CAMBRIDGE, Mass., Oct 28, 2010 (BUSINESS WIRE) --
Curis, Inc. (NASDAQ:CRIS), a drug development company seeking to develop next generation targeted small molecule drug candidates for cancer treatment, today reported its financial results for the third quarter ended September 30, 2010.
"We had a productive and encouraging third quarter, highlighted by our initiation of the Phase Ib expansion trial of CUDC-101, our first-in-class HDAC, EGFR and Her2 inhibitor in patients with specific types of cancer, including head and neck, breast, gastric, liver and non-small cell lung cancers," said Dan Passeri, Curis President and Chief Executive Officer. "To date, we have engaged five clinical centers and treated 14 patients in this 50 patient-study, and we are hopeful that we can continue to enroll this trial at a solid pace through enrollment completion and that the results will provide meaningful data to guide the continued development of CUDC-101. In addition to this Phase Ib study, we expect to initiate a Phase I study of CUDC-101 in combination with cisplatin and radiation in head and neck cancer patients later this year or early in 2011 and, assuming that an acceptable safety profile is achieved in this study, advance to a Phase II trial in 2011."
"Our other compounds also continue to advance. We are pleased with Genentech's recent initiation of a Phase II clinical trial in operable basal cell carcinoma (BCC), demonstrating Genentech's ongoing commitment to exploring the treatment of various forms of BCC with GDC-0449. Additionally, our partner Debiopharm has advanced Hsp90 inhibitor Debio 0932 in its ongoing Phase I clinical trial; we received $3 million upon Debiopharm's treatment of the fifth patient in this study during this quarter."
For the third quarter of 2010, Curis reported a net loss of $1.5 million, or ($0.02) per share on both a basic and fully diluted share outstanding basis, as compared to a net loss of $4.1 million or ($0.06) per share on both a basic and fully diluted share outstanding basis for the same period in 2009.
Revenues for the third quarter of 2010 were $3.2 million as compared to $800,000 for the same period in 2009. Curis received a $3.0 million contingent payment from Debiopharm during the third quarter of 2010 upon Debiopharm's treatment of the fifth patient in its ongoing Phase I clinical trial of Debio 0932.
Operating expenses for the third quarter of 2010 were $5.0 million as compared to $4.9 million for the same period in 2009.
Other income of $250,000 for the third quarter of 2010 primarily represents the change in the fair value of a warrant liability established in connection with Curis' January 2010 registered direct offering.
As of September 30, 2010, Curis' cash, cash equivalents and marketable securities totaled $43.7 million, and there were 75.6 million shares of common stock outstanding.
CUDC-101 (HDAC/EGFR/Her2 Inhibitor)
-- Initiated Phase Ib expansion clinical trial
In August 2010, Curis initiated a Phase I open-label expansion trial at five clinical sites within the U.S. of CUDC-101 in approximately 40 patients with advanced, refractory head and neck, gastric, breast and liver cancers. In October, the protocol was amended to include up to 10 additional patients with non-small cell lung cancer, so that a total of 50 patients will be studied in this trial. The primary objectives of the Phase Ib expansion trial are to obtain additional information on the safety and tolerability of CUDC-101 in this patient population. Secondary objectives are to assess the pharmacokinetics, to evaluate pharmacodynamic biomarkers and to assess the efficacy and ability of CUDC-101 to effectively inhibit histone deacetylase, or HDAC, epidermal growth factor receptor, or EGFR, and human epidermal growth factor receptor 2, or Her2, in this patient population.
GDC-0449 (Hedgehog Pathway Inhibitor in Collaboration with Genentech)
-- Announced initiation of Genentech's Phase II clinical trial in operable basal cell carcinoma
In October 2010, Curis announced that its collaborator Genentech, a member of the Roche Group, initiated a Phase II clinical trial of GDC-0449, an orally-administered small molecule Hedgehog Pathway Inhibitor, as a single-agent therapy for patients with operable nodular BCC. This Phase II clinical trial is in addition to the pivotal Phase II clinical trial currently being conducted by Genentech in patients with inoperable locally advanced or metastatic BCC.
-- Announced Roche and Genentech's Phase II clinical trial results in advanced ovarian cancer
In October 2010, Curis also announced that Genentech completed further analyses of results from its recently-completed Phase II clinical trial of GDC-0449 in advanced ovarian cancer. The median time to disease progression in the Phase II study was 7.5 months for patients who received GDC-0449 compared to 5.8 months for patients who received placebo (HR=0.791, p=0.3944). Genentech has concluded that these results did not demonstrate sufficient clinically meaningful improvement in progression-free survival to warrant additional clinical testing of GDC-0449 in ovarian cancer at this time. No obvious new safety signals were observed, and ongoing trials in other tumor types have not been impacted by this decision. Further research is needed to determine whether there is a role for GDC-0449 in the treatment of appropriately selected patients with ovarian cancer.
Debio 0932 (Hsp90 Inhibitor in Collaboration with Debiopharm S.A.)
-- Achieved Phase I milestone under Hsp90 collaboration with Debiopharm
In July 2010, Debiopharm treated the fifth patient in its ongoing Phase I clinical trial for small molecule heat shock protein 90 (Hsp90) inhibitor Debio 0932. Under the terms of the August 2009 license agreement between Curis and Debiopharm, Curis received a $3 million payment from Debiopharm in August 2010 for the achievement of this development objective.
Conference Call Information
Daniel Passeri, President and Chief Executive Officer of Curis, will host a conference call today, October 28, 2010, at 9:00 am EDT, to discuss Curis' financial results for the quarter, and corporate developments, plans and strategies.
To access the live conference call, please dial (866) 202-4367 from the United States or Canada or (617) 213-8845 from other locations, shortly before 9:00 am EDT. The conference ID number is 86361800. The conference call also can be accessed on the Curis website at www.curis.com in the Investors section. A replay will be available approximately two hours after the completion of the call through 12:00 pm EDT, Thursday, November 4, 2010. To access the replay, please dial (888) 286-8010 from the United States or Canada or (617) 801-6888 from other locations and reference conference ID number 32459588.
About Curis, Inc.
Curis is a drug development company that is committed to leveraging its innovative signaling pathway drug technologies to seek to create new targeted small molecule drug candidates for cancer. Curis is building upon its previous experiences in targeting signaling pathways, including in the Hedgehog pathway, in its effort to develop proprietary targeted cancer programs. For more information, visit Curis' website at www.curis.com.
Cautionary Note Regarding Forward-Looking Statements:
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, including without limitation statements regarding the Company's expectations regarding the further development and clinical and therapeutic utility of GDC-0449, Debio 0932 and CUDC-101. Forward-looking statements used in this press release may contain the words "believes", "expects", "anticipates", "plans", "seeks", "estimates", "assumes", "will", "may" or similar expressions. These forward-looking statements are not guarantees of future performance and involve risks, uncertainties, assumptions and other important factors that may cause the actual results to be materially different from those indicated by such forward-looking statements including, among other things:
In addition, any forward-looking statements represent the views only as of today and should not be relied upon as representing Curis' views as of any subsequent date. Curis disclaims any intention or obligation to update any of the forward-looking statements after the date of this press release whether as a result of new information, future events or otherwise.