WIXOM, Mich., March 15, 2017 (GLOBE NEWSWIRE) — Rockwell Medical, Inc. (NASDAQ:RMTI), a fully-integrated biopharmaceutical company targeting end-stage renal disease (ESRD) and chronic kidney disease (CKD) with innovative products and services for the treatment of iron replacement, secondary hyperparathyroidism and hemodialysis, reported results for the quarter and year ending December 31, 2016.
Q4 2016 Financial Highlights
- Sales were $13.4 million, or $0.7 million lower than Q4 2015, primarily due to lower domestic and lower contract manufacturing concentrate sales.
- Gross profit was $2.0 million compared to $2.1 million in Q4 2015.
- SG&A expense was $6.0 million compared $6.1 million in Q4 2015.
- R&D expense was $1.2 million compared to $2.0 million in Q4 2015.
- Net loss was $5.1 million or ($0.10) per share compared to a $5.8 million loss or ($0.12) per share in Q4 2015. Net loss was $0.7 million less year over year primarily due to lower R&D expense of $0.8 million.
- Cash and investments were $57.9 million as of December 31, 2016.
- Net working capital was $68.4 million as of December 31, 2016.
2016 Financial Highlights
- Sales were $53.3 million compared to $55.4 million in 2015, primarily due to lower contract manufacturing sales and lower international concentrate sales.
- Gross profit was $6.8 million compared to $8.9 million in 2015. Gross profit was impacted by increased drug product costs of $1.5 million, lower third party contract manufacturing revenue and a $0.2 million value add tax paid on the $4.0 million received from Wanbang Biopharma.
- SG&A expense was $21.1 million compared $19.1 million in 2015.
- R&D expense was $5.8 million compared to $5.0 million in 2015.
- Net loss was $19.8 million or ($0.39) per share versus $14.4 million or ($0.29) per share in 2015.
- Cash used in operating activities in 2016 was $12.5 million of which R&D related expense was $5.8 million and investment in Triferic inventory was $6.1 million.
2016 Corporate Highlights
- Made significant progress to secure transitional add-on reimbursement for Triferic.
- Formed wholly owned subsidiary in India to initiate commercialization activities of Triferic in India.
- Secured partnership in Canada for distribution of Triferic.
- Advanced clinical development with several new indications for Triferic, including peritoneal dialysis, total parenteral nutrition and orphan indication IRIDA.
- Triferic Phase-1 Healthy Volunteer Intravenous (IV) Pharmacokinetic Study published in the September 2016 edition of the Journal of Clinical Pharmacology.
- Received FDA approval to market Triferic powder packet.
- Built redundancy into Triferic product supply chain to manage anticipated customer demand.
- Entered into license agreement with ARAM Medical to market Triferic in Saudi Arabia, Egypt and Middle Eastern countries.
- Partnered with Wanbang Biopharma to commercialize Triferic and Calcitriol in the People’s Republic of China, receiving up to $39 million in milestone payments and ongoing profit on commercial product sales in China.
Mr. Robert L. Chioini, Chairman and Chief Executive Officer of Rockwell stated, “We are pleased and excited with our progress to obtain transitional add-on reimbursement for Triferic. Our effort and movement on the add-on reimbursement front has been very strong and we feel we are closer to our goal of securing it. We continue to garner support from key stakeholders for add-on reimbursement for Triferic. We are also very pleased with the response, and the positive clinical findings being reported from dialysis providers using Triferic through our drug sample program. Our marketing and education efforts on Triferic have been well received and continue to be very effective.” Mr. Chioini also stated, “We have advanced our clinical development work for Triferic in both the China and India markets, while implementing the necessary clinical steps to advance the use of Triferic in the Peritoneal dialysis, Total Parenteral Nutrition and Cancer markets.”
Conference Call Information
Rockwell Medical will be hosting a conference call to review its fourth quarter and year end 2016 results on Wednesday, March 15, 2017 at 4:30 pm ET. Investors are encouraged to call a few minutes in advance at (888) 438-5453, or for international callers (719) 457-2637, passcode # 8360933 or to listen to the call via webcast at the Rockwell Medical IR web page: http://ir.rockwellmed.com/
Triferic is the only FDA approved drug indicated to replace iron and maintain hemoglobin in hemodialysis patients suffering from anemia. Via dialysate during each dialysis treatment, Triferic replaces the 5-7 mg iron loss that occurs in all patients, effectively maintaining their iron balance. Unlike IV iron products, Triferic binds iron immediately and completely to transferrin (carrier of iron in the body) upon entering the blood and it is then transported directly to the bone marrow to be incorporated into hemoglobin, with no increase in ferritin (stored iron and inflammation) and no anaphylaxis, addressing a significant unmet need in overcoming Functional Iron Deficiency (FID) in ESRD patients. Please visit www.triferic.com to view the Triferic mode-of-action (MOA) video and for more information.
About Rockwell Medical
Rockwell Medical is a fully-integrated biopharmaceutical company targeting end-stage renal disease (ESRD) and chronic kidney disease (CKD) with innovative products and services for the treatment of iron replacement, secondary hyperparathyroidism and hemodialysis.
Rockwell’s recent FDA approved drug Triferic is indicated for iron replacement and maintenance of hemoglobin in hemodialysis patients. Triferic delivers iron to patients during their regular dialysis treatment, using dialysate as the delivery mechanism. Triferic has demonstrated that it safely and effectively delivers sufficient iron to the bone marrow and maintains hemoglobin, without increasing iron stores (ferritin). Rockwell intends to market Triferic to hemodialysis patients in the U.S. dialysis market and globally.
Rockwell’s FDA approved generic drug Calcitriol is for treating secondary hyperparathyroidism in dialysis patients. Calcitriol (active vitamin D) injection is indicated in the management of hypocalcemia in patients undergoing chronic renal dialysis. It has been shown to significantly reduce elevated parathyroid hormone levels. Reduction of PTH has been shown to result in an improvement in renal osteodystrophy. Rockwell intends to market Calcitriol to hemodialysis patients in the U.S. dialysis market.
Rockwell is also an established manufacturer and leader in delivering high-quality hemodialysis concentrates/dialysates to dialysis providers and distributors in the U.S. and abroad. As one of the two major suppliers in the U.S., Rockwell’s products are used to maintain human life by removing toxins and replacing critical nutrients in the dialysis patient’s bloodstream. Rockwell has three U.S. manufacturing/distribution facilities.
Rockwell’s exclusive renal drug therapies support disease management initiatives to improve the quality of life and care of dialysis patients and are intended to deliver safe and effective therapy, while decreasing drug administration costs and improving patient convenience. Rockwell Medical is developing a pipeline of drug therapies, including extensions of Triferic for indications outside of hemodialysis. Please visit www.rockwellmed.com for more information.
Certain statements in this press release constitute “forward-looking statements” within the meaning of the federal securities laws, including, but not limited to, Rockwell’s intention to sell and market Calcitriol and Triferic. Words such as “may,” “might,” “will,” “should,” “believe,” “expect,” “anticipate,” “estimate,” “continue,” “predict,” “forecast,” “project,” “plan”, “intend” or similar expressions, or statements regarding intent, belief, or current expectations, are forward-looking statements. While Rockwell Medical believes these forward-looking statements are reasonable, undue reliance should not be placed on any such forward-looking statements, which are based on information available to us on the date of this release. These forward looking statements are based upon current estimates and assumptions and are subject to various risks and uncertainties, including without limitation those set forth in Rockwell Medical’s SEC filings. Thus, actual results could be materially different. Rockwell Medical expressly disclaims any obligation to update or alter statements whether as a result of new information, future events or otherwise, except as required by law.
Triferic® is a registered trademark of Rockwell Medical, Inc.
|ROCKWELL MEDICAL, INC. AND SUBSIDIARIES|
|CONSOLIDATED INCOME STATEMENTS|
|For the three and twelve months ended December 31, 2016 and December 30, 2015|
|Three Months Ended
December 31, 2016
|Three Months Ended
December 31, 2015
|Cost of Sales||11,401,603||12,076,489||46,531,648||46,412,848|
|Selling, General and Administrative||6,049,663||6,089,606||21,120,901||19,078,867|
|Research and Product Development||1,200,729||2,029,736||5,840,346||4,961,313|
|Operating Income (Loss)||(5,262,209||)||(6,063,194||)||(20,208,729||)||(15,102,326||)|
|Interest and Investment Income||207,911||293,238||810,340||681,876|
|Income (Loss) Before Income Taxes||(5,054,298||)||(5,769,956||)||(19,398,389||)||(14,420,450||)|
|Income Tax Expense||—||—||(404,527||)||—|
|Net Income (Loss)||$||(5,054,298||)||$||(5,769,956||)||$||(19,802,916||)||$||(14,420,450||)|
|Basic Earnings (Loss) per Share||$||(0.10||)||$||(0.12||)||$||(0.39||)||$||(0.29||)|
|Diluted Earnings (Loss) per Share||$||(0.10||)||$||(0.12||)||$||(0.39||)||$||(0.29||)|
|ROCKWELL MEDICAL, INC. AND SUBSIDIARIES|
|CONSOLIDATED BALANCE SHEETS|
|As of December 31, 2016 and December 31, 2015|
|December 31,||December 31,|
|Cash and Cash Equivalents||$||17,180,594||$||31,198,182|
|Investments Available for Sale||40,759,703||39,482,732|
|Accounts Receivable, net of a reserve of $5,000 in 2016 and $75,000 in 2015||6,393,228||5,046,733|
|Other Current Assets||2,034,598||1,026,889|
|Total Current Assets||78,509,195||84,626,316|
|Property and Equipment, net||1,391,575||1,646,568|
|Other Non-current Assets||501,187||462,839|
|LIABILITIES AND SHAREHOLDERS’ EQUITY|
|Total Current Liabilities||10,145,602||8,091,451|
|Deferred License Revenue||20,051,737||17,410,852|
|Common Shares, no par value, 51,527,711 and 51,501,877 shares issued and outstanding||268,199,939||257,773,494|
|Accumulated Other Comprehensive Income||(902,548||)||(915,496||)|
|Total Shareholders’ Equity||52,956,299||62,319,822|
|Total Liabilities And Shareholders’ Equity||$||83,153,638||$||87,822,125|
|ROCKWELL MEDICAL, INC. AND SUBSIDIARIES|
|CONSOLIDATED STATEMENTS OF CASH FLOWS|
|For the years ended December 31, 2016 and December 31, 2015|
|Cash Flows From Operating Activities:|
|Adjustments To Reconcile Net Loss To Net Cash Used In Operating Activities:|
|Depreciation and Amortization||762,368||822,294|
|Share Based Compensation—Employees||10,346,284||8,887,977|
|Restricted Stock Retained in Satisfaction of Tax Liabilities||—||(2,912,859||)|
|Loss on Disposal of Assets||8,168||5,281|
|Loss on Sale of Investments Available for Sale||26,820||58,095|
|Changes in Assets and Liabilities:|
|(Increase) in Accounts Receivable||(1,162,469||)||(574,731||)|
|(Increase) in Inventory||(6,095,846||)||(3,951,595||)|
|(Increase) in Other Assets||(1,230,084||)||(360,303||)|
|(Decrease) in Accounts Payable||1,863,018||(1,299,299||)|
|(Decrease) in Other Liabilities||191,134||(413,652||)|
|Increase (decrease) in Deferred License Revenue||(2,065,785||)||(2,081,668||)|
|Increase (decrease) in Deferred Drug License Revenue||4,706,670||—|
|Changes in Assets and Liabilities||(3,793,362||)||(8,681,248||)|
|Cash (Used) In Provided By Operating Activities||(12,452,638||)||(16,240,910||)|
|Cash Flows From Investing Activities:|
|Purchase of Investments Available for Sale||(25,781,853||)||(21,800,000||)|
|Sale of Investments Available for Sale||24,491,677||1,468,656|
|Purchase of Equipment||(355,264||)||(815,002||)|
|Proceeds on Sale of Assets||1,000||4,800|
|Cash (Used In) Investing Activities||(1,644,440||)||(21,141,546||)|
|Cash Flows From Financing Activities:|
|Proceeds from Issuance of Common Shares and Purchase Warrants||80,161||2,780,187|
|Cash Provided By Financing Activities||80,161||2,780,187|
|Effects of exchange rate changes||(671||)||—|
|(Decrease) Increase In Cash||(14,017,588||)||(34,602,269||)|
|Cash At Beginning Of Period||31,198,182||65,800,451|
|Cash At End Of Period||$||17,180,594||$||31,198,182|
CONTACT: Michael Rice, Investor Relations; 646-597-6979