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NOT YET RECRUITING
NCT07607561
PHASE2

Phase 2a Study to Evaluate the Efficacy and Safety of SCAI-005 Ophthalmic Solution in Subjects With Neovascular Age-related Macular Degeneration

Sponsor: SCAI Therapeutics

View on ClinicalTrials.gov

Summary

Trial to Evaluate the Safety and Efficacy of SCAI-005 Ophthalmic solution in Patients with Neovascular Age-related Macular Degeneration. The purpose of this study is to investigate the efficacy, safety and tolerability of SCAI-005 Ophthalmic solution by dose in patients with neovascular Age-related Macular Degeneration (nAMD).

Official title: A Randomization, Double-blind, Placebo-controlled, Parallel, Multicenter, Phase 2a Study to Evaluate the Efficacy and Safety of SCAI-005 Ophthalmic Solution in Subjects With Neovascular Age-related Macular Degeneration

Key Details

Gender

All

Age Range

50 Years - Any

Study Type

INTERVENTIONAL

Enrollment

50

Start Date

2026-11-01

Completion Date

2027-08-31

Last Updated

2026-05-26

Healthy Volunteers

No

Interventions

DRUG

SCAI-005 0.04% 2drops TID

Axitinib 0.084mg/day

DRUG

SCAI-005 0.08% 2drops TID

Axinitib 0.168mg/day

DRUG

Placebo 2drops TID

vehicle