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BioWorld - Wednesday, January 21, 2026
Home » Topics » Disease categories and therapies » Ocular

Ocular
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Australian flag, coins, stock board

Opthea to raise AU$80M to continue phase III wet AMD trials for lead candidate OPT-302

Aug. 29, 2023
By Tamra Sami
Opthea Ltd. plans to raise AU$80 million (US$51.2 million) via a AU$10 million private placement and a AU$70 million entitlement offer to continue its pivotal phase III trials in wet age-related macular degeneration (wet AMD) for lead candidate OPT-302.
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Ocular

Merck Sharp & Dohme divulges new KLKB1 inhibitors

Aug. 28, 2023
Merck Sharp & Dohme Corp. has synthesized plasma kallikrein (KLKB1) inhibitors reported to be useful for the treatment of hereditary angioedema, diabetic macular edema, retinal vein occlusion, diabetic retinopathy, wet macular degeneration (exudative) and uveitis.
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Illustration of ophthalmoscopic view of diabetic retinopathy.
Ocular

FSCN1 inhibition using NP-G2-044 blocks ocular neovascularization in vivo

Aug. 28, 2023
Researchers from Nanjing Medical University have published data from a study that aimed to assess the potential of targeting fascin homologue 1 (FSCN1) as novel therapeutic strategy for the treatment of ocular neovascularization.
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Tarsier’s eye drop for uveitis misses phase III endpoint; silver lining?

Aug. 24, 2023
By Marian (YoonJee) Chu
A nonsteroidal eye drop formulation of dazdotuftide, TRS-01 missed its late-stage primary endpoint for controlling inflammation in uveitis, but developer Tarsier Pharma Ltd. said post-hoc analysis showing a boosted benefit-risk profile over steroids may be a ray of hope.
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Australian flag, coins, stock board

Opthea to raise AU$80M to continue phase III wet AMD trials for lead candidate OPT-302

Aug. 24, 2023
By Tamra Sami
Opthea Ltd. plans to raise AU$80 million (US$51.2 million) via a AU$10 million private placement and a AU$70 million entitlement offer to continue its pivotal phase III trials in wet age-related macular degeneration (wet AMD) for lead candidate OPT-302.
Read More
Close-up of elderly eye

Vision for future in crisp HD as Regeneron regenerates with new Eylea win

Aug. 21, 2023
By Randy Osborne
On the heels of the U.S. FDA clearance for Veopoz (pozelimab-bbfg) from Regeneron Pharmaceuticals Inc. to treat Chaple disease, the regulatory rollercoaster ride for the firm’s bid with higher-dose Eylea (aflibercept) ended with a green light for that compound as well. Eylea HD is indicated for wet age-related macular degeneration, diabetic macular edema, and diabetic retinopathy.
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Ocular

Novartis describes new complement factor B inhibitors for eye disorders

Aug. 17, 2023
Novartis AG has identified spirocyclic piperidinyl derivatives acting as complement factor B (CFB) inhibitors reported to be useful for the treatment of age-related macular degeneration (AMD), diabetic retinopathy and eye disorders.
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Illustration of the inside of an eye with macular degeneration
Ocular

Impact Biotech collaborates with Maastricht University to advance padeliporfin VTP research for pathological myopia

Aug. 14, 2023
Impact Biotech Ltd. has entered into an agreement with Maastricht University to collaborate on research focused on eye treatment to arrest the progression of pathological myopia, also known as myopic macular degeneration. The project will use Impact's padeliporfin vascular targeted photodynamic (VTP) therapy platform.
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Regeneron brings hearing loss gene therapy programs in-house in $213M Decibel buy

Aug. 9, 2023
By Jennifer Boggs
Six years of collaboration is ending in a buyout, as Decibel Therapeutics Inc. agreed to be acquired by Regeneron Pharmaceuticals Inc. in a deal valued at up to $213 million, including $109 million in equity, with additional payments via contingent value rights linked to clinical and regulatory milestones for DB-OTO, the lead gene therapy program targeting hearing loss.
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Izervay

Astellas-bought Iveric gains FDA clearance for eye drug Izervay

Aug. 8, 2023
By Marian (YoonJee) Chu
Iveric Bio Inc. is now the second biotech to gain U.S. clearance for geographic atrophy – snagging U.S. FDA approval on Aug. 4 for Izervay (avacincaptad pegol intravitreal solution) to treat GA secondary to age-related macular degeneration. The once-monthly Izervay 2-mg injection is anticipated to be available in the U.S. in two to four weeks, said Tokyo-based Astellas Pharma Inc., which recently acquired Iveric in May 2023.
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