in the past 6 months.
- You have a blood clotting disorder or are taking blood-thinning medication.
- You have significant levels of protein in your urine (confirm with trial site).
- Your doctor considers you unsuitable for other medical reasons not listed here.
Important: Always verify eligibility with the trial site directly before applying.
Based on publicly available eligibility criteria from ClinicalTrials.gov. Verify directly with the trial site before acting. This is not medical advice.
Contact this trial
Principal Investigator: Shunda Du, Peking Union Medical College Hospital (PUMCH)
Phone: 010-69152831
Contact details sourced from ClinicalTrials.gov. Verify directly with the trial site before attending.
GP referral letter
Print a one-page summary to share with your doctor.
Trial details
Where this trial is recruiting
Primary endpoints
Recurrence-Free Survival (RFS)
Can't join this trial?
Data last synced from ClinicalTrials.gov: 23 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.