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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT05022004
Other study ID # BRIN-20-01
Secondary ID
Status Completed
Phase Phase 3
First received
Last updated
Start date December 20, 2021
Est. completion date January 6, 2023

Study information

Verified date December 2023
Source Sun Pharmaceutical Industries Limited
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

This is a randomized, Investigator-masked, multi-center, parallel group, therapeutic equivalence study with clinical endpoint.


Recruitment information / eligibility

Status Completed
Enrollment 599
Est. completion date January 6, 2023
Est. primary completion date December 29, 2022
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria: - Male or nonpregnant female aged 18 years or older with chronic open angle glaucoma or ocular hypertension in both eyes. - Provide signed and dated informed consent in accordance with good clinical practice and local legislation prior to any study procedure. - Be able and willing to follow study instructions and complete all required visits. - Subject requires treatment of both eyes and is able to discontinue use of all ocular hypotensive medication(s) or switch ocular hypotensive medications and undergo appropriate washout period. Exclusion Criteria: - Subjects with angle closure glaucoma - Females who are pregnant, breast feeding, or planning a pregnancy. - Females of childbearing potential who do not agree to utilize an adequate form of contraception. - Current, or past history of, severe hepatic or renal impairment - Current, or history within 2 months prior to baseline of, significant ocular disease - Functionally significant visual field loss - Contraindication to brinzolamide or sulfonamide therapy or known hypersensitivity to any component of brinzolamide or sulfonamide therapy - Subjects currently in another clinical trial

Study Design


Intervention

Drug:
Brinzolamide ophthalmic suspension
dose: one drop of study medication; frequency: three times a day; route of administration: Topical ocular administration; duration of therapy: 6 weeks
Azopt®
dose: one drop of study medication; frequency: three times a day; route of administration: Topical ocular administration; duration of therapy: 6 weeks

Locations

Country Name City State
India Rising Retina Clinic Ahmedabad Gujarat
India Bhagwan Mahaveer Jain Hospital Bangalore Karnataka
India Dr. BR Ambedkar Medical College and hospital Bangalore Karnataka
India KLE's Dr. Prabhakar Kore Hospital & Medical Research Center Belgaum Karnataka
India Sankara Nethralaya Chennai Tamil Nadu
India Shanti Saroj Netralay Miraj Maharashtra
India Omkar Eye Care Center Mumbai Maharashtra
India K R Hospital, Mysore Medical College and Research Institute Mysuru Karnataka
India GMC, Srikakulam Srikakulam Andhra Pradesh
India Bhavna Super speciality Eye care Surat Gujarat
India Dr Agarwal's Eye Hospital Tirunelveli Tamil Nadu
India Heritage Institute of Medical Sciences Varanasi Uttar Pradesh
India Dr. RSPR Govt Regional Eye Hospital; Vishakapatnam Visakhapatnam Andhra Pradesh
India Acharya Vinoba Bhave Rural Hospital, Jawaharlal Nehru Medical College, Datta Meghe Institute of Medical Sciences Wardha Maharashtra
Russian Federation Federal State Autonomous Institution "Interdistrict Scientific and Technical Complex "Eye Microsurgery" named after Academician S.N. Fedorov" of the Ministry of Healthcare of the Russian Federation Cheboksary
Russian Federation Healthcare Organization "Eye Center", Limited Liability Company Chelyabinsk
Russian Federation Federal State Autonomous Institution "Interdistrict Scientific and Technical Complex "Eye Microsurgery" named after Academician S.N. Fedorov" of the Ministry of Healthcare of the Russian Federation Irkutsk
Russian Federation Ivanovo Regional Clinical Hospital Ivanovo
Russian Federation "Eye Microsurgery" n a Academician S.N. Fedorov" Kaluga
Russian Federation Republican clinical ophthalmological hospital of Ministry of Health of Republic of Tatarstan named after E.V. Adamyuk Kazan Republic Of Tatarstan
Russian Federation Federal State Autonomous Institution "Interdistrict Scientific and Technical Complex "Eye Microsurgery" named after Academician S.N. Fedorov" of the Ministry of Healthcare of the Russian Federation Khabarovsk
Russian Federation "Angris", Limited Liability Company Moscow
Russian Federation "Moscow Regional Clinical Research Institute named after M.F. Vladimirsky" Moscow
Russian Federation Federal State Autonomous Institution "Interdistrict Scientific and Technical Complex "Eye Microsurgery" named after Academician S.N. Fedorov" of the Ministry of Healthcare of the Russian Federation Moscow
Russian Federation Federal State Budgetary Educational Institution of Higher Education "Moscow State University of Medicine and Dentistry named after A.I. Evdokimov" of the Ministry of Healthcare of the Russian Federation Moscow
Russian Federation Moscow Medical university n.a. Sechenov Moscow
Russian Federation Federal budgetary healthcare institution Privolzhsky district medical center FMBA of Russia. Nizhny Novgorod
Russian Federation Federal Budgetary Healthcare Institution "Volga Region Medical Centre" of the Federal Medical and Biological Agency Novgorod
Russian Federation Federal State Autonomous Institution "Interdistrict Scientific and Technical Complex "Eye Microsurgery" named after Academician S.N. Fedorov" of the Ministry of Healthcare of the Russian Federation Novosibirsk
Russian Federation Budgetary Healthcare Institution of the Omsk Region "Clinical Eye Hospital named after V.P. Vykhodtsev Omsk
Russian Federation Institute of Human Brain of the Russian Academy of Science, 197376, Academ. Pavlov street 12 AP, StPetersburg, Russia Saint Petersberg Saint Petersburg
Russian Federation "X7 Clinical Research", Limited Liability Company Saint Petersburg
Russian Federation Federal State Autonomous Institution "Interdistrict Scientific and Technical Complex "Eye Microsurgery" named after Academician S.N. Fedorov" of the Ministry of Healthcare of the Russian Federation Saint Petersburg
Russian Federation Feral State Budgetary Healthcare Institution "Clinical Hospital No. 122 named after L.G. Sokolov of the Federal Medical and Biological Agency" Saint Petersburg
Russian Federation Samara medical university Samara
Russian Federation Nongovernmental Healthcare Institution "Clinical Hospital "RZhD [Russian Railways]- Saratov
Russian Federation State Budgetary Institution "Ufa Research Institute of Eye Diseases of the Academy of Sciences of the Republic of Bashkortostan Ufa
Russian Federation ZAO "Optimedservice" Ufa
Russian Federation Ulyanovsk ophthalmology clinical "Prozrenie" Ulyanovsk
Russian Federation Federal State Autonomous Institution "Interdistrict Scientific and Technical Complex "Eye Microsurgery" named after Academician S.N. Fedorov" of the Ministry of Healthcare of the Russian Federation Volgograd

Sponsors (1)

Lead Sponsor Collaborator
Sun Pharmaceutical Industries Limited

Countries where clinical trial is conducted

India,  Russian Federation, 

Outcome

Type Measure Description Time frame Safety issue
Primary Mean Difference in Intraocular Pressure of Both Eyes Between the Two Treatment Groups The recommended primary endpoint is the mean difference in Intraocular Pressure of both eyes between the two treatment groups at pre-specified time points. Baseline, Week 2 & Week 6
Secondary Change From Baseline in IOP of Both Eyes Between the 2 Treatment Groups. approximately 8:00 AM. (hour 0; before the morning drop) and 10:00 AM. (hour 2) at the Day 14 (Week 2) and Day 42 (Week 6) visits
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