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NCT03595865

Efficacy of Tafluprost as an Adjunct to Medical Therapy for Residual Glaucoma After Trabeculectomy

Status unknown NA Last updated 23 July 2018
What this trial tests

NA trial testing tafluprostin in Glaucoma; Drugs in 60 participants. Status unknown.

Timeline
1 August 2018
Primary endpoint
1 October 2019
1 June 2020

Quick facts

Lead sponsorwangdabo
PhaseNA
StatusStatus unknown
Study typeINTERVENTIONAL
Allocationnon randomized
Designparallel
Maskingnone
Primary purposetreatment
Enrollment60
Start date1 August 2018
Primary completion1 October 2019
Estimated completion1 June 2020

Drugs / interventions tested

Conditions studied

Sponsor

wangdabo — full company profile →

Who can join

Adults 18 to 75, any sex, with Glaucoma; Drugs. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

A 6-month, parallel-group study of the safety and efficacy of tafluprostin for Chinese patients with posttrabeculectomy residual primary angle-closure glaucoma or posttrabeculectomy residual primary open angle glaucoma.

Publications & conference data

No peer-reviewed publications indexed yet for this trial.

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Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT03595865.

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