Full Press Release Details
MEI PHARMA S MITOCHONDRIAL INHIBITOR ME-344 SHOWS PRELIMINARY EVIDENCE OF SINGLE-AGENT ACTIVITY IN
FIRST-IN-HUMAN CLINICAL STUDY
Extension of Progression-Free Survival Observed Compared to Last Prior Therapy
San Diego October 21, 2013 MEI Pharma, Inc. (Nasdaq: MEIP), an oncology company focused on the clinical development of novel therapies for
cancer, announced results from a Phase I first-in-human, single-agent clinical study of its investigational mitochondrial inhibitor drug candidate, ME-344, in patients with refractory solid tumors. The results, presented yesterday at the
AACR-NCI-EORTC International Conference on Molecular Targets and Cancer Therapeutics in Boston, indicated that five of 21 evaluable patients treated with ME-344 experienced progression free survival (34 to 61+ weeks) that was at least twice the
duration of their last prior treatment before entry into the study.
In addition, the presentation highlighted that one of these 5 patients, a heavily
pre-treated patient with small cell lung cancer, achieved a confirmed partial response. The patient received his first treatment of ME-344 in August 2012 and has now been on study for more than 61 weeks. His June 2013 scans showed a decrease of 32%
in target lesions, which was confirmed in his most recent scans (August 2013). This patient and three others remain on study and continue weekly dosing.
The observed radiographic partial response is promising, particularly in such a difficult-to-treat disease as small cell lung cancer, said
presenter and co-investigator Jeffrey R. Infante, MD, Director, Drug Development at Sarah Cannon Research Institute and Tennessee Oncology. In addition to tumor shrinkage, this patient has also demonstrated symptomatic improvement while on
study, including decreased cough, shortness of breath and improved performance status. The results of this single agent Phase I study are encouraging and further clinical development of ME-344 is warranted.
A copy of yesterday s poster presentation, entitled ME-344, a novel mitochondrial oxygenase inhibitor: Results from a first-in-human Phase I
study, is now available at www.meipharma.com.
ME-344 was generally well tolerated at doses equal to or less than 10 mg/kg delivered on a
weekly schedule for extended durations. Dose limiting toxicities were observed at both the 15 and 20 mg/kg dose levels, consisting primarily of Grade 3 peripheral neuropathy. Other medically significant adverse events observed in single patients
included angina and QTc prolongation at the 10 mg/kg dose.
We are encouraged by the results from this first-in-human study of ME-344,
said Robert D. Mass, MD, Chief Medical Officer of MEI Pharma. Not only did the trial show evidence of clinical activity, but the primary dose limiting toxicity was consistent with the proposed mechanism of
action of ME-344, namely mitochondrial inhibition, suggesting on-target activity. Based on these findings, we are now actively preparing for a Phase Ib clinical trial of ME-344 in combination
with Hycamtin (topotecan) in small cell lung cancer and ovarian cancer, which we expect to initiate during the second quarter of 2014.
The Phase Ib trial will be designed to evaluate the safety and tolerability of ME-344 in combination with
Hycamtin in a total of 45 patients with either small cell lung cancer or ovarian cancer. Hycamtin is a chemotherapy approved by the
U.S. Food & Drug Administration for the treatment of small cell lung cancer and ovarian cancer, as well as cervical cancer.
ME-344 is MEI Pharma s isoflavone-derived mitochondrial inhibitor drug candidate. In preclinical studies, ME-344 has been shown to cause
caspase-independent cell death in multiple human tumor cell lines, including ovarian cancer stem cells, by interfering with mitochondrial energy generation. In April 2013, Ayesha Alvero, MD, Yale University School of Medicine, presented data at the
American Association for Cancer Research Annual Meeting showing the ability of ME-344 to decrease tumor burden and delay recurrence in a pre-clinical in vivo model of recurrent epithelial ovarian cancer, the most lethal of all gynecologic
MEI Pharma owns exclusive worldwide rights to ME-344.
MEI Pharma, Inc. (Nasdaq: MEIP) is a
San Diego-based oncology company focused on the clinical development of novel therapies for cancer. The Company s lead drug candidate is Pracinostat, a potential best-in-class, oral HDAC inhibitor being developed for advanced hematologic
diseases, such as myelodysplastic syndrome (MDS) and acute myeloid leukemia (AML). The Company initiated a randomized, placebo-controlled Phase II trial of Pracinostat in combination with Vidaza (azacitidine) in patients with previously untreated
MDS in June 2013. An open-label Phase II trial of Pracinostat in combination with Vidaza in elderly patients with AML who are unsuitable for intensive chemotherapy is expected to initiate in the fall of 2013. In September 2013, the Company further
expanded its pipeline of drug candidates with the acquisition of PWT143, a highly selective PI3-kinase delta inhibitor. For more information, go to www.meipharma.com.
About Sarah Cannon Research Institute
Research Institute (SCRI) is a global strategic research organization focusing on advancing therapies for patients. It is one of the largest clinical research programs, conducting community-based clinical trials in oncology and cardiology through
affiliations with a network of more than 700 physicians in the United States and United Kingdom. Additionally, SCRI offers management, regulatory and other research support services to drug development sponsors and strategic investigator sites. For
more information, please visit sarahcannonresearch.com.
Under U.S. law, a new drug cannot be marketed until it has been investigated in clinical
trials and approved by the FDA as being safe and effective for the intended use. Statements included in this press release that are not historical in nature are forward-looking statements within the meaning of the safe harbor
provisions of the Private Securities Litigation Reform Act of 1995. You should be aware that our actual results could differ materially from those contained in the forward-looking statements, which are based on management s current expectations
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