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
May 10, 2018
Date of Report (Date of earliest event reported)
HTG Molecular Diagnostics, Inc.
(Exact name of registrant as specified in its charter)
Delaware |
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001-37369 |
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86-0912294 |
(State or other jurisdiction of incorporation) |
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(Commission File Number) |
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(IRS Employer Identification No.) |
3430 E. Global Loop Tucson, AZ |
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85706 |
(Address of principal executive offices) |
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(Zip Code) |
Registrant’s telephone number, including area code: (877) 289-2615
Check the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligations 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)) |
Indicate by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405 of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).
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 2.02 Results of Operations and Financial Condition
On May 10, 2018, HTG Molecular Diagnostics, Inc. issued a press release announcing its financial results for the quarter ended March 31, 2018. A copy of this press release is attached hereto as Exhibit 99.1.
The information in this Item 2.02 and the attached exhibit are being furnished and shall not be deemed to be “filed” for purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liability of that section, nor shall they be deemed incorporated by reference in any filing under the Securities Act of 1933, as amended, or the Exchange Act.
Item 9.01 Financial Statements and Exhibits
(d) Exhibits
Exhibit No. |
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Description |
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99.1 |
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Press release of HTG Molecular Diagnostics, Inc. dated May 10, 2018 |
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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HTG Molecular Diagnostics, Inc. |
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Dated: May 10, 2018 |
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By: |
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/s/ Shaun D. McMeans |
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Shaun D. McMeans |
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Senior Vice President and Chief Financial Officer |
Exhibit 99.1
FOR IMMEDIATE RELEASE
HTG Molecular Diagnostics Reports First Quarter 2018 Results
Revenue increased 203% compared to the three-month period in the prior year
Call scheduled for today, May 10, at 4:30 pm ET
TUCSON, Ariz., May 10, 2018 – HTG Molecular Diagnostics, Inc. (Nasdaq: HTGM) (HTG), a provider of instruments, reagents and services for molecular profiling applications, today reported financial results for the first quarter ended March 31, 2018.
Recent Accomplishments & Highlights:
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Entered into a third statement of work for a new clinical assay development program under its Master Assay Development, Commercialization and Manufacturing Agreement (the “Governing Agreement”) with QIAGEN Manchester Limited, a wholly owned subsidiary of QIAGEN N.V. |
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Announced the second amendment to the first statement of work for next phase development activities under the Governing Agreement, representing low, single-digit millions of dollars in development fees and profit sharing payments. |
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Entered into a non-exclusive license and supply agreement with Firalis S.A. (“Firalis”) enabling Firalis to develop and commercialize a theranostic test to predict a rheumatoid arthritis (RA) patient’s response to anti‑TNFα therapy, the primary therapy for millions of RA patients. The new assay using Firalis’ gene expression signature, BIOPRED, would be commercialized on the HTG EdgeSeq platform. |
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Announced a new Precision Immuno-Oncology panel of over 1,300 genes with an expected Q3 2018 availability, to be featured at the 2018 American Society of Clinical Oncology (ASCO) annual meeting. |
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Completed an underwritten public offering of 13,915,000 shares of its common stock at a price of $2.90 per share for aggregate net proceeds of approximately $37.7 million. |
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Entered into a senior debt facility for up to $30.0 million with MidCap Financial (MidCap), a healthcare technology firm, to replace its existing senior credit facility and provide additional working capital for the Company. |
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Announced the promotion of John Lubniewski to President and Chief Operating Officer. Mr. Lubniewski has served as HTG’s chief business officer for the past seven years, bringing over three decades of experience in the life science industry. |
“We are off to a solid start in 2018 and executing well, but continue to expect uneven quarterly revenue,” said TJ Johnson, Chief Executive Officer of HTG. “Our BioPharma programs are progressing as expected, we are launching an exciting new immuno-oncology panel early in the third quarter of 2018, and believe we have additional, potential catalysts in front of us.”
First Quarter 2018 Financial Results:
Total revenue for the first quarter of 2018 was $4.2 million, an increase of 203% over the same period in the prior year. The increase in current year revenue is primarily due to our BioPharma development programs and steady growth of our RUO profiling services.
Product and product-related services revenue was $1.7 million, compared to $1.4 million to the same period in 2017. Collaborative development services revenue was approximately $2.4 million compared to $0 for the same period in 2017.
Gross margin was $3.0 million for the first quarter of 2018 compared to $76,000 for the first quarter of 2017. Net loss from operations for the first quarter of 2018 was $5.2 million compared to $5.4 million for the first quarter of 2017. Net loss per share was $(0.22) for the first quarter of 2018 compared to $(0.73) for the first quarter of 2017.
HTG ended the first quarter with $45.6 million including cash, cash equivalents and short term, available-for-sale securities investments.
2018 Revenue Guidance:
HTG is increasing the lower end of the Company’s full-year revenue guidance to $21.0 to $25.0 million. Previous guidance was $20.0 to $25.0 million.
Conference Call and Webcast:
HTG will host an investment community conference call today beginning at 4:30 p.m. Eastern Time. Conference call and webcast details follow:
Date:Thursday, May 10, 2018
Time:4:30 p.m. Eastern Time
Toll Free:(866) 548-4713
International:(323) 794-2093
Conference ID:5477857
Webcast:http://public.viavid.com/index.php?id=129155
About HTG:
HTG is focused on next generation sequencing (NGS) based molecular profiling. The company’s proprietary HTG EdgeSeq technology automates complex, highly multiplexed molecular profiling from solid and liquid samples, even when limited in amount. HTG’s customers use its technology to identify biomarkers important for precision medicine, to understand the clinical relevance of these discoveries, and ultimately to identify treatment options. Our mission is to empower precision medicine at the local level.
Statements contained in this press release regarding matters that are not historical facts are “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995, including statements regarding our planned Precision Immuno-Oncology panel, and our revenue and operational expectations. Words such as “believes,” “anticipates,” “plans,” “expects,” “intends,” “will,” “goal,” “potential” and similar expressions are intended to identify forward-looking statements, although not all forward-looking statements necessarily contain these identifying words. These forward-looking statements are based upon management’s current expectations, are subject to known and unknown risks, and involve assumptions that may never materialize or may prove to be incorrect. Actual results and the timing of events could differ materially from those anticipated in such forward-looking statements as a result of various risks and uncertainties, including, without limitation, the risk that the Precision Immuno-Oncology panel may not function or provide benefits to our customers as expected, the risk that we may not achieve our revenue expectations for 2018 (including, without limitation, due to variations from our expectations in the amount or timing of work we perform under one or more companion diagnostic development programs with large pharma customers, which development programs comprise an increasing portion of our business and therefore have the ability to significantly impact the timing and amount of revenue recognized in one or more fiscal periods), the risk that we may not realize the benefits expected under our collaboration agreements, risks associated with our ability to successfully commercialize our products; the risk that our products and services may not be adopted by biopharmaceutical companies or other customers as anticipated, or at all; our ability to manufacture our products to meet demand; the level and availability of first party payor reimbursement for our products; our ability to effectively manage our anticipated growth; our ability to protect our intellectual property rights and proprietary technologies; our ability to operate our business without infringing the intellectual property rights and proprietary technology of first parties; competition in our industry; additional capital and credit availability; our ability to attract and retain qualified personnel; and product liability claims. These and other factors are described in greater detail in our filings with the Securities and Exchange Commission, including without limitation our Annual Report on Form 10-K for the year ended December 31, 2017. All forward-looking statements contained in this press release speak only as of the date on which they were made, and we undertake no obligation to update such statements to reflect events that occur or circumstances that exist after the date on which they were made.
-Financial tables follow-
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HTG Molecular Diagnostics, Inc. |
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Statements of Operations |
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(Unaudited) |
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Three Months Ended March 31, |
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2018 |
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2017 |
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Revenue: |
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Product and product-related services |
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$ |
1,733,546 |
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$ |
1,371,169 |
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Collaborative development services |
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2,425,106 |
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— |
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Total revenue |
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4,158,652 |
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1,371,169 |
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Cost of revenue |
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1,137,063 |
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1,295,302 |
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Gross margin |
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3,021,589 |
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75,867 |
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Operating expenses: |
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Selling, general and administrative |
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5,657,832 |
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4,238,467 |
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Research and development |
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2,589,286 |
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1,267,063 |
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Total operating expenses |
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8,247,118 |
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5,505,530 |
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Operating loss |
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(5,225,529 |
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(5,429,663 |
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Loss on settlement of Growth Term Loan |
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(105,064 |
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— |
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Other expense, net |
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(49,354 |
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(386,331 |
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Net loss before income taxes |
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(5,379,947 |
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(5,815,994 |
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Provision for income taxes |
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— |
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280 |
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Net loss |
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$ |
(5,379,947 |
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$ |
(5,816,274 |
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Net loss per share, basic and diluted |
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$ |
(0.22 |
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$ |
(0.73 |
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Shares used in computing net loss per share, basic and diluted |
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24,704,128 |
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7,971,097 |
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HTG Molecular Diagnostics, Inc. |
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Balance Sheets |
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March 31, |
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December 31, |
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2018 |
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2017 |
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Assets |
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(Unaudited) |
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Current assets: |
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Cash and cash equivalents |
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$ |
20,530,960 |
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$ |
9,968,600 |
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Short-term investments available-for-sale, at fair value |
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25,125,209 |
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— |
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Accounts receivable |
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2,836,526 |
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6,356,268 |
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Contract assets |
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167,835 |
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— |
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Inventory, net of allowance of $63,943 at March 31, 2018 and $62,142 at December 31, 2017 |
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1,042,017 |
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1,180,521 |
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Prepaid expenses and other |
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464,562 |
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443,068 |
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Total current assets |
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50,167,109 |
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17,948,457 |
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Deferred offering costs |
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— |
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2,953 |
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Deferred MidCap revolving loan costs |
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79,197 |
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— |
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Property and equipment, net |
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3,099,479 |
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3,304,890 |
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Total assets |
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$ |
53,345,785 |
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$ |
21,256,300 |
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Liabilities and stockholders' deficit |
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Current liabilities: |
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Accounts payable |
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2,216,115 |
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2,438,798 |
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Accrued liabilities |
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1,681,183 |
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3,746,786 |
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Contract liabilities - current |
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462,934 |
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665,882 |
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NuvoGen obligation - current |
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560,668 |
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496,442 |
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Growth Term Loan payable - current, net of discount and debt issuance costs |
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— |
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5,793,599 |
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Other current liabilities |
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202,564 |
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200,460 |
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Total current liabilities |
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5,123,464 |
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13,341,967 |
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NuvoGen obligation - non-current, net of discount |
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7,268,161 |
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7,520,913 |
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Convertible note, related party - net of debt issuance costs |
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2,964,123 |
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2,960,760 |
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MidCap Term Loan payable - net of discount and debt issuance costs |
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6,585,731 |
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— |
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Other non-current liabilities |
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435,017 |
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492,197 |
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Total liabilities |
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22,376,496 |
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24,315,837 |
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Commitments and Contingencies (Note 13) |
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Stockholders’ equity (deficit): |
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Common stock, $0.001 par value; 200,000,000 shares authorized at March 31, 2018 and December 31, 2017, 28,358,925 shares issued and outstanding at March 31, 2018 and 13,929,763 shares issued and outstanding at December 31, 2017 |
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28,359 |
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13,929 |
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Additional paid-in-capital |
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170,898,089 |
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131,492,595 |
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Accumulated other comprehensive loss |
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(11,151 |
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— |
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Accumulated deficit |
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(139,946,008 |
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(134,566,061 |
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Total stockholders’ equity (deficit) |
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30,969,289 |
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(3,059,537 |
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Total liabilities and stockholders' equity (deficit) |
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$ |
53,345,785 |
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$ |
21,256,300 |
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Ashley Robinson
LifeSci Advisors, LLC
Phone: (617) 775-5956
Email: arr@lifesciadvisors.com
TJ Johnson
CEO
HTG Molecular Diagnostics
Phone: (520) 547-2827 x130
Email: tjjohnson@htgmolecular.com
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