Amag Reports Third Quarter And Nine Month 2013 Financial Results
The following excerpt is from the company's SEC filing
WALTHAM, MA (October 23, 2013) AMAG Pharmaceuticals, Inc. (NASDAQ: AMAG), a specialty pharmaceutical company, today reported unaudited consolidated financial results for the third quarter and nine months ended September 30, 2013. Total revenues for the third quarter of 2013 were $21.6 million, of which $19.3 million were U.S. net Feraheme® (ferumoxytol) sales, the highest Feraheme quarterly sales since launch in 2009. AMAG generated positive cash flows during the quarter and ended the third quarter with $213.5 million in cash and investments.
Our ability to deliver another quarter of record growth as we entered the fifth year of Ferahemes launch in the chronic kidney disease (CKD) patient population is a testament to the features of the product, as well as the drive and determination of the AMAG commercial team, said William Heiden, president and chief executive officer. Physicians across the U.S. recognize Feraheme as the iron deficiency anemia (IDA) treatment of choice for their patients with CKD and we will continue our efforts to drive growth in the CKD segment as we seek regulatory approval to expand the indication for Feraheme.
· The company reported record U.S. net Feraheme product sales of $18.7 million in the third quarter of 2013, compared to $14.1 million in the third quarter of 2012, representing a 33 percent increase; the product sales and growth figures for each period exclude the positive impact of the reduction of reserves for Medicaid rebates and product returns. The growth in product sales was primarily driven by increased volume across all segments of the non-dialysis market. Increasing net revenue per gram also contributed to the growth in net product sales, driven by the continued execution of AMAGs pricing strategy.
· Total Feraheme provider demand for the third quarter of 2013 hit a record level for the second consecutive quarter at approximately 36,200 grams, compared to approximately 27,500 grams in the third quarter of 2012.(1) Several strategies led to the sales success during the third quarter of 2013, including an effective contracting strategy that provided incentives for physicians to have Feraheme in-stock and available, especially important in the face of a new competitor.
Wholesaler inventory levels at the end of the third quarter of 2013 remained consistent with levels at the end of the second quarter of 2013.
· During the third quarter of 2013, AMAG prepared for, and began promoting MuGard® Mucoadhesive Oral Wound Rinse, which the company licensed from Access Pharmaceuticals, Inc. in June 2013. The company revised the promotional messaging, developed new promotional materials, and trained its sales force.
· In October 2013, AMAG announced that it had received notice of a 3-month extension of the PDUFA action date for the supplemental new drug application (sNDA) for Feraheme. The sNDA is seeking to expand the label for Feraheme to include all adult IDA patients who have failed or could not tolerate oral iron. The FDA informed the company of a new PDUFA action date of January 21, 2014, and a target date of December 23, 2013 to enter label discussions.
Third Quarter and Nine Month 2013 Financial Results (unaudited)
The fundamentals of our business have improved every quarter for the past year and a half, commented Frank Thomas, chief operating officer. Now that we have managed the business to positive cash flow levels this quarter, future growth in revenue, combined with continuing operating expense discipline, should provide positive earnings and drive further cash generation for AMAG to deploy towards expanding our portfolio further.
The company reported record U.S. net Feraheme product sales of $18.7 million (excluding a $0.6 million reduction of Medicaid reserves) for the third quarter of 2013, compared to $14.1 million (excluding a $2.1 million reduction of product return and Medicaid reserves) for the third quarter of 2012. For the nine months ended September 30, 2013, AMAG reported U.S. net Feraheme product sales of $51.8 million (excluding a $0.6 million reduction of Medicaid reserves), compared to $40.7 million (excluding a $3.2 million reduction of product return and Medicaid reserves) for the corresponding period in 2012.
Total revenues for the quarter ended September 30, 2013 were $21.6 million, as compared to $17.7 million for the third quarter of 2012. For the nine months ended September 30, 2013, AMAG reported total revenues of $59.1 million, as compared to revenues of $64.2 million for the corresponding period in 2012; the 2012 nine-month period was favorably impacted by the recognition of a $15 million milestone payment from Takeda Pharmaceutical Company Ltd. in June 2012 following the European regulatory approval of ferumoxytol for patients with IDA and CKD.
Feraheme cost of goods sold (COGS) for the quarter ended September 30, 2013 was $2.5 million, or 13 percent of Feraheme net product revenues, compared to $4.3 million, or 31 percent of Feraheme net product revenues for the quarter ended September 30, 2012. For the nine months ended September 30, 2013, Feraheme COGS were $8.4 million, or 16 percent of Feraheme net product revenues, compared to $10.0 million, or 25 percent of Feraheme net product revenues, for the corresponding period in 2012. COGS for the 2012 periods included expenses associated with the closing of the companys Cambridge, Massachusetts manufacturing facility.
Total operating expenses for the quarter ended September 30, 2013 were $19.5 million, compared to $18.0 million for the third quarter of 2012. The increase in total operating expenses for the quarter ended September 30, 2013 was due to higher selling, general and administrative costs, including certain one-time costs related to the companys relocation to a new corporate headquarters, which is expected to result in
lower annual rent expense over the next several years. Total operating expenses for the nine months ended September 30, 2013 were $58.1 million, 14 percent lower than 2012 nine-month operating expenses of $67.5 million, including $1.6 million in restructuring expenses. The decrease in total operating expenses in the nine months ended September 30, 2013 was due primarily to decreased research and development costs associated with the companys global IDA registration program and the benefits of a leaner corporate infrastructure implemented in 2012.
The company reported a net loss of $0.1 million, or a loss of $0.01 per basic and diluted share, for the quarter ended September 30, 2013, as compared to net a loss of $4.0 million, or $0.19 per basic and diluted share, for the third quarter of 2012. AMAG reported a net loss for the nine months ended September 30, 2013 of $5.9 million, or $0.28 per basic and diluted share, as compared to a net loss of $13.1 million, or $0.61 per basic and diluted share, for the corresponding period in 2012.
As of September 30, 2013, the companys cash and investments totaled approximately $213.5 million, reflecting net cash generated during the quarter of approximately $1.1 million.
Improved 2013 Financial Outlook
The company has updated its financial guidance for the full year of 2013. AMAG has:
· Increased its total revenue forecast to between $78 million and $81 million, including:
· U.S. Feraheme net product sales of between $69 million and $71 million;
· Revenues from other sources of between $9 million and $10 million, including ex-U.S. Feraheme/Rienso product sales, royalties and amortization of milestones as well as MuGard product sales;
· Narrowed the range of forecasted Feraheme COGS to between 15 percent and 17 percent of net Feraheme global product sales. Total COGS reported includes those associated with sales of MuGard;
· Lowered its total operating expense forecast to between $76 million and $80 million; and
· Increased its 2013 year-end cash and investments forecast to between $209 million and $213 million, including the upfront costs of the MuGard licensing transaction, but excluding the impact of future business development transactions.
Conference Call and Webcast Access
AMAG Pharmaceuticals, Inc. will host a conference call and webcast with slides today at 8:00 a.m. EDT, during which management will discuss the companys financial results and commercial progress. To access the conference call via telephone, please dial (877) 412-6083 from the United States or (702) 495-1202 for international access. A telephone replay will be available from approximately 11:00 a.m. EDT on October 23, 2013 through midnight on October 30, 2013. To access a replay of the conference call, dial (855) 859-2056 from the United States or (404) 537-3406 for international access. The pass code for the live call and the replay is 78527930.
The call will be webcast with slides and accessible through the Investors section of the companys website at www.amagpharma.com. The webcast replay will be available from approximately 11:00 a.m. EDT on October 23, 2013 through midnight November 22, 2013.
AMAG Pharmaceuticals, Inc.
Condensed Consolidated Statements of Operations
(unaudited, amounts in thousands, except per share data)
Three Months Ended September 30,
Nine months Ended September 30,
U.S. Feraheme product sales, net
Other product sales and royalties
License fee and other collaboration revenues
Operating costs and expenses:
Cost of product sales
Research and development expenses
Selling, general and administrative expenses
Total operating costs and expenses
Interest and dividend income, net
Gains on sale of assets
Gains (losses) on investments, net
Net loss before income taxes
Income tax benefit
Net loss per share
Basic and diluted
Weighted average shares outstanding used to compute net loss per share:
Basic and diluted
AMAG Pharmaceuticals, Inc.
Condensed Consolidated Balance Sheets
(unaudited, amounts in thousands)
September 30, 2013
December 31, 2012
Cash and cash equivalents
Accounts receivable, net
Receivable from collaboration
Assets held for sale
Other current assets
Total current assets
Property and equipment, net
Intangible assets, net
Total current liabilities
Acquisition-related contingent consideration, net
Other long-term liabilities
Total long-term liabilities
Total stockholders equity
Total liabilities and stockholders equity
AMAG Pharmaceuticals, Inc. is a specialty pharmaceutical company that markets Feraheme® (ferumoxytol) Injection and MuGard® Mucoadhesive Oral Wound Rinse in the United States. Along with driving organic growth of its products, AMAG intends to expand its portfolio with additional commercial-stage specialty products. The company is seeking complementary products that leverage the companys commercial footprint and focus on hematology and oncology centers and hospital infusion centers. For additional company information, please visit www.amagpharma.com.
AMAG Pharmaceuticals and Feraheme are registered trademarks of AMAG Pharmaceuticals, Inc. MuGard is a registered trademark of Access Pharmaceuticals, Inc. Rienso is a registered trademark of Takeda Pharmaceutical Company Limited.
Such risks and uncertainties include: (1) uncertainties regarding our and Takedas ability to successfully compete in the intravenous iron replacement market both in the U.S. and outside the U.S., including the EU, (2) uncertainties regarding our ability to compete in the oral mucositis market in the U.S., (3) uncertainties regarding our ability to successfully and timely complete our clinical development programs and obtain regulatory approval for Feraheme/Rienso in the broader IDA indication both in the U.S. and outside of the US, including the EU, (4) the possibility that significant safety or drug interaction problems could arise with respect to Feraheme/Rienso, and in turn affect sales, regulatory approval or our ability to market the product both in the U.S. and outside of the U.S., including the EU, (5) uncertainties regarding the manufacture of Feraheme/Rienso or MuGard, (6) uncertainties relating to our patents and proprietary rights, both in the U.S. and outside of the U.S., (7) the risk of an Abbreviated New Drug Application (ANDA) filing following the FDAs draft bioequivalence recommendation for ferumoxytol, (8) the risk that we may not realize the anticipated benefits of our licensing arrangement for and continued integration of MuGard and (9) other risks identified in our Securities and Exchange Commission filings, including our Quarterly Report on Form 10-Q for the quarter ended June 30, 2013 and subsequent filings with the SEC. We caution you not to place undue reliance on any forward-looking statements, which speak only as of the date they are made.
We disclaim any obligation to publicly update or revise any such statements to reflect any change in expectations or in events, conditions or circumstances on which any such statements may be based, or that may affect the likelihood that actual results will differ from those set forth in the forward-looking statements.
The above information was disclosed in a filing to the SEC. To see this filing in its entirety, click here.
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