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David Anderson2024-05-07 05:00:362024-05-07 08:06:38iECURE Receives FDA Fast Track Designation for ECUR-506 for the Treatment of Neonatal Onset Ornithine Transcarbamylase (OTC) Deficiency
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David Anderson2024-04-04 08:00:252024-04-04 08:03:08iECURE Announces FDA Clearance of Investigational New Drug Application for ECUR-506 to Initiate OTC-HOPE Trial for Treatment of Neonatal Onset Ornithine Transcarbamylase Deficiency in the U.S.
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David Anderson2024-03-05 19:31:452024-03-05 19:33:00iECURE Secures Approval from U.K. Medicines & Healthcare Products Regulatory Agency to Expand the OTC-HOPE Study of ECUR-506
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eallison2023-12-12 18:17:352023-12-13 08:07:51iECURE Secures Clearance from Australian Therapeutic Goods Administration for its Clinical Trial Approval for the OTC-HOPE Phase 1/2 Study of ECUR-506
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David Anderson2023-03-21 18:54:482023-03-24 17:25:20European Commission Grants Orphan Designation for iECURE’s Lead Product Candidate GTP-506 for the Treatment of Ornithine Transcarbamylase (OTC) Deficiency
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David Anderson2023-03-15 19:15:252023-03-23 14:57:07iECURE Appoints Gabriel M. Cohn, M.D., as Chief Medical Officer
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David Anderson2022-11-30 00:00:412023-03-24 17:26:58iECURE Raises $65 Million to Advance In Vivo Gene Editing Programs for the Treatment of Rare Pediatric Liver Diseases
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David Anderson2022-10-19 08:00:312023-03-24 17:28:32Preclinical Data from iECURE’s GTP-506 Demonstrates Potential for the Treatment of Ornithine Transcarbamylase (OTC) Deficiency
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David Anderson2022-09-02 20:04:532023-03-24 17:30:23iECURE Receives FDA Orphan Drug Designation for GTP-506, an Investigational Gene Editing Product Candidate for the Treatment of Ornithine Transcarbamylase (OTC) Deficiency
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eallison2022-08-22 19:18:032023-03-24 17:37:04iECURE Receives FDA Rare Pediatric Disease Designation for GTP-506, an Investigational Gene Editing Product Candidate for the Treatment of Ornithine Transcarbamylase (OTC) Deficiency
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David Anderson2022-05-25 05:00:362022-05-25 08:00:43iECURE Enters Agreement with Center for Breakthrough Medicines (CBM) to Supply Materials for Future Clinical Programs
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David Anderson2022-05-18 08:00:012022-05-18 08:16:53Nonhuman Primate Data from iECURE’s Knock-in In Vivo Gene Editing Approach for Deadly Urea Cycle Disorder to be Presented in Presidential Symposium at ASGCT 2022
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David Anderson2022-05-02 19:02:112022-05-10 20:51:39iECURE Announces Presentation of Data on its Gene Editing Approach at the American Society of Cell and Gene Therapy Annual Meeting
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David Anderson2022-04-25 07:00:042022-05-10 20:48:21iECURE Appoints George Diaz, M.D., Ph.D., as VP, Therapeutic Area Lead for Urea Cycle Disorders
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David Anderson2022-02-01 08:11:062022-02-08 20:32:34iECURE Expands Leadership Team with the Appointment of Mark Semanick as VP and Head of Technical Operations and Brad Dickerson as VP of Project Management & Patient Advocacy
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eallison2021-12-16 08:00:052022-05-10 20:07:18iECURE Partners to Develop Next-Generation Liver-Targeted Lipid Nanoparticles with University of Pennsylvania
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eallison2021-12-07 12:29:012022-04-07 21:07:47iECURE Bolsters Senior Management Team with Appointment of David Garrett as Chief Financial Officer
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eallison2021-09-15 08:00:302022-05-10 20:08:16iECURE Appoints Brian Di Donato to Board of Directors
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eallison2021-09-15 08:00:072022-05-10 20:08:59iECURE Launches With $50 Million Series A Financing to Develop In Vivo Gene Insertion Approaches for Devastating Diseases
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David Anderson2024-08-05 18:51:242024-08-05 19:01:48Introducing Fierce Biotech’s 2024 Fierce 15
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eallison2024-05-29 17:19:002024-05-29 17:46:01University of Pennsylvania gene-editing spinout iEcure hits the FDA trifecta
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eallison2024-04-12 15:36:162024-04-12 15:49:23Exclusive: Jim Wilson startup gets FDA green light for first test of gene editing in babies
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eallison2021-12-01 19:30:422021-12-30 12:41:0634 healthcare and biotech startups that are set to take off in 2022, according to top investors
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eallison2021-12-01 19:29:062021-12-29 20:47:04Penn gene editing spinout iECURE just raised a $50M Series A
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David Anderson2021-09-09 08:00:322022-02-04 18:51:00This Startup Just Raised $50 Million To Deliver Gene Therapies For Rare Diseases
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eallison2021-12-01 19:29:522021-12-29 20:44:37Genetic meds pioneer James Wilson has a new startup, this time in gene editing
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eallison2021-12-01 19:26:302021-12-29 21:00:35Jim Wilson launches liver disease gene-editing company iECURE with $50 million
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eallison2021-12-01 19:25:272021-12-29 21:02:46iECURE emerges with $50M to search for ‘holy grail’ and ‘untapped frontier’ of gene editing
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eallison2021-09-09 08:00:552021-12-30 15:38:36The Tachi Yamada legacy tree continues to grow with a new gene editing biotech from Jim Wilson
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