UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
Washington, D.C. 20549
FORM 10-Q/A
(Amendment No. 1 to Form 10-Q)
(Mark One)
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QUARTERLY REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 |
For the quarterly period ended June 30, 2015
or
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TRANSITION REPORT PURSUANT TO SECTION 13 OR 15(d) OF THE SECURITIES EXCHANGE ACT OF 1934 |
For the transition period from
to
Commission File Number: 001-33827
BG MEDICINE,
INC.
(Exact name of registrant as specified in its charter)
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Delaware |
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04-3506204 |
(State or other jurisdiction of
incorporation or organization) |
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(I.R.S. Employer
Identification No.) |
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303 Wyman Street, Suite 300
Waltham, Massachusetts |
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02451 |
(Address of principal executive offices) |
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(Zip Code) |
(781) 890-1199
(Registrants telephone number, including area code)
Indicate by check mark whether the registrant (1) has filed all reports required to be filed by Section 13 or 15(d) of the
Securities Exchange Act of 1934 during the preceding 12 months (or for such shorter period that the registrant was required to file such reports), and (2) has been subject to such filing requirements for the past 90
days. Yes x No ¨
Indicate by check mark whether the registrant has submitted electronically and posted on its corporate Web site, if any, every Interactive
Data File required to be submitted and posted pursuant to Rule 405 of Regulation S-T (§232.405 of this chapter) during the preceding 12 months (or for such shorter period that the registrant was required to submit and post such
files). Yes x No ¨
Indicate by check mark whether the registrant is a large accelerated filer, an accelerated filer, a non-accelerated filer, or a smaller
reporting company. See the definitions of large accelerated filer, accelerated filer and smaller reporting company in Rule 12b-2 of the Exchange Act.
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Large accelerated filer |
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Accelerated filer |
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Non-accelerated filer |
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¨ (Do not check if a smaller reporting company) |
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Smaller reporting company |
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Indicate by check mark whether the registrant is a shell company (as defined
in Rule 12b-2 of the Exchange Act). Yes ¨ No x
As of July 31, 2015, the registrant had 8,742,638 shares of common stock outstanding.
EXPLANATORY NOTE
This Amendment No. 1 to the Quarterly Report on Form 10-Q/A (this Amendment) amends the Quarterly Report on Form 10-Q for the quarter ended
June 30, 2015 (the Original Report) filed by BG Medicine, Inc. with the Securities and Exchange Commission on August 14, 2015 at 5:15pm ET, which was the last business day prior to the time of this Amendment, which is being
filed when EDGAR reopens on August 17, 2015 at approximately 6:15am ET, which is the next possible filing opportunity. This Amendment is being filed solely for the purpose of adding Exhibit 10.6, which was inadvertently omitted from the
Original Report, to Item 6 of Part II of the Original Report.
Except as described above, no other changes have been made to the Original Report and
this Amendment does not modify or update disclosures in the Original Report and does not reflect subsequent events occurring after date of the Original Report. Accordingly, this Amendment should be read in conjunction with the Original Report, which
continues to speak as of the date of the Original Report.
(a) Exhibits
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Exhibit Number |
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Exhibit Description |
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Filed with this Report |
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Incorporated by Reference herein from Form or Schedule |
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Filing Date |
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SEC File/ Reg. Number |
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3.1.1 |
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Restated Certificate of Incorporation of BG Medicine, Inc. |
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Form 8-K (Exhibit 3.1) |
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2/11/11 |
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001-33827 |
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3.1.2 |
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Certificate of Amendment to Restated Certificate of Incorporation of BG Medicine, Inc., dated July 8, 2015. |
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Form 8-K (Exhibit 3.1) |
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7/8/15 |
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001-33827 |
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3.1.3 |
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Certificate of Designations of Series A Preferred Stock of BG Medicine, Inc. filed with the Secretary of State of the State of Delaware on July 14, 2015 |
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Form 8-K (Exhibit 3.1) |
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7/15/15 |
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001-33827 |
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4.1 |
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Form of Secured Convertible Promissory Note issued by BG Medicine, Inc. to each of the Purchasers |
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Form 8-K/A (Exhibit 4.1) |
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6/9/15 |
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001-33827 |
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4.2 |
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Form of Senior Indenture |
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Form S-3 (Exhibit 4.8) |
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5/19/15 |
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333-204307 |
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4.3 |
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Form of Subordinated Indenture |
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Form S-3 (Exhibit 4.9) |
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5/19/15 |
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333-204307 |
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10.1.1 |
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Securities Purchase Agreement by and between BG Medicine, Inc. and the purchasers named therein, dated May 12, 2015 |
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Form 8-K/A (Exhibit 10.1) |
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6/9/15 |
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001-33827 |
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10.1.2 |
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First Amendment to Securities Purchase Agreement by and between BG Medicine, Inc. and the purchasers named therein, dated July 14, 2015 |
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Form 8-K (Exhibit 10.1) |
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7/15/15 |
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001-33827 |
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10.2 |
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Security Agreement by and between BG Medicine, Inc. and the purchasers named therein, dated May 12, 2015 |
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Form 8-K/A (Exhibit 10.2) |
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6/9/15 |
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001-33827 |
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10.3 |
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Subordination and Intercreditor Agreement by and between BG Medicine, Inc., the purchasers named therein and General Electric Capital Corporation, dated May 12, 2015 |
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Form 8-K/A (Exhibit 10.3) |
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6/9/15 |
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001-33827 |
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10.4 |
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Second Amendment to Loan and Security Agreement by and between BG Medicine, Inc. and General Electric Capital Corporation, dated May 12, 2015 |
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8-K/A (Exhibit 10.4) |
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6/9/15 |
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001-33827 |
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10.5 |
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Fifth Amended and Restated Investor Rights Agreement by and between BG Medicine, Inc. and the stockholders named therein, dated July 14, 2015. |
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Form 8-K (Exhibit 10.2) |
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7/15/15 |
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001-33827 |
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10.6+ |
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Third Amendment to Galectin-3 License and Distribution Agreement by and between BG Medicine, Inc. and Abbott Laboratories, dated May 8, 2015. |
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31.1 |
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Certification of the Registrants Principal Executive Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002. |
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31.2 |
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Certification of the Registrants Principal Financial Officer pursuant to Section 302 of the Sarbanes-Oxley Act of 2002. |
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32** |
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Certification of Principal Executive Officer and Principal Financial Officer pursuant to Section 906 of the Sarbanes-Oxley Act of 2002. |
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99.1** |
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Temporary Hardship Exemption per Regulation S-T. |
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101* |
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The following materials from the Registrants Quarterly Report on Form 10-Q for the quarter ended June 30, 2015, formatted in XBRL (eXtensible Business Reporting Language): (i) Unaudited Condensed Consolidated Balance Sheets as
of June 30, 2015 and December 31, 2014, (ii) Unaudited Condensed Consolidated Statements of Operations for the three and six month periods ended June 30, 2015 and 2014, (iii) Unaudited Condensed Consolidated Statements of Cash Flows for the six
month periods ended June 30, 2015 and 2014, and (iv) Notes to Unaudited Condensed Consolidated Financial Statements. |
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(*) |
To be filed or furnished by amendment per Temporary Hardship Exemption under Regulation S-T. |
(+) |
Confidential treatment has been requested for portions of this exhibit which have been filed separately with the Securities and Exchange Commission. |
(**) |
Previously filed as part of the Companys Quarterly Report on Form 10-Q for the quarter ended June 30, 2015 with the Securities and Exchange Commission on August 14, 2015, which is being amended by this
Amendment No. 1 to the Quarterly Report on Form 10-Q/A. |
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 thereunto duly authorized.
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BG MEDICINE, INC. |
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Date: August 17, 2015 |
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By: |
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/s/ Paul R. Sohmer |
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Paul R. Sohmer, M.D. |
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President and Chief Executive Officer |
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Date: August 17, 2015 |
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By: |
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/s/ Stephen P. Hall |
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Stephen P. Hall |
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Executive Vice President, Chief Financial Officer and Treasurer |
EXHIBIT 10.6
THIRD AMENDMENT TO
GALECTIN-3 LICENSE AND DISTRIBUTION AGREEMENT
THIS THIRD AMENDMENT TO GALECTIN-3 LICENSE
AND DISTRIBUTION AGREEMENT (this Third Amendment) is entered into as of May 8, 2015, by and between Abbott Laboratories, a corporation of the state of Illinois, having its
principal place of business at 100 Abbott Park Road, Abbott Park, Illinois 60064-3500 (Abbott) and BG Medicine, Inc., a corporation of the state of Delaware, having its principal place of business at 880 Winter Street, Suite 210,
Waltham, Massachusetts 02451 (BGM).
RECITALS
A. Abbott and BGM are parties to that certain Galectin-3 License and Distribution Agreement, dated as of November 11, 2009, as amended,
(the Agreement), pursuant to which BGM granted Abbott a license under BGMs Patent Rights to commercialize Products in the Territory.
B. The Parties now desire to amend the Agreement to replace the Product Fee, Test Rebate, marketing service fee and certain exhibits among
other things.
NOW, THEREFORE, in consideration of the mutual covenants and agreement contained herein, and
upon the terms and subject to the conditions set forth below, Abbott and BGM hereby agree as follows:
AMENDMENT
1. Except as modified by this Amendment, capitalized terms used and not otherwise defined herein shall have the meanings given to them in the Agreement.
2. Section 1.2, AUP, is hereby deleted in its entirety and replaced with the following:
1.2 AUP is the total sales of Tests to unaffiliated Third Parties (as hereinafter defined), calculated in Dollars, in an
arms length transaction, divided by the number of Tests sold to unaffiliated Third Parties in an arms length transaction by Abbott or its Affiliates.
3. A new Section 1.6A is hereby added to the Agreement to read as follows:
1.6A Dollar, $ and Dollars means a United States Dollars or United States Dollars, as
applicable.
4. Section 1.7 is hereby deleted in its entirety and is replaced with the following:
1.7 First Commercial Sale means April 01, 2013.
Page 1 of
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Portions of this Exhibit, indicated by the mark [***], were omitted and have been filed separately with the
Securities and Exchange Commission pursuant to the Registrants application requesting confidential treatment pursuant to Rule 24b-2 of the Securities Exchange Act of 1934, as amended.
5. Section 1.13 is hereby deleted in its entirety and is replaced with the following:
1.13 Product means individually and collectively, any Galectin-3 assay kits; any Galectin-3 control kit; and any Galectin-3
calibrator kit; in each case whether sold alone or as a part of another product; as well as any individual Galectin-3 assay test, control test or calibrator test.
6. Section 1.17 is hereby deleted in its entirety and is replaced with the following:
1.17 Test means an individual Galectin-3 assay test or Galectin-3 assay kit for a single determination of Galectin-3, sold
by Abbott or its Affiliates, that would infringe one or more Valid Claims of a Patent Right in the country where such product is sold; provided, however, that a Test does not include Galectin-3 control kits or Galectin-3 calibrator kits.
7. The first sentence of Section 2.1 is hereby deleted in its entirety and is replaced with the following:
2.1 License Grant. BGM hereby grants to Abbott and its Affiliates a royalty-bearing license under Patent Rights to make, have made, use,
offer for sale, sell, have sold, import, distribute and have distributed Products in the Territory.
8. Section 2.2 is hereby deleted in its entirety
and is replaced with the following:
2.2 Additional Licensees; Most Favored Terms. BGM shall have the right to license Patent Rights
to no more than four (4) Third Parties (Other Licensees, and together with Abbott, the BGM Licensees) for such Other Licensees to make, have made, use, offer for sale, sell, have sold, import, distribute, have
distributed a Galectin-3 assay, whether on an automated system or not; provided, that such Other Licensees Galectin-3 assays may be commercialized only under the Other Licensees names and brands and only with respect to platforms or
technology that are owned or controlled by such Other Licensees, unless Abbott otherwise consents after considering in good faith an alternative proposal by BGM; provided, further, that (a) beginning five (5) years after the date of First
Commercial Sale, BGM may license Patent Rights to additional Third Parties (who shall then be considered Other Licensees) to offer for sale, sell, have sold, import, distribute or have distributed a Galectin-3 assay; and (b) no Other Licensee
shall receive more favorable financial terms than those set forth in this Agreement for Abbott. If BGM enters into an arrangement with any Other Licensee for a Galectin-3 assay that contains more favorable financial terms than those set forth in
this Agreement, BGM shall so inform Abbott within ten (10) days of entering such arrangement, and Abbott shall be entitled to elect to receive the benefit of the more favorable financial terms of such other arrangement from the date of the
arrangement with the Other Licensee. In the event Abbott desires to elect such financial terms, Abbott will notify BGM within ten (10) days of learning of these terms, after which the Parties will develop and execute the necessary amendments to
incorporate the more favorable financial terms into this Agreement. Other Licensees shall not have the right to grant sublicenses to any Third Party. For avoidance
Page 2 of
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Portions of this Exhibit, indicated by the mark [***], were omitted and have been filed separately with the
Securities and Exchange Commission pursuant to the Registrants application requesting confidential treatment pursuant to Rule 24b-2 of the Securities Exchange Act of 1934, as amended.
of doubt, BGM and the BGM Licensees shall be free to enter into agreements for development, manufacturing or distribution of their products, and such agreements shall not be considered licenses
to Patent Rights for purposes of this Section 2.2.
9. Section 3.1 is hereby deleted in its entirety and is replaced with the following:
3.1 Product Fee.
(a)
[***], as consideration for the rights and licenses granted by BGM to Abbott and its Affiliates and BGMs agreement to the other terms and conditions set forth in this Agreement, Abbott shall pay to BGM a fee as set forth in this
Section 3.1, and as shown below in Table 3.1 (the Product Fee) for Tests sold to Third Parties in the Territory.
(b) The Product Fee [***], the following tiers shall apply:
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(i) |
Cumulative Test sales by Abbott or its Affiliates to unaffiliated Third Parties from [***]; |
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(ii) |
Cumulative Test sales by Abbott or its Affiliates to unaffiliated Third Parties from [***]; and |
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(iii) |
Cumulative Test sales by Abbott or its Affiliates to unaffiliated Third Parties from [***]. |
[***], Abbott shall pay the Product Fee stipulated in this Section 3.1(b) subject to the provisions of Section 3.13 on completion of
the renegotiation.
(c) Subject to the other terms and conditions of this Agreement, if there is any unlicensed competitor selling
Galectin-3 products and, that unlicensed competitors product is covered by a Valid Claim, in any country in which a Test is then being sold, the Parties shall renegotiate the Product Fee to be paid, if any.
(d) [***]. Provided that, however, in no [***]that was being paid by Abbott immediately prior to the [***].
Page 3 of
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Portions of this Exhibit, indicated by the mark [***], were omitted and have been filed separately with the
Securities and Exchange Commission pursuant to the Registrants application requesting confidential treatment pursuant to Rule 24b-2 of the Securities Exchange Act of 1934, as amended.
10. Section 3.2 is hereby deleted in its entirety and replaced with the following:
3.2 [***].
(a) Abbott
shall be entitled to [***] per Test by Abbott to BGM [***].
(b) [***], Abbott, in its sole discretion, shall have the right to terminate
this Agreement under Section 11.2(j), and upon such termination, Abbott shall have no further rights and no further obligation to BGM, financial or otherwise hereunder, except as expressly set forth herein
11. Section 3.3, Test Rebate, is hereby deleted in its entirety.
12. Section 3.4 is hereby deleted in its entirety and replaced with the following:
3.4 [***]. The Product Fee set forth in Section 3.1 shall be payable hereunder only once with respect to a Test, regardless of the
number of Valid Claims or patents set forth in Patent Rights pertaining thereto.
13. Section 3.7 is hereby deleted in its entirety and replaced with
the following:
3.7 Product Fee Reports. With each payment hereunder, Abbott shall deliver to BGM a report describing on either a
country-by-country basis the number of Tests sold by Abbott and its Affiliates, the gross invoice price for such sales and resultant Product Fees.
Table 3.1AUP
Cumulative Test sales volume from [***] TIER 1 [***] TIER 2[***] TIER 3 [***] (baseline Product Fee) [***] [***] Product Fee [***] Product Fee [***] Product Fee [***] [***] [***] [***] [***] [***] [***] [***] [***] [***] [***] [***] [***] [***]
[***] [***] [***] [***] [***] [***] [***] [***] [***] [***] [***] [***] [***] [***] [***][***] [***] [***] [***] [***] [***] [***] [***] [***] [***] [***] [***] [***] [***] [***] [***] [***] [***] [***] [***] [***]
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Portions of this Exhibit, indicated by the mark [***], were omitted and have been filed separately with the
Securities and Exchange Commission pursuant to the Registrants application requesting confidential treatment pursuant to Rule 24b-2 of the Securities Exchange Act of 1934, as amended.
14. Section 3.13 shall be added to the Agreement as follows:
3.13 True-Up. In the event that Abbott has paid an incorrect amount of Product Fee as a result of applying the wrong Tier, AUP or total
sales; or that, pursuant to Section 3.1(b) above, [***]: (i) the amount of any such overpayment shall be applied either as an off-set against future Product Fees owed, or Abbott may request a refund, at its discretion; and (ii) Abbott
will pay to BGM the amount of any such underpayment within sixty (60) days of the amount of any such underpayment being agreed upon by the Parties.
15. Section 6.2 is hereby deleted in its entirety and replaced with the following:
6.2 Abbotts Galectin-3 Intellectual Property. If Abbott solely conceives and reduces to practice any new Product Inventions or
Indication Inventions that result in new patents being sought to cover such new reagents or indications, Abbott shall own such Product Inventions and Indication Inventions, and shall make such Product Inventions and Indication Inventions available
to BGM and the Other Licensees on a non-exclusive, royalty-free basis during the Term, so long as Abbott is compensated for the use of such Product Inventions and Indication Inventions. Abbott, in its sole discretion and for its own benefit, shall
have the right to exploit such Abbott-owned Product Inventions and Indication Inventions in the Territory.
16. Section 11.2, Abbott
Termination, is hereby amended as follows:
(a) 11.2(i) is hereby deleted in its entirety and replaced with the following:
11.2(i) A new marker shows superior clinical utility and is adopted by the physician community, or
17. Section 11.2(j) is hereby added to the Agreement as follows:
11.2(j) Abbott terminates this Agreement pursuant to Section 3.2(b).
18. Section 11.5 is hereby deleted in its entirety and replaced with the following:
11.5 Survival. The following Articles and Sections shall survive the expiration or termination of this Agreement: Articles 1, 8, 9, 10
and 11 and Sections 3.4, 3.10, 3.11, 3.12, 3.13, 6.1, 6.2, 6.5, 7.1.4 and 7.1.5. All provisions that survive termination, that are irrevocable or that arise due to termination shall survive in accordance with their terms. Any provisions of this
Agreement contemplated by their terms to pertain to a period of time following termination or expiration of this Agreement shall survive only for the specified period of time.
Page 5 of
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Portions of this Exhibit, indicated by the mark [***], were omitted and have been filed separately with the
Securities and Exchange Commission pursuant to the Registrants application requesting confidential treatment pursuant to Rule 24b-2 of the Securities Exchange Act of 1934, as amended.
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A new Section 11.6, Termination for Challenge of Patents is hereby added to the Agreement as follows: |
11.6 Termination for Challenge of Patents. Subject to the exceptions set forth in 11.6(a), in the event that Abbott or any of its
Affiliates initiates, or assists a Third Party in initiating, a patent re-examination, inter parties review, post grant or other patent office proceeding, opposition, litigation, or other court proceeding challenging the validity of any issued U.S.
patent within the Patent Rights licensed under this Agreement (a Patent Challenge), BGM may terminate this Agreement upon sixty (60) days written notice to Abbott, unless such Patent Challenge is terminated or withdrawn
by the end of such 60-day notice period.
(a) BGM shall have no right to terminate this Agreement under this Section 11.6 in the
following circumstances:
(1) If there are no Other Licensees as defined in Section 2.2;
(2) If BGM is unable to obtain the same commitment set forth in Section 11.6 from any and all Other Licensees;
(3) If BGM asserts or threatens to assert the Patent Rights against an Abbott Indemnitee, a distributor or customer of an Abbott Indemnitee; or
(4) If BGM chooses not to enforce any and all claims of infringement of any BGM patents included in the Patent Rights, or any related
proprietary rights, under the provisions of Section 7.1.2.
20. A new Section 11.7, Bankruptcy, is hereby added to the
Agreement as follows:
11.7 Bankruptcy. All rights and licenses granted by BGM under this Agreement are and shall be deemed to be
rights and licenses to intellectual property, as such term is used and interpreted under Section 365(n) of the United States Bankruptcy Code (the Code) (11 U.S.C. § 365(n)). Abbott shall have all rights, elections
and protections under the Code and all other applicable bankruptcy, insolvency and similar laws with respect to the rights and licenses granted under this Agreement.
21. Section 12.7, Notices, shall be amended to replace the Parties contact information as follows:
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If to Abbott: |
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With a copy to: |
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Abbott Laboratories |
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Abbott Laboratories |
100 Abbott Park Road |
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100 Abbott Park Road |
Abbott Park, IL 60064-6095 |
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Abbott Park, IL 60064-6049 |
Attn: [***] |
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Attn: [***] |
[***] |
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Dept. [***] |
Facsimile: [***] |
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Facsimile: [***] |
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Portions of this Exhibit, indicated by the mark [***], were omitted and have been filed separately with the
Securities and Exchange Commission pursuant to the Registrants application requesting confidential treatment pursuant to Rule 24b-2 of the Securities Exchange Act of 1934, as amended.
If to BGM:
BG Medicine, Inc.
Suite 210
880 Winter Street
Waltham, MA.
02451
Tel: 781-890-1199
Fax: 781-895-1119
Attn:
President & CEO
22. Exhibit 1.12, Patent Rights is hereby deleted in its entirety and is replaced with the Exhibit 1.12 attached to
this Amendment as Schedule B.
23. Exhibit 4.4, BGM Promotional Activities, is hereby deleted in its entirety and is replaced with the Exhibit
4.4 attached to this Amendment as Schedule A.
24. Except as expressly amended by this Third Amendment, all of the terms and conditions of the Agreement
remain in full force and effect.
25. This Third Amendment may be executed in two (2) original counterparts, each of which shall be deemed an
original, but all of which together shall constitute one and the same instrument.
IN WITNESS
WHEREOF, the Parties have executed this Third Amendment as of the date first above written.
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ABBOTT LABORATORIES |
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BG MEDICINE, INC. |
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By: |
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/s/ Brian J. Blaser |
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By: |
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/s/ Paul R. Sohmer, M.D. |
Name: |
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Brian J. Blaser |
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Name: |
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President & CEO |
Title: |
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Executive Vice President |
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Title: |
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Paul R. Sohmer, M.D. |
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President Diagnostics |
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Page 7 of
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Portions of this Exhibit, indicated by the mark [***], were omitted and have been filed separately with the
Securities and Exchange Commission pursuant to the Registrants application requesting confidential treatment pursuant to Rule 24b-2 of the Securities Exchange Act of 1934, as amended.
Schedule A
Exhibit 4.4
BGM Promotional Activities
BGM
agrees to use Commercially Reasonable Efforts, as set forth in Section 4.4, to accomplish the following activities in support of Galectin-3 marker development. These activities shall be reviewed at the quarterly Steering Committee meetings and
adjusted by mutual written agreement of the Parties.
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1) |
Continue to develop and execute a [***] of Galectin-3 [***] and [***] in [***], the US, [***]. Activities shall include: |
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Development and training of [***] to [***] of Galectin-3 products. |
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b. |
Continue to work with [***] where Galectin-3 [***]. |
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c. |
Continued [***] for Galectin-3 [***]. |
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2) |
Create and execute a [***] in [***] and US. Activities shall include: |
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Develop, test and refine Galectin-3 [***] and [***]. |
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b. |
Create, train and deploy a [***] for Galectin-3. |
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3) |
Develop and implement a [***] for Galectin-3 in [***] Galectin-3 [***]. Activities shall include: |
|
a. |
Conduct a [***] in the above countries [***] of Galectin-3 [***] and [***], the key [***] and [***]. Develop and execute a [***] in the above countries. |
Page 8 of
12
Portions of this Exhibit, indicated by the mark [***], were omitted and have been filed separately with the
Securities and Exchange Commission pursuant to the Registrants application requesting confidential treatment pursuant to Rule 24b-2 of the Securities Exchange Act of 1934, as amended.
Schedule B - Exhibit 1.12
Patent Rights - BG MEDICINE PATENTS and PATENT APPLICATIONS RELATING TO GALECTIN-3
PATENT TITLE
DOCKETNo.
COUNTRY
SERIAL or PATENT No.
FILING DATE
STATUS [***] PCT [***] [***] Nationalized [***] US Issued US Issued US Pending
Canada Granted Canada Pending Australia Granted Australia Granted Australia Pending Japan Granted Japan Granted Japan Pending China Granted China Pending India Pending Europe Granted Europe Granted Europe Pending Hong Kong Granted Hong Kong Pending
[***] US Provisional [***] [***] Expired [***] US Pending PCT Nationalized Europe Pending Japan Pending Japan Pending Australia Granted Brazil Pending Canada Granted China Allowed China Pending Hong Kong Pending
Page 9 of
12
Portions of this Exhibit, indicated by the mark [***], were omitted and have been filed separately with the
Securities and Exchange Commission pursuant to the Registrants application requesting confidential treatment pursuant to Rule 24b-2 of the Securities Exchange Act of 1934, as amended.
India Korea Mexico Singapore Pending Pending Granted Allowed [***] [***] US Provisional [***] [***] Expired PCT
Nationalized US Pending Europe Granted [***] [***] US Provisional [***] [***] Expired US Provisional Expired US Pending PCT Nationalized Europe Pending Japan Pending [***] [***] US Provisional [***] [***] Expired US Issued PCT Nationalized Japan
Allowed Europe Pending Australia Granted Canada Pending Hong Kong Pending [***] [***] US Provisional [***] [***] Expired US Pending PCT Nationalized Europe Pending Japan Pending Australia Pending Canada Pending Mexico Pending
Page 10 of
12
Portions of this Exhibit, indicated by the mark [***], were omitted and have been filed separately with the
Securities and Exchange Commission pursuant to the Registrants application requesting confidential treatment pursuant to Rule 24b-2 of the Securities Exchange Act of 1934, as amended.
Exhibit 31.1
CERTIFICATIONS UNDER SECTION 302
I, Paul R.
Sohmer, certify that:
1. I have reviewed this Amendment No. 1 to the Quarterly Report on Form 10-Q/A of BG Medicine, Inc.; and
2. Based on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact necessary to
make the statements made, in light of the circumstances under which such statements were made, not misleading with respect to the period covered by this report.
Date: August 17, 2015
|
/s/ Paul R. Sohmer |
Paul R. Sohmer, M.D. |
President and Chief Executive Officer |
(principal executive officer) |
Exhibit 31.2
CERTIFICATIONS UNDER SECTION 302
I, Stephen P.
Hall, certify that:
1. I have reviewed this Amendment No. 1 to the Quarterly Report on Form 10-Q/A of BG Medicine, Inc.; and
2. Based on my knowledge, this report does not contain any untrue statement of a material fact or omit to state a material fact necessary to
make the statements made, in light of the circumstances under which such statements were made, not misleading with respect to the period covered by this report.
Date: August 17, 2015
|
/s/ Stephen P. Hall |
Stephen P. Hall |
Executive Vice President, Chief Financial Officer
and Treasurer
(principal financial officer) |
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