Celluris participates in the Bioconvention 2022

On July 24, 2022 Celluris reported that participated this june in the largest biotechnology fair in World, the BioConvention in San Diego (Press release, (Press release, Celluris, JUL 24, 2022, View Source [SID1234616887]), JUL 24, 2022, View Source [SID1234616887]). These were intense days, with more than 30 meetings with industry players, such as related companies and innovation agents from other countries. In addition to the participation we made a presentation pitch on Brazilian Startup Day. Together with the Brazilian delegation in the event, there was the publication of the 6th edition of bioBr Magazine that was shared with everyone during the event and can be accessed digitally via the link to next: CLICK HERE In addition, Brazilian startups had a published article in Yahoo Finance : SEE HERE

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June 2022 Quarterly Activity Report

On July 22, 2022 Race Oncology reported that The June 2022 quarter (Q4 FY 2022) was highlighted by the successful completion of the Phase 1b stage of the relapsed or refractory Acute Myeloid Leukaemia (R/R AML) trial of Zantrene (bisantrene dihydrochloride) running at the Chaim Sheba Medical Centre, Israel (ASX announcement: 27 May 2022) (Press release, Race Oncology, JUL 22, 2022, View Source [SID1234617042]). Encouraging clinical responses were observed in a very heavily pre-treated AML patient population with 3 of the 6 patients bridged to a stem cell transplant. The study led by Professor Arnon Nagler now advances to the Phase 2 efficacy stage with the intention of recruiting up to 17 patients.

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A second highlight was the discovery that Zantrene protects the hearts of mice from the damaging effects of anthracyclines (specifically doxorubicin)-even when the chemotherapeutic dose was increased and without significant additional toxicity or bone marrow suppression (ASX announcement: 30 June 2022).

Our extramedullary AML clinical trial received all ethics and regulatory approvals and is expected to treat the first patient in the current quarter-Q3 CY 2022 (ASX announcements: 6 April 2022 and 12 May 2022). This is the first clinical trial in the world to investigate the targeting of FTO as a potential cancer therapy.

Highly promising melanoma preclinical results in cells, organoids and mice was announced, showing Zantrene is able to aid overcoming immune therapy resistance, and synergise with BRAF and MEK kinase inhibitors (ASX announcements: 22 June 2022; 28 June 2022).

Race announced an on-market share buyback for up to 4 million Race Oncology ordinary shares over the next 12 months (ASX announcement: 9 June 2022). The on-market buyback allows the company to take advantage of share price volatility through opportunistic share purchases during periods when the share price does not reflect the robust outlook for the company. Race Oncology Ltd ABN 61 149 318 749 Registered office: L36, 1 Macquarie Place, Sydney NSW 2000 www.raceoncology.com Race continues to progress its Three Pillar Strategy to capitalise on the RNA therapeutics opportunity in cancer and cardioprotection provided by Zantrene.

Management commentary Race CEO Phillip Lynch said: "We were particularly pleased to see the human heart cell data corroborated in a whole mouse model, confirming that Zantrene when used with doxorubicin protects from cardiac damage, while also improving anti-cancer efficacy. We are now developing clinical programs as we pursue realisation of this high value opportunity for Zantrene." Race CSO Daniel Tillett said: "Race made major advances this quarter, both in the clinic and in the lab. Advancement of the relapsed / refractory AML clinical trial at Chaim Sheba from Phase 1 to Phase 2 and progressing the EMD AML trial through the regulatory process were important clinical milestones achieved in the quarter. The mouse cardioprotection, melanoma immunotherapy and kinase inhibitor results have further highlighted the outstanding potential of Zantrene."

Race Chairman John Cullity said: "The Race team has again delivered for Shareholders. While preclinical, the reported cardioprotection data are groundbreaking. As a former clinician, I’m entirely alert to the impact that select chemotherapies have on the heart. It is remarkable that Zantrene might both enhance cancer cell kill while protecting the heart – so potentially reshaping cancer therapeutics. We possess an obligation to take this program forward with all purpose." –––– Key events of the quarter 

On 6 April 2022, Race announced that it had human ethics approval for its open label clinical trial of Zantrene in patients with extramedullary Acute Myeloid Leukaemia (AML) or high-risk Myelodysplastic Syndrome (MDS)(BISECT). This is the first clinical trial in the world to investigate the targeting of FTO as a potential cancer therapy. 

On 12 May 2022, Race announced it had received Research Governance Office (RGO) approval from the Calvary Mater Newcastle Hospital for its open label clinical trial of Zantrene in patients with extramedullary Acute Myeloid Leukaemia or high-risk Myelodysplastic Syndrome (BISECT). A site meeting was scheduled for 31 May 2022 to initiate the trial and allow recruitment of the first patient. 

On 18 May 2022, Race announced that it had appointed Dr James Guy Breitenbucher to its Scientific Advisory Board (SAB). Dr Breitenbucher brings to Race an extensive drug discovery and clinical development history, having spent more than 26 years in scientific leadership positions at a range of large and small pharmaceutical companies, including Johnson & Johnson, Convelo Therapeutics, Libra Therapeutics, Dart Neuroscience, Axys Pharmaceuticals, and Bristol Myers Squibb. Race Oncology Ltd ABN 61 149 318 749 Registered office: L36, 1 Macquarie Place, Sydney NSW 2000 www.raceoncology.com 

On 27 May 2022, Race announced results from the dose escalation Phase 1b stage of the relapsed or refractory Acute Myeloid Leukaemia (R/R AML) trial running at the Chaim Sheba Medical Centre, Israel. Phase 1b successfully completed after the treatment of the first six patients. Encouraging clinical responses were observed in this very heavily pre-treated AML patient population with 3 of the 6 patients bridged to stem cell transplants. The study led by Professor Arnon Nagler now advances to the Phase 2 efficacy stage with the intention of recruiting up to 17 patients. 

On 8 June 2022, Race announced it was expanding the FTO-targeted BISECT (RAC006) clinical trial in extramedullary Acute Myeloid Leukaemia (EMD AML) and Myelodysplastic Syndromes (MDS) to include five additional trial sites in Spain and Italy and had also signed a new clinical support agreement with global Clinical Research Organisation, Parexel International to support the additional trial monitoring activities. The total study costs are expected to be in the range of A$7.7 million to a maximum of A$15.4 million. The final cost is dependent on the location and number of patients screened and enrolled in the trial. 

On 9 June 2022, Race announced the Board has approved an on-market share buyback for up to 4 million Race Oncology ordinary shares over the next 12 months. All committed clinical and preclinical programs as outlined in the November 2021 Share Purchase Plan remain fully funded. The structure of an on-market buyback allows the company to take advantage of share price volatility through opportunistic share purchases during periods in which the share price does not reflect the robust outlook for the company. 

On 21 June 2022, Race announced that two peer reviewed research poster abstracts detailing new preclinical data on the anti-cancer uses of Zantrene (also known as bisantrene or CS1) had been published in the prestigious scientific journal, Cancer Research. Publication followed their recent presentation at the American Association of Cancer Research (AACR) (Free AACR Whitepaper) Annual Conference in New Orleans, from April 8 – 13, 2022. The first abstract demonstrates Zantrene’s ability to target FTO in the suppression of pancreatic cancer. The second abstract discusses the potential use of Zantrene as an adjunctive treatment to 5-FU based chemotherapy for colorectal cancer patients. These independent results add to Race’s own reported preclinical and clinical data, showing Zantrene’s potential in targeting FTO in AML, melanoma and kidney cancer. 

On 22 June 2022, Race announced further interim results from its preclinical melanoma research program (ASX announcement: 19 March 2021). Used at low concentrations, Zantrene was found to enhance cancer immunotherapy in three distinct and complementary ways:
(1) direct killing of melanoma cells;
(2) activation of immune cells targeting the tumour, and
(3) reducing the expression of immune evasion genes in the tumour. The results were supportive of future clinical trials using Zantrene in combination with immune therapy treatments to potentially improve melanoma patient outcomes. 

On 28 June 2022, Race announced final results of the preclinical melanoma research program in collaboration with the University of Newcastle. Zantrene in combination Race Oncology Ltd ABN 61 149 318 749 Registered office: L36, 1 Macquarie Place, Sydney NSW 2000 www.raceoncology.com with BRAF and MEK protein kinase inhibitors was found to improve the killing of human melanoma cells and to better target melanoma in organoid and animal tumour models. These discoveries offer potential non-immunotherapeutic pathways for the use of Zantrene in melanoma treatment. 

On 30 June 2002, Race announced additional interim results from our preclinical cardioprotection program in collaboration with researchers from the University of Newcastle (ASX announcement: 28 April 2021). Zantrene was found to protect the hearts of mice from the damaging effects of anthracyclines (specifically doxorubicin)-even when the chemotherapeutic dose was increased-without significant additional toxicity or bone marrow suppression.

Other news from the quarter  Chief Executive Officer (CEO) Phillip Lynch and Chief Scientific Officer (CSO) Daniel Tillett moved to 0.75 FTE level from 1 April 2022. Bonus and Option conditions remain unchanged and will be assessed according to the company’s incentive scheme and assessment of performance versus established goals.  Dr Daniel Tillett, Race CSO, presented at the Gold Coast Investment Showcase on 22 and 23 June 2022, and met with both existing and new shareholders through the event. Summary of cash flow and quarterly activity As of 30 June 2022, Race held cash and equivalents of $33.54 million, compared with $35.68 million on 31 March 2022. The net change in cash reserves of $2.14 million reflects continued research expenditure, an expansion of Zantrene inventory for clinical trials, and advancement of other drug development programs. Listing rule 4.7C.3 Payments during the quarter to Related Parties amounted to $208k, comprising payments of salaries and superannuation to executive directors of $165k and board fees to non-executive directors of $43k.

Revolution Medicines Announces Closing of Upsized Public Offering of Common Stock and Full Exercise of Underwriters’ Option to Purchase Additional Shares

On July 22, 2022 Revolution Medicines, Inc. (Nasdaq: RVMD), a clinical-stage oncology company developing targeted therapies for RAS-addicted cancers, reported the closing of an underwritten public offering of 13,225,000 shares of common stock at a public offering price of $20.00 per share, before underwriting discounts and commissions (Press release, Revolution Medicines, JUL 22, 2022, View Source [SID1234616889]). The shares of common stock issued and sold in the offering include 1,725,000 shares issued upon exercise in full by the underwriters of their option to purchase additional shares of common stock at the public offering price, less underwriting discounts and commissions. The gross proceeds from the offering, before deducting underwriting discounts and commissions and other offering expenses payable by Revolution Medicines, were $264.5 million. All shares in the offering were offered by Revolution Medicines.

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J.P. Morgan, Cowen and Guggenheim Securities acted as the joint book-running managers for the offering.

A shelf registration statement relating to these securities was filed with the U.S. Securities and Exchange Commission on March 2, 2021, and automatically became effective upon filing. This offering was made solely by means of a prospectus. A copy of the final prospectus supplement and the accompanying prospectus relating to this offering may be obtained by contacting: J.P. Morgan Securities LLC, c/o Broadridge Financial Solutions, 1155 Long Island Avenue, Edgewood, NY 11717, by telephone at (866) 803-9204 or by email at [email protected]; Cowen and Company, LLC, c/o Broadridge Financial Solutions, 1155 Long Island Avenue, Edgewood, NY, 11717, Attn: Prospectus Department, by telephone at (833) 297-2926 or by email at [email protected]; or Guggenheim Securities, LLC, Attn: Equity Syndicate Department, 330 Madison Avenue, 8th Floor, New York, NY 10017, by telephone at (212) 518-9544, or by email at [email protected].

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.

Immune Therapeutics, Inc. Appoints Dr. Stephen Wilson as Chief Executive Officer

On July 22, 2022 Immune Therapeutics, Inc. (OTC Pink: IMUN) ("Immune" or "IMUN"), a specialty pharmaceutical company involved in the acquisition, development and commercialization of pharmaceutical and biotechnology products that have a short and well-defined path to market, reported the appointment of Dr. Stephen "Steve" Wilson as Immune’s Chief Executive Officer (CEO), President, and interim Chief Financial Officer (CFO) effective July 19, 2022; he will continue to serve as a member of the Company’s Board of Directors (Press release, Immune Therapeutics, JUL 22, 2022, View Source [SID1234616888]).

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Dr. Wilson brings over 20 years of experience in biomedical research, executive management, and corporate governance. He is a trained immunologist. In addition, he is, among other things, an Associate Clinical Professor at the University of California, San Diego, and he previously served as the Chief Operating Officer at the La Jolla Institute for Immunology as it grew to become an international powerhouse.

Immune also announced that Kevin Phelps has stepped down from his positions as the company’s CFO, President, and CEO, but he will remain a member of Immune’s Board of Directors.

The appointment of Dr. Wilson as Immune’s CEO, President, and interim CFO is expected to further strengthen IMUN’s global executive leadership team to drive its next phase of growth and operational success within a new operational model, initially focused on regulatory approval and commercialization of existing assets that treat patients with inflammatory disease.

Dr. Wilson stated, "Our strategy is to lever the global need for affordable and effective therapeutics and modern financial tools; this hinges on acquisition, development and commercialization of pharmaceutical and biotechnology products that have a short and well-defined path to market. We have assets that fit this profile, and our business objectives fit immediate patient needs. Going forward, we will take a measured portfolio approach to investment, development and commercialization that will mandate each additional program be hyper focused, capital efficient and small-scale with clear paths to regulatory approval. Financing these programs through modern investment vehicles and partnerships, we plan to deploy in markets that include, but are not dependent upon, US commercialization."

GenFleet Receives CTAs Approval for Two Phase II Combination Studies of TGF-β R1 Inhibitor (GFH018) with PD-1 Inhibitor

On July 22, 2022 GenFleet Therapeutics, a clinical-stage biotechnology company focusing on cutting-edge therapies in oncology and immunology, reported that China’s National Medical Products Administration (NMPA) has approved the Clinical Trial Applications (CTAs) for GFH018 in two clinical studies for combination therapies (Press release, GenFleet Therapeutics, JUL 22, 2022, View Source;r1-inhibitor-gfh018-with-pd-1-inhibitor-301591532.html [SID1234616885]).

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One study is a phase Ib/II trial of GFH018 with PD-1 inhibitor treating patients with advanced solid tumors; the other study is a phase II trial of GFH018, PD-1 inhibitor with concurrent chemoradiotherapy treating patients with locally advanced & unresectable NSCLC. GenFleet has completed a phase I trial of GFH018 monotherapy treating solid tumors in early 2022, and the data will soon be published in relevant international medical conference.

"Pre-clinical in-vivo data have demonstrated desirable anti-tumor effects of GFH018 in combination with PD-1 inhibitors; the combo study(GFH018X0201)being conducted in Australia and China’s Taiwan has completed the dose escalation phase (phase Ib), with the dose expansion phase (phase II) currently ongoing. From this multi-regional, multi-center clinical trial, we expect to collect additional evidence to further confirm the efficacy of combination therapies with GFH018 in cancer patients. In the study of GFH018, PD-1 inhibitor with concurrent chemoradiotherapy(GFH018X1202), we will investigate the combination’s potential in improving the immunosuppressive microenvironment and reducing the side effects from concurrent chemoradiotherapy." said Yu Wang, M.D./Ph.D., Chief Medical Officer of GenFleet.

"GFH018 is GenFleet’s first product that has moved into clinical development stage. The progress of GFH018’s multi-regional studies clearly demonstrates GenFleet’s capability in global regulatory registration, patient enrollment and market positioning, and will substantially accelerate GFH018’s global clinical development. TGF-β signaling pathway has been studied as a critical target in multiple solid tumors; however, no drugs have been approved to date for this pathway. GFH018 is a small molecule drug designed to specifically target and inhibit TGF-β R1, and the discovery and development of GFH018 truly reflects GenFleet’s strategy of novel mechanism-focused innovation in drug development. GenFleet expects the development of the GFH018 to bring a novel therapy with great clinical benefit to cancer patients. "said Jiong Lan, Ph.D., Chief Executive Officer of GenFleet.

Both studies are multi-center, single-arm, and open-label trials designed to evaluate the safety/tolerability and efficacy of the GFH018 in combination therapies. Shanghai Oriental Hospital and Sun Yat-Sen University Cancer Center will lead the phase Ib/II study evaluating the combination of GFH018 and anti-PD-1 monoclonal antibody conducted in over 20 domestic hospitals. The safety/tolerability and efficacy of combination of GFH018, anti-PD-1 monoclonal antibody, concurrent chemoradiotherapy will be evaluated in the phase II study, which will be conducted at over 10 hospitals including West China Hospital of Sichuan University, Peking Union Medical College Hospital.

About GFH018 and TGF-β R1

Developed by GenFleet Therapeutics, GFH018 is an orally administered TGF-β R1 inhibitor and entered into phase I clinical trial in 2019. Preclinical data showed evidence of GFH018’s good anti-tumor properties against cancer cells in vivo and in vitro. Besides, translational and mechanistic studies confirmed it effectively acts on TGF-β signaling pathway and synergizes with checkpoint inhibitors.

In the microenvironment of advanced solid tumors, TGF-β signaling pathway can promote epithelial mesenchymal transition (EMT) & metastasis, induce the formation of cancer stem cells and their functional maintenance, inhibit anti-tumor immunity, enhance vasculature and fibrosis, and ultimately result in tumor progression. Among patients of hepatocellular carcinoma, glioma, colorectal cancer, lung cancer, pancreatic cancer, urothelial cancer and other solid tumors, high expression of genes related to TGF-β signaling pathway is frequently discovered in their blood and tumor tissues. The expression level is positively correlated to the malignancy & poor differentiation of tumor and unfavorable prognosis in patients.