Inactive Instrument

Freeline Therapeutics Holdings plc Stock

Equities

FRLN

US35655L2060

Biotechnology & Medical Research

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Freeline Presents Positive New Data from Phase 1/2 Trial of FLT201, Its Novel Gene Therapy Candidate for Gaucher Disease, in Late-Breaking Oral Presentation at ASGCT 27th Annual Meeting CI
Syncona’s Takeover of Freeline Therapeutics Becomes Effective MT
Freeline Therapeutics Holdings plc Announces Resignation of Julia Gregory, Martin Andrews, Jeffrey Chodakewitz, Colin Love and Paul Schneider from the Board CI
Freeline Therapeutics Holdings plc(NasdaqCM:FRLN) dropped from NASDAQ Composite Index CI
Syncona Investment Management Limited completed the acquisition of the remaining 42.08% stake in Freeline Therapeutics Holdings plc. CI
Freeline shareholders approve Syncona acquisition AN
Freeline Therapeutics' Shareholders Approve Acquisition by Syncona MT
Syncona says Freeline trial for Gaucher disease treatment positive AN
European Equities Traded in the US as American Depositary Receipts Gain Friday MT
Freeline Therapeutics Holdings plc Reports Earnings Results for the Nine Months Ended September 30, 2023 CI
HC Wainwright Downgrades Freeline Therapeutics to Neutral From Buy, Adjusts Price Target to $6.50 From $15 MT
Sector Update: Health Care Stocks Advance Late Afternoon MT
Sector Update: Health Care Stocks Higher in Afternoon Trading MT
FTSE 100 Closes Down 0.17% After Autumn Statement DJ
Syncona agrees to buyout deal with Freeline Therapeutics AN
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Latest transcript on Freeline Therapeutics Holdings plc

Managers TitleAgeSince
Founder - 14-12-31
Chief Executive Officer 49 21-03-14
Director of Finance/CFO 54 22-05-15
Members of the board TitleAgeSince
Chairman 50 15-11-30
Chief Executive Officer 49 21-03-14
Director of Finance/CFO 54 22-05-15
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Freeline Therapeutics Holdings plc is a United Kingdom-based clinical-stage biotechnology company. The Company is developing transformative adeno-associated virus (AAV) vector-mediated gene therapies. It is focused on improving patient lives through one-time treatments for chronic debilitating diseases. It uses its rationally designed AAV vector and capsid (AAVS3), along with promoters and transgenes, to deliver a functional copy of a therapeutic gene into human liver cells, thereby expressing a persistent functional level of the missing or dysfunctional protein into the patient's bloodstream. Therapeutic AAV vectors consist of two main components, the capsid and the expression cassette (that contains the gene and the promoter). The Company is advancing clinical programs in Fabry disease and Gaucher disease Type 1. The Company's pipeline includes Fabry Disease FLT190 for the treatment of Fabry disease and Gaucher Disease FLT201 for the treatment of type 1 Gaucher disease.
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