Current Report Filing (8-k)
March 19 2019 - 5:26PM
Edgar (US Regulatory)
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): March 19, 2019
Cocrystal
Pharma, Inc.
(Exact
name of registrant as specified in its charter)
Delaware
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001-38418
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35-2528215
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(State
or other Jurisdiction
of
Incorporation)
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(Commission
File
Number)
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(IRS
Employer
Identification
No.)
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19805
N. Creek Parkway
Bothell,
WA
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98011
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(Address
of principal executive offices)
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(Zip
Code)
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Registrant’s
telephone number, including area code: (786) 459-1831
(Former
name or former address, if changed since last report.): N/A
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:
[ ]
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Written
communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)
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[ ]
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Soliciting
material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12)
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[ ]
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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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[ ]
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Pre-commencement
communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c))
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Indicate
by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (17 CFR
§230.405) or Rule 12b-2 of the Securities Exchange Act of 1934 (17 CFR §240.12b-2).
Emerging
growth company [ ]
If
an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for
complying with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. [ ]
Item
8.01. Other Information.
Cocrystal
Pharma, Inc. (the “Company”) is in the process of finalizing certain accounting matters and its assessment of its
internal control over financial reporting. The Company’s independent registered public accounting firm is still completing
their audit procedures in regards to those matters. As a result, the Company is filing the extension notice under Rule 12b-25
of the Securities Exchange Act of 1934 which gives the Company an automatic 15-day extension to file its Form 10-K.
The
Company expects to report a total loss of approximately $63 million which will include a $54 million non-cash write off of our
remaining in-process research and development (“IPR&D”) intangible asset. Our research and development expenses
of approximately $59 million included the $54 million write off of IPR&D. Excluding the $54 million write off of IPR&D,
our research and development expenses primarily consisted of compensation-related costs for our employees dedicated
to research and development activities and for our Scientific Advisory Board, as well as lab supplies, CRO costs, lab services,
facilities and equipment costs. We abandoned the compounds associated with the IPR&D intangible asset, which were acquired
in our November 2014 merger with RFS Pharma. Since the compounds which were licensed to RFS Pharma by Emory University (“Emory”)
were no longer needed in our HCV program we terminated our license agreement of these compounds with Emory (see additional information
below regarding Emory license agreement). Our HCV program, including clinical trials (as well as the clinical trial scheduled
to begin in Hong Kong), only use our CC-31244 compound in combination with approved drugs. Our CC-31244 compound was created in
our labs and was not one of the IPR&D compounds licensed from Emory. Our HCV program is now focused on combining our CC-31244
compound with approved products rather than in combination with our own products still in early development. The goal of developing
ultra-short treatments of four-six weeks remains the same.
On
December 6, 2018, we notified Emory of the termination of our License Agreement with Emory, dated March 7, 2013 (the “License
Agreement”). The License Agreement covered patents and patent applications for HCV inhibitors, which we no longer consider
essential to our HCV program. As part of our HCV program, we continue to focus our efforts on CC-31244. The Company had the right
to terminate the License Agreement at its sole discretion upon 90 days’ prior written notice and upon payment of all amounts
due Emory under the License Agreement through the date of termination. As of the date of this filing, the License Agreement has
been terminated, no amounts were due under the License Agreement and none will be owed in the future.
The
above financial data is preliminary, based upon the Company’s estimates and subject to completion of the Company’s
evaluation of the matters described under Part III above. Moreover, this data has been prepared on the basis of currently available
information. The Company’s independent registered public accounting firm has not audited or reviewed, and does not express
an opinion with respect to, this data. This data does not constitute a comprehensive statement of the Company’s financial
results for the year ended December 31, 2018, and the Company’s final numbers for this data may differ materially from
these estimates.
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.
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Cocrystal
Pharma, Inc.
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Dated:
March 19, 2019
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By:
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/s/
James Martin
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James
Martin
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Chief
Financial Officer
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