Phase 2 Macular Degeneration Trial, Recruiting NCT07547228 Sponsor: Intra-IMMUSG Pte Ltd Condition: Macular Degeneration
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Phase 2 Macular Degeneration Trial, Recruiting

NCT07547228
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 diagnosed with Neovascular Age-related Macular Degeneration (a type of eye condition where abnormal blood vessels grow under the retina).
  • People who are willing to sign a consent form agreeing to take part in the study.
  • People who have already tried at least two standard eye injection treatments (Ranibizumab, Aflibercept, or Faricimab) without sufficient success, and are currently receiving these injections every 8 weeks or more frequently.
  • People who are able to complete a required "wash-out period" (a waiting period after stopping their current eye injection) before joining — the length of this waiting period depends on which medication they are currently receiving (ranging from approximately 4 to 8 weeks depending on the drug).
  • People whose eye scans show abnormal blood vessel activity in or near the central area of the retina, with signs such as fluid or abnormal tissue.
  • People whose vision in the study eye falls within a specific range — roughly equivalent to being able to read between the 20/32 and 20/320 lines on a standard eye chart.
  • People whose vision loss in the study eye is considered to be mainly caused by their retinal condition.
  • People whose eye scans show the presence of fluid or certain structural changes in the central area of the retina.
  • People whose liver, kidney, and blood test results are within an acceptable range (based on tests done within 7 days of starting treatment).

Who may not be able to join:

  • People who have scarring, fibrous tissue, tissue wasting, or tears in the central part of the retina in the study eye.
  • People with glaucoma (high pressure in the eye) that is not well controlled, even with medication (confirm with trial site).
  • People with a history of a particular type of eye inflammation called uveitis that has no known cause or is linked to an immune system condition, in the study eye.
  • People with a high degree of short-sightedness (at least 8 diopters) in the study eye, measured before any corrective eye surgery.
  • People who have an active infection or inflammation around or outside the eye in either eye at the time of their initial assessment.
  • People with high blood pressure that is not well controlled (specifically, a top reading above 160 or a bottom reading above 95).
  • People currently taking steroid tablets (above a certain dose) or other medications that suppress the immune system for an ongoing condition.

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: Prof Qi Zeng, Intra-IMMUSG Pte Ltd

Phone: +65 65869661

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
Intra-IMMUSG Pte Ltd
Registry
ClinicalTrials.gov
Start date
11 October 2025
Est. completion
7 February 2027

Where this trial is recruiting

🇸🇬 Singapore

Primary endpoints

Safety: Adverse Events according to CTCAE; Recommended Phase 2 Dose (PR2D); Efficacy: Best Corrected Visual Acuity (BCVA) measured by ETDRS letter score; Efficacy: Subfield Retinal Thickness (CST) measured by Optical Coherence Tomography (OCT)

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