Full Press Release Details
ZIOPHARM Reports First-Quarter 2014 Financial Results and
Reviews Recent Activities
May 8, 2014 ZIOPHARM Oncology, Inc. (Nasdaq: ZIOP) today announced financial results for the first quarter ended March 31, 2014, and provided an update on the company s product development activities.
ZIOPHARM, together with our channel partner Intrexon Corporation, continues to advance a portfolio of immuno-oncology programs, with the goal of
enabling a paradigm shift in cancer treatment, said Jonathan Lewis, M.D., Ph.D., chief executive officer of ZIOPHARM. We continue to work at a rapid pace toward elucidating the enormous potential of the transformative technology driving
this pipeline in a data-driven and efficient manner. We also look forward to a number of important, value-creating clinical, preclinical and strategic milestones over the balance of the year and beyond.
Recent Corporate Highlights
ZIOPHARM is advancing a
number of clinical- and preclinical-stage, gene- and cell-based therapies with related technologies to allow precise regulation of protein expression and control of cellular function. Controlled expression and delivery of DNA and therapeutic
proteins is achieved through Intrexon Corporation s (NYSE: XON) RheoSwitch Therapeutic System (RTS ) technology, the most advanced clinical method for precisely modulating protein
production in gene based therapies.
ZIOPHARM recently presented results from a study demonstrating the anti-tumor effects and tolerability of the
Company s lead therapeutic, Ad-RTS-mIL-12, as well as the ability for the activator ligand Veledimex to cross the blood-brain-barrier, in a glioblastoma (brain cancer) murine model. Ad-RTS-IL-12 is a novel DNA-based therapeutic candidate for
the controlled, local expression of IL-12, an important protein for stimulating an anti-cancer T cell immune response. These data, presented at the 2014 American Association for Cancer Research annual meeting in April 2014, add to multiple
preclinical studies demonstrating that Ad-RTS-IL-12 enables localized, controlled delivery of IL-12 in the brain and can produce a dose-dependent reduction in tumor growth with prolonged survival.
ZIOPHARM is currently conducting or planning Phase 2 studies of Ad-RTS-IL-12, alone or in combination with existing treatment standards, in melanoma and
breast cancer, with plans to initiate a Phase 1 study in high-grade gliomas (brain cancer). The Company also expects to file several investigational new drug (IND) applications for novel, multigenic gene therapies.
First-Quarter 2014 Financial Results
About ZIOPHARM Oncology, Inc.:
ZIOPHARM Oncology is a
Boston, Massachusetts-based biotechnology company employing novel gene expression and control technology to deliver DNA for the treatment of cancer. ZIOPHARM s technology platform employs Intrexon Corporation s RheoSwitch Therapeutic
System technology to turn on and off, and precisely modulate, gene expression at the cancer site in order to improve the therapeutic index. This technology is currently being evaluated in
Phase 2 clinical studies of the immune system cytokine interleukin-12 for the treatment of breast cancer and advanced melanoma. Multiple new Investigational New Drug Applications for new targets using synthetic biology technology are expected
through 2015. ZIOPHARM is also developing novel small molecules as potential cancer therapeutics.
Forward-Looking Safe-Harbor Statement:
This press release contains certain forward-looking information about ZIOPHARM Oncology, Inc. that is intended to be covered by the safe harbor for
forward-looking statements provided by the Private Securities Litigation Reform Act of 1995, as amended. Forward-looking statements are statements that are not historical facts. Words such as expect(s), feel(s),
may, anticipate(s) and similar expressions are intended to identify forward-looking statements. These statements include, but are not limited to, statements regarding our
ability to successfully develop and commercialize our therapeutic products; our ability to expand our long-term business opportunities; financial projections and estimates and their underlying assumptions; and future performance. All of such
statements are subject to certain risks and uncertainties, many of which are difficult to predict and generally beyond the control of the company, that could cause actual results to differ materially from those expressed in, or implied or projected
by, the forward-looking information and statements. These risks and uncertainties include, but are not limited to: whether Ad-RTS-IL-12, palifosfamide, darinaparsin, indibulin, or any of our other therapeutic products will advance further in the
clinical trials process and whether and when, if at all, they will receive final approval from the U.S. Food and Drug Administration or equivalent foreign regulatory agencies and for which indications; whether Ad-RTS-IL-12, palifosfamide,
darinaparsin, indibulin, and our other therapeutic products will be successfully marketed if approved; whether any of our other therapeutic product discovery and development efforts will be successful; our ability to achieve the results contemplated
by our collaboration agreements; the strength and enforceability of our intellectual property rights; competition from other pharmaceutical and biotechnology companies; the development of, and our ability to take advantage of, the market for our
therapeutic products; our ability to raise additional capital to fund our operations on terms acceptable to us; general economic conditions; and the other risk factors contained in our periodic and interim SEC reports filed from time to time with
the Securities and Exchange Commission, including but not limited to, our Annual Report on Form 10-K for the fiscal year ended December 31, 2013 and our Quarterly Report on Form 10-Q for the quarter ended March 31, 2014. Readers are
cautioned not to place undue reliance on these forward-looking statements that speak only as of the date hereof, and we do not undertake any obligation to revise and disseminate forward-looking statements to reflect events or circumstances after the
date hereof, or to reflect the occurrence of or non-occurrence of any events.
RheoSwitch Therapeutic System (RTS )
technology is a registered trademark of Intrexon Corporation.
ZIOPHARM Oncology, Inc.
Condensed Statements of Operations
(in thousands except share and per share data)
| Three Months Ended March 31, | ||||||||
| 2014 | 2013 | |||||||
| Revenue | $ | 200 | $ | 200 | ||||
| Operating expenses: | ||||||||
| Research and development | 6,542 | 19,112 | ||||||
| General and administrative | 3,442 | 4,671 | ||||||
| Total operating expenses | 9,984 | 23,783 | ||||||
| Loss from operations | (9,784 | ) | (23,583 | ) | ||||
| Other income (expense), net | (9 | ) | (4 | ) | ||||
| Change in fair value of warrants | 82 | 10,788 | ||||||
| Net loss | $ | (9,711 | ) | $ | (12,799 | ) | ||
| Basic and diluted net loss per share | $ | (0.10 | ) | $ | (0.15 | ) | ||
| Weighted average common shares outstanding used to compute basic and diluted net loss per share | 100,229,200 | 82,906,080 |
ZIOPHARM Oncology, Inc.
| March 31, 2014 | December 31, 2013 | |||||||
| Cash and cash equivalents | 60,385 | 68,204 | ||||||
| Working capital | 54,647 | 62,506 | ||||||
| Total assets | 63,325 | 71,754 | ||||||
| Total stockholders equity | 41,732 | 49,383 |
Lori Ann Cafarella-Occhiogrosso