RAPT Therapeutics Announces Private Placement Financing of $50 Million

On May 25, 2022 RAPT Therapeutics, Inc. (Nasdaq: RAPT), a clinical-stage, immunology-based biopharmaceutical company focused on discovering, developing and commercializing oral small molecule therapies for patients with significant unmet needs in inflammatory diseases and oncology, reported a $50 million private investment in public equity (PIPE) financing from the sale of pre-funded warrants to purchase up to 4 million shares of its common stock at a price per pre-funded warrant of $12.4999 to Redmile Group, based on the closing price per share of RAPT on May 24, 2022 (Press release, RAPT Therapeutics, MAY 25, 2022, https://investors.rapt.com/news-releases/news-release-details/rapt-therapeutics-announces-private-placement-financing-50 [SID1234615023]). Gross proceeds from the PIPE financing total approximately $50 million, before deducting offering expenses. The closing of the PIPE financing is subject to customary closing conditions and is expected to close on May 27, 2022.

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The shares of common stock underlying the pre-funded warrants have not been registered under the Securities Act of 1933, as amended, and may not be offered or sold in the United States except pursuant to an effective registration statement or an applicable exemption from the registration requirements. RAPT has agreed to file a registration statement with the Securities and Exchange Commission registering the resale of the shares of common stock underlying the pre-funded warrants.

This press release shall not constitute an offer to sell or a solicitation of an offer to buy these securities, nor shall there be any sale of these securities in any state or other jurisdiction in which such offer, solicitation or sale would be unlawful prior to the registration or qualification under the securities laws of any such state or other jurisdiction.

Oxford Vacmedix announces Innovate UK funding for development of novel T-cell potency assays

On May 25, 2022 Oxford Vacmedix UK Limited (OVM) reported the award of a Small Business Research Initiative contract from Innovate UK to fund research into the development of novel T-cell based potency assays (Press release, Oxford Vacmedix, MAY 25, 2022, View Source;utm_medium=rss&utm_campaign=innovate-uk-funding-for-development-of-novel-t-cell-potency-assays [SID1234615022]). These assays will support the development of vaccines for diseases of epidemic potential using the company’s proprietary recombinant overlapping peptide (ROP) technology and will pave the way for more cost-effective, rapid testing and improved control of manufacturing for vaccines. This is particularly important in the development of new vaccines for low- and middle-income countries and the findings may also be important in cancer research.

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One of the key issues in vaccine development is the need for potency assays for Quality Control release and stability testing. Traditionally, in vivo testing is used to determine vaccine potency; however, these assays are time-consuming and costly and can show high variability. Cell-based potency assays are typically more reliable and have significantly reduced costs. This project will demonstrate a platform application, so that the assay format can be modified for use with different vaccine antigens including those with epidemic potential. The research will be carried out in collaboration with the Department of Oncology at the University of Oxford and with RSSL.

Spun out from the University of Oxford, OVM is commercialising the research on ROPs developed initially in the University. The principal application of the ROP platform technology is the development of novel therapeutic cancer vaccines with the potential for increased efficacy, simpler regulatory pathways and lower costs. OVM’s lead cancer vaccine, OVM-200 which targets survivin, is in a Phase 1 clinical trial in the UK for solid tumours.

This research is funded by the Department of Health and Social Care as part of the UK Vaccine Network (UKVN), a UK Aid programme to develop vaccines for diseases with epidemic potential in low- and middle-income countries.

Dr Shisong Jiang, CSO and Founder of OVM, said:

"We are very pleased to have received the support from Innovate UK and this funding from the UK Vaccine Network to enable work on this important project to be undertaken. The development of this novel potency assay technology could demonstrate real utility in the development of vaccines for diseases of epidemic potential and be a valuable addition for the progression of all vaccines that employ T cells in the immune response, such as our cancer vaccines."

Professor Xiao-Ning Xu, Chair in Human Immunology, Imperial College, London: added:

"This project is an excellent opportunity to widen the applications of the Oxford Vacmedix’s ROP technology and to build on the company’s expertise in immunology and infectious disease. We look forward to a successful outcome and to these novel assays being able to speed up the development of new vaccines as prophylactics or therapies for cancer and infectious disease".

Genomic Testing Cooperative Hematology Profile Plus, Solid Tumor Profile Plus, and Liquid Biopsy Profiles Receive CE-IVD Mark

On May 25, 2022 Genomic Testing Cooperative (GTC) reported it received CE-IVD marks for its Hematology Profile Plus, Solid Tumor Plus as well as its liquid biopsy profiles for both solid tumors and hematology that are designed to provide a wide range of clinically actionable insights about a patient’s tumor (Press release, Genomic Testing Cooperative, MAY 25, 2022, View Source [SID1234615021]). The CE mark will allow GTC and its partner, TherapySelect (Heidelberg, Germany), to make available GTC’s menu of DNA and targeted transcriptome profiling for patients in Europe. The Solid Tumor Profile Plus provides information on targetable mutations, fusion genes, tumor cell of origin, and the presence or absence of homologous recombination deficiency (HRD). The Hematology Profile Plus provides molecular data for selecting targeted therapy and also accurate diagnosis and classification of various myeloid and lymphoid neoplasms including gene fusions, chromosomal gains and losses, and molecular immunoprofiling. The Hematology Liquid Biopsy Profile is designed to reduce the need for bone marrow biopsy in certain circumstances. The Solid Tumor Liquid Biopsy Profile is designed for tumor-informed monitoring.

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"We are excited to expand our molecular profiling offerings to Europe and to make membership in the Cooperative available internationally. This will strengthen the network and accelerate innovation by building broader knowledge-based artificial intelligence algorithms," stated Dr. Maher Albitar, Founder, Chief Executive Officer and Chief Medical Officer, GTC.

Dr. Frank Kischkel, Managing Director and Scientific Director at TherapySelect stated, "We elected to partner with GTC because of the superior quality and comprehensive offering of the tests along with their commitment to innovation. GTC tests are designed with patients and best practices in oncology in mind. In addition, the co-op business model allows us to internalize the testing in our laboratories as our volumes grow in Europe. We are very excited to be GTC’s authorized representative in Europe and look forward to growing our partnership."

TherapySelect will be the authorized representative in the EU to offer CE certified in vitro diagnostic medical devices. Membership in the Co-Op allows other member labs to internalize GTC testing, which now includes the EU and countries recognizing the CE mark.

AbbVie to Present at the Bernstein 38th Annual Strategic Decisions Conference

On May 25, 2022 AbbVie (NYSE: ABBV) reported that it will participate in the Bernstein 38th Annual Strategic Decisions Conference on Wednesday, June 1, 2022 (Press release, AbbVie, MAY 25, 2022, View Source [SID1234615020]). Richard A. Gonzalez, chairman and chief executive officer, will present at 10:00 a.m. Central Time.

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A live audio webcast of the presentation will be accessible through AbbVie’s Investor Relations website at investors.abbvie.com. An archived edition of the session will be available later that day.

Interim report for the period January 1, 2022 – March 31, 2022

On May 25, 2022 Vivesto reported that Interim report for the period January 1, 2022 – March 31, 2022 (Press release, Vivesto, MAY 25, 2022, View Source [SID1234615013])

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SIGNIFICANT EVENTS DURING THE FIRST QUARTER
With the purpose to finance the continued development of Vivesto and its projects in accordance with its business plan and strategy, the Board of Directors resolved on a fully secured rights issue of approximately SEK 151 million in January, subject to approval at an Extraordinary General Meeting.
In January, Vivesto announced progress on the development of XR-18 and that the company had identified and synthesized a promising novel candidate for use in the drug delivery platform.
On February 21, an Extraordinary General Meeting approved the Board of Directors’ resolution on 19 January 2022 on a new issue of shares with preferential rights for existing shareholders, and approved an amendment to the Articles of Association whereby the company’s corporate name would change to Vivesto AB.
In February, Vivesto provided an update on the progress of the SAKK investigator-initiated Phase 1b trial of Docetaxel Micellar in advanced prostate cancer.
In March, Vivesto announced that Fredrik Järrsten would leave his role of Chief Financial Officer later in the year, following a notice period of six months, to pursue new opportunities.
In March Vivesto announced that the intellectual property (IP) portfolio had been strengthened considerably in terms of XR-17, the company’s primary drug delivery technology.
In March Vivesto expanded its R&D ability with a planned laboratory upgrade in Uppsala.
In March Vivesto signed a manufacturing agreement with Lonza for drug candidate Cantrixil. Under the agreement, Lonza will deliver cGMP-standard drug substance for clinical supply.
On March 25 Vivesto announced the final results from the company’s fully secured rights issue. 48,367,120 shares, corresponding to approximately 54 percent of the shares offered, were subscribed for by the exercise of subscription rights. 1,519,430 shares, corresponding to approximately 1.7 percent of the shares offered, were allotted to persons who have subscribed for shares without the use of subscription rights. The remaining 39,787,359 shares offered, corresponding to approximately 44 percent, were allotted to guarantors. Vivesto receives approximately SEK 151 million through the rights issue before issue costs.
On March 28 the company announced the completion of its name change to Vivesto AB.
SIGNIFICANT EVENTS AFTER THE REPORTING PERIOD
In April Daniel Tesfa was appointed as Chief Medical Officer.
In April Vivesto signed an agreement with leading US CRO Visikol Inc. to evaluate anti-cancer drug formulations using its proprietary drug delivery platforms.
In April the Nomination Committee of Vivesto proposed the re-election of Board members Hege Hellström and Peter Zonabend, and the election of Pål Ryfors and Roger Tell as new Board members. Further, the Nomination Committees proposed the election of Peter Zonabend as the new Chairman of the Board. The Board members Anders Härfstrand, Andrea Buscaglia and Birgit Stattin Norinder have declined re-election.
FIRST QUARTER: JANUARY 1, 2022 – MARCH 31, 2022
Consolidated net sales amounted to TSEK 0 (37)
Operating profit/loss var TSEK -26,329 (-40,842)
Net profit/loss after tax amounted to TSEK -26,457 (-41,209)
Earnings per share amounted to SEK -0.06 (-0.09)
CEO REVIEW
Creating a solid foundation for the future

The first quarter of 2022 has seen us deliver significant progress, completing the turnaround and, with the recent financing, securing a solid foundation for the future.

Over the last eighteen months, my team and I have rightsized the business and eliminated unnecesary costs to conserve cash, reduced risk by settling legacy litigation, added new development and regulatory capabilites, and initiated our ‘string of pearls’ strategy to build our pipeline through in-licensing and M&A.

Most recently, during the reporting period and despite global geopolitical tensions and a challenging financing environment, we were able to raise SEK 151m through a rights issue, strengthening our balance sheet and securing the short to medium-term finances of the business. This money will be used to fund existing operations and help us achieve potential value inflection points for our development programs.

To mark the completion of the turnaround in the business and the new chapter in our journey, we changed the company name to Vivesto following a vote at an extraordinary general meeting earlier this year. Vivesto comes from Vivo, or to live, in Spanish and Latin, and esto which infers investment. This reflects our focus and commitment to improve survival and quality of life for patients with cancer through investment in R&D and innovation.

Progressing our internal oncology R&D programs
There are still many cancer patients with limited or no treatment options or whose cancers have become resistant to treatment. Our programs, which address these hard to treat cancers, are progressing well in clinical development.

We are preparing for the initation of a Phase 2 trial of our most advanced internal development program, Cantrixil, a potent and selective third generation benzopyran SMETI inhibitor encapsulated in a cyclodextrin, for advanced ovarian cancer. Cantrixil, an intraperitoneally administered drug, was in-licensed from Kazia Therapeutics last year and represents the first program to be brought in-house through our ‘string of pearls’ strategy.

Cantrixil is complicated to manufacture so we have had to engage with multiple parties to secure the supply of clinical trial material. I’m pleased to report that during the quarter we made substantial progress with the signing of an agreement with Lonza, the Swiss multinational manufacturing company, for large-scale production of the main drug intermediate. We also expanded our research facility in Uppsala and broadened our capabilities to develop new Cantrixil formulations using our proprietary drug delivery platform which we believe may provide benefits for patients. Cantrixil is particularly exciting as it is believed to target a wide spectrum of cancer cells, including chemotherapy-resistant tumor-initiating cells that are thought to be responsible for disease relapse.

Docetaxel micellar is currently in an investigator-initiated Phase 1b trial for advanced prostate cancer with the non-profit making Swiss Group for Clinical Cancer Research (SAKK). Prostate cancer is a significant and increasingly prevalent health problem worldwide and is the leading cause of male cancer deaths. Docetaxel micellar is a solvent-free formulation of docetaxel, developed to avoid the need for the solubility enhancers in solvent-based docetaxel, and the mandatory high-dose steroid premedication, while providing an effective treatment option.

The SAKK 67/20 trial is an open-label, multicenter, single-stage Phase 1b trial at major hospitals in Switzerland, recruiting 18 chemotherapy-naïve patients with metastatic castration resistant prostate cancer (mCRPC) with adequate bone marrow, liver, and renal function. The primary objective of this trial is to determine the maximum tolerated dose of Docetaxel micellar in patients with mCRPC and the secondary objectives are to evaluate safety, assess the preliminary anti-tumor activity, and to characterize the pharmacokinetics in this population. During the quarter we announced that the first patient had fully completed the study. Furthermore, the first two of three dosing groups in the trial had been successfully recruited and the first patient for dose group three is in screening phase. We look forward to updating you as the trial progresses.

Maximising value from our partnered commercial oncology program
Our partnered program Apealea (paclitaxel micellar) for late stage ovarian cancer is an intravenously injectable, non-Cremophor based formulation of paclitaxel using our proprietary drug platform that can be given without premedication such as steroids and with a shorter infusion time. Paclitaxel is a well-known chemotherapy agent used to treat breast, ovarian, lung, bladder, prostate, melanoma, and oesophageal cancer, as well as other types of solid tumour cancers and is often formulated with Cremophor-EL, which is associated with allergic reactions.

Apealea is outlicensed globally to Elevar Therapeutics and other regional partners. It is expected to be launched in the UK through Elevar’s European partner Inceptua in the first half of 2022, with the launch in Germany to follow in the second half of 2022. This could lead to us receiving royalties on sales during the second half of 2022. Following feedback from the FDA Elevar has decided to conduct clinical studies prior to filing a registration application for Apealea in the US. A Phase II/III trial is planned to investigate the safety and efficacy of Apealea in epithelial ovarian cancer. Elevar is working closely with the US Gynecologic Oncology Group (GOG) Foundation through its GOG Partners program. We are in regular contact with Elevar and will keep you informed as the program progresses.

Exploring the full potential of our technologies
Our proprietary drug solubilization technology platform, XR-17, together with our next-generation, development-stage platform, XR-18, provide a vital constituent of our Apealea and Docetaxel micellar formulations.

During the quarter we were pleased to announce a significant expansion of our intellectual property (IP) portfolio associated with XR-17. XMeNa patents were granted in Japan, Singapore, Russia and in several other jurisdictions, protecting an improved method for the manufacturing of the unique XR-17 components. The XMeNa patent adds to Vivesto’s broad IP portfolio and provides patent protection for the XR‑17 technology and Apealea to 2036.

We also announced that we have identified and synthesized a promising novel candidate for use in the XR-18 drug delivery platform, which we believe could offer enhanced capabilities compared with the XR-17 technology. The next-generation formulation applied in XR-18 is already being tested in combination with a widely used oncology compound, which we cannot disclose for competitive reasons while steps to secure intellectual property are being taken.

Building on these advances post period end, we announced the signing of a research agreement with Visikol Inc., a leading U.S. contract research services provider, to evaluate the cellular effects of new and existing anti-cancer drug formulations developed using Vivesto’s XR-17 and XR-18 technologies. As a result of this research, we will be able to assess anti-cancer compounds formulated with our XR-17 drug delivery platform as well as line extensions formulated with our XR-18 technology with regard to their therapeutic properties and underlying biologic effects. This research will allow us to select promising developmental drug candidates and further expand our current and future oncology pipeline.

Looking ahead
I am pleased with the progress the business has made during the first quarter of the year in difficult market conditions. We’ve raised finances to secure our short to medium term future and launched a new identity to mark our focus and commitment to improve survival and quality of life for patients with cancer through investment in R&D and innovation.

As our internal development program progresses through the clinic it is vital that we employee the very best capabilities to maximize the chances of success. I am therefore looking forward to welcoming our new Chief Medical Officer, Dr. Daniel Tesfa in the summer. Daniel’s extensive and first-hand experience working in clinical development and oncology makes him a perfect fit for Vivesto.

The next stage in our journey focusses on the execution of our ‘string of pearls’ strategy, in-licensing and M&A to build our oncology pipeline. We remain in discussion with several companies, and I look forward to updating you when I can.

I’d like to thank my team for their continued dedication without whom it would have been impossible to deliver the changes that led to our transformation.

I would also like to thank you all for continuing to invest in a business that is now more streamlined and focused than ever before and which, I believe, is well positioned to deliver value over time.