Positive 24-Week Clinical Data for ALD403 in Chronic Migraine Continues to Demonstrate a Best-In-Class Profile as Company Advances Toward a BLA Submission
Advances Second Program Directed at Migraine Prevention, ALD1910, into IND-Enabling Studies
BOTHELL, Wash., July 26, 2016 (GLOBE NEWSWIRE) -- Alder BioPharmaceuticals, Inc. (NASDAQ:ALDR), a clinical-stage biopharmaceutical company developing monoclonal antibody therapeutics, today provided a corporate update and reported its financial and operating results for the second quarter ended June 30, 2016.
"Led by the positive top-line 24 week data in chronic migraine announced yesterday, we continue to execute successfully against our plan to advance ALD403 toward an FDA submission and the goal of marketing a best-in-class migraine prevention antibody therapy," said Randall C. Schatzman, Ph.D., president and chief executive officer of Alder. "We are on schedule to initiate our second pivotal study of ALD403, PROMISE 2, later this year and to advance our alternate ALD403 formulation suitable for administration as a single quarterly sub-cutaneous or intra-muscular injection into advanced studies. Lastly, we are doubling our efforts to meet the needs of millions of people living with migraine by bringing forward a second drug candidate directed at migraine prevention, ALD1910, our PACAP-38 directed antibody. This action further reinforces our strategy to build a specialty sales force capable of successfully marketing multiple agents in the CNS arena, thereby increasing shareholder value."
Recent Pipeline and Corporate Highlights
ALD403 — Pivotal-stage monoclonal antibody candidate inhibiting the calcitonin gene-related peptide (CGRP) and being evaluated for migraine prevention
Clazakizumab — Monoclonal antibody, discovered by Alder, designed to block interleukin-6 (IL-6), which plays a key role in the inflammatory cascade
Expected Upcoming Events and Milestones
Second Quarter Ended June 30, 2016 Financial Results
For the second quarter ended June 30, 2016, Alder recorded approximately $0.1 million of revenue under license agreement with Vitaeris relating to a sale of clazakizumab inventory to Vitaeris at cost. Alder did not record any revenue in the second quarter of 2015.
Research and development expenses for the second quarter ended June 30, 2016, totaled $33.8 million, compared to $14.1 million for the same period in 2015. The increase in spending was primarily due to the ALD403 development program, and consisted of costs related to PROMISE 1 and other ongoing clinical trials and manufacturing costs of drug supplies in support of existing and planned pivotal clinical trials. In addition, Alder incurred increased compensation costs due to an increase in Alder's research and development headcount to support the pivotal trial program for ALD403 and an increase in stock-based compensation.
General and administrative expenses for the second quarter ended June 30, 2016, totaled $6.5 million, compared to $3.9 million for the same period in 2015. The increase was primarily due to compensation costs as a result of an increase in stock-based compensation and general and administrative headcount, as well as increases in market research and other administrative costs.
Alder recognized a gain of $1.1 million on licensing clazakizumab to Vitaeris in the second quarter ended June 30, 2016.
Net loss for the second quarter ended June 30, 2016, totaled $38.9 million, or $0.79 per share, compared to a net loss of $17.7 million, or $0.46 per share, on a fully-diluted basis, for the same period in 2015.
As of June 30, 2016, Alder had $450.1 million in cash, cash equivalents and investments which included net proceeds from Alder's April 2016 public offering, compared to $353.3 million as of March 31, 2016.
Conference Call and Webcast
Alder will host a conference call today at 5:00 p.m. ET to discuss these financial results and provide a general business update. The live call may be accessed by dialing (877) 430-4657 for domestic callers or (484) 756-4339 for international callers, and providing conference ID number 29548578. The webcast will be broadcast live on the Events & Presentations page of the Investors section of Alder's website at www.alderbio.com and will be available for replay following the call for 30 days.
About Alder BioPharmaceuticals, Inc.
Alder BioPharmaceuticals, Inc., is a clinical-stage biopharmaceutical company that discovers, develops and seeks to commercialize therapeutic antibodies with the potential to meaningfully transform current treatment paradigms. ALD403, Alder's lead pivotal-stage product candidate being evaluated for migraine prevention, is a genetically engineered monoclonal antibody that inhibits calcitonin gene-related peptide. Alder is additionally evaluating ALD1910, a preclinical product candidate also in development as a migraine prevention therapy. ALD1910 is a monoclonal antibody targeting pituitary adenylate cyclase-activating polypeptide-38 (PACAP-38), a protein that is active in mediating the initiation of migraine. Clazakizumab, Alder's third program, is a monoclonal antibody candidate designed to block interleukin-6 and is licensed to Vitaeris, Inc. For more information, please visit http://www.alderbio.com.
This press release contains forward-looking statements, including, without limitation, statements relating to: the continued development and clinical, therapeutic and commercial potential of ALD403 and ALD1910; the initiation of future clinical trials and studies; future regulatory filings; the anticipated commercialization of ALD403; Alder's marketing strategy and expected increase in shareholder value; and Alder's potential receipt of royalties and other payments under the license agreement with Vitaeris. Words such as "continues," "demonstrate," "advance," "plan," "toward," "goal," "on schedule," "initiate," "meet," "bringing forward," "directed," "strategy," "build," "value," "confirm," "extend," "eligible," "will," "believes," "potential," "may," "expected," "upcoming," "intended," "support," "objective," "announce," or other similar expressions, identify forward-looking statements, but the absence of these words does not necessarily mean that a statement is not forward-looking. In addition, any statements that refer to expectations, projections or other characterizations of future events or circumstances are forward-looking statements. The forward-looking statements in this press release are based upon Alder's current plans, assumptions, beliefs, expectations, estimates and projections, and involve substantial risks and uncertainties. Actual results and the timing of events could differ materially from those anticipated in the forward-looking statements due to these risks and uncertainties as well as other factors, which include, without limitation: risks related to the potential failure of ALD403 and ALD1910 to demonstrate safety and efficacy in clinical testing; Alder's ability to conduct clinical trials of ALD403 and ALD1910 sufficient to achieve a positive completion; the availability of data at the expected times; the clinical, therapeutic and commercial value of ALD403 and ALD1910; risks and uncertainties related to regulatory application, review and approval processes and Alder's compliance with applicable legal and regulatory requirements; the uncertain timing and level of expenses associated with the development of ALD403 and ALD1910; the sufficiency of Alder's capital and other resources; Alder's reliance on Vitaeris for the development of clazakizumab; market competition; changes in economic and business conditions; and other factors discussed under the caption "Risk Factors" in Alder's Quarterly Report on Form 10-Q for the quarterly period ended June 30, 2016, which was filed with the Securities and Exchange Commission (SEC) on July 26, 2016, and is available on the SEC's website at www.sec.gov. Additional information will also be set forth in Alder's other reports and filings it will make with the SEC from time to time. The forward-looking statements made in this press release speak only as of the date of this press release. Alder expressly disclaims any duty, obligation or undertaking to release publicly any updates or revisions to any forward-looking statements contained herein to reflect any change in Alder's expectations with regard thereto or any change in events, conditions or circumstances on which any such statements are based.
|Condensed Consolidated Balance Sheets|
|(Amounts in thousands)|
|June 30,||December 31,|
|Cash, cash equivalents and investments||$||450,107||$||381,012|
|Prepaid expenses and other assets||24,270||19,015|
|Total stockholders' equity||458,067||387,517|
|Total liabilities and stockholders' equity||$||474,377||$||400,027|
|Condensed Consolidated Statements of Operations|
|(Amounts in thousands, except share and per share data)|
|Three Months Ended||Six Months Ended|
|June 30,||June 30,|
|Revenue under license agreement||$||113||$||—||$||113||$||—|
|Cost of sales||113||—||113||—|
|Research and development||33,833||14,088||61,480||25,123|
|General and administrative||6,466||3,930||12,511||7,607|
|Total operating expenses||40,412||18,018||74,104||32,730|
|Gain on license of clazakizumab||1,050||—||1,050||—|
|Loss from operations||(39,249||)||(18,018||)||(72,941||)||(32,730||)|
|Other income, net||383||363||712||422|
|Net loss per share - basic and diluted||$||(0.79||)||$||(0.46||)||$||(1.55||)||$||(0.86||)|
|Weighted average number of common shares used in net loss per share - basic and diluted||49,284,573||38,162,226||46,519,045||37,536,331|
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