Efficacy and Safety of PRO-118 Ophthalmic Solution in Allergic Conjunctivitis

Conjunctivitis, Allergic Clinical Trial

— PRO-118  

Official title:

STUDY TO EVALUATE THE EFFICACY AND SAFETY OF PRO-118 OPHTHALMIC SOLUTION IN ALLERGIC CONJUNCTIVITIS

Clinical Trial Details — Status: Withdrawn

Administrative data

• NCT number: NCT01541904
• Other study ID #: LVO1209FII
• Secondary ID: PRO-118
• Status: Withdrawn
• Phase: Phase 2
• Start date: March 2011
• Est. completion date: February 2012

Study information

• Verified date: October 2018
• Source: Laboratorios Sophia S.A de C.V.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

The purpose of this study is to evaluate the efficacy and safety of four doses of PRO-118 ophthalmic solution ophthalmic solution compared with placebo, for the treatment of seasonal (SAC) and perennial (PAC) allergic conjunctivitis.

Description:

A phase II, double-masked, randomized, placebo-controlled, parallel-group and multicenter clinical trial, to evaluate and compared the clinical efficacy and safety of four doses of PRO-118 ophthalmic solution ( PRO-118 0.015% qd, PRO-118 0.015% twice daily , PRO-118 0.020% qd, PRO-118 0.020% twice daily) for the treatment of seasonal (SAC) and perennial (PAC) allergic conjunctivitis.

Recruitment information / eligibility

• Status: Withdrawn
• Enrollment: 0
• Est. completion date: February 2012
• Est. primary completion date: February 2012
• Accepts healthy volunteers: No
• Gender: All
• Age group: 6 Years and older

Eligibility

Inclusion Criteria:

• Patients with diagnosis of seasonal or perennial allergic conjunctivitis.

• Age = 6 years old at screening visit.

• Male or female patients.

Applicable in patients = 18 years old.

• Patient has signed the Informed Consent Form (ICF) prior to any screening procedures.

Applicable in patients with age = 18 years old.

• Patients Patients'parents or legal guardians signed an Informed Consent Form (ICF).

• The patients also provided written assent.

Exclusion Criteria:

• Presence of any form of allergic conjunctivitis other than seasonal or perennial allergic conjunctivitis (Atopic keratoconjunctivitis, giant papillary conjunctivitis).

• Any other ophthalmic medication within seven days prior to randomization.

• Patient with one blind eye.

• Visual acuity of 20/40 in any eye.

• Patients with history of active stage of any other concomitant ocular disease.

• Contraindications or sensitivity to any component of the study treatments.

• Contact lens users.

• Ocular surgery within the past 3 months.

• Women who were not using an effective means of contraception or who were pregnant or nursing.

• Participation in any studies of investigational drugs within 90 days previous to the inclusion.

Discontinuation criteria:

• Patients could be discontinued before the completion of the study because of use of prohibited medications, adverse events, pregnancy, protocol violations, lack of efficacy, or administrative reasons.

Related Conditions & MeSH terms

• Conjunctivitis
• Conjunctivitis, Allergic
• Ocular Allergy
• Ocular Itching
• Perennial Allergic Conjunctivitis
• Seasonal Allergic Conjunctivitis

Intervention

Drug:
• PRO-118 Ophthalmic Solution 0.015%
PRO-118 Ophthalmic Solution 0.015 % applied qd during 21 days
• PRO-118 Ophthalmic Solution 0.015 %
PRO-118 Ophthalmic Solution 0.015 % applied twice to day during 21 days
• PRO-118 Ophthalmic Solution 0.020 %
PRO-118 Ophthalmic Solution 0.020 % applied qd during 21 days
• PRO-118 Ophthalmic Solution 0.020 %
PRO-118 Ophthalmic Solution 0.020 % applied twice to day during 21 days
• Placebo Ophthalmic Solution
Placebo Ophthalmic Solution applied qd during 21 days

Locations

Country	Name	City	State
Mexico	Antiguo Hospital Civil de Guadalajara "Fray Antonio Alcalde"	Guadalajara	Jalisco
Mexico	"Instituto de Oftalmología Fundación Conde de Valenciana, I.A.P	Mexico City

Sponsors (1)

Lead Sponsor	Collaborator
Laboratorios Sophia S.A de C.V.

Country where clinical trial is conducted

Mexico, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Efficacy of PRO-118 ophthalmic solution.	Primary efficacy measure: Evaluation of ocular itching.; Secondary efficacy measures: Evaluation of symptoms(redness eye,ocular irritation, foreign body sensation, photophobia and lacrimation) and signs(conjunctival hyperaemia,chemosis, mucous discharge ocular and presence of follicles/papillae).	21 days.
Secondary	Safety of PRO-118 Ophthalmic Solution.	Evaluation of ocular symptoms and signs, visual acuity (VA), biomicroscopy, intraocular pressure (IOP), funduscopy and cup disc-ratio.; Frequency, severity and relationship to study medication of all adverse events occurring during the course of the study.	21 days.