Full Press Release Details
Fate Therapeutics Reports Second Quarter 2016 Financial Results
Opened Patient Enrollment in Phase 1/2 Clinical Trial of ProTmune for Prevention of
Acute GvHD and CMV Infection
IND Filing for Allogeneic Memory-Like NK Cell Cancer Immunotherapy Planned for 2016
Announced $10.3 Million Common Stock Private Placement
San Diego, CA - August 8, 2016 - Fate Therapeutics, Inc. (NASDAQ: FATE), a biopharmaceutical company dedicated to the development of programmed cellular immunotherapies for cancer and immune disorders, today reported business highlights and financial results for the second quarter ended June 30, 2016.
"With the opening of enrollment in our Phase 1/2 clinical trial, we believe we are well-positioned in 2016 to complete the initial safety assessment and begin evaluating the potential of ProTmune for the prevention of life-threatening immunological conditions, including acute GvHD, in cancer patients undergoing allogeneic transplant for which there is a clear unmet and urgent medical need," said Scott Wolchko, President and Chief Executive Officer of Fate Therapeutics. "Additionally, we plan to collaborate with the University of Minnesota in filing an IND later this year for our Adaptive NK Cell cancer immunotherapy, which has shown persistent and potent tumor killing independent of antigen recognition in preclinical studies. We believe our allogeneic memory-like NK cell approach is a novel and promising intervention strategy for combating both liquid and solid tumors."
Recent Highlights & Program Updates
Second Quarter 2016 Financial Results
Today's Conference Call and Webcast
The Company will conduct a conference call today, Monday, August 8, 2016 at 5:00 p.m. ET to review financial and operating results for the quarter ended June 30, 2016. In order to participate in the conference call, please dial 1-877-303-6235 (domestic) or 1-631-291-4837 (international) and refer to conference ID 52471261. The live webcast can be accessed under "Events & Presentations" in the Investors & Media section of the Company's website at www.fatetherapeutics.com. The archived webcast will be available on the Company's website beginning approximately two hours after the event.
ProTmune is an investigational programmed cellular immunotherapy undergoing clinical development for the prevention of acute GvHD and CMV infection in patients undergoing allogeneic HCT. The cell therapy is produced by modulating a donor-sourced, human mobilized peripheral blood graft ex vivo with two small molecules (FT1050 and FT4145) to enhance the biological properties and therapeutic function of the graft's immune cells. The programmed mobilized peripheral blood graft is adoptively transferred and administered to a patient as a one-time intravenous infusion.
About Fate Therapeutics, Inc.
Fate Therapeutics is a biopharmaceutical company dedicated to the development of programmed cellular immunotherapies for cancer and immune disorders. The Company's cell therapy pipeline is
comprised of immuno-oncology programs, including off-the-shelf NK- and T-cell cancer immunotherapies derived from engineered induced pluripotent cells, and immuno-regulatory programs, including hematopoietic cell immunotherapies for protecting the immune system of patients undergoing hematopoietic cell transplantation and for regulating autoimmunity. Its adoptive cell therapy programs are based on the Company's novel ex vivo cell programming approach, which it applies to modulate the therapeutic function and direct the fate of immune cells. Fate Therapeutics is headquartered in San Diego, CA. For more information, please visit www.fatetherapeutics.com.
Forward-Looking Statements
This release contains "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995, including statements regarding the Company's advancement of, and the anticipated timing, progress, milestones and plans related to, the Company's product candidates, clinical studies, research and development programs and partnerships, the timing of the consummation of the private placement and the expected receipt and use of proceeds from the private placement, and the Company's projected cash expenditures. These and any other forward-looking statements in this release are based on management's current expectations of future events and are subject to a number of risks and uncertainties that could cause actual results to differ materially and adversely from those set forth in or implied by such forward-looking statements. These risks and uncertainties include, but are not limited to, the risk that results observed in prior studies, including preclinical studies of ProTmune , will not be observed in ongoing or future studies involving these product candidates, the risk that the Company may cease or delay preclinical or clinical development activities for any of its existing or future product candidates for a variety of reasons (including requirements that may be imposed by regulatory authorities and requirements for regulatory approval, difficulties or delays in patient enrollment in current and planned clinical trials, and any adverse events or other negative results that may be observed during preclinical or clinical development), the risk that the Company's research collaborations, including with Juno Therapeutics, may not be successful or may be terminated, the risk that the closing of the private placement transaction may not be consummated, the risk that the resale registration statement covering the common stock issued pursuant to the private placement is not timely filed by the Company or declared effective by the Securities and Exchange Commission (SEC), and the risk that the Company's expenditures may exceed current expectations for a variety of reasons. For a discussion of other risks and uncertainties, and other important factors, any of which could cause our actual results to differ from those contained in the forward-looking statements, see the risks and uncertainties detailed in the Company's periodic filings with the Securities and Exchange Commission, including but not limited to the Company's most recently filed periodic report, and from time to time the Company's other investor communications. Fate Therapeutics is providing the information in this release as of this date and does not undertake any obligation to update any forward-looking statements contained in this release as a result of new information, future events or otherwise.
Availability of Other Information about Fate Therapeutics, Inc.
Investors and others should note that the Company routinely communicates with investors and the public using its website (www.fatetherapeutics.com) and its investor relations website (ir.fatetherapeutics.com), including without limitation, through the posting of investor presentations, SEC filings, press releases, public conference calls and webcasts on these websites. The information
posted on these websites could be deemed to be material information. As a result, investors, the media, and others interested in Fate Therapeutics are encouraged to review this information on a regular basis. The contents of the Company's website, or any other website that may be accessed from the Company's website, shall not be deemed incorporated by reference in any filing under the Securities Act of 1933, as amended.
Condensed Consolidated Statements of Operations and Comprehensive Loss
(in thousands, except share and per share data)
| Three Months Ended June 30, | Six Months Ended June 30, | |||||||
| 2016 | 2015 | 2016 | 2015 | |||||
| (unaudited) | ||||||||
| Collaboration revenue | $ 1,027 | $ 329 | $ 2,349 | $ 329 | ||||
| Operating expenses: | ||||||||
| Research and development | 6,782 | 4,857 | 13,418 | 9,425 | ||||
| General and administrative | 2,249 | 2,690 | 4,851 | 5,446 | ||||
| Total operating expenses | 9,031 | 7,547 | 18,269 | 14,871 | ||||
| Loss from operations | (8,004) | (7,218) | (15,920) | (14,542) | ||||
| Other income (expense): | ||||||||
| Interest income | 31 | 2 | 58 | 3 | ||||
| Interest expense | (435) | (563) | (923) | (1,121) | ||||
| Total other expense, net | (404) | (561) | (865) | (1,118) | ||||
| Net loss | $ (8,408) | $ (7,779) | $ (16,785) | $ (15,660) | ||||
| Other comprehensive income (loss): | ||||||||
| Unrealized gain (loss) on available-for-sale securities, net | (3) | - | 11 | - | ||||
| Comprehensive loss | $ (8,411) | $ (7,779) | $ (16,774) | $ (15,660) | ||||
| Net loss per common share, basic and diluted | $ (0.29) | $ (0.33) | $ (0.58) | $ (0.70) | ||||
| Weighted-average common shares used to compute basic and diluted net loss per share | 28,868,464 | 23,920,630 | 28,823,127 | 22,246,832 |
Condensed Consolidated Balance Sheets
| June 30, | December 31, | |||
| 2016 | 2015 | |||
| (unaudited) | ||||
| Assets | ||||
| Current assets: | ||||
| Cash and cash equivalents | $ 35,870 | $ 64,809 | ||
| Short-term investments | 10,060 | - | ||
| Prepaid expenses and other current assets | 1,162 | 843 | ||
| Total current assets | 47,092 | 65,652 | ||
| Long-term assets | 2,086 | 2,306 | ||
| Total assets | $ 49,178 | $ 67,958 | ||
| Liabilities and stockholders' equity | ||||
| Current liabilities: | ||||
| Accounts payable and accrued expenses | $ 4,353 | $ 3,435 | ||
| Long-term debt, current portion | 7,864 | 7,550 | ||
| Current portion of deferred revenue | 2,105 | 2,401 | ||
| Other current liabilities | 5 | 55 | ||
| Total current liabilities | 14,327 | 13,441 | ||
| Long-term debt, net of current portion | 6,676 | 10,688 | ||
| Deferred revenue | 3,881 | 4,934 | ||
| Other long-term liabilities | 1,165 | 857 | ||
| Stockholders' equity | 23,129 | 38,038 | ||
| Total liabilities and stockholders' equity | $ 49,178 | $ 67,958 |
Jesse Baumgartner, Stern Investor Relations, Inc.
212.362.1200, jesse@sternir.com