Conference Call Scheduled Today at 8:30 a.m. ET
WILMINGTON, Del.--(BUSINESS WIRE)-- Incyte Corporation (Nasdaq:INCY) today reported first quarter 2010 financial results and provided an update on recent clinical accomplishments, including positive top-line results from an ongoing six-month, dose-ranging Phase II trial to evaluate INCB28050 in rheumatoid arthritis (RA) patients.
Paul A. Friedman, M.D., Incyte's President and Chief Executive Officer, stated, "We have achieved positive three-month Phase II results for INCB28050, our oral JAK1/JAK2 inhibitor, for rheumatoid arthritis. The efficacy results from this study are very encouraging and compare favorably not only with marketed RA treatments, in particular biologics, but also with oral molecules in development. We look forward to presenting the full six-month results from this trial at the American College of Rheumatology meeting in November.”
To preserve Incyte’s ability to present the final data from this study at the American College of Rheumatology (ACR) meeting, only top-line efficacy and safety results are being described at this time. The three-month results from the ongoing six-month Phase II trial involving 125 rheumatoid arthritis patients considered to be inadequately controlled by any disease modifying anti-rheumatic drug (DMARD) therapy, including patients previously treated with biologics, are as follows:
Summary of Safety Results2
INCB28050 was generally well tolerated in this study. Nearly all adverse events were mild to moderate in intensity with frequency similar to that observed in patients treated with placebo. The only serious adverse event in the study was an unrelated gastrointestinal bleed. There were no cases of thrombocytopenia. Hemoglobin and hematocrit levels remained steady in patients treated with 4 mg or 7 mg once daily while the 10 mg once daily dose showed a modest decrease over time.
Richard Levy, Incyte’s Executive Vice President, Chief Drug Development and Medical Officer, added, "Given the efficacy and safety seen with the lowest dose, 4 mg once-daily, it’s possible that even lower doses may be effective, suggesting that INCB28050 could provide a wide therapeutic window.”
Below is a summary of other recent accomplishments:
JAK1/JAK2 Inhibitor: INCB18424 (oral formulation) for Myelofibrosis (MF), Polycythemia Vera (PV) and Essential Thrombocythemia (ET)
JAK1/JAK2 Inhibitor: INCB18424 (topical formulation) for Psoriasis
Sheddase Inhibitor: INCB7839 for Breast Cancer
cMET Inhibitor: INCB28060 for Solid Tumors
CCR2 Antagonist Program
1 ACR American College of Rheumatology (ACR) score
2 Safety and tolerability as measured by adverse events, vital signs, clinical laboratory tests and electrocardiography
3 Copies of the poster and oral presentation will be available immediately after each session at: www.incyte.com:
First Quarter 2010 Financial Results
As of March 31, 2010, cash, short-term and long-term marketable securities totaled $422.3 million, excluding $56.5 million in restricted cash for an escrow account reserved for the first three years of interest payments on the 4.75% Convertible Senior Notes, compared to $473.9 million as of December 31, 2009. The Company used $43.0 million in cash and marketable securities during the first quarter of 2010, excluding $158.6 million used for the redemption of the remaining 3 1/2% Convertible Senior and Subordinated Notes, the $60 million milestone payment from Novartis for the initiation of the COMFORT II clinical trial and the $90 million upfront payment related to its collaborative agreement with Lilly.
Total revenues for the quarter ended March 31, 2010 were $17.3 million as compared to $0.7 million for the same period in 2009. The increase was primarily the result of revenues recognized under the Company's collaborative agreements with Novartis and Lilly.
As a result of the $33 million in payments expected to be received in connection with milestones from Lilly and Pfizer, we are increasing our revenue guidance from $66 to $68 million to $99 to $101 million for 2010.
The net loss for the quarter ended March 31, 2010 was $35.7 million, or $0.30 per share, as compared to $40.0 million, or $0.41 per share, for the same period in 2009. Included in the net loss for the quarter ended March 31, 2010 was a non-cash charge of $4.0 million or $0.03 per share related to the redemption of the 3 1/2% Convertible Senior and Subordinated Notes.
Also included in the net loss for the quarter ended March 31, 2010 was $3.1 million of non-cash expense related to the impact of expensing share-based payments, including employee stock options, as compared to $3.4 million for the same period in 2009.
Research and development expenses for the quarter ended March 31, 2010 were $31.4 million as compared to $29.6 million for the same period last year. Included in research and development expenses for the quarter ended March 31, 2010 was $2.2 million of non-cash expense related to the impact of expensing share-based payments, including employee stock options, as compared to $2.5 million for the same period in 2009. The Company expects its research and development expenses to vary from quarter to quarter, primarily due to the timing of its clinical development activities.
Selling, general and administrative expenses for the quarter ended March 31, 2010 were $5.8 million as compared to $4.8 million for the same period last year. Increased selling, general and administrative expenses for the quarter ended March 31, 2010 reflected the Company's initial sales and marketing activities for the potential commercialization of INCB18424 for myelofibrosis. Also included in selling, general and administrative expenses for the quarter ended March 31, 2010 and 2009 was $0.9 million of non-cash expense related to the impact of expensing share-based payments, including employee stock options.
Interest expense for the three months ended March 31, 2010 was $11.8 million as compared to $6.3 million for the comparable period last year. Included in interest expense for the quarter ended March 31, 2010, was $0.5 million of non-cash charges to amortize the discount on the Company's 3 1/2% Convertible Senior Notes as compared to $2.3 million for the same period in 2009. Also included in interest expense for the quarter ended March 31, 2010 was $4.8 million of non-cash charges to amortize the discount on the Company's 4.75% Convertible Senior Notes.
Conference Call Information
Incyte will hold its first quarter 2010 financial results conference call this morning at 8:30 a.m. ET. To access the conference call, please dial 877-407-8037 for domestic callers or 201-689-8037 for international callers. When prompted, provide the passcode, which is 349566.
If you are unable to participate, a replay of the conference call will be available for thirty days. The replay dial-in number for the U.S. is 877-660-6853 and dial-in number for international callers is 201-612-7415. To access the replay you will need the conference account number 278 and the ID number 349566.
Incyte Corporation is a Wilmington, Delaware-based drug discovery and development company focused on developing proprietary small molecule drugs for oncology and inflammation. Incyte's most advanced compound, INCB18424, is in Phase III development for myelofibrosis. For additional information on Incyte, visit the Company's web site at www.incyte.com.
Except for the historical information contained herein, the matters set forth in this press release, including statements with respect to the top-line three-month results of INCB28050 comparing favorably with other marketed RA treatments and molecules in development, Incyte’s intent to present full six-month results for INCB28050 at the ACR meeting in November, the possibility that lower doses of INCB28050 may be effective and that INCB28050 could provide a wide therapeutic window, the presentation of results for topical INCB18424 for mild-to-moderate psoriasis at the Society of Dermatology Meeting in May, the poster presentation for INCB7839 at the 2010 ASCO Annual Meeting in June and Best of ASCO San Francisco Meeting in July, financial guidance about expected revenue and the expected variability of quarterly research and development expenses, are all forward-looking statements within the meaning of the "safe harbor" provisions of the Private Securities Litigation Reform Act of 1995.
These forward-looking statements are subject to risks and uncertainties that may cause actual results to differ materially, including the high degree of risk and uncertainty associated with drug development and clinical trials, the uncertainty associated with the regulatory approval processes, risks related to the timing of and patient enrollment in clinical trials, unanticipated developments in and risks related to the efficacy or safety of Incyte's compounds in clinical trials, the results of further research and development, risks associated with Incyte's dependence on its relationships with its collaboration partners, risks and uncertainties that may cause the parties not to achieve some or all of the commercial and developmental milestones set forth in the collaborative agreements, the risks related to market competition, and other risks detailed from time to time in Incyte's filings with the Securities and Exchange Commission, including its Annual Report on Form 10-K for the year ended December 31, 2009. Incyte disclaims any intent or obligation to update these forward-looking statements.
Condensed Consolidated Statements of Operations
(in thousands, except per share amounts)
Three Months Ended
|License and royalty revenues||551||671|
|Costs and expenses:|
|Research and development||31,439||29,587|
|Selling, general and administrative||5,794||4,821|
|Total costs and expenses||37,118||34,917|
|Loss from operations||(19,830||)||(34,246||)|
|Interest and other income (expense), net||195||548|
|Loss on debt redemption||(3,988||)||—|
|Loss before income taxes||(35,402||)||(40,036||)|
|Provision for income taxes||327||—|
|Basic and diluted net loss per share:||$||(0.30||)||$||(0.41||)|
|Shares used in computing basic and diluted net loss per share||119,727||97,340|
Condensed Consolidated Balance Sheet Data
|Cash, cash equivalents, and short-term and long-term marketable securities||$||422,254||$||473,931|
|Convertible senior notes||261,408||308,059|
|Convertible subordinated notes||16,292||135,079|
|Total stockholders’ deficit||(114,413||)||(102,384||)|
Pamela M. Murphy, Vice President, Investor Relations/Corporate Communications, 302-498-6944
KEYWORDS: United States North America Delaware Pennsylvania
INDUSTRY KEYWORDS: Health Biotechnology Clinical Trials Fitness & Nutrition Oncology Pharmaceutical Other Health Research Other Science Science General Health