Targovax ASA: Registration of share capital increase following the settlement of RSUs

On May 26, 2021 Targovax ASA (OSE:TRVX) ("Targovax" or the "Company") reported that regarding the board of directors’ resolution to increase the share capital of the Company following the settlement of RSUs (Press release, Targovax, MAY 26, 2021, View Source [SID1234580590]).

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The share capital increase has today been registered with the Norwegian Register of Business Enterprises (Nw. Foretaksregisteret). The Company’s new share capital is NOK 8,658,240.50, divided into 86,582,405 shares, each with a par value of NOK 0.10.

Defence therapeutics accuvac-d001 cancer vaccine generates effective long-lasting anti-tumoral response

On May 25, 2021 Defence Therapeutics reported the completion of its AccuVAC-D001 cancer vaccine preclinical study (Press release, Defence Therapeutics, MAY 25, 2021, View Source [SID1234626234]). The AccuVAC-D001 cancer vaccine demonstrated a 70% cure rate of mice with pre-established solid tumors, this AccuVAC-D001 cancer vaccine confirms an effective antitumoral response.

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Non-specific degradation of endocytosed cancer antigens by endo-lysosomal organelles in dendritic cells (DCs) is a major limitation in the field of cancer vaccination. Defence AccuVACTM addresses this with its engineered novel antigen formulation. The AccuVACTM protects endocytosed antigen from non-specific endosomal degradation by promoting its escape via endosomal membrane disruption. As such, endocytosed antigens accumulate – in their closest native state – in the cytosol of DC cells consequently resulting in efficient antigen crosspresentation to responding immune cells.

AccuVACTM dramatically improved protein processing and cross-presentation by ex vivo developed monocyte-derived DCs, which elicited potent CD4 and CD8 T-cell responses compared to the use of naked antigen. The net outcome culminates into effective anti-tumoral responses curing 70% of animals with pre-established solid tumors.

"The solid results of the AccuVACTM study demonstrates how this strategy can be positively adapted to engineered universal DC vaccines. This puts Defence and its technology on the path for future development of universal therapeutic vaccines for cancer and infectious diseases vaccines", says Mr. Plouffe, CEO of Defence Therapeutics.

Vaccines Market Size 2021, is Projected to Reach USD $104.87 Billion by 2027, exhibiting a CAGR of 10.7% according to Future Business Insights.

PureTech to Present at the Jefferies Virtual Healthcare Conference

On May 25, 2021 PureTech Health plc (Nasdaq: PRTC, LSE: PRTC) ("PureTech" or the "Company"), a clinical-stage biotherapeutics company dedicated to discovering, developing and commercializing highly differentiated medicines for devastating diseases, reported that Daphne Zohar, Founder and CEO, will participate in a fireside chat at the Jefferies Virtual Healthcare Conference on Wednesday, June 2nd at 9:00 AM EST (Press release, PureTech Health, MAY 25, 2021, View Source [SID1234584764]). A webcast of the presentation will be available at View Source

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NuCana to Present at the Jefferies Virtual Healthcare Conference

On May 25, 2021 NuCana plc (NASDAQ: NCNA) reported that Hugh Griffith, Chief Executive Officer, and Don Munoz, Chief Financial Officer, will present and host one-on-one meetings at the Jefferies Virtual Healthcare Conference being held from June 1 to June 4, 2021 (Press release, Nucana BioPharmaceuticals, MAY 25, 2021, View Source [SID1234584208]).

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Event: Jefferies Virtual Healthcare Conference
Date: Tuesday, June 1, 2021
Time: 9:30 AM ET

The presentation will be webcast live and available for replay under "Events & Presentations" in the Investors section of the Company’s website at www.nucana.com.

UK Says ‘Not So Fast’ on AstraZeneca’s $39 Billion Alexion Acquisition

On May 25, 2021 AstraZeneca reported that $39 billion acquisition of Alexion is now being investigated by the UK’s Competition and Markets Authority (CMA), to determine if the deal is anti-competitive (Press release, AstraZeneca, MAY 25, 2021, View Source [SID1234583260]). On March 17, 2021, it was reported that the U.S. Federal Trade Commission (FTC) organized a multinational working group to evaluate pharmaceutical mergers.

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Along with the FTC, the group included the CMA, the Canadian Competition Bureau, the European Commission Directorate General for Competition, the U.S. Department of Justice Antitrust Division, and Offices of State Attorneys General.

The commission’s goal is to "identify concrete and actionable steps to review and update the analysis of pharmaceutical mergers."

At that time, the FTC was reviewing the AstraZeneca-Alexion deal. Alexion had filed with the U.S. Securities and Exchange Commission (SEC) at the time, indicating it planned to withdraw and refile its notification and report form under the Hart-Scott-Rodino Antitrust Improvements Act of 1976, "in order to give the FTC additional time to review the proposed transaction."

The deal has since received the greenlight from the U.S., Canada, Brazil and Russia, but decisions are still pending from the UK, the EU and Japan. The deal was announced in December 2020. AstraZeneca wanted to bolster its immunology presence.

Two weeks ago, Alexion shareholders approved the deal.

"We’re very pleased with today’s affirmative shareholder vote, which brings us one step closer to completing a transaction that will accelerate the combined company’s ability to develop and provide access to life-changing medicines for patients with rare and devastating diseases around the world," said Ludwig Hantson, Alexion’s chief executive officer, at the time.

Under the terms of the deal, Alexion shareholders would receive $60 in cash and 2.1243 AstraZeneca American Depositary Shares (ADS), with each ADS worth half of an ordinary AstraZeneca share. That comes to about $175 per share.

AstraZeneca’s market presence has typically been on oncology, cardiovascular, renal and metabolism and respiratory diseases. It increased its immunology R&D efforts in immune-mediated diseases.

Alexion’s focus is on complement inhibition, a part of the human immune system. Its branded products focus on immune-mediated rare diseases caused by abnormal activation of the complement system. These include Soliris (eculizumab), a first-in-class anti-complement component 5 (C5) monoclonal antibody.

Soliris is approved in several countries for paroxysmal hemoglobinuria (PNH), atypical hemolytic uremic syndrome, generalized myasthenia gravis and neuromyelitis optica spectrum disorder. The company’s Ultomiris (ravulizumab) is a second-generation C5 monoclonal antibody. Other products include Strensiq (asfotase alfa) and Kanuma (sebelipase alfa).

If the merger is finalized, the two companies will work to advance Alexion’s pipeline of 11 molecules across more than 20 clinical programs, many in rare diseases. Alexion’s immunology expertise is expected to support AstraZeneca’s presence in immunology and rare diseases.

At the time of the announcement, Pascal Soriot, AstraZeneca’s chief executive officer, said, "Alexion has established itself as a leader in complement biology, bringing life-changing benefits to patients with rare diseases. This acquisition allows us to enhance our presence in immunology. We look forward to welcoming our new colleagues at Alexion so that we can together build on our combined expertise in immunology and precision medicines to drive innovation that delivers life-changing medicines for more patients."