Macular Degeneration Trial, Recruiting NCT06859515 Sponsor: Guangzhou Jiayin Biotech Ltd Condition: Macular Degeneration
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Macular Degeneration Trial, Recruiting

NCT06859515
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:

  • People who previously received treatment with EXG102-031 in the related study (EXG102-031-111)
  • People who have given informed consent and are willing to follow the procedures set out in the study protocol

Who may not be able to join:

  • People who are unwilling or unable to take part in long-term follow-up visits or check-ins

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

Principal Investigator: Mingwei ZHAO, PhD, Peking University People's Hospital

Phone: +86 13957164092

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
Guangzhou Jiayin Biotech Ltd
Registry
ClinicalTrials.gov
Start date
13 March 2025
Est. completion
15 May 2030

Where this trial is recruiting

🇨🇳 China

Primary endpoints

long-term safety:the types, severity, and incidence of serious adverse events (SAEs), adverse events (AEs).

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