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BioWorld - Tuesday, July 21, 2026
Home » Topics » Disease categories and therapies » Ocular

Ocular
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Nasdaq building

Australia’s Opthea lists on Nasdaq in $128M IPO, gears up for phase III wet AMD trials

Oct. 28, 2020
By Tamra Sami
PERTH, Australia – Opthea Ltd. completed a $128.2 million IPO on the U.S. Nasdaq market, which will fund two phase III trials in wet age-related macular degeneration (AMD) and bring the company’s lead candidate, OPT-302, to market if successful.
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FDA approves Eysuvis for short-term treatment of dry eye disease

Oct. 28, 2020
Close-up of eye

Azura Ophthalmics raises $20M series C for registration study in Meibomian gland dysfunction

Oct. 27, 2020
By Tamra Sami
PERTH, Australia – Azura Ophthalmics Ltd. raised a $20 million series C round with existing investors, including Brandon Capital’s Medical Research Commercialization Fund (MRCF), Orbimed, TPG Biotech and Ganot Capital.
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FDA clears Kala DED therapy; stock sinks as payer, pandemic concerns aired

Oct. 27, 2020
By Randy Osborne
Kala Pharmaceuticals Inc.’s anticipated win with Eysuvis (loteprednol etabonate ophthalmic suspension) 0.25% for the short-term (up to two weeks) treatment of the signs and symptoms of dry eye disease (DED) didn’t help shares (NASDAQ:KALA), which closed Oct. 27 at $6.28, down $1.44, or 18.7%, on word of the FDA approval.
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FDA approves IND for phase II study of VSJ-110 for allergic conjunctivitis

Oct. 27, 2020
Close-up of eye

Azura Ophthalmics raises $20M series C for registration study in Meibomian gland dysfunction

Oct. 23, 2020
By Tamra Sami
PERTH, Australia – Azura Ophthalmics Ltd. raised a $20 million series C round with existing investors, including Brandon Capital’s Medical Research Commercialization Fund (MRCF), Orbimed, TPG Biotech and Ganot Capital.
Read More
Face with digital focus on eye

Gene therapy approaches tackle multiple forms of blindness

Oct. 22, 2020
By Anette Breindl
New gene therapy approaches may be able to treat forms of vision loss that currently have no treatment options, and improve the treatment of others.
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Gene therapy approaches tackle multiple forms of blindness

Oct. 22, 2020

Apellis reports 18-month data on pegcetacoplan in advanced geographic atrophy

Oct. 21, 2020
Rays of light beaming from eye

Sparingvision adds $52.5M for gene therapy trial, expansion to U.S.

Oct. 20, 2020
By Nuala Moran
LONDON – Sparingvision SAS has raised €44.5 million (US$52.5 million) to advance SPVNo6, a gene therapy designed to be effective for all retinitis pigmentosa patients regardless of the underlying mutation, with a phase I dose-ranging study now due to start in 2021.
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