Oxford Vacmedix announces filing of new patent for Anti-Microbial Resistance diagnostic test

On July 27, 2022 Oxford Vacmedix (OVM), the UK clinical stage biopharma company, focused on the development of a new generation of cancer vaccines, reported that project work to develop a novel diagnostic test for anti-microbial resistance, funded by Innovate UK, has been filed as a patent in the UK (Press release, Oxford Vacmedix, JUL 27, 2022, View Source;utm_medium=rss&utm_campaign=new-patent-for-anti-microbial-resistance-diagnostic-test [SID1234616989]).

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The need to monitor and control resistance to antimicrobial therapy has been identified as an urgent global priority by both the WHO and UN. The rise in carbapenem resistance has been identified as of particular concern given the importance of this class of antibiotics.

The research project carried out in collaboration with Imperial College in London and the Ditan hospital in Beijing, has been to develop a fast and economic lateral flow immune assay (LFIA) diagnostic test to detect bacterial resistance to carbapenem antibiotics. This has advantages in terms of speed, simplicity and cost-effectiveness, especially important for low- and middle-income countries. The prototype assays, produced at Changzhou Biotech under contract to OVM, have been trialled at several leading hospitals in Beijing where antibiotic resistance is a serious problem, particularly in intensive care patients. Preliminary clinical tests show that the kits can detect the bacteria of antibiotic resistance directly from clinical samples in about 15 minutes, without prior bacterial culture.

The AMR diagnostic project has been mainly outsourced and run alongside OVM’s main development programmes to allow the company to focus on the development of its two lead cancer vaccines; OVM-100, an HPV vaccine targeted at cervical cancer; and OVM-200 a new type of vaccine based on survivin that targets solid tumours, and which is in Phase 1. Both vaccines address areas of significant unmet medical need with potential both as single agents and also in combination with other immune-oncology agents.

William Finch CEO of Oxford Vacmedix said:

"Whilst our primary focus is in the development of cancer vaccines, our technology also has applications for infectious diseases and this novel diagnostic test addresses an important need in treating seriously ill patients. We have a lot of confidence in our initial results and with a patent application now made, we look forward to working with a partner to complete development and to commercialise the test."

Shisong Jiang, Founder and CSO of Oxford Vacmedix said:

"I am very pleased that we have been able to use the Innovate UK funding and work with our collaboration partners to develop this AMR test. I would like particularly to recognise the development work at Changzhou Biotech where the team has done an excellent job. The sensitivity and specificity of the diagnostic test demonstrate its potential and I look forward to seeing this work taken further, to help patients."

IN8bio Observes Durable Morphologic Complete Responses in Ongoing Phase 1 Clinical Trial of INB-100, an Allogeneic Gamma-Delta T Cell Therapy in High-Risk Leukemia Patients

On July 27, 2022 IN8bio, Inc. (Nasdaq: INAB), a clinical-stage biopharmaceutical company focused on the discovery and development of innovative gamma-delta T cell therapies utilizing its DeltEx platform, reported a clinical update from the ongoing Phase 1 trial of INB-100 (Press release, In8bio, JUL 27, 2022, View Source [SID1234617007]). This program is an allogeneic, or donor-derived, gamma-delta T cell therapeutic candidate in development for patients with high-risk leukemias undergoing haploidentical hematopoietic stem cell transplant (HSCT). William Ho, Chief Executive Officer of IN8bio, will be discussing these results at the 3rd Annual Gamma-Delta T Therapies Summit, being held July 26-28, in Boston.

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"We are excited about the early signals of long-term durable responses from gamma-delta T cell therapy in these high-risk AML patients with complex cytogenetics," said Trishna Goswami, M.D., Chief Medical Officer of IN8bio. "Despite the up to 51% anticipated one-year relapse rate of the patients enrolled in the trial, all three remain alive and disease free for more than one-year post-transplant. These data are highly encouraging, with the potential to increase the rates of cures in AML patients without significant added toxicities observed to date."

The Phase 1 clinical trial continues to show positive clinical trends with the first three patients remaining alive and progression-free. Despite multiple cytogenetic abnormalities and a high risk of relapse, these patients remain in remission 26.5, 24.2 and 12.5 months post-transplant, respectively. Immune system reconstitution at six months post-treatment demonstrates continued normal function including observed elevations in T cells, B cells, and gamma-delta T cells. No treatment emergent serious adverse events (SAEs), including graft-vs-host disease (GvHD), cytokine release syndrome (CRS) or immune effector cell-associated neurotoxicity syndrome (ICANS) have been observed. The clinical trial is ongoing and additional patients have been recruited, with updated data expected in late 2022.

As of June 30, 2022

About the INB-100 Phase 1 Trial

The Phase 1 clinical trial (NCT03533816) is a dose-escalation trial of allogeneic derived, gamma-delta T cells from matched related donors that have been expanded and activated ex vivo and administered systemically to patients with leukemia following haploidentical HSCT. Three high-risk AML patients with complex cytogenetics have been treated to-date. The single-institution clinical trial is currently being conducted at the University of Kansas Cancer Center (KUCC). The primary endpoints of this trial are safety and tolerability, and secondary endpoints include rates of GvHD, relapse rate and overall survival.

Agenus to Provide Corporate Update and Second Quarter 2022 Financial Report

On July 27, 2022 Agenus (NASDAQ: AGEN) an immuno-oncology company with an extensive pipeline of therapeutics designed to activate the immune response to cancers and infections, reported it will release its second quarter 2022 financial results before the market opens on Tuesday, August 9, 2022 (Press release, Agenus, JUL 27, 2022, View Source [SID1234617023]). Agenus executives will host a conference call and webcast at 8:30 a.m. ET that morning to discuss the results and to provide a corporate update.

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Webcast
A webcast and replay of the conference call will be accessible from the Events & Presentations page of the Company’s website at View Source and via View Source

PULSE BIOSCIENCES SCHEDULES SECOND QUARTER 2022 FINANCIAL RESULTS CONFERENCE CALL FOR AUGUST 10, 2022

On July 27, 2022 Pulse Biosciences, Inc. (Nasdaq: PLSE), a novel bioelectric medicine company commercializing the CellFX System powered by Nano-Pulse Stimulation (NPS) technology, reported it will report financial results for the second quarter of 2022 after market close on Wednesday, August 10, 2022 (Press release, Pulse Biosciences, JUL 27, 2022, View Source [SID1234617096]). Company management will host a corresponding conference call beginning at 1:30pm PT.

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Investors interested in listening to the conference call may do so by dialing 1-877-704-4453 for domestic callers or 1-201-389-0920 for international callers. A live and recorded webcast of the event will be available at View Source

TRACON to Report Second Quarter 2022 Financial Results and Provide Corporate Update on August 10, 2022

On July 27, 2022 TRACON Pharmaceuticals (Nasdaq: TCON), a clinical stage biopharmaceutical company utilizing a cost-efficient, CRO-independent product development platform to advance its pipeline of novel targeted cancer therapeutics and to partner with other life science companies, reported that it will report its second quarter 2022 financial and operating results after the close of U.S. financial markets on Wednesday, August 10, 2022 (Press release, Tracon Pharmaceuticals, JUL 27, 2022, View Source [SID1234616990]). In addition, management will host a conference call to provide an update on corporate activities and discuss the financial results.

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A replay of the webcast will be available for 60 days on the website.