SEC Comment Letter for Armata Pharmaceuticals, Inc. (ARMP) (CIK 0000921114) (ARMP) — Feb 25, 2014
Armata Pharmaceuticals, Inc. (ARMP) (CIK 0000921114)
Date: Feb. 25, 2014 · CIK: 0000921114 · Accession: 0000000000-14-009378
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February 24, 2014 Via E -Mail Philip J. Young President and CEO AmpliPhi Biosciences Corporation 4870 Sadler Road, Suite 300 Glen Allen, Virginia 23060 Re: AmpliPhi Biosciences Corporation Amendment No. 1 to Registration Statement on Form 10 Filed February 4, 2014 File No. 000 -23930 Dear Mr. Young: We have reviewed your amended filing and have the following comments. In some of our comments, we may ask you to provide us with information so we may better understand your disclosure. Please respo nd to this letter within ten business days by amending your filing, by providing the requested information, or by advising us when you will provide the requested response. If you do not believe our comments apply to your facts and circumstances or do not believe an amendment is appropriate, please tell us why in your response. After reviewing any amendment to your filing and the information you provide in response to these comments, we may have additional comments. Item 1. Business Product Candidates, page 5 1. We note your response to our prior comment 6 and reissue the comment in part. Please revise your disclosure to explain what a p -value is and what it measures at your first reference. Anti-Infective Treatments with Bacteriophages, page 10 2. We note your response to prior comment 13 and reissue the comment in part. Please revise your disclosure to identify the current development status of the study started by the Polish Academy of Sciences in 2005. Please also revise your disclosure to identify how the study conducted by the Polish Academy of Sciences and the study sponsored by the European Union suggest that phage therapy shows promise for treating infectious Philip J. Young AmpliPhi Biosciences Corporation February 24, 2014 Page 2 diseases. In this regard, please discuss how the specific results of these s tudies support your stated conclusion. Sale of Assets to Celladon Corporation, page 16 3. We note your revised disclosure in response to our prior comment 16 and reissue the comment in part. Please revise your disclosure to disclose the $0.3 million sublic ense fee received in May 2013. Please also discuss the extent to which Celladon has an on -going obligation to provide future sublicense payments and, if so, the circumstances in which further payments may be required. Intellectual Property, page 16 4. We n ote your response to prior comment 16. Please revise the description of your license agreement with the U.K. Health Protection Agency to identify the duration of the agreement and the circumstances in which it may be terminated by the parties to the agree ment. Item 15. Financial Statements and Exhibits Consolidated Financial Statements For The Years Ended December 31, 2012 and 2011 7. Stock Options and Warrants , page F -10 5. Comment 31 requested you to tell us how you accounted for each issuance of warrants (including those accounted for as equity) so we repeat that request. Also disclose the fair value recognized for the warrants accounted for as equity and disclose the assumptions used to determine fair value. Report of Independent Registered Public Accounting Firm, page F -14 6. Please explain to us why your accountants did not make reference to correction of all the errors in your restated financial statements in their report. Clarify use of the term “misstatement”. Consolidated Statements o f Stockholders’ Equity (Deficit), page F -17 7. Please explain your accounting for the $3.4 million added to stockholders’ equity and goodwill for shares held in escrow for the SPH Holdings acquisition. Philip J. Young AmpliPhi Biosciences Corporation February 24, 2014 Page 3 9. Business Combinations, page F -27 8. Refer to your response to our prior comment 34 regarding your purchase of Biocontrol Limited on January 6, 2011 for $8.584 million and Special Phage Services on November 9, 2012 for $7.2 million. You indicate that you did acquire know -how, patents and phage libraries but were unable to determine fair value of these intangible assets. In explaining your accounting for these two transactions: State specifically what assets were acquired. Tell us how AmpliPhi is using the acquired assets in its R&D processes to develop bacteriophage -based products and whether the assets have alternative future uses. Tell us what information was used by AmpliPhi in determining how much to pay for the acquired companies. In not determining the fair value of the know -how, patents and phage l ibraries, and thus allocating 100% of the acquisition price to goodwill, tell us how you complied with the guidance in ASC 805 -20-20 which states that an asset is identifiable if it meets either of the following criteria: o It is separable, that is, capabl e of being separated or divided from the entity and sold, transferred, licensed, rented, or exchanged, either individually or together with a related contract, identifiable asset, or liability, regardless of whether the entity intends to do so. o It arises from contractual or other legal rights, regardless of whether those rights are transferable or separable from the entity or from other rights and obligations. Whereas goodwill is defined in ASC 805 -20-20 as an asset representing the future economic benefi ts arising from other assets acquired in a business combination that are not individually identified and separately recognized. Explain why you did not recognize any in -process research and development assets. Tell us if you referred to the AICPA Guide Assets Acquired in a Business Combination to Be Used in Research and Development Activities: A Focus on Software, Electronic Devices, and Pharmaceutical Industries in determining your accounting. Tell us how many full time employees, including management, the acquired businesses had when you acquired them and how many were retained by AmpliPhi. 9. With regard to your response to comment 35, tell us why two years of financial statements for SPH Holdin gs are not required by Rule 8 -04 of Regulation S -X. Philip J. Young AmpliPhi Biosciences Corporation February 24, 2014 Page 4 12. Correction of an Error, page F -29 10. Please amend your filing to include the required format and disclosures provided in ASC 250-10-50 paragraphs 7 through 11 for error corrections. Mark those col umns restated as “restated” on the face of the financial statements. We urge all persons who are responsible for the accuracy and adequacy of the disclosure in the filing to be certain that the filing includes the information the Securities Exchange Act o f 1934 and all applicable Exchange Act rules require. Since the company and its management are in possession of all facts relating to a company’s disclosure, they are responsible for the accuracy and adequacy of the disclosures they have made. In resp onding to our comments, please provide a written statement from the company acknowledging that: the company is responsible for the adequacy and accuracy of the disclosure in the filing; staff comments or changes to disclosure in response to staff comment s do not foreclose the Commission from taking any action with respect to the filing; and the company may not assert staff comments as a defense in any proceeding initiated by the Commission or any person under the federal securities laws of the United States. You may contact James Peklenk at (202) 551 -3661 or Lisa Vanjoske at (202) 551 -3614 if you have questions regarding comments on the financial statements and related matters. Please contact Amy Reischauer at (202) 551 -3793, Bryan Pitko at (202) 551 -3203, or me at (202) 551 - 3715 with any other questions. Sincerely, /s/ Bryan J. Pitko for Jeffrey P. Riedler Assistant Director cc: Via E -Mail Stephen B. Thau Morrison & Foerster LLP 755 Page Mill Road Palo Alto, CA 94304 -1018