Freeline Announces September 2022 Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
Freeline Therapeutics Holdings plc (Nasdaq: FRLN) announced the granting of non-statutory options for 416,850 ordinary shares to five newly hired employees on September 30, 2022. These awards, compliant with Nasdaq Listing Rule 5635(c)(4), were approved by an independent subcommittee and are part of the 2021 Equity Inducement Plan. The options have an exercise price of $0.68 per share, vesting over four years. Freeline focuses on innovative gene therapies for inherited diseases, with ongoing clinical programs in hemophilia B, Fabry disease, and Gaucher disease Type 1.
- Granting of 416,850 share options indicates growth and expansion due to new hires.
- Inducement awards align with Nasdaq rules, highlighting regulatory compliance.
- The exercise price of $0.68 reflects the company's market value as of the grant date.
- None.
LONDON, Oct. 05, 2022 (GLOBE NEWSWIRE) -- Freeline Therapeutics Holdings plc (Nasdaq: FRLN) today announced that on September 30, 2022, the Company granted five newly hired employees non-statutory options to purchase an aggregate of 416,850 of the Company’s ordinary shares.
The awards were granted as an inducement material to the employees entering into employment with the Company in accordance with Nasdaq Listing Rule 5635(c)(4) and were approved by an independent subcommittee of the remuneration committee of Freeline’s board of directors. The awards were granted pursuant to the terms of Freeline’s 2021 Equity Inducement Plan, which was adopted by Freeline’s board of directors in September 2021.
Each of the options has an exercise price of
About Freeline Therapeutics
Freeline is a clinical-stage biotechnology company developing transformative adeno-associated virus (AAV) vector-mediated systemic gene therapies. The company is dedicated to improving patient lives through innovative, one-time treatments that may provide functional cures for inherited systemic debilitating diseases. Freeline uses its proprietary, rationally designed AAV vector and capsid (AAVS3), along with novel 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. The company has clinical programs in hemophilia B, Fabry disease, and Gaucher disease Type 1. Freeline is headquartered in the UK and has operations in Germany and the U.S.
Media Contact:
Arne Naeveke, PhD
Vice President, Head of Corporate Communications
arne.naeveke@freeline.life
+1 617 312 2521
IR Contact:
Naomi Aoki
naomi.aoki@freeline.life
Senior Vice President, Head of Investor Relations & Communications
+ 1 617 283 4298
FAQ
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