UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 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): | May 18, 2011 |
La Jolla Pharmaceutical Company
__________________________________________
(Exact name of registrant as specified in its charter)
Delaware | 0-24274 | 33-0361285 |
_____________________ (State or other jurisdiction |
_____________ (Commission |
______________ (I.R.S. Employer |
of incorporation) | File Number) | Identification No.) |
4365 Executive Drive, Suite 300, San Diego, California | 92121 | |
_________________________________ (Address of principal executive offices) |
___________ (Zip Code) |
Registrants telephone number, including area code: | (858) 452-6600 |
Not Applicable
______________________________________________
Former name or former address, if changed since last report
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:
[ ] Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
[ ] Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
[ ] Pre-commencement communications pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b))
[ ] Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))
Item 8.01 Other Events.
On May 18, 2011, La Jolla Pharmaceutical Company (the Company) received preliminary data from Charles River Laboratories, the Companys clinical research organization (the CRO), regarding the confirmatory pre-clinical study of the Companys LJP1485 compound being studied for tissue regeneration (the Preclinical Study). Based on the preliminary data from the Preclinical Study, the Company expects that the predetermined study endpoints, as set forth on the Purchase Agreement (defined below), will not be met and that the LJP1485 compound will not show statistically significant improvement in the study endpoints as compared to vehicle (placebo).
The Company expects the CRO to issue its final report on the Preclinical Study (the Study Report) on or about May 25, 2011. If the Companys existing holders of Series C-11 Convertible Preferred Stock (the Preferred Stockholders) do not exercise their cash warrants (the Cash Warrants) within five days from their receipt of the Study Report, as contemplated in the Purchase Agreement, then GliaMed, Inc. will have the right under the Purchase Agreement to reacquire the 1485 compound and all related assets in consideration for paying the Company a nominal cash sum. The Preferred Stockholders will have no obligation to exercise the Cash Warrants if the Study Report concludes that the endpoints were not met, which we expect will be the case.
Unless and until the Preferred Stockholders exercise the Cash Warrants, the Preferred Stockholders have the right to require the Company to redeem all outstanding shares of Series C-11 Convertible Preferred Stock for an aggregate sum of approximately $5.4 million. If the Preferred Stockholders exercise these redemption rights, the Company would have insufficient cash to sustain its operations and the Company would likely need to wind down all activities.
The Preclinical Study was being conducted pursuant the Asset Purchase Agreement, dated March 29, 2011, by and among the Company, Jewel Merger Sub, Inc. and GliaMed, Inc. (the Purchase Agreement). Additional information relating to the Purchase Agreement can be found in the Companys Current Report on Form 8-K filed on April 5, 2011.
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SIGNATURES
Pursuant to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
La Jolla Pharmaceutical Company | ||||
May 20, 2011 | By: |
/s/ Gail A. Sloan
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Name: Gail A. Sloan | ||||
Title: Chief Financial Officer and Secretary |