Akorn, Inc. Receives U.S. IND Clearance for the Clinical Development of AK-1015, an NDA Drug Product for Ocular Anesthesia
01 Agosto 2006 - 8:00AM
Business Wire
Akorn, Inc. (AMEX:AKN) today announced that it has received U.S.
IND clearance to initiate the pivotal, clinical trial for AK-1015
in 200 patients. AK-1015, an ophthalmic new drug application (NDA)
will pursue an indication for ocular anesthesia. The clinical trial
will begin in August 2006. Akorn has signed an agreement with a CRO
firm for the deployment of the protocol and monitoring of the
clinical trial. Akorn intends to file the NDA in 2007 with a
potential product launch in 2008. The AK-1015 formulation was
developed internally at the Somerset, NJ facility. Akorn already
has a targeted sales force to optimize and create market
penetration. The U.S. market for this drug is approximately 5
million ophthalmic procedures per year. Akorn recently filed a U.S.
patent for AK-1015 with supporting claims. Arthur S. Przybyl,
Akorn's President and Chief Executive Officer stated, "AK-1015 is
our first internally developed NDA drug supported through an IND
with clinical trials to help build our ophthalmic specialty
pharmaceutical product line. The four arm clinical trial in 200
patients is intended to support the NDA filing for the indication
of ocular anesthesia." About Akorn, Inc. Akorn, Inc. manufactures
and markets sterile specialty pharmaceuticals. Akorn has
manufacturing facilities located in Decatur, Illinois and Somerset,
New Jersey and markets and distributes an extensive line of
hospital and ophthalmic pharmaceuticals. Additional information is
available at the Company's website at www.akorn.com. Materials in
this press release may contain information that includes or is
based upon forward-looking statements within the meaning of the
Securities Litigation Reform Act of 1995. Forward-looking
statements give our expectations or forecasts of future events. You
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