HanxBio Presents Latest Clinical Data on Anti-CD47/PD-1 Bifunctional Antibody Injection (HX0090) at the 2021 American Society of Clinical Oncology (ASCO) Annual Meeting

On October 20, 2021 HanX Biopharmaceuticals reported the latest clinical data for its recombinant humanized anti-CD47/PD-1 bifunctional antibody HX009 injection at the 2021 American Society of Clinical Oncology (ASCO) (Free ASCO Whitepaper) Annual Meeting (Press release, HanX Biopharmaceuticals, OCT 20, 2021, View Source [SID1234655941]). Professor Aflah Roohullah, the clinical lead PI at Southwestern Medical Center in Sydney, Australia, presented the favorable safety and tolerability clinical trial results of HX009 in an oral poster presentation.

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About the HX009 Australian Clinical Trial
Selected Study: First-in-Human Phase 1 Dose-Escalation Study of HX009, a Novel Recombinant Humanized Anti-CD47/PD-1 Bispecific Antibody, in Patients with Advanced Malignancies (Abstract No. 2517)

HX009 underwent a Phase I clinical study in Australia to evaluate the safety, tolerability, and pharmacokinetic (PK) properties of HX009 injection in patients with advanced solid tumors, and to assess its preliminary anti-tumor efficacy in solid tumors using the RECIST1.1 standard.

As of April 2021, enrollment in the seven dose-escalation cohorts in Australia has been completed, with a total of 21 patients enrolled. No dose-limiting toxicities or maximum tolerated doses have been observed, and safety and tolerability are good. Among the 20 patients who completed at least one tumor assessment, three patients (15%) achieved partial response (PR), with an objective response rate (ORR) of 15%, and seven patients (35%) achieved stable disease (SD), with a disease control rate (DCR) of 50%.

About HX009
HX009 Injection is a novel humanized antibody fusion protein injection independently developed by Hangzhou Hans. The HX009 antibody fusion protein simultaneously targets PD-1 and CD47. Through interaction between CD47’s ligand protein SIRPa and CD47 on tumor cells, it enhances macrophage phagocytosis and activates the immune response of CD8+ T cells. Anti-PD-1 antibodies then stimulate the replication of previously exhausted T cells, thereby enhancing both innate and cellular immune responses through multiple steps.

Doma landed in BioBAY to jointly create new drug research and development innovation highland

On October 20, 2021 Doma announced the official start of its operation and plans to build its new drug development headquarters in Suzhou Industrial Park (Press release, Doma Biopharmaceutical, OCT 20, 2021, View Source [SID1234636132]). Doma was established in Suzhou BioBAY in September 2021. Led by Biocytogen and supported by three major central enterprises, China Life, PICC and State Development and Investment Corp., as well as CMB International and Suzhou Industrial Park, the project involves the joint construction of an innovative drug incubation center and the investment of the first phase is expected to exceed RMB 1 billion.

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By leveraging the innovative pipelines branched from the project integrum platform, Doma is committed to incubating new antibody drug companies in the park and establishing a new cradle of innovation for new drug development in China. the goal of the project integrum is to discover numerous potential first-in-class targets and novel antibody molecules over a period of 3-5 years. Incubatees in their early stages can leverage the large number of promising new targets and antibodies identified by the platform to reduce early-stage R&D spending and move their pipelines quickly into clinical stages, thereby greatly accelerating the R&D process

Licence agreement with TRx Biosciences Limited

On October 20, 2021 Oxilio reported that it signed an exclusive global licensing agreement with TRx Biosciences Ltd, a privately held pharmaceutical development company, for its patent rights and know-how connected with the TRx platform technology (Press release, Oxilio, OCT 20, 2021, View Source [SID1234621599]). Oxilio will use this technology for the development and commercialisation of an optimised compound formulation in the field of cancer treatment.

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The TRx technology enables targeted oral drug delivery to specific organs, cells and tissues in cancer using a clinically and commercially proven approach.

Roche reports strong growth in the first nine months – outlook for 2021 raised

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OncoMyx Announces Presentations at SITC 2021 of New Data Demonstrating the Potential of a Multi-Armed Myxoma Virus as a Novel Oncolytic Immunotherapy for Solid Tumors and Heme Malignancies

On October 19, 2021 OncoMyx Therapeutics, a privately-held oncolytic immunotherapy company, reported two poster presentations at the upcoming Society for Immunotherapy of Cancer (SITC) (Free SITC Whitepaper)’s (SITC) (Free SITC Whitepaper) 36th Annual Meeting being held November 10-14, 2021, both virtually and in Washington, D.C (Press release, OncoMyx Therapeutics, OCT 19, 2021, View Source [SID1234594855]).

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Onsite posters will be presented in the Poster Hall at the Walter E. Washington Convention Center. The posters will be available for onsite viewing November 12-14 from 7am to 5pm EST. Even numbered posters will be presented Saturday, November 13. ePosters will be on display on the SITC (Free SITC Whitepaper) 2021 virtual meeting platform from 7am EST on Friday, November 12 until the virtual meeting platform is closed on January 9, 2022.

Titles of the presentations are as follows:

(742) Multi-armed myxoma virus induces potent anti-tumor responses in vitro and in vivo
(744) Multi-armed myxoma virus has therapeutic potential for treatment of multiple myeloma
Full abstracts will be available on November 9th on the SITC (Free SITC Whitepaper) 2021 Annual Meeting website. Posters for both presentations will be available on OncoMyx’s website on November 12th.

About Oncolytic Immunotherapy and Myxoma Virus

Oncolytic viruses (OV) selectively replicate in and lyse tumor cells and provide stimulation to the immune system, representing a promising therapeutic option in development to treat cancers that do not respond well tOncolytic viruses (OV) selectively replicate in and lyse tumor cells and provide stimulation to the immune system, representing a promising therapeutic option in development to treat cancers that do not respond well to treatment with immune checkpoint inhibitors. Myxoma virus (MYXV) is a member of the Pox family of double stranded DNA viruses. The natural host of MYXV is a subset of rabbits and hares, but MYXV is able to infect cancer cell lines of humans and other species. The genome of MYXV is relatively large and is amenable to engineering for expression of transgenic proteins, making it an excellent oncolytic virus for introduction of immunomodulatory proteins.