Phase 2RecruitingAge-related condition

Efficacy and Safety of BRIMOCHOL PF and CARBACHOL PF in Chinese Presbyopia Patients

A Multicenter, Randomized, Double-Blind, Crossover, Placebo-Controlled Phase II Clinical Study to Evaluate the Efficacy and Safety of BRIMOCHOL PF, CARBACHOL PF in Chinese Patients With Presbyopia

Sponsor
Zhaoke (Guangzhou) Ophthalmology Pharmaceutical Ltd. (Industry)
Enrollment
119 planned
Conditions
Presbyopia
Interventions
BRIMOCHOL PF eye drops; CARBACHOL PF eye drops; Brimonidine eye drops; Placebo
Ages
adults, older adults
Registry
NCT06948357

Full record on ClinicalTrials.gov

From the registry

A multicenter, randomized, double-Blind, crossover, placebo-controlled Phase II clinical Study to evaluate the efficacy and safety of BRIMOCHOL PF and CARBACHOL PF in the treatment of Chinese patients with presbyopia.

Primary outcomes

  • Changes in MCNVA(monocular corrected near visual acuity) ETDRS letters and MCDVA (monocular corrected distance visual acuity) ETDRS letters from baseline in the study eyes after administration

History

  1. Study completion

  2. Primary completion

  3. Registered

  4. Started