BD Announces Live Webcast Of First Fiscal Quarter Earnings Conference Call

On January 9, 2020 BD (Becton, Dickinson and Company) (NYSE:BDX) reported that it will conduct a live webcast of its first fiscal quarter 2020 earnings conference call on Thursday, February 6, 2020, at 8:00 a.m. (ET) (Press release, BD Pharmaceutical Systems, JAN 9, 2020, View Source [SID1234552945]). BD will issue a press release detailing the quarter’s earnings earlier that morning.

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The webcast of the conference call, along with related slides, will be accessible through BD’s website at www.bd.com/investors and will be available for replay through Thursday, February 13, 2020.

Novavax to Present at the 38th Annual J.P. Morgan Healthcare Conference

On January 9, 2020 Novavax, Inc. (NASDAQ: NVAX), a late-stage biotechnology company developing next-generation vaccines for serious infectious diseases, reported that it will present at the 38th Annual J.P. Morgan Healthcare Conference (Press release, Novavax, JAN 9, 2020, View Source [SID1234552984]).

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Presentation details are as follows:

Date and Time: Thursday, January 16, 11:00 – 11:25 a.m. P.T.
Location: California West, Westin St. Francis Hotel, San Francisco
Live webcast: www.novavax.com, "Investors"/"Events"

A replay of the presentation will also be accessible under the "Investors/Events" section www.novavax.com.

Samyang Biopharmaceuticals Corporation Signed Technology Transfer Contract for Metabolism-Modulating Anticancer Drug Candidate

Samyang Biopharmaceuticals Corporation is developing a metabolism-modulating anticancer drug through open innovation (Press release, Samyang Biopharmaceuticals, JAN 9, 2020, View Source [SID1234570884]). A metabolism-modulating anticancer drug refers to a treatment which works on cancer cells’ energy metabolism to prevent cancer growth or induce apoptosis.

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Samyang Biopharmaceuticals Corporation recently announced that the company had a signing ceremony of a technology transfer contract for a metabolism-modulating anticancer drug candidate with the innovative drug discovery biotech startup LMITO Therapeutics on January 9 in Samyang Discovery Center, Pangyo, Seongnam.

This contract allows Samyang Biopharmaceuticals Corporation to have the exclusive right to introduce the drug candidate LMT503 and its technology from LMITO Therapeutics, develop, conduct a clinical trial for, manufacture, and commercialize them. With the goal of filing an investigational new drug (IND) application in 2022 to enter the clinical phase, Samyang Biopharmaceuticals Corporation is seeking to develop a metabolism-modulating anticancer drug based on this candidate and technology.

In addition to down payment, Samyang Biopharmaceuticals Corporation pays LMITO Therapeutics for the success of each stage (milestone) including clinical trial, marketing authorization, and sales and a certain portion of revenue as operating royalties after it begins to be sold in the market. Both companies, however, agreed to not disclose the exact payment conditions including down payment.

LMT503 is a low-molecular weight compound expected to treat cancer by regulating cancer cells’ energy metabolism while activating immune cells. In particular, the cancer cell energy metabolism regulation mechanism in LMT503 was suggested for the Nobel Prize in Physiology or Medicine in 2019 as a new cancer treatment method, so many studies are being conducted in Korea and around the world.

President Tae-ung Eom of Samyang Biopharmaceuticals Corporation explained the significance of this contract, "With the aim of developing a first-in-class drug (drug with a new mechanism of action), Samyang Group is employing a two-track strategy where Samyang Biopharmaceuticals Corporation is focusing on new chemical entities and Samyang Biopharm USA is focusing on biopharmaceuticals. To increase development speed and success likelihood, we are using open innovation by actively cooperating with other companies."

CEO Whee-sung Lee of LMITO Therapeutics said, "Thanks to technology transfer to Samyang Biopharmaceuticals Corporation, LMITO Therapeutics is able to increase the development speed for a metabolism-modulating anticancer drug in our pipeline. We will be actively supporting Samyang Biopharmaceuticals Corporation so that they can successfully develop an innovative anticancer drug."

Meanwhile, Samyang Biopharm USA, a subsidiary of Samyang Biopharmaceuticals Corporation, recently cooperated with global companies, signed contracts one after another to introduce an antibody drug candidate and conduct joint research, and is speeding up biopharmaceutical drug development.

Grey Wolf completes £2.5 million Series A2 financing for development of therapies targeting ERAP2

On January 9, 2020 Grey Wolf Therapeutics, a drug discovery biotechnology company focused on developing first-in-class therapies for immuno-oncology (IO), reported it has completed a £2.5 million ($3.3 million) Series A2 financing round with existing leading international healthcare investors Andera Partners and Canaan (Press release, Grey Wolf Therapeutics, JAN 9, 2020, View Source [SID1234552910]).

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The new funding – all from existing investors – will allow the company to accelerate development of therapies targeting endoplasmic reticulum aminopeptidase 2 (ERAP2), following many positive signals of its potential. Funds will also be used to continue to drive the lead endoplasmic reticulum aminopeptidase 1 (ERAP1) modulator program. For context, both of Grey Wolf’s novel ERAP approaches are aimed at directly altering tumor cells, illuminating them for attack and destruction by the immune system. The goal is to exploit this increased tumor visibility in monotherapy and to extend the therapeutic benefit of already approved immunotherapies to many more cancers. The company is developing small molecule modulators of ERAP1 and ERAP2, two key proteins in the antigen presentation pathway, to change the antigen repertoire of tumors and thereby increase the number and range of cancer-related antigens, including neoantigens, presented on tumor cells available to engage an immune response.

"We are delighted to have the continued support of Andera and Canaan." said Peter Joyce, Chief Executive Officer and Co-Founder. "The financing reflects growing potential in both our ERAP1 and ERAP2 approaches. We continue to see momentum, both in our own work and in the broader scientific community. These funds will allow us to further capitalize on this opportunity and expand our leadership position in the discovery and development of both ERAP1 and ERAP2 modulators."

Grey Wolf is expanding efforts around ERAP2 for two reasons. First, clinical data continues to demonstrate that tumors which are more visible to the immune system show improved responses to checkpoint inhibitors. One such example is the recent November 2019 paper published in Nature Medicine by the Chan group at MSKCC. The results are consistent across patients which either have a higher tumor mutational burden, heterozygosity of the Class I HLA locus or greater structural / sequence divergence at the Class I HLA locus. Second, the company has developed unique insight into the targeting of the ERAP enzymes through the lead program ERAP1 and validated the role for ERAP inhibition in modulating the cancer-related antigen repertoire. These in-house data provide compelling evidence that the therapies could have a real impact in the treatment of oncology.

"We have continued to generate data showing that modulation of both ERAP pathways drives change to the cancer-related antigen repertoire," said Tom McCarthy, Executive Chairman and Co-Founder of Grey Wolf Therapeutics. "Data clearly demonstrates that modulation of ERAP2 drives an altogether different change to the antigen repertoire, when compared with ERAP1 modulation, due to ERAP2’s clearly differentiated peptide substrate specificities. With this investment and the prior knowledge base within Grey Wolf we will be able to accelerate the ERAP2 program quickly through optimization, building on our leading position in ERAP disease-related biology."

The additional funds represent further confidence from investors. "Grey Wolf have already provided compelling insight into the potential of ERAP1 modulation," said Raphaël Wisniewski, Partner at Andera Partners. "This timely investment further underlines our excitement in these approaches. Grey Wolf are fast becoming true experts in modulation of ERAP biology for treatment of cancer." Brent Ahrens, General Partner at Canaan, added: "Canaan continues to be excited by the potential of targeting the ERAP pathway and are impressed with the progress the team has made in such a short space of time since closing Series A. The additional A2 investment enables the Company to push forward ERAP2 whilst maintaining the momentum on the lead ERAP1 program."

Portola Announces Preliminary Full Year 2019 Andexxa Global Net Revenues of Approximately $111 Million

On January 9, 2020 Portola Pharmaceuticals, Inc. (Nasdaq: PTLA) reported preliminary unaudited Andexxa global net revenues for the fourth quarter and full year 2019 (Press release, Portola Pharmaceuticals, JAN 9, 2020, View Source [SID1234552930]). For the fourth quarter, the Company expects Andexxa global net revenues to be approximately $28 million. For the full year 2019, the Company expects Andexxa global net revenues to be approximately $111 million.

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In the U.S., net revenues of Andexxa in the fourth quarter 2019 were approximately $24 million, which compares to net revenues of $14.0 million in the same period a year ago and $33.0 million in third quarter 2019.

In Europe, net revenues of Ondexxya were approximately $4 million, which compares to net revenues of $2.7 million in the third quarter of 2019. Fourth quarter 2019 was Ondexxya’s first full quarter of sales following its launch in July 2019 in Europe, where it is now marketed in Germany, Austria, the U.K., the Netherlands, Sweden, Denmark and Finland.

During the fourth quarter, approximately 90 new accounts, and over 425 new accounts in 2019, ordered Andexxa in the U.S. This brings the total number of accounts now ordering Andexxa to approximately 640 at the end of 2019. There continues to be a significant hospital penetration opportunity within the Company’s 2,100 target accounts in 2020 and beyond. Also in the fourth quarter, re-ordering accounts contributed 80% of U.S. revenues, compared to 76% of revenues in the third quarter.

Fourth quarter Andexxa net sales in the U.S. were impacted primarily by two factors:

A $5 million gross to net adjustment due to a return reserve for short-dated product. The Company expects this to be mitigated going forward by its current longer-dated, 36-month product, which began shipping in November 2019.

Flat quarter over quarter demand due to a decrease in utilization, primarily in tier 1 accounts. While physician demand remains strong, the Company believes that in certain of these accounts, hospital pharmacies curtailed use of Andexxa following drug utilization reviews in an effort to manage pharmacy budgets. Following this reduction, re-ordering patterns are stabilizing in many of these accounts.

"While we are disappointed in the fourth quarter net revenues for Andexxa in the U.S., 2019 was a year of significant growth. We exceeded $100 million in revenues, including encouraging contributions from our global launch of Ondexxya, and Andexxa remains on track as one of the top five hospital drug launches in the U.S. in the last 30 years," said Scott Garland, Portola’s president and chief executive officer. "Our belief in the long-term potential of Andexxa remains

strong, and we maintain our projection that this highly innovative, orphan drug has an over $2 billion opportunity in the rapidly growing FXa-inhibitor market in the U.S. and Europe. We look forward to continuing to build long-term revenue growth and value for our shareholders as we establish Andexxa as the standard for care for doctors addressing the urgent needs of patients facing serious, life-threatening bleeds."

"Physician support for Andexxa and Ondexxya in the U.S. and Europe has been tremendous, and we continue to receive outstanding feedback from members of the medical community who have seen first-hand the benefits of Andexxa in treating DOAC-related bleeds," said Sheldon Koenig, Portola’s chief commercial officer. "The drug has excellent efficacy, works fast and is the only FDA-approved agent available. In 2020, we are moving aggressively to execute on our launch strategy and build greater awareness of the life-saving benefits of Andexxa by further educating hospitals on its value."

2020 Growth Drivers

The Company expects continued strong demand of Andexxa, driven by the growth of the Factor Xa inhibitor market in the U.S. and Europe. In 2019, the Factor Xa inhibitor market volume grew by 27% globally to reach $24 billion. In addition, growth in new hospital customers and deeper hospital utilization of Andexxa is expected in 2020 driven by:

Presentation and publication of newly generated health economics and outcomes research data at multiple medical meetings starting with three abstracts at the American College of Cardiology’s Annual Scientific Session together with the World Congress of Cardiology, showing the impact of Andexxa on inpatient mortality, burden of illness, budget impact model and cost effective analysis

Presentation and publication of data demonstrating 4-factor PCC’s, which are only approved to reverse warfarin, are not effective for reversing Factor Xa related bleeds

The launch of key educational initiatives to raise awareness of best practices for the various access and reimbursement pathways available, including: The New Technology Add-on Payment (NTAP) for Medicare beneficiaries in the inpatient setting; a pass through C-code for Medicare and commercial patients in the outpatient setting; participation in both Medicaid and the 340B drug pricing program; and consignment opportunities

Initiation of a single arm study in patients taking Factor Xa inhibitors that require urgent surgery, providing experience to inform the design of a randomized clinical trial

Conclusion of reimbursement discussions in European Wave 1 countries

Expansion of European launch into Wave 2 countries

The Company has a strong cash position to continue to invest in the launch of Andexxa and Ondexxya. As of December 31, 2019, the Company’s cash position totaled $464 million, compared with $317 million as of December 31, 2018.

These preliminary results are based on management’s initial analysis of operations for the quarter ended December 31, 2019. The Company expects to issue full financial results for the fourth quarter and fiscal year 2019 in late February.

Conference Call Details

The Company will host a live conference call on Thursday, January 9, 2020, at 5:00 p.m. ET, which can be accessed by phone by calling (844) 452-6828 from the United States and Canada or 1 (765) 507-2588 internationally and using the passcode 3995797. The webcast can also be accessed live on the Investor Relations section of the Company’s website at View Source

Corporate Update on January 14, 2020

As previously announced, Portola will provide a corporate update on Tuesday, January 14, at 7:00 a.m. PT (10:00 a.m. ET). The live webcast will be available on the Company’s website at View Source A replay of that presentation will remain available on the website after the live webcast.