SINGAPORE, July 25, 2012 /PRNewswire-Asia/ -- Biosensors International Group, Ltd. ("Biosensors" or the "Company", Bloomberg: BIG SP; Reuters: BIOS.SI; SGX: B20), a developer, manufacturer and marketer of innovative medical devices, today announced financial results for its first fiscal quarter ended 30 June 2012 ("Q1 FY13").
Q1 FY13 Highlights:
"We have achieved yet another quarter of strong growth in our revenues, profits and operating cash flow. This is due to the sustained robust growth in the IVP sales, consolidation of the operating results of JW Medical System Ltd. ("JWMS"), and increased licensing revenue," commented CEO Dr. Jack Wang. "During the EuroPCR, we announced four-year data from the DIVERGE study, which showed that the use of our Axxess™ bifurcation DES resulted in positive clinical results.(2) We continue to see encouraging growth in physicians' adoption of Axxess™. At the same time, we also announced that our BioMatrix Flex™ was chosen as the stent platform for GLOBAL LEADERS, the largest ever clinical trial involving a DES, and also our plans for LEADERS FREE, the first large-scale study for our BioFreedom™ DCS, which is awaiting CE Mark approval. This demonstrates our commitment to build a significant body of clinical evidence before commercializing BioFreedom."
Performance Summary for Q1 FY13
For Q1 FY13, Biosensors reported total revenue, including licensing and royalties, of US$86.3 million, a 51% increase over US$57.0 million in the first quarter of fiscal year 2012 ("Q1 FY12"). Correspondingly, IVP sales rose to US$65.7 million, up 74% from US$37.7 million in Q1 FY12. This was largely due to the full-quarter consolidation of JWMS' results and continued growth in the sales of the Company's BioMatrix™ family of DES. Sales revenue of critical care products ("CCP") was US$3.3 million, compared to US$3.7 million in the same period last year.
Licensing and royalties revenue grew to US$17.3 million, a year-on-year increase of 10% from US$15.6 million in Q1 FY12.
Gross margin on total revenue rose to 85% for the quarter from 82% in the previous quarter and 81% in Q1 FY12. Gross margin on total product sales was 81%, compared to 76% in the previous quarter and 74% in Q1 FY12. Reduction in manufacturing cost, favorable geographical and product mix contributed to the improvement in the gross product margin.
Overall operating expense as a percentage of total revenue for the quarter was 46% compared to 40% in Q1 FY12.
In detail, the quarter's sales and marketing ("S&M") expense was US$22.3 million; general and administrative ("G&A") expense was US$10.1 million; research and development ("R&D") expense, which included costs for new product development and testing, clinical trials, patent registration and regulatory approval, was US$6.3 million. As a percentage of total revenue, Q1 FY13 S&M expense was 26%, compared to 28% in Q1 FY12; G&A expense was 12% compared to 11%, while R&D expense was 7% versus 8%.
For the quarter, the Group's operating profit was US$33.7 million, representing a 44% year-on-year increase compared to the same period last year.
Excluding exceptional items, which comprise fair value adjustments for warrants and provisions for restructuring expenses, net profit for Q1 FY13 would have been US$28.3 million or basic earnings per share ("basic EPS") of 1.65 US cents and diluted earnings per share ("diluted EPS") of 1.62 US cents. This compares to a net profit of US$24.1 million or basic EPS of 1.80 US cents and diluted EPS of 1.76 US cents for Q1 FY12 after excluding the fair value adjustments for warrants.
Including exceptional and non-operating items, net profit for Q1 FY13 was US$32.6 million or basic EPS of 1.90 US cents and diluted EPS of 1.86 US cents compared to a net profit of US$22.6 million or basic EPS of 1.68 US cents and diluted EPS of 1.64 US cents for Q1 FY12.
The Company maintains its full-year financial guidance. For the fiscal year ending 31 March 2013 ("FY13"), management anticipates total revenue to grow by 20% to 30% over FY12, driven by continued strong DES revenue growth as well as modest licensing and royalty revenue increase. The Company expects FY13 profitability, excluding exceptional items, to increase overall but anticipates that the higher revenues will be partially offset by increased expenses required to support revenue growth and development of future products.
"Looking ahead, despite the challenging global macro economic developments, we remain confident about our growth prospects for the fiscal year," concluded Dr. Wang. "Our DES growth stays strong. At the same time, we are committed to continue boosting our competitiveness by demonstrating more positive clinical evidence with our existing and pipeline products. On the merger and acquisition front, we will continue to explore various opportunities to grow Biosensors to greater heights."
About Biosensors International Group, Ltd
Biosensors International develops, manufactures and markets innovative medical devices for interventional cardiology and critical care procedures. We aim to improve patients' lives through pioneering medical technology that pushes forward the boundaries of innovation.
With the increasing use of the BioMatrix™ family of drug-eluting stents and the recent launch of our Axxess™ self-expanding bifurcation drug-eluting stent, we are rapidly emerging as a leader in the global coronary stent market. The development of the BioFreedom™ drug-coated stent will further reinforce our market position.
All three stents incorporate Biolimus A9™ (BA9™), an anti-restenotic drug developed and patented by Biosensors specifically for use with drug-eluting stents. Both the BioMatrix stent family and the Axxess stent feature a unique abluminal biodegradable polymer coating, which fully degrades into carbon dioxide and water after six to nine months as it releases BA9. The BioMatrix stent family features workhorse stent platforms for a broad range of lesions, and the Axxess stent employs a self-expanding stent platform specifically designed for treating bifurcation lesions. BioFreedom, a completely polymer‐free stent abluminally coated with BA9, is currently undergoing clinical evaluation.
For more information, please visit www.biosensors.com.
Certain statements herein include forward-looking statements within the meaning of the U.S. Private Securities Litigation Reform Act of 1995. Forward-looking statements generally can be identified by the use of forward-looking terminology, such as "may," "will," "expect," "intend," "estimate," "anticipate," "believe," "project" or "continue" or the negative thereof or other similar words. All forward looking statements involve risks and uncertainties, including, but not limited to, customer acceptance and market share gains, competition from companies that have greater financial resources; introduction of new products into the marketplace by competitors; successful product development; dependence on significant customers; the ability to recruit and retain quality employees as Biosensors grows; and economic and political conditions globally. Actual results may differ materially from those discussed in, or implied by, the forward-looking statements. The forward-looking statements speak only as of the date of this release and Biosensors assumes no duty to update them to reflect new, changing or unanticipated events or circumstances.
Biosensors International Group
Mr. Wong Teck Yenn
Director, Investor Relations
|SOURCE Biosensors International Group, Ltd.|
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