Earnings Release • Aug 9, 2017
Earnings Release
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Pursuant to Section 13 or 15(d) of the Securities Exchange Act of 1934
Date of Report (Date of Earliest Event Reported): August 3, 2017
__________________________________________ (Exact name of registrant as specified in its charter)
_____________________
Delaware 001-33528 75-2402409 ______________
(I.R.S. Employer
(State or other jurisdiction of incorporation) File Number) Identification No.)
4400 Biscayne Blvd., Miami, Florida 33137
_________________________________ (Address of principal executive offices)
Registrant's telephone number, including area code: (305) 575-4100
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))
___________ (Zip Code)
_____________ (Commission
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. [ ]
On August 8, 2017, OPKO Health, Inc., a Delaware corporation (the "Company"), issued a press release announcing operating and financial highlights for the quarter ended June 30, 2017. A copy of the press release is attached hereto as Exhibit 99.1.
The information included herein and in Exhibit 99.1 shall not be deemed "filed" for purposes of Section 18 of the Securities Exchange Act of 1934 as amended ("Exchange Act") or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated by reference in any filing under the Securities Act of 1933 as amended ("Securities Act") or the Exchange Act, except as expressly set forth by specific reference in such a filing.
On August 3, 2017, the Company issued a press release announcing that it will hold a conference call to provide a business update and discuss its second quarter financial and operating results. A copy of the press release is attached hereto as Exhibit 99.2.
The information included herein and in Exhibit 99.2 shall not be deemed "filed" for purposes of Section 18 of the Exchange Act or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated by reference in any filing under the Securities Act or the Exchange Act, except as expressly set forth by specific reference in such a filing.
(d) Exhibits
| Exhibit No. | Description |
|---|---|
| 99.1 | Press Release of the Company dated August 8, 2017 |
| 99.2 | Press Release of the Company dated August 3, 2017 |
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.
OPKO Health, Inc.
August 8, 2017 By: Adam Logal
Name: Adam Logal Title: Senior Vice President-Chief Financial Officer
| Exhibit No. | Description | |||||
|---|---|---|---|---|---|---|
| 99.1 | Press Release of the Company dated August 8, 2017 | |||||
| 99.2 | Press Release of the Company dated August 3, 2017 |

MIAMI (August 8, 2017) – OPKO Health, Inc. (NASDAQ: OPK) ("OPKO" or "the Company"), reports business and financial results for the three and six months ended June 30, 2017.
Sales force expansion for RAYALDEE underway. OPKO has made substantial progress in obtaining formulary access for RAYALDEE, with more than 68% of potential patient lives now covered under insurance plans. With the more extensive insurance coverage available, OPKO is continuing to expand its field-based sales force to 70 representatives from the original 35.
Phase 2a trial for intravenously administered Factor VII-CTP and Phase 1 trial for subcutaneously administered Factor VII-CTP ongoing . These long-acting forms of Factor VII utilizing OPKO's CTP technology are expected to better support prophylaxis, provide easier administration and decrease dosing frequency for hemophilia patients.
Enrollment for global pediatric Phase 3 hGH-CTP clinical trial continues and a Japanese pediatric registration trial for hGH-CTP is now underway.
Clinical trials of Claros point-of-care (POC) prostate specific antigen (PSA) test completed and Premarket Approval (PMA) filing anticipated this fall . Analytic and clinical validation studies of OPKO's proprietary POC diagnostic test for PSA have been completed; PMA application to the FDA is planned for 4Q 2017. OPKO expects to begin an additional multicenter study of its POC testosterone test in late 2017 or early 2018, followed by a 510(k) submission to FDA.
Initiation of five Phase 2 clinical trials anticipated in 2H 2017 and early 2018 .
Investigational New Drug application was approved for a Phase 2a trial of OPK88002 and OPKO expects to initiate this study later this year.
• OPK88001, an oligonucleotide based AntagoNAT for the treatment of Dravet Syndrome: OPK88001 has received orphan drug designation in the U.S. and Europe. OPKO plans to file an IND for a Phase 2 clinical trial in 2H 2017 and plans to initiate that study by the end of the year. Currently, there is no globally approved treatment for Dravet Syndrome. AntagoNAT, anti-Natural Antisense Transcripts, is an in-house developed OPKO platform technology in which single strand oligonucleotide molecules are designed to interfere with regulatory gene expression in order to enhance production of endogenous functional proteins.
Expanded relationship with the University of California Health System to offer genetic, genomic and molecular testing services.
Implemented a unique clinician-focused test ordering portal to provide better management and tracking of data.
Revenue for the three months ending June 30, 2017 was \$314.2 million, which included a \$10.0 million milestone payment from TESARO related to the commercial launch of VARUBY® in Europe. This compares with revenue of \$357.1 million for the comparable 2016 period, which included a \$50 million payment related to a RAYALDEE license to Vifor Fresenius.
During the three months ended June 30, 2017, operating expenses included significant investment in the activities supporting the commercial launch of RAYALDEE®, as well as continued investment in the Company's pharmaceutical pipeline.
For the three months ending June 30, 2017, net loss was \$17.5 million compared with net income of \$15.5 million for the comparable 2016 period, which benefited from a \$50 million payment for RAYALDEE from Vifor Fresenius.
Cash, cash equivalents and marketable securities were \$130.5 million as of June 30, 2017.
OPKO's senior management will provide a business update and discuss results in greater detail in a conference call and live audio webcast at 4:30 p.m. Eastern time today. The conference call dial in information is listed below. To access the webcast, please log on to the OPKO website at www.opko.com.
WHEN: Tuesday, August 8, 2017, 4:30 p.m. Eastern time. DOMESTIC DIAL-IN: (866) 634-2258 INTERNATIONAL DIAL-IN: (330) 863-3454 PASSCODE: 65755948 WEBCAST: http://investor.opko.com/events.cfm
For those unable to participate in the live conference call or webcast, a replay will be available beginning August 8, 2017 two hours after the close of the conference call. To access the replay, dial (855) 859-2056 or (404) 537-3406. The replay passcode is: 65755948. The replay can be accessed for a period of time on OPKO's website at http://investor.opko.com/events.cfm.
OPKO Health is a diversified healthcare company that seeks to establish industry-leading positions in large, rapidly growing markets. Our diagnostics business includes Bio-Reference Laboratories, the nation's third-largest clinical laboratory with a core genetic testing business and a 400-person sales and marketing team to drive growth and leverage new products, including the 4Kscore® prostate cancer test and the Claros® 1 in-office immunoassay platform. Our pharmaceutical business features RAYALDEE, an FDA-approved treatment for SHPT in stage 3-4 CKD patients with vitamin D insufficiency (launched in November 2016), VARUBI® for chemotherapy-induced nausea and vomiting (oral formulation launched by partner TESARO and IV formulation pending FDA approval), OPK88003, a once or twice weekly oxyntomodulin for type 2 diabetes and obesity which is a clinically advanced drug candidate among the new class of GLP-1 glucagon receptor dual agonists, and OPK88004, an androgen receptor modulator for androgen deficiency indications. Our biologics business includes hGH-CTP, a once weekly human growth hormone injection (in phase 3 and partnered with Pfizer), and a long-acting Factor VIIa drug for hemophilia in phase 2a. We also have production and distribution assets worldwide, multiple strategic investments and an active business development strategy. More information available at www.opko.com.
This press release contains "forward-looking statements," as that term is defined under the Private Securities Litigation Reform Act of 1995 (PSLRA), which statements may be identified by words such as "expects," "plans," "projects," "will," "may," "anticipates," "believes," "should," "intends," "estimates," and other words of similar meaning, including statements regarding expected financial performance and expectations regarding the market for and sales of our products, whether 4Kscore test utilization will continue to grow, our product development efforts and the expected benefits of our products, including whether our ongoing and future clinical trials will be successfully completed on a timely basis or at all and whether the data from any of our trials will support submission or approval, validation and/or reimbursement for our products, the expected timing for launch of our products in development, whether the data for hGH-CTP will support approval of a BLA, the expected timing of commencing and concluding our clinical trials, enrollment in clinical trials, and disclosure of results for the trials, the timing of our regulatory submissions, our ability to market and sell any of our products in development, expectations about developing RAYALDEE for dialysis patients, our ability to obtain broad reimbursement coverage for the 4Kscore test, expectations regarding revenue growth and operating margins for BioReference for the remainder of 2017 and 2018, as well as other non-historical statements about our expectations, beliefs or intentions regarding our business, technologies and products, financial condition, strategies or prospects. Many factors could cause our actual activities or results to differ materially from the activities and results anticipated in forward-looking statements. These factors include those described in our Annual Reports on Form 10-K filed and to be filed with the Securities and Exchange Commission and in our other filings with the Securities and Exchange Commission, as well as integration challenges for Bio-Reference, EirGen, Transition, and other acquired businesses, the risks inherent in funding, developing and obtaining regulatory approvals of new, commercially-viable and competitive products and treatments, that earlier clinical results of effectiveness and safety may not be reproducible or indicative of future results, that the 4Kscore, RAYALDEE, Varubi™, hGH-CTP, OPKO88003, OPK88004, and/or any of our compounds or diagnostic products under development may fail, may not achieve the expected results or effectiveness and may not generate data that would support the approval or marketing of products for the indications being studied or for other indications, that currently available over-the-counter and prescription products, as well as products under development by others, may prove to be as or more effective than our products for the indications being studied. In addition, forwardlooking statements may also be adversely affected by general market factors, competitive product development, product availability, federal and state regulations and legislation, the regulatory process for new products and indications, manufacturing issues that may arise, patent positions and litigation, among other factors. The forward-looking statements contained in this press release speak only as of the date the statements were made, and we do not undertake any obligation to update forward-looking statements. We intend that all forward-looking statements be subject to the safe-harbor provisions of the PSLRA.
Company OPKO Health, Inc. David Malina, 305-575-4100 Investor Relations [email protected]
LHA Anne Marie Fields, 212-838-3777 [email protected] or Bruce Voss, 310-691-7100 [email protected]
Tables to Follow
| As of | ||
|---|---|---|
| June 30, | December 31, | |
| 2017 | 2016 | |
| Assets: | ||
| Cash, cash equivalents and marketable securities | \$ 130.5 |
\$ 168.7 |
| Other current assets | 342.0 | 314.9 |
| Total Current Assets | 472.5 | 483.6 |
| In-process Research and Development and Goodwill | 1,358.0 | 1,349.3 |
| Other assets | 938.2 | 933.7 |
| Total Assets | \$2,768.7 | \$ 2,766.6 |
| Liabilities and Equity: | ||
| Current liabilities | \$ 283.1 |
\$ 263.3 |
| 2033 Senior Notes, net | 34.8 | 43.7 |
| Deferred tax liabilities | 142.2 | 165.3 |
| Other long-term liabilities, principally | 201.8 | 202.5 |
| deferred revenue and contingent consideration | ||
| Total Liabilities | 661.9 | 674.8 |
| Equity | 2,106.8 | 2,091.8 |
| Total Liabilities and Equity | \$2,768.7 | \$ 2,766.6 |
| Condensed Consolidated Statements of Operations | ||
|---|---|---|
| (unaudited) | ||||||||
|---|---|---|---|---|---|---|---|---|
| (in millions, except share and per share data) | ||||||||
| For the three months ended June 30, | For the six months ended June 30, | |||||||
| 2017 | 2016 | 2017 | 2016 | |||||
| Revenues | ||||||||
| Revenue from services | \$ | 256.7 | \$ | 266.0 | \$ | 512.0 | \$ | 518.5 |
| Revenue from products | 29.0 | 22.8 | 51.2 | 42.7 | ||||
| Revenue from transfer | ||||||||
| of intellectual property | 28.5 | 68.3 | 47.1 | 86.9 | ||||
| Total revenues | 314.2 | 357.1 | 610.3 | 648.1 | ||||
| Costs and expenses | ||||||||
| Cost of revenues | 157.4 | 153.4 | 312.2 | 301.0 | ||||
| Selling, general and | ||||||||
| administrative | 128.3 | 117.5 | 265.0 | 245.5 | ||||
| Research and | ||||||||
| development | 32.6 | 31.3 | 58.6 | 59.1 | ||||
| Contingent | ||||||||
| consideration | 4.4 | 10.8 | 6.7 | 12.5 | ||||
| Amortization of | ||||||||
| intangible assets | 18.0 | 15.8 | 35.9 | 29.2 | ||||
| Total Costs and | ||||||||
| expenses | 340.7 | 328.8 | 678.4 | 647.3 | ||||
| Operating income (loss) | (26.5) | 28.3 | (68.1) | 0.8 | ||||
| Other income and |
| (expense), net | 3.6 | 5.1 | 9.4 | 2.5 | |||
|---|---|---|---|---|---|---|---|
| Income (loss) before | |||||||
| income taxes and | (22.9) | 33.4 | (58.7) | 3.3 | |||
| investment losses | |||||||
| (Provision for) benefit | |||||||
| from income taxes | 11.0 | (15.9) | 17.9 | 4.6 | |||
| Income (loss) before | |||||||
| investment losses | (11.9) | 17.5 | (40.8) | 7.9 | |||
| Loss from investments in | |||||||
| investees | (5.6) | (2.0) | (7.7) | (4.3) | |||
| Net income (loss) | \$ | (17.5) | \$ 15.5 |
\$ | (48.5) | \$ | 3.6 |
| Earnings (loss) per share: | |||||||
| Earnings (loss) per | |||||||
| share, basic | \$ | (0.03) | \$ 0.03 |
\$ | (0.09) | \$ | 0.01 |
| Earnings (loss) per | |||||||
| share, diluted | \$ | (0.04) | \$ 0.02 |
\$ | (0.10) | \$ | 0.00 |
| Weighted average | |||||||
| common shares | |||||||
| outstanding, basic | 559,347,540 | 547,558,800 | 558,892,375 | 546,691,117 | |||
| Weighted average | |||||||
| common shares | |||||||
| outstanding, diluted | 564,163,808 | 557,040,435 | 563,617,274 | 556,735,862 | |||
| # ## | |||||||

MIAMI (August 3, 2017) – OPKO Health, Inc. (NASDAQ: OPK), a multinational biopharmaceutical and diagnostics company, will announce operating and financial results for the three months and six months ended June 30, 2017, after the close of the U.S. financial markets on Tuesday, August 8, 2017.
OPKO's senior management will provide a business update and discuss its financial results in a conference call and live audio webcast beginning at 4:30 p.m. Eastern time on Tuesday, August 8, 2017.
WHEN: Tuesday, August 8, 2017, 4:30 p.m. Eastern time. DOMESTIC DIAL-IN: (866) 634-2258 INTERNATIONAL DIAL-IN: (330) 863-3454 PASSCODE: 65755948 WEBCAST: http://investor.opko.com/events.cfm
For those unable to participate in the live conference call or webcast, a replay will be available beginning August 8, 2017 two hours after the close of the conference call. To access the replay, dial (855) 859-2056 or (404) 537-3406. The replay passcode is: 65755948. The replay can be accessed for a period of time on OPKO's website at http://investor.opko.com/events.cfm.
OPKO Health is a diversified healthcare company that seeks to establish industry-leading positions in large, rapidly growing markets. Our diagnostics business includes Bio-Reference Laboratories, the nation's third-largest clinical laboratory with a core genetic testing business and a 400-person sales and marketing team to drive growth and leverage new products, including the 4Kscore® prostate cancer test and the Claros® 1 in-office immunoassay platform. Our pharmaceutical business features RAYALDEE, an FDA-approved treatment for SHPT in stage 3-4 CKD patients with vitamin D insufficiency (launched in November 2016), VARUBI™ for chemotherapy-induced nausea and vomiting (oral formulation launched by partner TESARO and IV formulation pending FDA approval), OPK88003, a once or twice weekly oxyntomodulin for type 2 diabetes and obesity which is a clinically advanced drug candidate among the new class of GLP-1 glucagon receptor dual agonists, and OPK88004, an androgen receptor modulator for androgen deficiency indications. Our biologics business includes hGH-CTP, a once weekly human growth hormone injection (in phase 3 and partnered with Pfizer), and a long acting Factor VIIa drug for hemophilia in Phase 2a. More information available at www.opko.com.
OPKO Health, Inc. David Malina, 305-575-4137 Investor Relations [email protected]
Investors LHA Anne Marie Fields, 212-838-3777 [email protected]
Or Bruce Voss, 310-691-7100 [email protected]
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