Emeryville, CA, November 3, 2008 -- Bionovo, Inc. (NASDAQ: BNVI) today announced results for the third quarter of 2008.
Quarter Results
The company did not report any revenue for the three and nine months ended September 30, 2008.
Total operating expenses for the three and nine months ending September 30, 2008 were $5.2 million and $13.7 million, respectively, compared to $3.6 million and $9.9 million, respectively, for the same period in 2007. This reflects the increase in costs related to the clinical trials of our leading drug candidates.
The Company reported a net loss for the three and six months ended September 30, 2008 of $5.1 million, or $0.07 per share, and $13.2 million, or $0.17 per share, respectively, compared with a net loss of $3.2 million, or $0.05 per share, and $9.2 million, or $0.15 per share, respectively, for the same periods in 2007.
The Company ended the quarter with $17.3 million in cash, cash equivalents and short term investments, and began the quarter with $24.6 million, a difference of $7.3 million. This difference includes $3.4 million in non-recurring capital expenditures associated with tenant improvements for laboratory and production capability expansion.
Company Highlights
The Company has continued the scientific and clinical development of its drug candidates for the treatment of advanced breast cancer, menopausal hot flashes, and menopausal vaginal atrophy. Recent advances have included:
· | The phase 1 portion of the BZL101 Phase 1/2 clinical trial for advanced metastatic breast cancer has now been completed successfully, showing positive safety and tolerability profiles, as well as the early signs of clinical efficacy. The Phase 2 part of the trial is now open for enrollment at 17 clinical.sites in the US, and is expected to enroll 80 patients in the trial. There are currently over 160,000 women living with metastatic breast cancer in the U.S. |
· | The Company presented an analysis of the metabolism of one of the active chemical ingredients of MF101, the Company’s drug candidate for the treatment of menopausal hot flashes. The presentation, to the American Society for Pharmacology and Experimental Therapeutics, Drug Metabolism and Disposition, adds to the growing body of data supporting MF101’s mechanism of action, safety and potential potency, as well as furthering the intellectual property protection for the Company. |
· | Also on MF101, the Company released data from its previous Phase 2 study that showed MF101’s superior efficacy with respect to “night sweats” or “night awakenings due to hot flashes” – a particularly debilitating form of hot flash for which many women seek medical treatment and improved quality of life. This adds to the increasing evidence of the possible efficacy of MF101 and the market opportunity awaiting MF101 if and when it is approved by the FDA and put on the market. |
· | The Company is currently in discussions with the FDA on the specific requirements for progression to Phase 3 pivotal trials of MF101. The Company expects to have resolution, and to be in a position to continue the clinical development and trials for MF101, by the end of the year. |
· | The Company presented a report to the North American Menopause Society (NAMS), showing laboratory results of superior efficacy for VG101, the Company’s drug candidate for menopausal vaginal dryness, over other treatments. The Company expects to begin human clinical trials for VG101 late in 2008 or early in 2009. |
“The third quarter of the year continued the positive scientific progress for Bionovo,” said Dr. Isaac Cohen, O.M.D., Bionovo’s Chairman and Chief Executive Officer. “After much preparation and discussion with the FDA and our advisors, we are now poised to begin the next phase of clinical testing for our portfolio of women’s health and oncology drug candidates. We are also continuing promising discussions with potential pharmaceutical partners.”
“With over seventeen million dollars in cash, cash equivalents and short term investments, and a lower than industry clinical trial cost profile, we are poised to progress our lead drug candidates through these challenging economic times,” added Tom Chesterman, Bionovo’s Senior Vice President and Chief Financial Officer. "Given our current plans and expectations, this funding will be sufficient for at least the next 12 months".
A full financial report on Form 10-Q is expected to be filed by Tuesday, November 4, 2008.