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BioWorld - Thursday, February 12, 2026
Home » Keywords » geographic atrophy

Items Tagged with 'geographic atrophy'

ARTICLES

Eye and DNA illustration
Ocular

Meiragtx licenses Zipbio’s gene therapies for geographic atrophy

Feb. 4, 2026
No Comments
Zipbio has signed an exclusive license agreement with Meiragtx Holdings plc to advance an AAV gene therapy for geographic atrophy. Under the agreement, Meiragtx will receive exclusive rights to Zipbio’s first-in-class therapies targeting the complement pathway for geographic atrophy.
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Eye, DNA double helix illustration.
Ocular

Complement Therapeutics’ CTx-001 gains IND clearance

Oct. 8, 2025
No Comments
Complement Therapeutics GmbH has obtained clearance for CTx-001, a gene therapy candidate.
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Close-up of elderly eye
Ocular

Pulsesight seeks clinical trial clearance for PST-611 for dry AMD/geographic atrophy

Jan. 14, 2025
Pulsesight Therapeutics SAS has submitted a clinical trial authorization (CTA) to the French authority ANSM seeking to conduct a first-in-human phase I trial of PST-611 for dry age-related macular degeneration (AMD)/geographic atrophy (GA).
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FDA hands complete response letter to Astellas’ Izervay sNDA

Nov. 19, 2024
By Marian (YoonJee) Chu
The U.S. FDA issued a complete response letter Nov. 15 for Izervay’s (avacincaptad pegol intravitreal solution, ACP) supplemental NDA, which sought to include positive two-year data for the Astellas Pharma Inc. therapy, previously approved for use in a treatment for geographic atrophy secondary to age-related macular degeneration.
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Astellas withdraws its EU MAA for geographic atrophy

Oct. 29, 2024
By Tamra Sami
Astellas Pharma Inc. has withdrawn its marketing authorization application from the EMA for its avacincaptad pegol intravitreal solution for the treatment of geographic atrophy secondary to age-related macular degeneration. “The company's decision to withdraw its application followed interactions” with the EMA’s Committee for Medicinal Products for Human Use, an Astellas spokesperson told BioWorld.
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EMA icons

EMA’s CHMP recommends Hympavzi for hemophilia, Elahere for cancer

Sep. 23, 2024
By Nuala Moran
For once, the EMA appears to have pipped the U.S. FDA to the post, with Pfizer Inc.’s hemophilia A and B therapy Hympavzi (marstacimab) recommended for approval in Europe on Sept. 20, while the U.S. PDUFA date is set for the fourth quarter of the year.
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Théa ends deal with Olix, returns rights of ocular drugs

June 25, 2024
By Marian (YoonJee) Chu
France’s Théa Open Innovation, a subsidiary of Laboratoires Théa SAS, terminated its licensing agreement with South Korea’s Olix Pharmaceuticals Inc., and returned global rights of Olix’s ocular small interfering RNA (siRNA) biologic agents, OLX-301D and OLX-301A.
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Close up of man's eye
Ocular

4D Molecular Therapeutics’ 4D-175 gains FDA clearance for phase I trial in geographic atrophy

June 25, 2024
4D Molecular Therapeutics Inc. has obtained IND clearance by the FDA for 4D-175, an R100 vector-based intravitreal genetic medicine, for the treatment of patients with geographic atrophy.
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Théa ends deal with Olix, returns rights of ocular drugs

June 24, 2024
By Marian (YoonJee) Chu
France’s Théa Open Innovation, a subsidiary of Laboratoires Théa SAS, terminated its licensing agreement with South Korea’s Olix Pharmaceuticals Inc., and returned global rights of Olix’s ocular small interfering RNA (siRNA) biologic agents, OLX-301D and OLX-301A.
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Obesity, fat cell research concept image
Endocrine/metabolic

Aldeyra Therapeutics expands RASP modulator pipeline

June 21, 2024
Aldeyra Therapeutics Inc. has expanded its novel reactive aldehyde species (RASP) modulator pipeline with the discovery and advancement of new RASP modulators for the treatment of inflammatory and metabolic diseases.
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