Viridian Therapeutics Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)
06 Giugno 2024 - 10:01PM
Business Wire
Viridian Therapeutics, Inc. (Nasdaq: VRDN) (the “company” or
“Viridian”), a biopharmaceutical company focused on discovering and
developing potential best-in-class medicines for serious and rare
diseases, today announced that a majority of the independent
directors serving on the Compensation Committee of the company’s
Board of Directors approved the grant of non-qualified stock
options to purchase an aggregate of 450,000 shares of the company’s
common stock to two new employees (the “Inducement Grants”) on June
3, 2024 (the “Grant Date”). The Inducement Grants have been granted
outside of the company’s Amended and Restated 2016 Equity Incentive
Plan (the “Plan”) but remain subject to the terms and conditions of
such Plan. The Inducement Grants were granted as an inducement
material to these individuals entering into employment with
Viridian in accordance with Nasdaq Listing Rule 5635(c)(4).
The Inducement Grants have an exercise price per share that is
equal to the closing price of Viridian’s common stock on the Grant
Date. The Inducement Grants will vest over a four-year period, with
25% of the shares vesting on the one-year anniversary of the
employee’s start date, and thereafter the remainder of the shares
vest in 36 equal monthly installments, subject to each employee’s
continued employment with Viridian through the applicable vesting
dates.
About Viridian Therapeutics
Viridian is a biopharmaceutical company focused on engineering
and developing potential best-in-class medicines for patients with
serious and rare diseases. Viridian’s expertise in antibody
discovery and protein engineering enables the development of
differentiated therapeutic candidates for previously validated drug
targets in commercially established disease areas.
Viridian is advancing multiple candidates in the clinic for the
treatment of patients with thyroid eye disease (TED). The company
is conducting two global Phase 3 clinical trials (THRIVE and
THRIVE-2) to evaluate the safety and efficacy of VRDN-001 in
patients with active and chronic TED. Viridian’s goal is to advance
VRDN-001 as a potential best-in-class intravenous therapy followed
by VRDN-003 as a potential first- and best-in-class subcutaneous
therapy for the treatment of TED.
In addition to its TED portfolio, Viridian is advancing a novel
portfolio of neonatal Fc receptor (FcRn) inhibitors, including
VRDN-006 and VRDN-008, which has the potential to be developed in
multiple autoimmune diseases.
Viridian is based in Waltham, Massachusetts. For more
information, please visit www.viridiantherapeutics.com. Follow
Viridian on LinkedIn and X.
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version on businesswire.com: https://www.businesswire.com/news/home/20240606422492/en/
Louisa Stone, 617-272-4604 Manager, Investor Relations
IR@viridiantherapeutics.com
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