Phase 2 Pulmonary Hypertension Trial, Recruiting NCT07632235 Sponsor: Shanghai 6th People's Hospital Condition: Pulmonary Hypertension
Back to Pulmonary Hypertension

Phase 2 Pulmonary Hypertension Trial, Recruiting

NCT07632235
Recruiting Phase 2

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:

  • Adults aged 18 years or older
  • People who have been diagnosed with intrahepatic cholangiocarcinoma (a type of bile duct cancer that starts inside the liver), confirmed through a tissue or cell sample
  • People whose cancer cannot be surgically removed, has come back, or has spread to other parts of the body
  • People who have not yet received any systemic (whole-body) treatment, such as chemotherapy, for their advanced cancer
  • People who have at least one tumour that can be measured using standard imaging guidelines
  • People who are relatively well and able to carry out daily activities, as measured by a standard health scale (ECOG score of 0 or 1)
  • People for whom enough tumour tissue is available before treatment starts, for review by a central laboratory
  • People whose tumour tissue shows a specific protein marker result (CK5/6 H-score of 1.0 or higher), as tested by a central laboratory
  • People whose liver, kidneys, and bone marrow are functioning well enough to meet the trial's laboratory requirements
  • People who have a blocked bile duct must have had it successfully drained and their condition stabilised before joining
  • People who are able to give written consent to participate

Who may not be able to join:

  • People who have another type of primary cancer, including bile duct cancer outside the liver, gallbladder cancer, or cancer of the ampulla (a small opening where the bile duct meets the small intestine)
  • People whose tumour tissue shows a CK5/6 H-score below 1.0
  • People who have already received systemic treatment for advanced or metastatic disease
  • People with active gastrointestinal bleeding, stomach ulcers, or a high risk of a hole developing in the stomach or bowel
  • People who have recently had a serious heart or blood vessel event, such as a heart attack, stroke, uncontrolled high blood pressure, or severe heart failure
  • People with a known allergy or sensitivity to celecoxib, sulfonamide medicines, anti-inflammatory medicines (NSAIDs), or aspirin — including those who have breathing problems triggered by aspirin
  • People with an active autoimmune disease or any condition that would make treatment with pembrolizumab unsafe
  • People with severely reduced kidney function
  • People with advanced liver impairment classified as Child-Pugh class C
  • People with an active infection that is not under control
  • People who have any other condition that, in the treating doctor's judgement, would interfere with taking part in or interpreting the results of the trial

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.

This is a simplified plain English summary of the eligibility criteria. Full criteria are set by the trial investigators and may include additional requirements not shown here. Never self-exclude from a trial based on this summary. Contact the trial site directly to confirm your eligibility.
Last synced 26 July 2026
Phase 2: approximately ~30% of drugs entering this phase reach regulatory approval, based on published industry-wide historical data. This is not specific to this trial.
Phase success rates shown are historical industry-wide averages based on published data. They are not a prediction for this specific trial or your individual situation.

Contact this trial

Principal Investigator: Cun Wang, State Key Laboratory of Systems Medicine for Cancer, Shanghai Cancer Institute & Department of Liver Surgery, Renji Hospital, Shanghai Jiao Tong University School of Medicine, Shanghai, China.

Phone: 86 18160747569

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

Status
Recruiting
Phase
Phase 2
Sponsor
Shanghai 6th People's Hospital
Registry
ClinicalTrials.gov
Start date
1 July 2026
Est. completion
31 December 2029

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Progression-Free Survival (PFS)

Can't join this trial?

Expanded access pathways

If this trial is not available to you, other access pathways may exist. In Australia, the TGA Special Access Scheme allows access to unapproved therapeutic goods for individual patients.

TGA Special Access Scheme information

Find other recruiting trials on ClinicalTrials.gov

Data last synced from ClinicalTrials.gov: 26 July 2026. Trial status can change. Always verify current status directly with the trial site before making any decision.

Trial recruitment status can change without notice between our nightly data updates. Always contact the trial site directly to confirm current recruitment status before making any decisions or travel arrangements.

View original record on ClinicalTrials.gov