Clinical Trials Directory

Trials / Completed

CompletedNCT01535443

Safety and Tolerability of PRO-155 Ophthalmic Solution 0.09% in Healthy Volunteers.

Fase 1 Study to Evaluate the Safety and Tolerability of PRO-155 Ophthalmic Solution 0.09% in Healthy Volunteers.

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
35 (actual)
Sponsor
Laboratorios Sophia S.A de C.V. · Industry
Sex
All
Age
18 Years
Healthy volunteers
Accepted

Summary

Study to evaluate the safety and tolerability of PRO-155 Ophthalmic Solution 0.09 % in healthy volunteers.

Detailed description

A phase I, open label and unicentric clinical trial to evaluate the safety and tolerability of PRO-155 Ophthalmic Solution 0.09 % in healthy volunteers.

Conditions

Interventions

TypeNameDescription
DRUGBromfenacDrug: Bromfenac Other names: PRO-155

Timeline

Start date
2011-09-01
Primary completion
2011-10-01
Completion
2011-10-01
First posted
2012-02-17
Last updated
2019-10-16
Results posted
2019-07-19

Locations

1 site across 1 country: Mexico

Source: ClinicalTrials.gov record NCT01535443. Inclusion in this directory is not an endorsement.