Phase 2 Interstitial Lung Disease 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:
- People aged between 18 and 85 years old
- Tumor patients who are able to have surgery or a biopsy to get a confirmed tissue diagnosis
- People who are able to understand and sign a consent form agreeing to take part
- People whose doctors estimate they are likely to live for more than 6 months and who are able to attend follow-up appointments
- Healthy volunteers who do not have a long-term history of conditions such as high blood pressure, diabetes, heart disease, kidney disease, or cancer
Who may not be able to join:
- Women who are pregnant or currently breastfeeding
- People who have a known allergy to the ingredients in the study drug
- People with serious liver or kidney problems, specifically those with blood creatinine levels above 159 µmol/L (confirm with trial site for exact measurement details)
- People who are already taking part in another clinical trial that could affect the results of this study
- People whose illness is so severe that they are unable to cooperate with the required tests and examinations
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
Phone: +86-13021115973
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
Analysis of PET/CT Images of [68Ga] Ga-NI-FAPI-04
Can't join this trial?
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.