UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, DC 20549
FORM 8-K
CURRENT REPORT
Pursuant to Section 13 or 15(d) of
the Securities Exchange Act of 1934
Date of Report (Date of earliest event reported): January 29, 2008
DUSA PHARMACEUTICALS, INC.
(Exact name of registrant as specified in its charter)
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New Jersey
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0-19777
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22-3103129 |
(State or other jurisdiction of
incorporation)
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(Commission File Number)
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(IRS Employer
Identification Number) |
25 Upton Drive
Wilmington, Massachusetts 01887
(Address of principal executive offices, including ZIP code)
(978) 657-7500
(Registrants telephone number, including area code)
Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the
filing obligation of the registrant under any of the following provisions (see General Instruction
A.2. below):
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Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425) |
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Soliciting material pursuant to Rule 14a-12 under the Securities Act (17 CFR 240.14a-12) |
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Pre-commencement communications pursuant to Rule 14d-2(b) under the
Exchange Act (17 CFR 240.14d-2(b)) |
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Pre-commencement communications pursuant to Rule 13e-4(c) under the
Exchange Act (17 CFR 240.13e-4(c)) |
Item 1.01 Entry into a Material Definitive Agreement
On January 29, 2008, Sirius Laboratories, Inc. (Sirius), a wholly-owned subsidiary of DUSA
Pharmaceuticals, Inc. (DUSA), entered into the 2006 Micanol Transition License Agreement (the
Transition License Agreement) with Winston Laboratories, Inc. (Winston). The Transition
License Agreement amends the original 2006 Micanol License Agreement, dated as of January 30, 2006,
between Sirius and Winston, which DUSA has previously filed, related to DUSAs
Psoriatec® product. The original 2006 Micanol License Agreement was due to expire
pursuant to its terms on January 31, 2008. The parties entered into the Transition License
Agreement to extend the term of the 2006 Micanol License Agreement to September 30, 2008, to reduce
the period of time that Sirius is required to maintain product liability insurance with respect to
its distribution and sale of the Product (as defined in the 2006 Micanol License Agreement) after
the termination of the Transition License Agreement and to confirm the allocation of certain costs
and expenses relating to the product during and after the transition period.
The foregoing is a summary of the material terms of the Transition License Agreement and is
qualified by reference to the Transition License Agreement attached here to as Exhibit 10.1 and
incorporated herein by reference.
Except for historical information, this report contains certain forward-looking statements
that involve known and unknown risk and uncertainties, which may cause actual results to differ
materially from any future results, performance or achievements expressed or implied by the
statements made. These forward-looking statements relate to the risks relating to the expected
term of the agreement. These forward-looking statements are further qualified by important factors
that could cause actual results to differ materially from those in the forward-looking statements.
These factors include, without limitation penetration of the market by Psoriatec, reliance on third
parties to manufacture Psoriatec, and any liabilities assumed by DUSA related thereto and the other
risks identified in DUSAs SEC filings from time to time.
Item 9.01 Financial Statement and Exhibits.
(d) Exhibits
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Item No. |
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Description |
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10.1
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2006 Micanol Transition License Agreement, dated as of January 29, 2008, by and between
Winston Laboratories, Inc. and Sirius Laboratories, Inc. portions of which have been omitted
pursuant to a request for confidential treatment under Rule 24(b)-2 of the Securities Exchange
Act of 1934, as amended. |