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BioWorld - Tuesday, May 26, 2026
Home » Topics » Ocular, BioWorld

Ocular, BioWorld
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Eye socket: Market sees good fit for Outlook’s made-to-measure bevacizumab in wet AMD

Aug. 3, 2021
By Randy Osborne
Outlook Therapeutics Inc. CEO Russell Trenary said positive results from the phase III study called Norse Two represent “the final step we need” to proceed with the BLA in the first quarter of next year for an ophthalmic formulation of the VEGF binder bevacizumab to treat wet age-related macular degeneration (AMD).
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Woman taking Amsler grid eye exam

Through Infinity and beyond, Adverum gene therapy keeps buzz alive in AMD

July 23, 2021
By Randy Osborne
Adverum Biotechnologies Inc. CEO Laurent Fischer said the firm chose the more prudent route in scrapping development of gene therapy ADVM-022 (AAV.7m8-aflibercept) for diabetic macular edema (DME) as a result of dose-limiting toxicity in the phase II Infinity trial.
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DNA illustration

No drama as Horama raises $25M, becomes Coave Therapeutics to reflect wider focus

July 21, 2021
By Cormac Sheridan
DUBLIN – Coave Therapeutics unveiled a new identity and a new gene therapy platform, as it closed a €21.2 million (US$25 million) extension to its long-running series B round, which takes the total raise to €33 million.
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Eye and DNA

Eluminex brings in late-stage biosynthetic cornea from Fibrogen in $108M deal

July 20, 2021
By Elise Mak
In a deal worth up to $108 million, ophthalmic startup Eluminex Biosciences Ltd. has licensed the global rights to Fibrogen Inc.’s biosynthetic cornea derived from recombinant human collagen (RHC) type III intended to tackle corneal blindness.
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Eye mites

Tarsus eyes FDA filing on positive phase II/III trial in Demodex blepharitis

June 21, 2021
By Richard Staines
Tarsus Pharmaceuticals Inc. announced results from a pivotal trial of its therapy for Demodex blepharitis, which could lead to an FDA filing to treat the common eye disease for which there are no FDA-approved medications.
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Eye chart

A farsighted solution? Lenz launches with $47M for presbyopia drug

June 21, 2021
By Cormac Sheridan
Lenz Therapeutics Inc. emerged from stealth mode with $47 million in series A financing to fund its mission to bring a drug therapy to bear on farsightedness, a problem that affects much of humanity, at one point or another.
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Biogen’s Nightstar buy questioned as depression drug makes progress in phase III

June 15, 2021
By Richard Staines
Biogen Inc. has announced contrasting results from phase III trials of therapies for a rare eye disease and depression, following last week’s controversial FDA approval of Alzheimer’s drug Aduhelm. The Cambridge, Mass.-based firm said a phase III gene therapy study in the rare retinal disease choroideremia missed its primary and secondary endpoints, although the news was better from a potential therapy for major depressive disorder.
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Lungs and eye wireframe illustration

$20M up front: Pieris shares climb on Genentech deal in respiratory disease, ophthalmology

May 25, 2021
By Cormac Sheridan
Pieris Pharmaceuticals Inc. is banking $20 million up front and could receive up to $1.4 billion more in preclinical, clinical and commercial milestones from a multi-program collaboration and license agreement in respiratory disease and ophthalmology with Genentech.
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Eye and DNA

Vedere successor launches with $77M series A financing

May 18, 2021
By Michael Fitzhugh
Less than a year after Novartis AG's acquisition of optogenetics specialist Vedere Bio Inc., its successor Vedere Bio II Inc. is launching with $77 million in series A financing, led by Octagon Capital. The company will develop earlier-stage assets than those Novartis purchased, including new, mutation-agnostic optogenetics technology to improve upon current gene therapies aimed at restoring functional vision to people with vision loss due to photoreceptor death.
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Blind alley? Biogen’s gene therapy misses primary endpoint in inherited retinal disease

May 14, 2021
By Lee Landenberger
Little more than two years ago, Biogen Inc. plunked down about $800 million for gene therapy developer Nightstar Therapeutics plc, which had an X-linked retinitis pigmentosa drug in its pipeline. Top-line results from the phase II/III Xirius study of cotoretigene toliparvovec (BIIB-112), administered by subretinal injection, show the one-time therapy missed its primary endpoint of producing a statistically significant improvement in the proportion of treated study eyes.
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