Phase 2 Interstitial Lung Disease Trial, Recruiting NCT07121413 Sponsor: Shanghai Synvida Biotechnology Co.,Ltd. Condition: Interstitial Lung Disease
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Phase 2 Interstitial Lung Disease Trial, Recruiting

NCT07121413
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:

  • People who have a confirmed diagnosis of IPF (idiopathic pulmonary fibrosis) and whose lung function test results meet the specific requirements set out in the trial protocol.
  • People who agree to use highly effective birth control during the trial and for 6 months after the last dose of the study drug.
  • People who are able to understand the study, freely agree in writing to take part, and are willing and able to follow all the trial's required procedures.

Who may not be able to join:

  • People who have a known history of drug or other allergies, or whom the trial doctor believes may be allergic to the study drugs.
  • People who have another significant lung disease in addition to IPF at the time of screening.
  • People for whom lung function testing is not considered safe or appropriate at the time of screening.
  • People who have had a respiratory or whole-body infection requiring antibiotic or antiviral treatment in the month before joining the trial.
  • People who have had a sudden worsening (acute exacerbation) of their IPF in the 4 months before joining the trial.
  • People who have taken any medication known to cause or worsen lung scarring in the 3 months before screening.
  • People who have smoked in the 3 months before screening, or who are unwilling to remain smoke-free throughout the trial.
  • People who have a significant heart, brain, blood, nerve, mental health, or metabolic condition at screening, or who are planning major surgery during the trial period.
  • People whose blood test results show certain abnormalities at screening (confirm specific values with trial site).
  • People who show signs of significant kidney impairment or who require dialysis at screening.
  • People with an active hepatitis virus infection, or a history of an immune deficiency condition (whether acquired or present from birth).
  • People who have had a cancer diagnosis within the 5 years before screening.
  • People who have difficulty with blood draws, or who have a history of needle phobia or fear of blood.
  • People who have a positive pregnancy test or who are currently breastfeeding at screening.
  • People who have taken part in another clinical trial or received another experimental drug within the 3 months before joining this trial.
  • People whom the trial doctor considers unsuitable for participation for any other reason.

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 27 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

Phone: 86-21-62483180

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 Synvida Biotechnology Co.,Ltd.
Registry
ClinicalTrials.gov
Start date
4 November 2025
Est. completion
31 December 2026

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Incidence of Treatment-Emergent Adverse Events

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: 27 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