Acadia Pharmaceuticals Enters Into an Agreement to Sell its Rare Pediatric Disease Priority Review Voucher for $150 Million
05 Noviembre 2024 - 3:05PM
Business Wire
Acadia Pharmaceuticals Inc. (Nasdaq: ACAD) today announced that
it entered into a definitive asset purchase agreement to sell its
Rare Pediatric Disease Priority Review Voucher (PRV) for $150
million upon the closing of the transaction.
Acadia was granted the PRV in March 2023 following approval by
the U.S. Food and Drug Administration (FDA) of DAYBUE™
(trofinetide) for the treatment of Rett syndrome. DAYBUE was
initially licensed by Acadia from Neuren Pharmaceuticals Limited in
August 2018. Pursuant to the license agreement, Acadia is required
to pay Neuren one-third of the net proceeds.
Acadia plans to invest proceeds from the sale of the PRV to
support its commercial operations, R&D programs in central
nervous system and rare disease, and future business
development.
The transaction is subject to customary closing conditions,
including expiration of applicable waiting period under the
Hart-Scott Rodino (HSR) Antitrust Improvements Act. Jefferies LLC
acted as financial advisor to Acadia on this transaction.
About Acadia Pharmaceuticals
Acadia is advancing breakthroughs in neuroscience to elevate
life. Since our founding we have been working at the forefront of
healthcare to bring vital solutions to people who need them most.
We developed and commercialized the first and only FDA-approved
drug to treat hallucinations and delusions associated with
Parkinson’s disease psychosis and the first and only approved drug
in the United States and Canada for the treatment of Rett syndrome.
Our clinical-stage development efforts are focused on Prader-Willi
syndrome, Alzheimer’s disease psychosis and multiple other programs
targeting neuropsychiatric symptoms in central nervous system
disorders. For more information, visit us at Acadia.com and follow
us on LinkedIn and X.
Forward-Looking Statements
This press release contains forward-looking statements within
the meaning of the Private Securities Litigation Reform Act of
1995. Forward-looking statements include all statements other than
statements of historical fact and can be identified by terms such
as “intends,” “may,” “will,” “should,” “could,” “would,” “expects,”
“plans,” “anticipates,” “believes,” “estimates,” “projects,”
“predicts,” “potential” and similar expressions (including the
negative thereof) intended to identify forward-looking statements.
Forward-looking statements contained in this press release,
include, but are not limited to, statements about: (i) the closing
of the transaction and any expectations with respect to the timing
for such closing, (ii) HSR clearance of the transaction and the
timing of any such clearance, and (iii) the use of the proceeds
from the transaction. Forward-looking statements are subject to
known and unknown risks, uncertainties, assumptions and other
factors that may cause our actual results, performance or
achievements to differ materially and adversely from those
anticipated or implied by our forward-looking statements. Such
risks, uncertainties, assumptions and other factors include, but
are not limited to: our ability to satisfy or waive all required
closing conditions for the transaction and ultimately close the
transaction, our ability to obtain HSR clearance in a timely manner
or at all, our ability to successfully deploy the proceeds of the
transaction as anticipated, our ability to continue to successfully
commercialize DAYBUE, the timing, enrollment and results of ongoing
and future clinical trials and our ability to continue to stay in
compliance with applicable laws and regulations. Given these risks
and uncertainties, you should not place undue reliance on these
forward-looking statements. For a discussion of these and other
risks, uncertainties, assumptions and other factors that may cause
our actual results, performance or achievements to differ, please
refer to our quarterly report on Form 10-Q for the period ended
June 30, 2024 filed with the Securities and Exchange Commission on
August 7, 2024, as well as our subsequent filings with the
Securities and Exchange Commission from time to time. The
forward-looking statements contained herein are made as of the date
hereof, and we undertake no obligation to update them after this
date, except as required by law.
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version on businesswire.com: https://www.businesswire.com/news/home/20241105089742/en/
Investor Contact: Acadia Pharmaceuticals Inc. Al Kildani (858)
261-2872 ir@acadia-pharm.com
Media Contact: Acadia Pharmaceuticals Inc. Deb Kazenelson (818)
395-3043 media@acadia-pharm.com
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