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RecruitingGeographic Atrophy Secondary to Age-related Macular Degeneration

An Optimised GA Interventional Trial (Opti-GAIN) to Test if Treatment With CTx001 is Safe and Works for People With Geographic Atrophy (GA)

Eligible age

55+ yrs

Accepts

All genders

Locations

4 states

Healthy volunteers

No

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About this study

This is a clinical study to evaluate the safety, tolerability and efficacy of CTx001, administered via a single subretinal injection, for GA (secondary to AMD). Safety and efficacy will be measured at regular intervals for 2 years after which long-term safety will be assessed annually for up to 5 years.

Sponsor: Complement Therapeutics

You may qualify if…

  • Meet protocol-defined age eligibility
  • Have bilateral geographic atrophy secondary to AMD, confirmed by the Reading Center
  • Meet baseline lesion size requirements, as assessed by fundus autofluorescence imaging
  • Meet best-corrected visual acuity and low-luminance visual acuity criteria, as measured by ETDRS charts
  • Meet retinal sensitivity criteria, as measured by microperimetry
  • Have sufficient fellow-eye visual function to ensure navigational vision
  • Have adequate historical SD-OCT imaging available for longitudinal assessment
  • Meet reproductive status and contraception requirements, where applicable

You may not qualify if…

  • Macular atrophy or retinal disease not attributable to AMD
  • Evidence of current or prior choroidal neovascularization (wet AMD)
  • Prior intraocular, macular, or retinal surgery or laser treatment that may confound assessments
  • Prior AMD-directed or intravitreal therapy in the study eye, except permitted supplements
  • Prior exposure to complement inhibitor therapies
  • Ocular conditions, infections, inflammation, or media opacities that interfere with safety or retinal imaging
  • Uncontrolled glaucoma, diabetic retinopathy, or clinically significant refractive error
  • Aphakia or compromised posterior capsule, except as permitted by protocol

Where it's recruiting

Indiana

Carmel

Nevada

Reno

Texas

Dallas

Wisconsin

La Crosse

Source: ClinicalTrials.gov · NCT07392255 · last updated 2026-06-22