Phase 4 Interstitial Lung Disease Trial, Recruiting NCT05841758 Sponsor: Hospices Civils de Lyon Condition: Interstitial Lung Disease
Back to Interstitial Lung Disease

Phase 4 Interstitial Lung Disease Trial, Recruiting

NCT05841758
Recruiting Phase 4

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 are at least 18 years old
  • You have been diagnosed with sarcoidosis confirmed by tissue testing, following internationally recognised medical guidelines
  • You have a non-severe form of sarcoidosis affecting the eyes that needs treatment taken by mouth or injection (systemic treatment)
  • You have a non-severe form of sarcoidosis affecting the skin that needs systemic treatment
  • You have a non-severe form of sarcoidosis affecting the bones that needs systemic treatment
  • You have a non-severe form of sarcoidosis affecting the joints that needs systemic treatment
  • You have a non-severe form of sarcoidosis causing high calcium levels in the blood that needs systemic treatment
  • You have a non-severe form of sarcoidosis affecting the nerves outside the brain and spinal cord that needs systemic treatment
  • You have a non-severe form of sarcoidosis affecting the ears, nose, or throat that needs systemic treatment
  • You have higher-than-normal calcium levels in your urine, as measured by a 24-hour urine test or a standard urine sample (confirm with trial site for exact values)
  • You are willing and able to sign a consent form agreeing to take part
  • You are registered with the French national social security system

Who may not be able to join:

  • You have a severe form of sarcoidosis that requires stronger treatments such as certain immune-suppressing drugs, anti-TNF antibody therapy, or high-dose steroid injections into a vein
  • You have used immune-suppressing medications within the last 3 months, or are currently taking them
  • You have taken steroid tablets (such as cortisone or prednisone) and have not been off them for at least 3 months
  • You have previously taken antimalarial drugs such as hydroxychloroquine or chloroquine, and have not been off them for at least 12 months
  • You are currently taking any of the following medications: citalopram, escitalopram, hydroxyzine, domperidone, or piperaquine
  • You have a known allergy or intolerance to hydroxychloroquine, chloroquine, related drugs, or prednisone
  • You have a heart rhythm problem shown on a heart tracing (ECG), specifically a prolonged QT interval (note: atrial fibrillation alone does not automatically exclude you — confirm with trial site)
  • You have severe eye problems, eye problems that would prevent regular eye monitoring during the trial, or a history of damage to the central part of the retina (maculopathy or retinopathy)
  • You have end-stage (very advanced) disease of the lungs, liver, heart, or kidneys
  • Your sarcoidosis affects the brain or spinal cord (central nervous system)
  • Your sarcoidosis affects the heart
  • You have signs of an active infection (including herpes or chickenpox viruses), a serious unstable health condition (such as moderate to severe heart failure), or unstabilised psychosis
  • You have a long-term infection with HIV or hepatitis B virus (HBV)
  • You have tuberculosis (TB) that has not been treated, whether it is active or a latent (dormant) infection
  • You are pregnant or breastfeeding (a pregnancy blood test will be done at the start of the trial)
  • You need to receive a live vaccine during the period you are in the trial
  • You are unable to understand the trial information or to give informed consent, or are otherwise unable to meet the requirements of the study
  • You are already taking part in another clinical trial involving a treatment intervention
  • You are under legal court protection
  • You are not able or willing to use effective contraception throughout the duration of the trial (confirm with trial site for the full list of accepted contraceptive methods)

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
Phase 4 trials study a drug that has already been approved, monitoring long-term safety and effectiveness in real-world use.

Contact this trial

Phone: 04.26.73.26.29

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 4
Registry
ClinicalTrials.gov
Start date
30 July 2024
Est. completion
1 July 2029

Where this trial is recruiting

🇫🇷 France

Primary endpoints

Evaluate the steroid-sparing effect of hydroxychloroquine as an add-on therapy in patients with non severe extra-pulmonary sarcoidosis requiring a systemic treatment.

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