Innovation Pharmaceuticals Receives New Patent for Compounds for Use in Treatment of Oral Mucositis

On February 19, 2019 Innovation Pharmaceuticals, (OTCQB:IPIX) ("the Company"), a clinical stage biopharmaceutical company, is reported that the U.S. Patent & Trademark Office issued today a new patent to the Company for the treatment of oral mucositis (Press release, Innovation Pharmaceuticals, FEB 19, 2019, View Source [SID1234533476]). The patent (U.S. Patent Number 10206894) covers methods for treating and/or preventing mucositis with one or more compounds, or pharmaceutically acceptable salts.

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The new patent broadens the Company’s Intellectual Property footprint in the oral mucositis therapeutic area, and further builds on other recently assigned patent protections for Brilacidin, the Company’s defensin-mimetic drug candidate. Brilacidin has been successfully evaluated in clinical trials in oral mucositis, inflammatory bowel disease and serious skin infections, with planned extension into dermatological diseases.

Recent patents assigned to Brilacidin include: a patent covering Brilacidin oral, buccal and sublingual pharmaceutical compositions, including liquid compositions, such as rinses; a patent covering Brilacidin in combination with additional medicaments, such as antibiotics, anti-inflammatory agents, etc.

"As the Company prepares to advance Brilacidin into Phase 3 development for the prevention and treatment of oral mucositis, initially in Head and Neck Cancer, this new patent provides additional key protections," commented Arthur P. Bertolino, MD, PhD, MBA, President and Chief Medical Officer at Innovation Pharmaceuticals. "Oral mucositis represents a large area of unmet need and a substantial market opportunity. We, along with potential Pharma partners, feel Brilacidin—as a conveniently-administered oral rinse—is well-positioned possibly to emerge one day as a frontline, go-to treatment for this common, costly and debilitating side-effect of chemoradiation."

About Brilacidin and Severe Oral Mucositis

There currently are no FDA-approved drugs for the prevention of Severe OM (SOM) (WHO Grade ≥ 3) in Head and Neck Cancer (HNC) patients receiving chemoradiation. The additional expenses incurred by patients suffering from SOM are estimated to be as high as $18,000 to $25,000 per case in the U.S. when hospitalization is required. These factors contribute to SOM qualifying as an area of significant unmet medical need. According to published statistics, the number of new annual HNC cases in the U.S. is estimated to be 65,000, and on a worldwide basis, ~750,000 cases. Between 60 and 70 percent of these HNC patients typically will develop Severe OM, with the overall incidence of HNC patients developing some grade of OM (WHO Grades 1 to 4) approaching 100 percent. Because it cannot be predicted which patients will develop SOM, a preventative treatment, such as Brilacidin oral rinse, would begin in all patients as soon as starting chemoradiation and continue until its completion (typically a seven-week course). Given Brilacidin is administered as a convenient oral rinse, with plans to package it in an easily transportable sachet form, the Company believes it would be attractive both to doctors and patients—likely translating to widespread and rapid market adoption should Brilacidin oral rinse gain regulatory approval.

VBL Therapeutics to Present Data on its Novel VB-600 Platform at Keystone Conference on February 26

On February 12, 2019 VBL Therapeutics (Nasdaq: VBLT), reported that the Company will present new data on the potential of its VB-600 platform targeting MOSPD2 for inflammatory and oncology indications, at the Keystone Symposia on Myeloid Cells, to be held February 24—28, 2019 at the Eldorado Hotel & Spa in Santa Fe, New Mexico (Press release, VBL Therapeutics, FEB 19, 2019, View Source [SID1234533475]).

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Oral Presentation Details:
Title: MOSPD2: Key Regulator of Myeloid Cell Migration and a Novel Target for Treatment of Inflammatory Diseases
Presenter: Itzhak Mendel, PhD
Date: Tuesday, February 26, 2019
Time: 8:00 – 11:00 AM MST
Session: Myeloid Cells in Metabolic and Inflammatory Diseases
Location: Eldorado Grand Ballroom

Poster Presentation Details:
Abstract: MOSPD2: Key Regulator of Myeloid Cell Migration and a Novel Target for Treatment of Inflammatory Diseases
Session title: Poster Session 2
Date: Tuesday, February 26, 2019
Time: 7:30 – 10:00 PM MST
Poster #: 2028
For more information on the Keystone Symposium on Myeloid Cells, including a detailed program, refer to View Source;meetingid=1553

About VBL’s VB-600 Platform

VBL is conducting two parallel drug development programs that are exploring the potential of MOSPD2, a protein that VBL has identified as a key regulator of cell motility, as a therapeutic target for inflammatory diseases and cancer. Our VB-600 platform comprises classical anti-MOSPD2 monoclonal antibodies for inflammatory indications, as well as bi-specific antibody candidates for oncology.

Blueprint Medicines to Report Fourth Quarter and Full Year 2018 Financial Results on Tuesday, February 26, 2019

On February 19, 2019 Blueprint Medicines Corporation (NASDAQ: BPMC), a precision therapy company focused on genomically defined cancers, rare diseases and cancer immunotherapy, reported that it will host a live conference call and webcast at 8:30 a.m. ET on Tuesday, February 26, 2019 to report its fourth quarter and full year 2018 financial results and provide a corporate update (Press release, Blueprint Medicines, FEB 19, 2019, View Source [SID1234533474]).

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To access the live conference call, please dial (855) 728-4793 (domestic) or (503) 343-6666 (international), and refer to conference ID 26735762. A webcast of the call will also be available under "Events and Presentations" in the Investors & Media section of Blueprint Medicines’ website at View Source The archived webcast will be available on Blueprint Medicines’ website approximately two hours after the conference call and will be available for 30 days following the call.

Ophthotech Corporation to Report Fourth Quarter and Full Year 2018 Financial Results and Host Conference Call on Tuesday, February 26, 2019

On February 19, 2019 Ophthotech Corporation (Nasdaq: OPHT) reported that it will report its fourth quarter and full year 2018 financial and operating results on Tuesday, February 26, 2019 (Press release, Ophthotech, FEB 19, 2019, View Source [SID1234533473]). Following the announcement, Ophthotech’s management team will host a live conference call and webcast at 8:00 a.m. Eastern Time to discuss the Company’s financial results and provide a general business update.

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To participate in this conference call, dial 888-224-1005 (USA) or 323-994-2093 (International), passcode 6840989. A live, listen-only audio webcast of the conference call can be accessed on the Investor Relations section of the Ophthotech website at: www.ophthotech.com. A replay will be available approximately two hours following the live call for two weeks. The replay number is 888-203-1112 (USA Toll Free), passcode 6840989.

Merck Receives First U.S. Patent for Improved CRISPR Genome-Editing Method

On February 19, 2019 Merck, a leading science and technology company and leader in genome editing, reported that the United States Patent and Trademark Office has issued a formal notice allowing Merck’s patent application directed to its proxy-CRISPR technology (Press release, Merck & Co, FEB 19, 2019, View Source [SID1234533472]).

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"This our first U.S. patent for CRISPR, and as a leading innovator of CRISPR technology, we will continue to collaborate with scientists around the world to ensure that the full potential of this powerful tool is realized, responsibly and ethically," said Udit Batra, member of the Merck Executive Board and CEO, Life Science. "This is great news for researchers in the U.S., as they now have more gene-editing options that accelerate drug development."

Merck’s proxy-CRISPR is a new genome-editing technique that makes CRISPR more efficient, flexible and specific by opening the genome for modification of DNA.

The technology can help scientists modify regions of the genome which are difficult to access.

This U.S. patent allowance marks Merck’s 13th CRISPR patent worldwide. The company’s CRISPR patent portfolio includes granted patents in Australia, Canada, Europe, Singapore, China, Israel and South Korea. Those patents are for CRISPR-related technologies covering foundational and alternative genome-editing methods.

To deploy the proxy-CRISPR method, two CRISPR systems are designed to target the genome in proximity to each other and work together. One CRISPR system opens a regional "door," pushing away blocking chromatin proteins, while the other walks through it to find the exact location for modification. Since the resulting modification requires two CRISPR binding events, the proxy-CRISPR method can enable twice the specificity of individual CRISPR systems.

Merck has received patents for its CRISPR paired nickase technology (cleaving opposite strands of a chromosomal sequence to create a double-stranded break) in Australia, Canada and Europe. Patents for Merck’s CRISPR integration technology (chromosomal cutting of the sequence of eukaryotic cells and insertion of a DNA sequence) have been granted in Australia, Canada, Europe, Singapore, China, Israel and South Korea. Merck is licensing its entire patent portfolio for all fields of use.

CRISPR technology is a core competency for Merck, which has 15 years’ experience with genome editing, spanning from discovery to manufacturing. Merck recognizes that genome editing has resulted in major advancements in biological research and medicine. At the same time, the growing potential of genome-editing technologies has opened scientific, legal and societal concerns. The company supports research with genome editing under careful consideration of ethical and legal standards. Merck has established an independent, external Bioethics Advisory Panel to provide guidance for research in which its businesses are involved, including research on or using genome editing, and has developed, defined and transparently published a clear operational position taking into account scientific and societal issues to inform promising therapeutic approaches for use in research and applications.

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