WHO ICTRP trial

To study the safety,tolerability and effect of Pilocarpine Hydrochloride…

CTRI/2025/07/090630 · Clinical Trials Registry India (CTRI) · Not Recruiting

Key facts

Trial ID CTRI/2025/07/090630
Public title To study the safety,tolerability and effect of Pilocarpine Hydrochloride Ophthalmic Solution USP 1.25 percentage w/v for the treatment in Participants with Presbyopia.
Scientific title A Multicenter, Open Label, Single-Arm, Phase IV Clinical Study to Evaluate the Safety, Tolerability and Efficacy of Pilocarpine Hydrochloride Ophthalmic Solution USP 1.25 percentage w/v for the treatment in Participants with Presbyopia. - NIL
Primary sponsor Entod Pharmaceuticals Ltd.
Registry Clinical Trials Registry India (CTRI)
Recruitment status Not Recruiting
Study type Interventional
Phase Phase 4
Countries India
Conditions Health Condition 1: H524- Presbyopia
Interventions Intervention1: Pilocarpine Hydrochloride Ophthalmic solution USP 1.25 % w/v: One drop of Pilocarpine Hydrochloride Ophthalmic solution USP 1.25 % w/v once daily in each eye (preferably in morning) for 120 days of treatment duration. Control…
Registration date Oct 7, 2025
Target size 206
Secondary IDs BCR-EPL-003, Version 2.0, 1st amendment, dated 24 Apr 2025
Registry page ctri.nic.in

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Source: World Health Organization (WHO), International Clinical Trials Registry Platform (ICTRP) · Source date:

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