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Sarepta Therapeutics Names Art Krieg, M.D., Chief Scientific Officer
01/09/14 4:06 PM EST
“We are excited to welcome Art to Sarepta as we advance the field of RNA
medicine with our proprietary technologies,” said
Dr. Krieg joins Sarepta from RaNA Therapeutics, where he served as chief
executive officer since he co-founded the company in 2011. Prior to
RaNA, he was chief scientific officer of Pfizer’s Oligonucleotide
Therapeutics Unit from 2008 to 2011. Previously, he was the chief
scientific officer, executive vice president of research and
development, and co-founder of
Dr. Krieg discovered the immune stimulatory CpG DNA motif in 1994, which
led to a new approach to immunotherapy and vaccine adjuvants. Based on
this technology, he co-founded
“The recent resurgence in the field of RNA therapeutics has been due in part to the excitement around Sarepta’s exon skipping therapies and their potential for patients with Duchenne,” said Dr. Krieg. “I look forward to joining the Sarepta team as we seek to advance these programs and realize the full potential of Sarepta’s technologies to address other serious and life-threatening diseases.”
In connection with Dr. Krieg’s hire, the Compensation Committee of the
Board of Directors of Sarepta approved an inducement stock option grant
to Dr. Krieg under Nasdaq Listing Rule 5635(c)(4), with a grant date of
About
Forward-Looking Statements and Information
This press release contains forward-looking statements. These forward-looking statements generally can be identified by use of words such as "believes or belief," "anticipates," "plans," "expects," "will," "intends," "potential," "possible," "advance" and similar expressions. These forward-looking statements include statements about the development of our Duchenne muscular dystrophy platform, our product pipeline based on RNA technologies and management contributions towards the same.
Each forward-looking statement contained in this press release is
subject to risks and uncertainties that could cause actual results to
differ materially from those expressed or implied by such statement.
Applicable risks and uncertainties include, among others: Any of
Sarepta's drug candidates, including eteplirsen, may fail in
development, may not receive required regulatory approvals (including
Subpart H accelerated approval), or may not become commercially viable
within expected time frames or at all due to delays or other reasons;
and those risks identified under the heading "Risk Factors" in Sarepta's
Annual Report on Form 10-K for the full year ended
Any of the foregoing risks could materially and adversely affect
Sarepta's business, results of operations and the trading price of
Sarepta's common stock. For a detailed description of risks and
uncertainties Sarepta faces, you are encouraged to review the Company's
filings with the
Source:
Sarepta Investor Contact:
Erin Cox, 857-242-3714
ecox@sarepta.com
or
Sarepta
Media Contact:
Jim Baker, 857-242-3710
jbaker@sarepta.com
This section of our website may contain dated or archived information which should not be considered current and may no longer be accurate. For current information, you are encouraged to review our most recent official corporate documents on file with the U.S. Securities and Exchange Commission.