Portola Pharmaceuticals to Participate in Two Upcoming Investor Conferences

On August 30, 2018 Portola Pharmaceuticals, Inc. (Nasdaq:PTLA) reported that the company will participate in the following conferences in September (Press release, Portola Pharmaceuticals, AUG 30, 2018, View Source;p=RssLanding&cat=news&id=2365495 [SID1234529231]):

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Citi’s 13th Annual Biotech Conference on Thursday, September 6, 2018 in Boston, MA. The Company will conduct one-on-one meetings with institutional investors at this conference.

Morgan Stanley 16th Annual Global Healthcare Conference on Wednesday, September 12, 2018, at 2:15 p.m. Eastern Time in New York, NY. The Company will participate in a fireside chat presentation at the conference, which will be webcast live and available for replay from Portola’s website at www.portola.com in the Investor Relations section.

MEI Pharma Reports Fiscal Year 2018 Results and Operational Highlights

On August 30, 2018 MEI Pharma, Inc. (Nasdaq: MEIP), a late-stage pharmaceutical company focused on advancing new therapies for cancer, reported results for its fiscal year ended June 30, 2018 (Press release, MEI Pharma, AUG 30, 2018, View Source [SID1234529228]).

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"We begin the 2019 fiscal year in our strongest position ever, with progress across all four clinical-stage oncology candidates, and with particular focus on the planned initiation of the ME-401 Phase 2 accelerated approval study by year-end. With ME-401 joining pracinostat as the second candidate in a global study to support marketing authorization, along with our robust cash position, we are well situated to pursue our development strategy," said Daniel P. Gold, Ph.D., president and chief executive officer of MEI Pharma.

Dr. Gold continued, "We are also very pleased to report that in recent discussions with FDA on a ME-401 accelerated approval registration strategy, FDA expressed support of our proposed randomized Phase 2 trial in which we will evaluate continuous and intermittent dosing schedules in patients with relapsed or refractory follicular lymphoma. As we execute on our plans to start this study around year-end, we also look forward to reporting additional progress across our pipeline over the coming quarters, including clinical data from our CDK9 inhibitor, voruciclib, and clinical updates on pracinostat and ME-344."

Fiscal Year 2018 and Recent Company Highlights

Financial

In May 2018, the Company completed a private placement of common stock, along with warrants to purchase common stock, resulting in net proceeds to MEI of approximately $70 million.
As of June 30, 2018, MEI had $102.7 million in cash, cash equivalents and short-term investments, with no outstanding debt. The cash balance includes the proceeds of our private placement completed in May 2018.
Research and development expenses were $17.0 million for the year ended June 30, 2018, compared to $7.2 million for 2017. The increase was primarily related to increased activities in all clinical programs including the acquisition and development costs associated with voruciclib.
General and administrative expenses were $9.8 million for the year ended June 30, 2018, compared to $8.6 million for 2017. The increase primarily relates to professional services expenses, share-based compensation, and general corporate expenses incurred during the year ended June 30, 2018.
The Company recognized revenues of $1.6 million for the year ended June 30, 2018. Revenues resulted from the recognition of fees allocated to research and development activities related to the Helsinn License Agreement. Revenue decreased due to lower levels of research and development activities during the year ended June 30, 2018.
Cash expenditures for operations were $21.3 million for the year ended June 30, 2018, compared to $16.5 million for 2017. Cash expenditures were $3.8 million for the fourth quarter ended June 30, 2018, compared to $3.1 million for the same period in 2017.
Net loss was $40.1 million, or $0.97 per share, for the fiscal year ended June 30, 2018, compared to net income of $2.7 million, or $0.07 per share for 2017. The Company’s net loss includes a $9.7 million change in the fair value of the warrants issued in connection with the May 2018 financing and $2.4 million in transaction costs related to the May 2018 financing recorded as financing expense on the statement of operations. The Company is required to calculate the change in fair value of the warrants and record the non-cash charge to the statement of operations at each reporting date.
ME-401 – a next-generation selective oral inhibitor of PI3K delta

In June 2018, the Company presented results from a Phase 1b study evaluating ME-401 in patients with relapsed/refractory follicular lymphoma, chronic lymphocytic leukemia and small lymphocytic lymphoma at the 2018 American Society of Clinical Oncology (ASCO) (Free ASCO Whitepaper) Annual Meeting as well as the European Hematology Association (EHA) (Free EHA Whitepaper) Congress. The data demonstrated a 90% overall objective response rate in patients. Based on these data, the Company is advancing ME-401 into a Phase 2, single-agent study for the treatment of adults with relapsed or refractory follicular lymphoma. The Phase 2 study is intended to support accelerated approval and is planned to begin around the end of 2018.
In July 2018 the Company discussed with FDA a ME-401 monotherapy accelerated approval strategy in patients with relapsed or refractory follicular lymphoma (FL). The FDA communicated support for the Company’s proposed randomized Phase 2 trial evaluating continuous and intermittent dosing schedules. Accelerated approval of ME-401 will be subject to FDA review of the improvement provided by ME-401 over other therapies available at the time of the regulatory action.
MEI expects to report data updates from the Phase 1b study, including at a medical meeting late in Q4 2018. By year-end 2018, MEI also plans to initiate the Phase 2 study to support accelerated approval of ME-401 in relapsed or refractory follicular lymphoma.
Pracinostat – an oral HDAC inhibitor (partnered with Helsinn Healthcare, SA)

In January 2018, the European Medicines Agency granted Orphan Drug Designation to pracinostat, currently in a Phase 3 study in combination with azacitidine for the treatment of acute myeloid leukemia (AML) in adult patients unfit for induction chemotherapy.
In May 2018, the Company and Helsinn announced a successful interim analysis from the Phase 2 study evaluating the combination of pracinostat and azacitidine in high and very high-risk myelodysplastic syndrome (MDS) patients previously untreated with hypomethylating agents. Based on the successful planned interim analysis, the study expanded open-label enrollment to 60 patients. MEI is responsible for the conduct of the Phase 2 study, the cost of which will be shared by Helsinn. Helsinn is responsible for funding any further studies.
MEI expects to provide updates to the pracinostat program at a medical meeting late in Q4 2018.
Voruciclib – an oral, selective CDK inhibitor with robust CDK9 inhibition

In January 2018, the U.S. Food and Drug Administration cleared the Company’s Investigational New Drug Application (IND) for voruciclib.
MEI expects to report updates regarding the ongoing Phase 1 study, and the initiation of dosing of voruciclib in combination with VENCLEXTA (venetoclax) in relapsed or refractory B-cell malignancies, at medical meetings in 2019.
ME-344 – a novel mitochondrial inhibitor

In June 2018, the Company presented interim results from an investigator-initiated Phase 1 study in HER2 negative breast cancer in combination with bevacizumab (marketed as Avastin) at ASCO (Free ASCO Whitepaper). ME-344 in combination with Avastin demonstrated inhibition of tumor proliferation as measured by Ki-67 reductions in HER2 negative breast cancer patients. These results support continuation of the ongoing Phase 1 study.
MEI expects to report additional data from the investigator-sponsored Phase 1 study at medical meetings in 2019.
Operational Highlights

In February 2018, the Company announced the appointment of industry veteran Frederick W. Driscoll to the board of directors. Mr. Driscoll serves on the audit committee.
In July 2018, the Company announced that David M. Urso, J.D., senior vice president of corporate development and general counsel, was promoted to chief operating officer. Mr. Urso is also continuing as the Company’s general counsel and head of corporate development.
Conference Call and Webcast

MEI Pharma will host a conference call with simultaneous webcast today, August 30, 2018, at 5:00 p.m. Eastern time to provide a corporate update. To access the live call, please dial (866) 939-3921 (United States) or (678) 302-3550 (International), conference ID 47469059. The conference call will also be webcast live and can be accessed at www.meipharma.com. A replay of the webcast will be available approximately one hour after the conclusion of the call.

SOTIO and PPF complete acquisition of Cytune Pharma

On August 30, 2018 SOTIO, a biotechnology company owned by the PPF Group, reported the completion of the acquisition of Cytune Pharma by PPF (Press release, SOTIO, AUG 30, 2018, View Source [SID1234529225]). SOTIO will continue to develop the lead program SO-C101 (RLI-15) within its pipeline and intends to initiate first-in- human clinical trials in early 2019. SOTIO is spearheading all of PPF’s activities in the biotech sector and closely cooperated during Cytune’s acquisition process. All Cytune projects will be developed as part of SOTIO’s pipeline.

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Cytune Pharma develops IL-15 based therapies for the treatment of cancer. The lead molecule of Cytune’s pipeline, SO-C101 (RLI-15), is a human fusion protein of IL-15 and the high-affinity binding domain of IL-15Rα and acts as a specific IL-2/IL-15Rβγ agonist.

The deal announced in 2015 between PPF Group and Cytune involved investments into Cytune and a staged-acquisition of the company, which has now been completed with the acquisition of all outstanding shares of Cytune. Cytune becomes an important part of SOTIO’s activities in the biotech sector and will also closely collaborate with its affiliate Accord Research on the future development of the lead program SO-C101, and other earlier-stage targeted RLI-15 programs. SOTIO is planning to initiate a first-in-human study with SO-C101 in selected European countries and the US in early 2019. A key part of this early clinical program is the combination with immune checkpoint inhibitors.

"We are excited about the completion of the acquisition and welcome Cytune to the PPF Group. Cytune and SOTIO have been closely and very successfully collaborating over the course of the last few years and we very much look forward to initiating the first clinical trials with SO-C101 in a few months," commented Radek Spisek, CEO of SOTIO. "SO-C101 will become a core program of our pipeline, together with our clinical programs in ovarian, lung and prostate cancer based on our autologous dendritic cell therapy platform DCVAC."

"I’m proud that our products, originating from INSERM and the University of Nantes and supported by Bpifrance and Atlanpole Biotherapies, hold the potential to lead to new therapeutic options for the treatment of cancer patients. Such IL-2/IL-15Rβγ agonists represent a new and very promising class of drugs in the immune-oncology segment as they have shown to re-induce responses in patients after failure to checkpoint inhibitors treatment," adds David Bechard, President and COO of Cytune. "The continued financial support by PPF combined with SOTIO’s clinical development expertise will be instrumental in accelerating the development of SO-C101 in multiple clinical trials, ultimately for the benefit of cancer patients."

The financial terms of the transaction are not disclosed.

About SO-C101
Molecule SO-C101 (RLI-15) is a human fusion protein of IL-15 and the high-affinity binding domain of IL-15Rα which acts as a specific agonist of the intermediate-affinity IL-2/IL-15Rβγ. It is a novel immunotherapeutic approach with potential applications in a variety of oncology indications. In preclinical experiments, SO-C101 has been shown to stimulate and induce proliferation of immune effector cells, such as cytotoxic T cells and NK cells, without expanding the CD4+ T regulatory cells. Based on the preclinical experiments, SO-C101 is more potent and better tolerated compared to the unmodified IL-15 or IL-2. SO-C101 and other products based on this platform allow for combinations with other immunotherapeutic strategies, including checkpoint inhibitors.

Cerus to Present at the Baird 2018 Global Healthcare Conference

On August 30, 2018 Cerus Corporation (Nasdaq: CERS) reported that Kevin D. Green, Cerus’ vice president, finance and chief financial officer, will present and provide a corporate update at the Baird 2018 Global Healthcare Conference in New York City on Thursday, September 6, 2018 at 8:30 a.m. ET (Press release, Cerus, AUG 30, 2018, View Source [SID1234529224]).

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A live webcast of the presentation will be available from the Investor Relations page of the Cerus web site at View Source A replay will be available for approximately two weeks following the completion of the event.

Celyad to participate at upcoming healthcare conferences in September

On August 30, 2018 Celyad (Euronext Brussels and Paris, and NASDAQ: CYAD), a clinical-stage biopharmaceutical company focused on the development of CAR-T cell therapies, reported that management will participate at both the 13th Annual Wells Fargo Healthcare Conference and the 16th Annual Morgan Stanley Global Healthcare Conference in September (Press release, Celyad, AUG 30, 2018, View Source [SID1234529223]).

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The Wells Fargo Healthcare Conference will take place in Boston, MA on September 4–6, 2018. The Company presentation is scheduled on Thursday, September 6 at 10:20 a.m. ET.

The Morgan Stanley Global Healthcare Conference will take place in New York, NY on September 12–14, 2018.