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BioWorld - Thursday, February 26, 2026
Home » diabetic macular edema

Articles Tagged with ''diabetic macular edema''

Close up of man's eye

Going Ollin on AMD, DME: Vabysmo in phase Ib crosshairs

Jan. 9, 2026
By Randy Osborne
No Comments
Ollin Biosciences Inc. is gearing up for global phase III trials this year after disclosing favorable top-line results from its randomized, head-to-head phase Ib Jade study comparing OLN-324, a next-generation VEGF/Ang2 bispecific antibody, to Vabysmo (faricimab, Roche AG), which takes aim at the same targets. The drugs were tested in more than 160 patients with diabetic macular edema (DME) or wet age-related macular degeneration (AMD).
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Oculis eyes MS as privosegtor gets FDA breakthrough status in AON

Jan. 6, 2026
By Nuala Moran
No Comments
Eye disease specialist Oculis SA is laying plans to branch out into multiple sclerosis (MS) after the phase II trials of its acute optic neuritis (AON) drug, privosegtor, showed it reduced levels of neurofilament release, a key biomarker of neuronal damage and neurodegeneration.
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Fundus image of eye with age-related macular degeneration.
Ocular

Coave nominates lead gene therapy for retinal vascular diseases

Nov. 17, 2025
No Comments
Coave Therapeutics SA has nominated a lead gene therapy program, CoTx-101, for the treatment of retinal vascular diseases, such as wet age-related macular degeneration and diabetic macular edema.
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Close-up of eye with digital focus
Newco news

Ollin eyes next-gen ophthalmology space, launches with $100M

Sep. 17, 2025
By Jennifer Boggs
No Comments
To say the team at Ollin Biosciences Inc. has some experience in ophthalmology would be an understatement. The company, which emerged from stealth with $100 million in venture capital and two in-licensed assets with plans to add more, brings to the table years of expertise from work on blockbuster retinal disease drugs Lucentis (ranibizumab, Roche AG) and Vabysmo (faricimab, Roche AG).
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Ocular

Rezolute patents new KLKB1 inhibitors

Aug. 19, 2025
Rezolute Inc. has disclosed plasma kallikrein (KLKB1) inhibitors reported to be useful for the treatment of diabetic macular edema and uveitis.
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Therini Bio locks in another $39M for its fibrin-targeting immunotherapies

May 16, 2025
By Brian Orelli
No Comments
Therini Bio raised an additional $39 million in its series A financing round, bringing the total for the round to $75 million. The capital will be used to advance its fibrin-targeting immunotherapies for neurodegenerative diseases.
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Unity eyes path forward for UBX-1325 despite missed DME endpoint

March 24, 2025
By Jennifer Boggs
Shares of Unity Biotechnology Inc. (NASDAQ:UBX) sank 28.8% to close at $1.30 March 24 as a top-line readout of its phase IIb Aspire study testing UBX-1325 head-to-head against aflibercept in diabetic macular edema (DME) fell short of statistical noninferiority on the primary analysis endpoint. But that’s not the full story, according to company executives, who have plans for moving the senolytic Bcl-xL inhibitor into late-stage studies.
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Eye wireframe illustration
Ocular

DP Technology nominates Lp-PLA2 inhibitor candidates

July 9, 2024
Beijing DP Technology Co. Ltd. has nominated DPT-0415, a novel small molecule targeting lipoprotein‐associated phospholipase A2 (Lp-PLA2), as a preclinical candidate for the treatment of diabetic retinopathy (DR) and diabetic macular edema (DME).
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Eye wireframe illustration
Ocular

DP Technology nominates Lp-PLA2 inhibitor candidates

July 8, 2024
Beijing DP Technology Co. Ltd. has nominated DPT-0415, a novel small molecule targeting lipoprotein‐associated phospholipase A2 (Lp-PLA2), as a preclinical candidate for the treatment of diabetic retinopathy (DR) and diabetic macular edema (DME).
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Celltrion president Young ho Yoo and Kukje Pharm President and CEO Nam Tae-Hoon

Celltrion gains Korea approval of Eylea biosimilar

June 4, 2024
By Marian (YoonJee) Chu
Celltrion Inc., of Incheon, South Korea, gained MFDS clearance of Eydenzelt (CT-P42) as a biosimilar referencing Regeneron Pharmaceuticals Inc./Bayer AG’s Eylea (aflibercept) on May 30. The news comes on the heels of the U.S. FDA approving the first Eylea interchangeable biosimilars on May 20.
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