Catch up on what happened in optometry during the week of June 3-June 7.
Catch up with what Optometry Times shared this week:
By Martin David Harp, Associate Editor, Ophthalmology Times
Bausch + Lomb Corporation has announced the official US launch of its Blink NutriTears, a nutritional supplement for the treatment of dry eyes.
According to the company, Blink NutriTears “target the key root causes of dry eyes, promote healthy tear production and provide noticeable relief of dry eye symptoms in as little as 2 to 4 weeks.”
By David Hutton, Managing Editor, Ophthalmology Times
Harrow announced results from its ESSENCE 2 open-label extension (OLE) clinical study for cyclosporine ophthalmic solution (Vevye) 0.1% to treat the signs and symptoms of dry eye disease (DED).
According to a news release, ESSENCE-2 OLE was a Phase 3, prospective, multicenter, open-label, clinical study with 202 patients, who had previously completed the ESSENCE 2 study, receiving cyclosporine ophthalmic solution in each eye twice a day for 52 weeks.
By Jordana Joy, Associate Editor
Nordic Group BV’s subsidiary Nordic Pharma announced the commercial launching of its Lacrifill canalicular gel, a novel therapy for dry eye disease (DED) in the US.1 The gel is a cross-linked hyaluronic acid derivative and has been cleared by the FDA to temporarily block tear drainage by the occlusion of the canalicular system, according to a news release.
By Jordana Joy, Associate Editor
Quantel Medical, a division of Lumibird Medical, has announced the launch of its new POCKET III handheld pachymeter. According to a news release, the pachymeter is the lightest handheld product on the market, weighing in at 60 grams.1
"In addition to the importance of being able to calculate corneal thickness in pre-refractive surgery, pachymetry is essential to calculate and correlate with intraocular pressure. In fact, 80 million* people suffer from glaucoma,” said François Checinski, Ultrasound product manager, in the release.
By Jordana Joy, Associate Editor
Clinical-stage biopharmaceutical company Azura Ophthalmics announced that the first patient has been enrolled in the company’s Phase 3 clinical trial for its Assessment of Secretions and Treatment for Restoring Ocular Surface Health in Patients with Meibomian Gland Dysfunction (ASTRO) study.1 The trial is aiming to evaluate the efficacy, safety, and tolerability of sterile ophthalmic ointment (AZR-MD-001) 0.5% compared to vehicle in patients with abnormal meibomian gland function (MGD) and associated symptoms of dry eye disease (DED), according to a news release.