Phase 2 Macular Degeneration Trial, Recruiting NCT07185841 Sponsor: Fujian Haixi Pharmaceuticals Co., Ltd. Condition: Macular Degeneration
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Phase 2 Macular Degeneration Trial, Recruiting

NCT07185841
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:

  • You are between 50 and 80 years old (for Phase I) or between 50 and 85 years old (for Phase II) at the time of signing the consent form, and you are male or female
  • You have been diagnosed with active abnormal blood vessel growth under the retina (called choroidal neovascularization, or CNV) caused by age-related macular degeneration (AMD), confirmed by special eye imaging tests
  • The affected area in your eye is below a certain size limit, as measured by an eye imaging test called fluorescein angiography
  • You have either never been treated for this condition before, or you previously received anti-VEGF eye injections that worked, stopped them more than 3 months ago, and now have fluid in the retina shown on a scan
  • Your vision in the eye being studied falls within a specific range — roughly between 20/32 and 20/400 on a standard eye chart
  • There may be additional requirements set by the trial site (confirm with trial site)

Who may not be able to join:

  • You have a specific type of blood vessel condition in the eye (polypoidal choroidal vasculopathy) that puts you at high risk of serious bleeding
  • You have a large amount of bleeding under the retina, or significant scarring or tissue loss affecting more than half the problem area or the central part of your vision
  • Your abnormal blood vessel growth is caused by something other than age-related macular degeneration
  • You have any other eye condition in the study eye that could affect your vision
  • You have active inflammation or infection in either eye, or a history of a specific type of eye inflammation related to the immune system (uveitis)
  • You have a high level of short-sightedness (prescription stronger than -6.00)
  • You had eye surgery in the study eye within the past 90 days before the screening visit
  • You have previously had certain eye treatments, including a light-based therapy (photodynamic therapy) within 120 days, radiation treatment, certain types of laser treatment, macular surgery, or heat-based eye therapy
  • You received certain anti-VEGF treatments given through the body (not the eye) within 90 days before starting the study
  • You are pregnant or breastfeeding
  • You have a known allergy or medical reason to avoid any of the study treatments or procedures
  • You have had serious heart problems — such as heart failure, unstable chest pain, a heart attack, a stroke-like heart event, a blood clot, or a major bleeding episode — within the past 6 months, or you have high blood pressure that is not well controlled, or a heart rhythm problem requiring ongoing treatment
  • You had a stroke within the past 12 months, or a mini-stroke (transient ischemic attack) within the past 6 months
  • You have poorly controlled diabetes, indicated by a blood sugar level measure (HbA1c) of 12% or higher
  • There may be additional reasons set by the trial site that could affect eligibility (confirm with trial site)

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 26 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

Principal Investigator: Hong Dai, Beijing Hospital

Phone: +86 0591-87519936

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
Fujian Haixi Pharmaceuticals Co., Ltd.
Registry
ClinicalTrials.gov
Start date
1 July 2025
Est. completion
1 July 2028

Where this trial is recruiting

🇨🇳 China

Primary endpoints

Phase I : Dose-Limiting Toxicity (DLT); Phase II: Mean change of letters from baseline in Best Corrected Visual Acuity(BCVA)

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: 26 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