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Macular Degeneration clinical trials in Virginia

7 studies for Macular Degeneration are looking for participants at sites in Virginia.

Cities in Virginia

A Clinical Trial of EYE201/MK-8748 in People With Macular Degeneration (MK-8748-002)

  • Piedmont Eye Center (Site 054), Lynchburg
RecruitingPhase 2/3
Ages 50 and older · All sexes · Updated Oct 2, 2026 · NCT07440225

A Long-term Extension Study of JNJ-81201887 (AAVCAGsCD59) Parent Studies in Participants With Geographic Atrophy (GA) Secondary to Age-related Macular Degeneration (AMD)

  • Piedmont Eye Center, Lynchburg
  • Wagner Kapoor Research institute, Norfolk
RecruitingPhase 2/3
Ages 60 and older · All sexes · Updated Sep 30, 2026 · NCT06635148

A Study Investigating Subcutaneously Administered Pozelimab in Combination With Cemdisiran or Cemdisiran Alone in Adult Participants With Geographic Atrophy

  • Southeastern Retina Associates, Bristol
  • Retina Group of Washington, Fairfax
  • Piedmont Eye Center, Lynchburg
  • and 1 more
RecruitingPhase 3
Ages 50 to 85 · All sexes · Updated Sep 18, 2026 · NCT06541704

Study to Evaluate Efficacy and Safety of ONL1204 in Patients With GA Associated With AMD

  • Piedmont Eye Center, Lynchburg
RecruitingPhase 2
Ages 55 and older · All sexes · Updated Sep 10, 2026 · NCT06659445

A Long-term Follow-up Study to Evaluate SKG0106 in the Treatment of Patients With nAMD

  • Wagner Macula & Retina Center, Norfolk
RecruitingObservational study
Ages 50 and older · All sexes · Updated Sep 1, 2026 · NCT06346600

A Clinical Trial of EYE201/MK-8748 in People With Macular Degeneration (MK-8748-003)

  • Vistar Eye Center (Site 129), Roanoke
RecruitingPhase 2/3
Ages 50 and older · All sexes · Updated Aug 6, 2026 · NCT07496567

Single Intravitreal (IVT) Injection of 4D-150 in Patients With Macular Neovascularization Secondary to Age-Related Macular Degeneration

  • Piedmont Eye Center, Lynchburg
RecruitingPhase 3
Ages 50 and older · All sexes · Updated Apr 16, 2026 · NCT07064759

From ClinicalTrials.gov, data retrieved Oct 5, 2026. Each study sets its own eligibility; the study team decides who can join.