AcelRx shares surge after
FDA staff says opioid safe
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[October 11, 2018]
(Reuters) - AcelRx Pharmaceuticals Inc's
shares surged 30 percent on Wednesday after U.S. Food and Administration
staff said the company's opioid treatment was safe and effective,
bringing it one step closer to a marketing approval.
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The FDA declined to approve the drug - Dsuvia - last October,
seeking additional safety data and asking for certain changes in
directions of use to ensure that the drug is administered properly.
The drug is a new formulation of the potent opioid sufentanil that
is meant to be taken orally through a pre-filled, single-dose
applicator for the management of acute pain in patients in a
medically supervised setting.
An advisory panel to the FDA will vote on the drug on Friday, before
the regulator's final decision by Nov. 3. The regulator generally
follows the advice of its experts, but is not obliged to do so.
With opioid abuse reaching epidemic proportions in the United
States, the FDA has been extremely cautious about issuing new
approvals and is looking to approve reformulated versions of opioids
that are harder to abuse.
The FDA, however, said the small tablet size of AcelRx's drug has
the risk of being dropped or misplaced during administration, which
increases the risk of accidental exposure, overdose, and death,
particularly in children.
"We determined that the benefit may outweigh the risk of accidental
exposure if sufentanil sublingual tablet 30 mcg is administered by a
healthcare provider only in certified medically supervised
settings," FDA staffers said.
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Oppenheimer analyst Leland Gershell expects focus of Friday's
discussion to be the risks associated with dropped tablets, given
their sesame-seed size and high-potency opioid contents.
The company's shares were up 30 percent at $3.45 by midday after
initially falling in premarket trading following the release of the
briefing documents.
"We believe there had been some confusion as the first review cycle
information had been included in the package," RBC Capital Markets
analyst Randall Stanicky said, adding the language in the staff's
review appeared supportive of an approval.
(Reporting by Manas Mishra and Aakash Jagadeesh Babu in Bengaluru;
Editing by Saumyadeb Chakrabarty and Shailesh Kuber)
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