Interstitial Lung Disease Trial, Recruiting NCT07371182 Sponsor: West China Second University Hospital Condition: Interstitial Lung Disease
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Interstitial Lung Disease Trial, Recruiting

NCT07371182
Recruiting Not Applicable

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:

  • Children from birth up to 18 years old, of any sex
  • Children who have been diagnosed with a condition called LCH (Langerhans cell histiocytosis), confirmed through laboratory testing, and who have not yet received any treatment specifically for LCH
  • Children whose LCH affects multiple spots in the bones, OR affects a single bone location in certain sensitive areas of the head (such as around the eyes, ears, or mouth — but not the parietal, occipital, or frontal bones), OR affects a single spot in the spine where it is pressing on the spinal cord
  • Children (and their parent or guardian) who are willing to sign a consent form, follow the treatment plan described in the trial, and attend follow-up appointments

Who may not be able to join:

  • Children who have other serious underlying health conditions, such as a weakened immune system from birth, heart failure, kidney problems, hepatitis, HIV infection, or who have had an organ transplant
  • Children who have a second, separate cancer diagnosis
  • Children whose heart electrical activity test (ECG) shows a reading above a certain level before joining the trial (confirm with trial site)
  • Children whose eye examination before joining the trial shows certain eye conditions, such as a blocked vein in the eye, a detached layer at the back of the eye, or other significant eye problems
  • Children whose LCH has a specific type of genetic change (called a category 3 MEK mutation) — there is a particular list of mutation types that would make a child ineligible (confirm with trial site)
  • Children (or their parent/guardian) who are not willing to sign the consent form

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 28 July 2026
This study is not part of the standard drug-approval phase pathway (for example an observational, device, behavioural, or registry study), so a phase success rate does not apply.

Contact this trial

Phone: 86+18280145819

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
Not Applicable
Sponsor
West China Second University Hospital
Registry
ClinicalTrials.gov
Start date
19 June 2026
Est. completion
31 December 2030

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Event-free survival rate

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: 28 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