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Preservative-Free Bimatoprost 0.01% Ophthalmic Gel for Glaucoma Therapy: A Phase III Randomized Controlled Trial.
Muñoz-Negrete, Francisco J; Topouzis, Fotis; Oddone, Francesco; Nisslé, Sylvie; Rokicki, Dariusz; Januleviciene, Ingrida; Harasymowycz, Paul; Stalmans, Ingeborg.
Afiliação
  • Muñoz-Negrete FJ; Department of Ophthalmology, Hospital Universitario Ramón y Cajal.
  • Topouzis F; Faculty of Medicine, University of Alcalá, IRYCIS, Madrid, Spain (Facultad de Medicina, Universidad de Alcalá, IRYCIS, Madrid, Spain).
  • Oddone F; Department of Ophthalmology, School of Medicine, Aristotle University of Thessaloniki, AHEPA Hospital, Thessaloniki, Greece.
  • Nisslé S; Clinical and Research Institute of Ophthalmology, IRCCS-Fondazione Bietti, Rome, Italy.
  • Rokicki D; Laboratoires Thea, Clermont-Ferrand, France.
  • Januleviciene I; Laboratoires Thea, Clermont-Ferrand, France.
  • Harasymowycz P; Department of Ophthalmology, Eye Clinic of Medical Academy of Lithuanian University of Health Sciences, Kaunas, Lithuania.
  • Stalmans I; Department of Ophthalmology, University of Montreal.
J Glaucoma ; 33(6): 422-430, 2024 Jun 01.
Article em En | MEDLINE | ID: mdl-38506750
ABSTRACT
PRCIS Noninferiority of efficacy was demonstrated for a preservative-free bimatoprost 0.01% compared with BAK-containing bimatoprost 0.01% following a 12-week treatment period in patients with open angle glaucoma or ocular hypertension. Improved tolerability, in particular conjunctival hyperemia, was also observed.

PURPOSE:

To evaluate the intraocular pressure (IOP)-lowering efficacy and safety of a preservative-free bimatoprost 0.01% ophthalmic gel (PFB 0.01% gel) compared with preserved bimatoprost 0.01% (PB 0.01%).

DESIGN:

Phase III, international, multicenter, randomized, 2-parallel group, investigator-masked, 3-month treatment duration.

METHODS:

Patients with glaucoma or ocular hypertension were randomized after a 7-week run-in/washout period to receive once-daily PFB 0.01% gel (n=236) or PB 0.01% (n=249) for 3 months. The primary efficacy measure was changed from baseline in IOP at week 12. Safety measures included adverse events (AEs) and assessment of conjunctival hyperemia.

RESULTS:

The mean changes from baseline in IOP at week 12 in the PFB 0.01% gel and PB 0.01% were -9.72±2.97 and -9.47±3.06 mm Hg, respectively, at 8 am , -9.41±3.03 and -9.19±3.12 mm Hg at 10 am , and -8.99±3.36 and -8.54±3.44 mm Hg at 4 pm . Noninferiority of PFB 0.01% gel to PB 0.01% was demonstrated at week 12 based on predetermined criteria (upper 95% CI margin of 1.5 mmHg at all time points). The most frequently reported AE was conjunctival hyperemia; 13 (5.5%) patients with PFB 0.01% gel and 17 (6.8%) patients with PB 0.01%. The percentage of patients experiencing a worsening from baseline in conjunctival hyperemia score was lower with PFB 0.01% gel compared to PB 0.01% at week 6 (20.1% vs. 29.3%, respectively) and week 12 (18.3% vs. 30.4%, respectively).

CONCLUSIONS:

PFB 0.01% ophthalmic gel has the same efficacy in lowering IOP as PB 0.01% and demonstrated less aggravation of conjunctival hyperemia at weeks 6 and 12.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Soluções Oftálmicas / Conservantes Farmacêuticos / Tonometria Ocular / Glaucoma de Ângulo Aberto / Hipertensão Ocular / Bimatoprost / Géis / Pressão Intraocular / Anti-Hipertensivos Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Soluções Oftálmicas / Conservantes Farmacêuticos / Tonometria Ocular / Glaucoma de Ângulo Aberto / Hipertensão Ocular / Bimatoprost / Géis / Pressão Intraocular / Anti-Hipertensivos Idioma: En Ano de publicação: 2024 Tipo de documento: Article