Macular Degeneration Trial, Recruiting NCT07005323 Sponsor: PharmaBio Corporation Condition: Macular Degeneration
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Macular Degeneration Trial, Recruiting

NCT07005323
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:

  • You are between 50 and 85 years old at the time of signing up for the trial
  • You have been diagnosed with a type of age-related macular degeneration (AMD) that involves abnormal blood vessel growth, in one or both eyes
  • The vision in your study eye (the eye being treated) is quite poor but not completely lost — within a specific range of reduced vision (confirm with trial site for exact details)
  • You meet at least one of the following eye conditions in your study eye: the central part of your retina (fovea) is affected by a tear or scarring in the back layer of the eye; or a specific area of damage has spread to the centre of your vision; or your eye has thinning of the tissue behind the retina with fluid that has not responded to standard treatment, but without certain signs of high-risk damage; or you have a specific type of fluid build-up and cell damage in the retina, again without certain high-risk signs (confirm details with trial site)
  • Your eye condition has not improved — or your vision has gotten worse — after two recent consecutive anti-VEGF injections (a common treatment for AMD) given 4 to 8 weeks apart

Who may not be able to join:

  • You have a specific type of raised tissue change (pigment epithelial detachment of a certain thickness) at the centre of your study eye (confirm with trial site)
  • You have hard deposits (hard exudates) in the layers of your study eye's retina
  • You currently have an eye infection in your study eye
  • You have a history of other retinal diseases, detached retina, a hole in the central part of your retina, inflammation inside the eye, or other eye diseases (other than AMD) in your study eye
  • You have damage to the optic nerve in your study eye
  • You have glaucoma in your study eye that is getting worse or is not well controlled
  • You have severe short-sightedness in your study eye, based on the size of your eye or your lens prescription
  • You have had surgery inside your study eye (cataract surgery may be acceptable if it went well, there were no complications, and it was more than 3 months ago — confirm with trial site)
  • The vision in your other (non-study) eye is very poor, below a certain level (confirm with trial site)
  • You are currently receiving or planning to receive anti-VEGF injections in your other (non-study) eye during the trial
  • You have abnormal results from screening tests that the trial team believes would affect your safe participation
  • You have tested positive for certain infections including Hepatitis B, Hepatitis C, HIV, HTLV-1, or syphilis
  • You have a known allergy to human serum albumin, antibiotics, or trypsin
  • You have serious conditions affecting your blood, heart, liver, or kidneys
  • You have been diagnosed with cancer within the last 5 years, or are currently receiving cancer treatment
  • You are pregnant, breastfeeding, or plan to become pregnant during the trial
  • You are taking blood-thinning or antiplatelet medications that you cannot stop before the trial
  • You have a history of drug addiction or alcoholism

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: Hitoshi Kusano, M.D., PhamaBio Coorporation

Phone: +81 44-589-6479

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
PharmaBio Corporation
Registry
ClinicalTrials.gov
Start date
12 September 2024
Est. completion
1 March 2027

Where this trial is recruiting

🇯🇵 Japan

Primary endpoints

Safety Evaluation: Incidence, type, and severity of Adverse Events (AE)

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