Non-inferiority of PRO-122 Ophthalmic Solution vs KRYTANTEK Ofteno® in Glaucoma or Ocular Hypertension (CONFORTK)

Ocular Hypertension Clinical Trial

— CONFORTK  

Official title:

Clinical Study to Evaluate the Non-inferiority of PRO-122 an Ophthlamic Solution Manufactured by Laboratorios Sophia, Previous Treatment With Krytantek Ofteno ®, in Subjects With Primary Open-Angle Glaucoma or Ocular Hypertension.

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03257813
• Other study ID #: SOPH122-0914/III
• Status: Completed
• Phase: Phase 3
• Start date: April 1, 2016
• Est. completion date: June 18, 2017

Study information

• Verified date: November 2019
• Source: Laboratorios Sophia S.A de C.V.
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Aim: To demonstrate the non-inferiority of the PRO-122 ophthalmic solution manufactured by Laboratorios Sophia S.A. de C.V. versus Krytantek Ofteno® ophthalmic solution like hypotensive therapy in subjects with primary open angle glaucoma or ocular hypertension.

Study design: a multicentric, prospective, crossover (2x2), double blind clinical study. Sample size: one hundred patients with primary open angle glaucoma or ocular hypertension. Patients in the period 1: In the first sequence 30 patients will be assigned to receive the ophthalmic solution: Krytantek Ofteno ® (timolol 0.5%%/brimonidine 0.2%/dorzolamide 2%) 1 drop B.I.D. during 30 days and the second sequence 30 patients will be assigned to receive the ophthalmic solution: PRO-122 1 drop B.I.D. during 30 days in the same period. Washout period: 20 hours. Patients in the period 2: the pharmacological intervention change to the opposite therapy for 30 days

Description:

The American Academy of Ophthalmology Glaucoma Panel: The primary open angle glaucoma (POAG) is a progressive, chronic optic neuropathy in adults in which intraocular pressure (IOP) and other currently unknown factors contribute to damage and in which, in the absence of other identifiable causes, there is a characteristic acquired atrophy of the optic nerve and loss of retinal ganglion cells and their axons. This condition is associated with an anterior chamber angle that is open by gonioscopic appearance.

This is a multicentric, crossover, double blind and prospective clinical study. The investigators will include patients with confirmed diagnosis of primary open-angle glaucoma or ocular hypertension, with target intraocular pressure (TIOP) within a range at which a patient is likely to remain stable or at which worsening of glaucoma will be slow enough that the risk of additional intervention is not justified.

Patients will be randomly divided into 2 groups, one of them treated with a known formulation of timolol 0.5%/brimonidine 0.2%/dorzolamide 2% (Krytantek Ofteno®, Laboratorios Sophia, Mexico) and the other one treated with PRO-122 ophthalmic solution. Patients will receive 1 drop B.I.D. into the lower conjunctival sac of either formulations and were examined at days: 1, 15, 30, 45 and 61 after initiation of treatment. A phone call security at day 75 will be performed.

Primary efficacy outcome: To evaluate the efficacy of PRO-122 versus Krytantek Ofteno® instilled onto the ocular surface in subjects with primary open angle glaucoma (POAG) or ocular hypertension (HTO), to control and maintenance of the target intraocular pressure (TIOP).

Recruitment information / eligibility

• Status: Completed
• Enrollment: 60
• Est. completion date: June 18, 2017
• Est. primary completion date: March 1, 2017
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• 18 years of age or older

• male or female.

• obtained in the external consultation.

• With diagnosis primary of open-angle glaucoma and / or hypertension classified as mild, moderate or severe glaucomatous damage, users of Krytantek Ofteno® at least two months prior to inclusion and under control of the target IOP.

• informed consent.

Exclusion Criteria:

General Criteria

1. Subjects with topical or systemic medication that interferes decisively in the results of the study. (Such as topical immunomodulators, lacrimal point tamponade, corticosteroids, ocular hypotensives other than those listed above, artificial tears with preservative).

2. Subjects (female) with an active sex life who are not using a contraceptive method.

3. Female Subjects in pregnancy or breastfeeding.

4. Female subjects with positive urine pregnancy test.

5. Positive drug addiction (verbal interrogation).

6. Subjects who have participated in any clinical research study in the last 40 days.

7. Legally or mentally disabled subjects to give informed consent for their participation in this study.

8. Subjects who can not comply with the appointments or with all the requirements of the protocol.

Ophthalmologic criteria

1. Subject with only one eye with vision.

2. Subjects with visual capacity 20/200 or worse.

3. Subjects with a narrow-angle history without treatment, with or without total or partial closure of the angle in either eye.

4. Subjects with corneal abnormalities that prevent applanation tonometry.

5. Subjects with ocular surgery or ocular trauma 6 months prior to inclusion.

6. Any ocular laser surgery 3 months prior.

7. Any uncontrolled or progressive retinal disease.

8. Inflammatory diseases of any kind.

9. Contact lens wearers.

10. Subjects with a history of hypersensitivity to any of the ingredients of the research product or its analogues.

Related Conditions & MeSH terms

• Glaucoma
• Glaucoma, Open-Angle
• Hypertension
• Ocular Hypertension
• Primary Open Angle Glaucoma

Intervention

Drug:
• PRO-122
1 drop every 12 hours for 30 days of alternating treatment with 30 days
• Krytantek Ofteno®
1 drop every 12 hours for 30 days of alternating treatment with 30 days

Locations

Country	Name	City	State
n/a

Sponsors (1)

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

Outcome

Type	Measure	Description	Time frame	Safety issue
Other	Adverse Events	The presence of adverse events by percentage between groups will be evaluated. the scale is present or absent.	75 days, includes the security call
Other	Conjunctival Hyperemia	the conjunctival hyperemia will be evaluated by the presence or absence of it and the percentage of affected by group will be reported.	Baseline (day 1) crossover visit (day 30) and final visit (day 60)
Other	Chemosis	Chemosis: qualitative ordinal variable, will be evaluated by the presence or absence of it and the percentage of affected by group will be reported.	Baseline (day 1) crossover visit (day 30) and final visit (day 60)
Other	Eye Burning	Eye ocular burning will be evaluated by the presence or absence of it and the number of affected by group will be reported.	Baseline (day 1) crossover visit (day 30) and final visit (day 60)
Other	Number of Eyes With Tearing	Tearing will be evaluated by the presence or absence of it and the number of affected by group will be reported	Baseline (day 1) crossover visit (day 30) and final visit (day 60)
Other	Number of Eyes With Foreign Body Sensation	Foreign body sensation will be evaluated by the presence or absence of it and the number of affected by group will be reported.	Baseline (day 1) crossover visit (day 30) and final visit (day 60)
Primary	Intraocular Pressure (IOP)	Intraocular pressure, Unit: Millimeters of mercury (mmHg) type of variable: Continuous, Measurement method: Goldman applanation tonometry. Normal intraocular pressure 11-21 mmHg.; The change between the IOP of both groups was compared (sequence 1 versus sequence 2) of the data obtained at the end of each period (day 30 and day 60).	Change from Baseline intraocular pressure at day 30 and 60.
Secondary	Visual Acuity (VA)	The VA will be evaluated basally, without refractive correction with the Snellen chart. A Snellen chart is placed at a standard distance: 20 ft. At this distance, the symbols on the line representing "normal" acuity subtend. This line, designated 20/20 is the smallest line that a person with normal acuity can read at a distance of 20fs. the scale consists of 11 lines of letters of different size, the size of the letter gives a fractional value according to the visual acuity of the patient, the value is inversely proportional to the visual acuity, if the denominator is greater the visual acuity will be less.; Line 1: 20/200 Line 2: 20/100, Line 3: 20/70, line 4: 20/50, line 5: 20/40, Line 6: 20/30, line 7: 20/25, Line 8: 20/20, line 9: 20/15, line 10: 20/13, line 11: 20/10. the differences between groups in the basal, cross over and final visit will be evaluated.	Visual Acuity at Baseline (day 1) crossover visit (day 30) and final visit (day 60)