We just know that it will.”Phase 3 trials, the last stage before regulatory submission and then marketing, are extremely expensive. If they get there, then BiondVax will probably increase production either through partnerships or licensing, he said, though it is still too soon to consider it.The flu is a universal experience. October: Began regulatory procedures with the European EMA (akin to the American FDA) regarding Phase 3 trial plans. BiondVax founder, president and CEO Ron Babecoff said, "This investment is a vote of confidence in BiondVax and its universal influenza vaccine candidate. aMoon Fund is an Israeli investment firm focused on innovative Israeli healthcare and life science…Ayala Pharmaceuticals has bought rights from international company Bristol-Myers Squibb (BMS) to develop a personalized treatment for cancer. “Israel waited in line, asked for vaccines and there were none.” Everyone was looking out for number one, he said. A year from now, at the end of 2020, we might get there for the first time, thanks to an Israeli company called BiondVax Pharmaceuticals that is currently holding phase 3 clinical trials for its universal influenza vaccine.The Northern Hemisphere is now entering flu season. Vaccinations started in July, and all participants had to sign an informed consent form committing to not receiving a seasonal vaccination this year. Bloomberg the Company & Its Products The Company & its Products Bloomberg Terminal Demo Request Bloomberg Anywhere Remote Login Bloomberg Anywhere Login Bloomberg Customer Support Customer Support

Most recently, in 2009, swine flu swept the world, killing almost 300,000 people, according to updated estimations.For this reason, the promise of a universal vaccine, one that will be able to grant immunity despite the mutating nature of the virus, has long been the holy grail of flu researchers and public health institutions. Throughout the winter, local caregivers from one of the 83 hospitals participating in BiondVax’s trial will collect samples from participants who report flu symptoms and send them to the Israeli Ministry of Health’s virology lab in Tel HaShomer, which is part of a global World Health Organization network of labs that monitor influenza. Following the placement, BiondVax has 3 large strategic investors holding a total of over 30%, with Marius Nacht’s aMoon Partners fund remaining our largest current shareholder. As it is not incubated in eggs but rather created in a lab using engineered E. coli bacterium, it both shortens the time needed to create the vaccine and solves a lot of logistical problems, making the process more of an industry standard.The US Food and Drug Administration (FDA) was somewhat flabbergasted, Babecoff recalled. The system is also very clean, people either receive our vaccine or they don’t receive any vaccine at all,” she said,“Since we have one vaccine, one formulation, we broke the connection between the vaccine and the season or a specific strain,” Babecoff said. Mr. Marius Nacht has fully subscribed for the entire allotment available to him in the rights offering through his wholly owned entity Angels Investments in High Tech Ltd. (“AIHT”). They really did not want to.

aMoon Fund, part of Angels High Tech Investments, a company fully owned by Marius Nacht, Co-founder and Chairman of Check Point (NASDAQ: CHKP), invested NIS 10.9 million (close to $3 million) in BiondVax, at the then-prevailing market price. Following the placement, BiondVax has 3 large strategic investors holding a total of over 30%, with Marius Nacht's aMoon Partners fund remaining our largest current shareholder. Both groups also received the standard seasonal influenza vaccine. “Each infected cell displays virus parts on its surface, as a sort of a red flag, causing the cellular arm of the immune system to attack and kill it, and the immune cells also release substances that have an antiviral effect,” she said.

Bloomberg the Company & Its Products The Company & its Products Bloomberg Terminal Demo Request Bloomberg Anywhere Remote Login Bloomberg Anywhere Login Bloomberg Customer Support Customer Support All Rights Reserved.Zebra Medical Vision said on Monday it received approval from the U.S. Food and Drug Administration for its artificial intelligence-based chest X-ray triage product.The FDA, which approves all medical devices and formulations in the U.S., has very few branches outside of the U.S.Marius is an Anchor Investor at aMoon.

“They said it was unprecedented and that we should continue. He also exercised his option to purchase, under the same terms of the rights offering, 2,203,640 ADSs and 141,538 ordinary shares offered in the rights offering that were not purchased by other shareholders. The final vaccine, currently in phase 3 clinical trial, combines those conserved epitopes into one protein that can then be used to invoke a much more expansive response towards the virus.

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