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LOGICBIO THERAPEUTICS INC. - More news...
LOGICBIO THERAPEUTICS INC. - More news...
- LogicBio Therapeutics to Present at Upcoming Investor Conferences
- LogicBio Therapeutics Reports Third Quarter 2020 Financial Results and Provides Business Update
- LogicBio Therapeutics Receives FDA Fast Track Designation for LB-001 for the Treatment of Methylmalonic Acidemia (MMA)
- LogicBio Therapeutics Announces Appointment of Veteran Biotech Executive Mariana Nacht, Ph.D., as Chief Scientific Officer and Kyle Chiang, Ph.D., Promoted to Chief Operating Officer
- LogicBio Therapeutics Announces Closing of Public Offering of Common Stock and Full Exercise of Underwriters’ Option to Purchase Additional Shares
- LogicBio Therapeutics Announces Pricing of Public Offering of Common Stock
- LogicBio Therapeutics Announces Proposed Public Offering of Common Stock
- LogicBio Therapeutics to Present at the Jefferies Virtual Gene Editing/Therapy Summit October 2, 2020
- LogicBio Therapeutics to Present at the 4th Annual Chardan Virtual Genetic Medicines Conference October 5, 2020
- LogicBio Therapeutics Announces SUNRISE Phase 1/2 Clinical Design for LB-001 for the Treatment of Methylmalonic Acidemia in Pediatric Patients
- LogicBio Therapeutics Reports Second Quarter 2020 Financial Results and Provides Business Updates
- LogicBio Therapeutics to Hold Virtual-Only Annual Meeting of Stockholders
- LogicBio Therapeutics to Present at the Jefferies Virtual Healthcare Conference
- LogicBio Therapeutics to Present New Data on GeneRide™ Platform and Next Generation Capsid Development Program at the American Society of Gene & Cell Therapy 2020 Annual Meeting
- LogicBio Reports First Quarter 2020 Financial Results and Provides Business Updates
- LogicBio Therapeutics Appoints Mark Enyedy to its Board of Directors
- LogicBio Reports Full Year 2019 Financial Results and Provides Business Updates
- LogicBio Therapeutics Provides Update on FDA Review of Investigational New Drug Application for LB-001 for Methylmalonic Acidemia
- LogicBio Therapeutics Announces Submission of Investigational New Drug Application (IND) for LB-001 for Methylmalonic Acidemia (MMA) and Highlights Key Corporate Milestones
- LogicBio Therapeutics Announces Collaboration with Takeda to Develop New Genome Editing Candidate LB-301 for the Treatment of Crigler-Najjar Syndrome
- LogicBio Therapeutics Extends Sponsored Research Agreement with Oregon Health & Science University to Explore Translation of Pharmaceutically-Driven Selective Advantage for Future GeneRide™ Candidates
- LogicBio Reports Third Quarter 2019 Financial Results and Provides Business Updates
- LogicBio Therapeutics to Present at November Conferences
- LogicBio Therapeutics to Present New Data on Next Generation Capsid Development Program and GeneRide™ Platform Program at the European Society of Gene and Cell Therapy 27th Annual Congress
- LogicBio Therapeutics to Present at October Conferences
- LogicBio Reports Second Quarter 2019 Financial Results and Provides Business Updates
- LogicBio Therapeutics Receives Rare Pediatric Disease Designation for LB-001 for the Treatment of Methylmalonic Acidemia
- LogicBio to Present at the Jefferies 2019 Healthcare Conference
- LogicBio Reports First Quarter 2019 Financial Results and Provides Business Updates
- LogicBio Therapeutics Receives FDA Orphan Drug Designation for LB-001 for the Treatment of Methylmalonic Acidemia