SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549
Pursuant to Section 13 or 15(d) of the
Securities Exchange Act of 1934
Date of Report (Date of earliest event reported): August 12, 2008
Achillion Pharmaceuticals, Inc.
(Exact name of registrant as specified in its charter)
(State or other jurisdiction
300 George Street
New Haven, CT
(Address of principal
Registrants telephone number, including area code: (203) 624-7000
(Former name or former address, if changed since last report)
Check the appropriate box if the Form 8-K is intended to simultaneously satisfy the filing obligation of the registrant under any of the following provisions:
|¨||Written communications pursuant to Rule 425 under the Securities Act (17 CFR 230.425)|
|¨||Soliciting material pursuant to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12).|
|¨||Pre-commencement communications pursuant to Rule 14a-2(b) under the Exchange Act (17 CFR 240.14d-2(b))|
|¨||Pre-commencement communications pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c)).|
Item 2.02. Results of Operations and Financial Condition
On August 12, 2008, Achillion Pharmaceuticals, Inc. (the Company) announced its financial results for the fiscal quarter ended June 30, 2008. The full text of the press release issued in connection with the announcement is furnished as Exhibit 99.1 to this Current Report on Form 8-K.
The information in this Form 8-K (including Exhibit 99.1) shall not be deemed filed for purposes of Section 18 of the Securities Exchange Act of 1934 (the Exchange Act) or otherwise subject to the liabilities of that section, nor shall it be deemed incorporated by reference in any filing under the Securities Act of 1933 or the Exchange Act, except as expressly set forth by specific reference in such a filing.
Item 9.01. Financial Statements and Exhibits
The following exhibit relating to Item 2.02 shall be deemed to be furnished, and not filed:
99.1 Press Release dated August 12, 2008
Pursuant to the requirements of the Securities Exchange Act of 1934, as amended, the registrant has duly caused this report to be signed on its behalf by the undersigned hereunto duly authorized.
Date: August 12, 2008
ACHILLION PHARMACEUTICALS, INC.
By: /s/ Mary Kay Fenton
Mary Kay Fenton
Chief Financial Officer
|99.1||Press Release dated August 12, 2008|
ACHILLION REPORTS SECOND QUARTER 2008 FINANCIAL RESULTS
Conference Call today at 4:30PM ET
NEW HAVEN, Conn., Aug 12, 2008 Achillion Pharmaceuticals, Inc. (Nasdaq: ACHN), a leader in the discovery and development of small molecule drugs to combat the most challenging infectious diseases, today reported financial results for the quarter and six months ended June 30, 2008.
For the six months ended June 30, 2008, the Companys net loss was $12.8 million, compared to a net loss of $15.3 million for the six months ended June 30, 2007. For the second quarter of 2008, the Company reported a net loss of $6.8 million, compared to a net loss of $7.7 million in the second quarter of 2007. Cash, cash equivalents and marketable securities at June 30, 2008 were $22.0 million.
Im quite pleased to report broad progress across Achillions diverse portfolio of anti-infective candidates in the second quarter of 2008, especially in our rapidly maturing HCV programs, said Michael Kishbauch, President and CEO of Achillion. Based on its promising pre-clinical profile, we nominated ACH-1625 as the first candidate from our internal HCV protease inhibitor program for clinical evaluation. ACH-1625 operates via a different, but potentially synergistic, mechanism from our NS4A antagonist candidate, ACH-1095, also now known as GS-9525, which we are developing in collaboration with Gilead Sciences.
Kishbauch continued, We also continue to make progress in our HIV and antibacterial programs, notably reporting the 48-week treatment segment in our longest running elvucitabine trial, as well as performing a full review of data from ACH-702 wherein we discovered a potentially more comprehensive profile for this potent compound which we plan to discuss with the Food and Drug Administration at a session scheduled for September 2008. Achillion has a depth of experience across multiple indications in the anti-infective area and, with the completion of our recent financing, we believe we have both the expertise and resources to successfully advance this portfolio.
Six month results
For the six months ended June 30, 2008, the Company reported a net loss of $12.8 million, compared to a net loss of $15.3 million in the same period in 2007. Total revenues were $1.0 million for the six months ended June 30, 2008, compared to $2.7 million for the six months ended June 30, 2007. Revenues consisted of amounts earned under a collaboration agreement with Gilead Sciences to develop compounds for use in treating chronic hepatitis C. The decrease in revenues from 2007 to 2008 was the result of fewer full-time equivalent hours incurred in the program as Gilead begins to take on more program responsibilities.
For the six months ended June 30, 2008, research and development expenses totaled $10.5 million, compared to $16.1 million during the same period in 2007. The decline in research and development expenses is related to the stage of the Companys phase II clinical trials for elvucitabine which are now substantially completed but were on-going during the first half of 2007, as well as pre-clinical testing of ACH-702 which is also now completed. General and administrative expenses were $3.3 million for the six months ended June 30, 2008, equivalent to $3.3 million in the same period in 2007.
Non-cash stock compensation expense totaled $1.1 million for the six months ended June 30, 2008, and is included in both research and development and general and administrative expenses.
Second quarter results
The Company reported a net loss of $6.8 million for the three months ended June 30, 2008, compared to a net loss attributable to common stockholders of $7.7 million for the three months ended June 30, 2007. Total revenues were $0.4 million for the second quarter of 2008, compared to $1.2 million for the second quarter of 2007. Total revenues decreased primarily as a result of fewer full-time equivalent hours incurred under the Companys collaboration with Gilead Sciences.
Research and development expenses were $5.5 million in the second quarter of 2008, compared to $7.7 million for the same period of 2007. Research and development expenses decreased primarily as the result of clinical studies of elvucitabine which were on-going during the second quarter of 2007 but which are now nearing completion.
For the three months ended June 30, 2008, general and administrative expenses totaled $1.6 million, compared to $1.7 for the same period in 2007.
Cash and cash equivalents and marketable securities at June 30, 2008 were $22.0 million. This amount does not include any amounts associated with the private placement financing announced by the Company on August 6, 2008. The first closing of this financing was held on August 12, 2008.
The Company will host a conference call to discuss these results at 4:30 PM ET on August 12, 2008. The call may be joined via telephone by dialing (877) 627-6555 or (719) 325-4942 (for international participants) at least 5 minutes prior to the start of the call and using the conference confirmation code 9701454. An audio replay will be available through August 15, 2008 by dialing (888) 203-1112 or (719) 457-0820 (international) and using the conference confirmation code 9701454.
A live audio webcast of the call will also be available on the Investor Relations section of the companys website, www.achillion.com. An archived audio webcast will be available on the Achillion website approximately two hours after the event and will be archived for three months.
Achillion is an innovative pharmaceutical company dedicated to bringing important new treatments to patients with infectious disease. The companys proven discovery and development teams have advanced multiple product candidates with novel mechanisms of action. Achillion is focused on solutions for the most challenging problems in infectious diseaseHIV, hepatitis and resistant bacterial infections. For more information on Achillion Pharmaceuticals, please visit the companys web site at www.achillion.com or call Achillion at 1-203-624-7000.
This press release includes forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995 that are subject to risks, uncertainties and other factors, including statements with respect to the timing, completion and success of Achillions preclinical studies and clinical trials of Achillions drug candidates. Among the factors that could cause actual results to differ materially from those indicated by such forward-looking statements are: unexpected regulatory actions or delays; uncertainties relating to results of clinical trials, including additional data relating to ongoing clinical trials; Achillions ability to obtain additional funding required to conduct its research, development and commercialization activities; Achillions ability to enter into successful collaboration arrangements; Achillions ability to obtain shareholder approval for its private placement financing, and Achillions dependence on its collaboration with Gilead Sciences. These and other risks are described in the reports filed by Achillion with the U.S. Securities and Exchange Commission, including its Annual Report on Form 10-K for the year ended December 31, 2007.
Mary Kay Fenton
Achillion Pharmaceuticals, Inc.
Tel. (203) 624-7000
MacDougall Biomedical Communications, Inc.
Tel. (781) 235-3060
- Financial results follow -
ACHILLION PHARMACEUTICALS INC. (ACHN)
Statements of Operations
(Unaudited, in thousands, except per share amounts)
|Three Months Ended
|Six Months Ended June
Research and development
General and administrative
Total operating expenses
Loss from operations
Other income (expense):
Net loss before tax benefits
Net loss per sharebasic and diluted
Weighted average shares outstandingbasic and diluted
|(Unaudited, in thousands)|
Cash and cash equivalents and marketable securities
Total stockholders equity