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Articles published by Atsena Therapeutics

Atsena Therapeutics Announces Positive Clinical Data from Part A of Phase I/II Trial Evaluating ATSN-201 Gene Therapy to Treat X-linked Retinoschisis (XLRS)
From Atsena Therapeutics
Via GlobeNewswire
Atsena Therapeutics to Present at May Scientific Conferences
From Atsena Therapeutics
Via GlobeNewswire
Atsena Therapeutics Granted U.S. FDA Regenerative Medicine Advanced Therapy Designation for ATSN-201 Gene Therapy to Treat X-linked Retinoschisis
From Atsena Therapeutics
Via GlobeNewswire
Atsena Therapeutics Announces Oversubscribed $150 Million Series C Financing to Further Advance Ocular Gene Therapy Programs
From Atsena Therapeutics
Via GlobeNewswire
Atsena Therapeutics Granted U.S. FDA Fast Track Designation for ATSN-201 Gene Therapy to Treat X-linked Retinoschisis
From Atsena Therapeutics
Via GlobeNewswire
Atsena Therapeutics to Present ATSN-201 Safety and Efficacy Data at The Macula Society’s 48th Annual Meeting
From Atsena Therapeutics
Via GlobeNewswire
Atsena Therapeutics Initiates Part B of Phase I/II Clinical Trial Evaluating Gene Therapy ATSN-201 to Treat X-linked Retinoschisis
From Atsena Therapeutics
Via GlobeNewswire
Atsena Therapeutics Announces Dosing Completed in Part A of Phase I/II Clinical Trial Evaluating Gene Therapy ATSN-201 to Treat X-linked Retinoschisis
From Atsena Therapeutics
Via GlobeNewswire
Nippon Shinyaku and Atsena Therapeutics enter into an Exclusive Strategic Collaboration for ATSN-101 in the U.S. and Japan
From Atsena Therapeutics
Via GlobeNewswire
Atsena Therapeutics to Present ATSN-201 Safety and Efficacy Data at the American Academy of Ophthalmology 2024 Annual Meeting
From Atsena Therapeutics
Via GlobeNewswire
Atsena Therapeutics to Present at Chardan’s 8th Annual Genetic Medicines Conference
From Atsena Therapeutics
Via GlobeNewswire
Atsena Therapeutics Receives Orphan Drug Designation from the U.S. FDA for ATSN-201 Gene Therapy to Treat X-linked Retinoschisis
From Atsena Therapeutics
Via GlobeNewswire
Atsena Therapeutics Announces 12-Month Safety and Efficacy Data from Phase I/II Clinical Trial of ATSN-101 in LCA1 Published in The Lancet
From Atsena Therapeutics
Via GlobeNewswire
Atsena Therapeutics Receives Rare Pediatric Disease Designation from the U.S. FDA for ATSN-201 Gene Therapy to Treat X-linked Retinoschisis
From Atsena Therapeutics
Via GlobeNewswire
Atsena Therapeutics Appoints Joseph S. Zakrzewski as Board Chair
From Atsena Therapeutics
Via GlobeNewswire
Atsena Therapeutics Announces Positive Clinical Data from the First Cohort of Phase I/II Trial Evaluating ATSN-201 Gene Therapy for the Treatment of X-linked Retinoschisis (XLRS)
From Atsena Therapeutics
Via GlobeNewswire
Atsena Therapeutics Announces Initiation of Dosing in Second Cohort of Phase I/II Clinical Trial Evaluating ATSN-201 Gene Therapy for the Treatment of X-linked Retinoschisis (XLRS)
From Atsena Therapeutics
Via GlobeNewswire
Atsena Therapeutics Receives Rare Pediatric Disease Designation from FDA for ATSN-101 Gene Therapy for GUCY2D-associated Leber Congenital Amaurosis (LCA1)
From Atsena Therapeutics
Via GlobeNewswire
Atsena Therapeutics Announces Positive 12-month Safety and Efficacy Data from Ongoing Phase I/II Clinical Trial of ATSN-101 in Patients with Leber Congenital Amaurosis Caused by Biallelic Mutations in GUCY2D (LCA1)
From Atsena Therapeutics
Via GlobeNewswire
Atsena Therapeutics Receives FDA Regenerative Medicine Advanced Therapy (RMAT) Designation for ATSN-101 Gene Therapy for GUCY2D-associated Leber Congenital Amaurosis (LCA1)
From Atsena Therapeutics
Via GlobeNewswire
Atsena Therapeutics Announces First Patient Dosed in Phase I/II Clinical Trial of ATSN-201 for the Treatment of X-linked Retinoschisis
From Atsena Therapeutics
Via GlobeNewswire
Atsena Therapeutics Receives FDA Clearance of IND Application for ATSN-201, an Investigational Gene Therapy for the Treatment of X-linked Retinoschisis
From Atsena Therapeutics
Via GlobeNewswire
Atsena Therapeutics Announces Positive 6-month Data from Ongoing Phase I/II Clinical Trial of ATSN-101 in Patients with Leber Congenital Amaurosis Caused by Biallelic Mutations in GUCY2D (LCA1)
From Atsena Therapeutics
Via GlobeNewswire
Atsena Therapeutics Announces Six-Month Data from Phase I/II Clinical Trial of ATSN-101 to be Presented at ARVO 2023 Annual Meeting
From Atsena Therapeutics
Via GlobeNewswire
Atsena Therapeutics to Present Positive Interim Encore Data from the Phase I/II Clinical Trial of ATSN-101 for the Treatment of GUCY2D-associated Leber Congenital Amaurosis (LCA1) at the 46th Annual Macula Society Meeting
From Atsena Therapeutics
Via GlobeNewswire
Atsena Therapeutics to Present at NewYorkBIO’s December 2022 Emerging Life Science Company Showcase
From Atsena Therapeutics
Via GlobeNewswire
Atsena Therapeutics Expands Leadership Team with Appointment of Lis Leiderman, MD, MBA, as Chief Financial Officer and Chief Business Officer
From Atsena Therapeutics
Via GlobeNewswire
Atsena Therapeutics Announces Positive Results from Phase I/II Clinical Trial of ATSN-101 for the Treatment of GUCY2D-associated Leber Congenital Amaurosis (LCA1)
From Atsena Therapeutics
Via GlobeNewswire
Atsena Therapeutics Announces Opening of New Office and Laboratory Space in North Carolina’s Research Triangle
From Atsena Therapeutics
Via GlobeNewswire
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