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Sunshine Heart Announces First Quarter 2015 Results and Provides Corporate Update EDEN PRAIRIE, Minn., May 5, 2015 (GLOBE NEWSWIRE) -- Sunshine Heart, Inc. (Nasdaq:SSH) announced today its financial results and provided a corporate update for the first quarter of 2015. The Company will host a conference call and webcast at 9:00 AM ET today to discuss its financial results and provide an update on its ongoing clinical studies. To access the live webcast, please visit the Investors page of the Sunshine Heart website at http://ir.sunshineheart.com. Alternatively, you may access the live conference call by dialing (877) 303-9826 (U.S.) or (224) 357-2194 (international) and using conference ID 33142990. An audio archive of the webcast will be available following the call at http://ir.sunshineheart.com."Resuming enrollment in the COUNTER HF™ study was our top priority during the quarter and remains our most important initiative. The Company's proposed minor protocol modifications will enhance an already robust protocol, and should increase the likelihood of study success. We are pleased with progress made with the FDA and remain confident that the Company will resolve this matter within 30 days," commented Dave Rosa, President and Chief Executive Officer of Sunshine Heart.First Quarter Corporate Highlights:
- 23 sites activated in the COUNTER HF U.S. pivotal study, up from 21 at the end of the fourth quarter of 2014
- Eight additional patients enrolled prior to pausing enrollment; Company had been trending to 20 enrollments for the first quarter of 2015
- FDA granted approval for an interim analysis for the COUNTER HF study
- Two additional implants completed in the OPTIONS HF EU post-market study bringing the total number of EU implants to 14
- The ISHLT accepted poster presentation authored by Dr.Mark Slaughter ofJewish Hospital inLouisville Kentucky on management of driveline infections for the C-Pulse System
- Hired Claudia Drayton as the Company's Chief Financial Officer
First Quarter Financial Highlights:
- Cash used in operations was$7.1 million in the first quarter 2015 vs.$6.7 million in the first quarter 2014
- Cash and cash equivalents on hand at March 31, 2015 was $37.0 million vs. $31.3 million at year-end 2014
Prior to the temporary pause in COUNTER HF's study enrollment which commenced on March 6, 2015, Sunshine Heart was on pace to record its most successful quarter of enrollment since initiating the study. The Company was trending to reach 20 patients in the first quarter of 2015 as an additional 50 patients were to be evaluated in March. In addition, the Company activated two new centers in the quarter, bringing the total number of activated sites to 23. The Company is also pleased to report that there have been no exit site infections in the study to-date.In accordance with the temporary pause in enrollment, the Company provided the U.S. Drug and Food Administration (FDA) with site documentation regarding the four patient deaths in the treatment arm of the study in an effort to establish a plan to resume enrollment. The Company reported that the four treatment arm deaths in COUNTER HF were adjudicated by an independent Clinical Events Committee (CEC) as being not device or therapy related. The independent Data Safety Monitoring Board (DSMB) has also recommended continuing the study. Upon review of the findings, the FDA did not indicate concern regarding device safety and requested submission of minor protocol changes prior to granting Sunshine Heart approval to resume enrollment.The Company submitted the requested minor protocol changes to the FDA on April 22, 2015 and approval of re-initiation of the study is expected by May 23, 2015. The most significant updates provided to the FDA included details on the Company's proposal to incorporate a Physician Subject Selection Committee into the study to ensure that patients meet the study entry criteria and address the targeted population that will most likely benefit from receiving C-Pulse therapy. The new committee will be comprised of cardiology heart failure experts and cardiothoracic surgeons familiar with the therapy. A COUNTER HF study investigator meeting will be held on May 7-8, 2015 to prepare for resumption of study enrollment.During the first quarter of 2015, the European based OPTIONS HF post-market study continued to advance and the Company is pleased to report that two additional patients were implanted during the period bringing the total number of implants under the European study to 14. Integral to this milestone is that it marks the first implant performed at the Company's German Tübingen site. Furthermore, with the initial patients in the study achieving the milestone of 18 months of therapy, only two of 14 patients have had reported exit site infections to-date.Also during the quarter, the Company continued to achieve meaningful progress with its next generation, fully implantable C-Pulse Heart Assist System. The first acute animal experiment with the complete fully implantable system was achieved, with successful power transfer through the skin to activate the pump. Finally, in terms of expanded opportunities beyond congestive heart failure, the Company has initiated a research program with Dr. Mark Slaughter and the Jewish Hospital of Louisville, Kentucky for the treatment of Pulmonary Arterial Hypertension.On the corporate development front, the Company continued to bolster its leadership team with the appointment of Claudia Drayton as its Chief Financial Officer. Prior to joining Sunshine Heart, Ms. Drayton spent fifteen years at Medtronic, Inc, a global leader in the medical device industry. During her tenure, she held multiple senior managerial finance positions culminating with an assignment in Europe serving as Chief Financial Officer of the Peripheral Vascular Business (2010-2012) and, most recently, as Chief Financial Person and Senior Finance Director of the Integrated Health Solutions Business. Another key milestone during the first quarter of 2015 was the closing of a loan and security agreement with Silicon Valley Bank for proceeds of up to $10.0 million.FINANCIALSThe Company's first quarter 2015 results include reimbursement revenue of $59,000 for an implant of the C-Pulse System under its U.S. COUNTER HF study, a comparable amount to the same period in 2014. Although the Company's C-Pulse System is not approved for commercial sale in the U.S., the FDA has assigned the C-Pulse System to a Category B designation, making it eligible for reimbursement at certain U.S. sites during clinical studies. Consequently, the Company is able to invoice some hospitals and clinics that are eligible for reimbursement by Medicare, Medicaid or private insurance companies. Many private insurance companies and certain governmental institutions have a non-coverage policy for experimental or investigational procedures, however, so the Company has not been successful in achieving reimbursement for some of its implant procedures.Product costs incurred for the Company's clinical studies are deemed to be development costs and, accordingly, are expensed to research and development as incurred.Operating expenses in the first quarter of 2015 totaled $7.1 million, compared to $6.4 million in the first quarter of 2014. Equity compensation expense included in operating expenses totaled $0.9 million and $0.7 million for the three months ended March 31, 2015 and 2014, respectively. Excluding equity compensation expense, non-GAAP operating expenses totaled $6.2 million and $5.7 million for the three months ended March 31, 2015 and 2014, respectively. The increase over the prior year was primarily attributable to increased development expenses associated with the Company's fully-implantable system, increased clinical research expenses related to the U.S. pivotal and EU post-market studies, and increased product purchases related to the manufacture of the C-Pulse System.Net loss in the first quarter of 2015 was $7.1 million, or $0.40 per share, compared to a net loss of $6.3 million, or $0.38 per share in the first quarter of 2014. Excluding equity compensation expense, first quarter 2015 and 2014 net non-GAAP losses totaled $6.2 million, or $0.35 per share and $5.6 million, or $0.33 per share, respectively.Cash used in operating activities totaled $7.1 million for the first quarter of 2015 compared to $6.7 million for the first quarter of 2014, with the increase driven primarily by higher research, development and clinical expenses. During the first quarter of 2015, the Company received net proceeds provided by financing activities of $12.9 million, as follows: $6.9 million from the sale of common shares under the Company's existing At-The-Market facility (ATM), and $6.0 million from borrowings under a $10.0 million debt facility with Silicon Valley Bank. In the first quarter of 2014, the Company had $16,000 in proceeds from the exercise of warrants. The Company ended the first quarter of 2015 with $37.0 million in cash and cash equivalents, compared to $31.3 million at December 31, 2014. The Company believes that the combination of the ATM and the debt facility should provide the Company with sufficient capital through 2016, assuming no acceleration to the fully implantable C-Pulse System development timeline.
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Column 1 |
0 |
SUNSHINE HEART, INC. AND SUBSIDIARIESCondensed Consolidated Statements of Operations and Comprehensive Loss (Unaudited)(In thousands, except per share amounts) |
|
|
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Three months ended |
March 31, |
2015 |
2014Net sales |
$ 59 |
$ 59 |
|
Operating expenses: |
|
Selling, general and administrative |
2,186 |
2,361Research and development |
4,865 |
4,063Total operating expenses |
7,051 |
6,424Loss from operations |
(6,992) |
(6,365)Other income (expense), net |
(66) |
33Loss before income taxes |
(7,058) |
(6,332)Income tax expense |
5 |
--Net loss |
$ (7,063) |
$ (6,332) |
|
Basic and diluted loss per share |
$ (0.40) |
$ (0.38) |
|
Weighted average shares outstanding - basic and diluted |
17,509 |
16,859 |
|
Other comprehensive income: |
|
Foreign currency translation adjustments |
$ 10 |
$ (19)Total comprehensive loss |
$ (7,053) |
$ (6,351) |
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|
|
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