Interstitial Lung Disease Trial, Recruiting NCT07431060 Sponsor: West China Second University Hospital Condition: Interstitial Lung Disease
Back to Interstitial Lung Disease

Interstitial Lung Disease Trial, Recruiting

NCT07431060
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:

  • The child must be between 0 and 18 years old (any sex).
  • The child must have a confirmed diagnosis of Langerhans cell histiocytosis (LCH) — a rare disease involving abnormal immune cells — proven by a laboratory test showing specific markers (CD1a and/or CD207), and must not have received any treatment for LCH before.
  • The child's LCH must affect more than one part or system of the body, as confirmed by medical tests and scans.
  • A parent or legal guardian must be willing and able to sign a consent form agreeing to take part, follow the treatment plan, and attend follow-up appointments (and the child may also be asked to give their agreement if old enough).

Who may not be able to join:

  • Children who have another serious underlying health condition, such as a weakened immune system from birth, heart failure, kidney problems, long-term hepatitis, HIV, or who have had an organ transplant.
  • Children who have had a second, separate type of cancer at any point.
  • Children whose heart electrical activity test (ECG) shows a specific measurement (called QTcF) above 0.47 seconds before joining the trial.
  • Children whose eye examination before joining the trial shows certain eye problems — such as a blocked vein in the eye or separation of eye tissue layers — that the doctor feels would make it unsafe to participate.
  • Children whose LCH has a specific type of gene change (called a Class 3 MEK pathway mutation — a particular list of genetic alterations) (confirm with trial site if unsure whether this applies).
  • Children whose parent or guardian is unwilling or unable to sign the required consent forms.

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
13 February 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