Aurinia Pharmaceuticals to Present at the Jefferies Virtual Healthcare Conference

On May 27, 2021 Aurinia Pharmaceuticals Inc. (NASDAQ: AUPH / TSX: AUP) (the "Company") reported that members of the executive management team will participate in a fireside chat during the Jefferies Virtual Healthcare Conference on Thursday, June 3, 2021 at 11:30 a.m. ET (Press release, Aurinia Pharmaceuticals, MAY 27, 2021, View Source [SID1234580667]).

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In order to participate in the audio webcast, interested parties can access the live webcast under "News/Events" through the "Investors" section of the Aurinia corporate website at www.auriniapharma.com. A replay of the webcast will be available on Aurinia’s website.

Aptose to Hold Corporate Update Friday, June 11th

On May 27, 2021 Aptose Biosciences Inc. ("Aptose") (NASDAQ: APTO, TSX: APS), a clinical-stage company developing highly differentiated therapeutics targeting the underlying mechanisms of cancer, reported that the company management team will provide a corporate update for the investment community on Friday, June 11th, at 8:00 AM ET, in conjunction with participation at the EHA (Free EHA Whitepaper)2021 Virtual Congress (Press release, Aptose Biosciences, MAY 27, 2021, View Source [SID1234580666]). The event will include an up-to-date review of clinical data available for Aptose’s clinical programs: luxeptinib (CG-806), Aptose’s oral, first-in-class FLT3 and BTK kinase inhibitor in two Phase 1 a/b trials, one in patients with relapsed or refractory acute myeloid leukemia (AML) and another in patients with relapsed or refractory B cell malignancies; and APTO-253, a first-in-class small molecule MYC repressor in a Phase 1 a/b trial in patients with relapsed or refractory AML or high risk myelodysplastic syndromes (MDS).

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Aptose Corporate Update Details

Date & Time: Friday, June 11th, 8:00 AM ET

Participant Webcast Link: LINK

The slides will be available on Aptose’s website here and a recording of the presentation will be archived shortly after the conclusion of the event.

Early clinical data for luxeptinib (CG-806) and APTO-253 also will be presented in posters at the EHA (Free EHA Whitepaper)2021 Virtual Congress, to be held virtually June 9 – 17, 2021. All e-posters will be made available in the Virtual Congress platform on Friday, June 11 at 09:00 CEST / 03:00 ET. The posters also will be available on the presentations page of Aptose website here.

Poster Presentation Details

Title: A Phase 1a/b dose escalation study of the mutation agnostic BTK/FLT3 inhibitor luxeptinib (CG-806) in patients with relapsed or refractory B cell malignancies
Topic: Chronic lymphocytic leukemia and related disorders – Clinical
Final Abstract Code: EP643
Poster Date & Time: Friday, June 11 at 09:00 CEST

Title: A Phase 1a/b dose escalation study of the MYC repressor APTO-253 in patients with relapsed or refractory AML or high-risk MDS
Topic: Acute myeloid leukemia – Clinical
Final Abstract Code: EP452
Poster Date & Time: Friday, June 11 at 09:00 CEST
Abstract Only

Title: A Phase 1a/b dose escalation study of the mutation agnostic BTK/FLT3 inhibitor luxeptinib (CG-806) in patients with relapsed or refractory acute myeloid leukemia
Topic: Acute myeloid leukemia – Clinical
Final Abstract Code: PB1391

ONK Therapeutics Secures Exclusive Global License to Patent for CISH Knockout in NK Cells for the Treatment of Cancer, from Australia’s WEHI

On May 27, 2021 ONK Therapeutics Ltd, an innovative natural killer (NK) cell therapy company, reported that it has entered into an exclusive global patent license agreement with Australia’s Walter and Eliza Hall Institute of Medical Research (WEHI) providing rights to CISH KO in the field of NK cells for the treatment of cancer (Press release, ONK Therapeutics, MAY 27, 2021, View Source [SID1234580662]).

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"Deletion of CISH in NK cells leads to an improved metabolic profile, greatly enhancing their proliferation, cytotoxicity, and persistence. In-vivo models of cancer have shown that CISH KO NK cells are much more efficient in eliminating cancer cells, making such cells a very attractive prospect for future clinical development," said Prof Michael O’Dwyer, CSO of ONK Therapeutics.

"This patent agreement builds on and strengthens the broad IP we have created at ONK Therapeutics against multiple NK cell checkpoints," added Prof O’Dwyer.

CIS (encoded by the gene CISH) is a member of the suppressor of cytokine signaling (SOCS) family of proteins. The research team at WEHI, led at the time by Prof Nick Huntington and Assoc Prof Sandra Nicholson, was the first to show the critical role that CIS plays in negatively regulating the function of NK cells. When NK cells are stimulated with growth factors, such as interleukin 15 (IL-15), which encourage their growth, survival, and killing capability, there is an increase in the activity of CIS protein, which acts as a brake or checkpoint, on further NK cell growth and function.

The WEHI team found that when CIS was removed from NK cells by deleting the CISH gene, the NK cells were more responsive to growth factors and had improved survival and killing capacity(1). Improving the metabolic fitness of NK cells to enhance glycolysis and oxidative phosphorylation is important for optimizing the anti-tumor activity of NK cells, especially against solid tumors(2-3).

"Uncovering the role of CIS as an intracellular NK cell checkpoint has been an essential discovery to further the understanding of NK cell homeostasis and turnover," said Dr. Anne-Laure Puaux, Head of Biotechnology and Commercialisation, WEHI. "We believe that our invention has the potential to improve the potency of the NK cell-based therapy platform developed by ONK Therapeutics and provide greater benefit to patients."

Under the terms of the agreement, ONK Therapeutics has secured exclusive global rights to WEHI’s patent covering the use of human NK cells lacking CISH for the purposes of researching, developing, manufacturing and commercializing NK cell therapies. The financial terms of the agreement include milestone payments and royalties on sales, the specifics of which are not disclosed.

ONK Therapeutics’ CEO Chris Nowers said, "We are very pleased that via this agreement with WEHI we have the unique ability to produce therapeutic NK cells lacking CISH for the treatment of cancer. This is another example of our innovative strategy to engineer a highly differentiated NK cell therapy platform that has broad potential across both hematological malignancies and solid tumors."

ONK Therapeutics is optimizing a unique off-the-shelf, dual-targeted NK cell therapy platform, combining the expression of a chimeric antigen receptor (CAR) and a TRAIL variant (TRAILv) and anticipates using CISH KO as a core feature of this platform. The pipeline currently has four programs in pre-clinical development across hematological malignancies and solid tumors. The Company is also exploring engineering strategies to enhance tumor homing, to optimize persistence and metabolism, and to overcome exhaustion in the tumor microenvironment, including the exploration of proprietary gene edits, such as the deletion of checkpoint receptors in NK cells, including extracellular proteins CD96, TIGIT, Siglec-7 and PD-1.

1. Delconte, R., Kolesnik, T., Dagley, L. et al. CIS is a potent checkpoint in NK cell–mediated tumor immunity. Nat Immunol 17, 816–824 (2016) View Source

2. Daher et al., Targeting a cytokine checkpoint enhances the fitness of armored cord blood CAR-NK cells Blood Sept 9, 2020

3. Zhu et al., Metabolic Reprograming via Deletion of CISH in Human iPSC-Derived NK Cells Promotes In Vivo Persistence and Enhances Anti-tumor Activity Cell Stem Cell Sept 3, 2020″

BioTheryX Announces $92M Series E Financing to Accelerate Development of Targeted Protein Degradation Pipeline and Technology Platform in Oncology

On May 27, 2021 BioTheryX, Inc., a clinical-stage company focused on degrading proteins to create life-saving cancer medicines, reported a $92 million Series E financing led by Farallon Capital Management, with participation from additional new investors Avidity Partners, Deep Track Capital, Irving Investors, Janus Henderson Investors, Lumira Ventures, Point72, Rock Springs Capital, Surveyor Capital, Tekla Capital Management, Alexandria Venture Investors and Wedbush Healthcare Partners, and existing investors (Press release, BioTheryX, MAY 27, 2021, View Source [SID1234580406])The proceeds from the financing will be used to advance multiple molecular glues, PHM-based PROTACs and monovalent degraders, including BTX-1188, toward clinical development. BioTheryX also plans to advance the clinical development of its lead multi-kinase inhibitor, BTX-A51, for the treatment of acute myeloid leukemia, myelodysplastic syndromes and solid tumors.

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"We are pleased to have the support of an elite group of investors who share BioTheryX’s vision of realizing the promise of targeted protein degradation and delivering benefit to patients," said Robert Williamson, President and CEO of BioTheryX. "With this financing, we are well positioned to execute our plans to bring our first molecular glue program BTX-1188 into the clinic by the end of 2021, expand our platform of molecular glues, PROTACs and monovalent degraders and progress our lead program BTX-A51 through Phase 1."

Cue Biopharma to Present a Corporate and Clinical Progress Update at the Upcoming Jefferies Virtual Healthcare Conference

On May 26, 2021 Cue Biopharma, Inc. (Nasdaq: CUE), a clinical-stage biopharmaceutical company engineering a novel class of injectable biologics designed to selectively engage and modulate targeted T cells directly within the patient’s body, reported that it will present at the Jefferies Virtual Healthcare Conference being held June 1-4, 2021 (Press release, Cue Biopharma, MAY 26, 2021, https://cuebiopharma.gcs-web.com/news-releases/news-release-details/cue-biopharma-present-corporate-and-clinical-progress-update [SID1234608278]).

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Cue Biopharma will provide a corporate update highlighting clinical progress with CUE-101, representative of the CUE-100 series and the Company’s lead Immuno-STAT (Selective Targeting and Alteration of T cells) platform-based therapeutic, in clinical trials for the treatment of patients with HPV+ recurrent/metastatic head and neck cancer. The presentation will also focus on other platform developments as well as pipeline progress including CUE-102, Cue Biopharma’s drug candidate targeting Wilms Tumor 1 (WT1). CUE-102 is scheduled for an Investigational New Drug (IND) filing in 1H 2022.

Presentation Details
Jefferies Virtual Healthcare Conference
Date and Time: Thursday, June 3, 2021 at 8:30 a.m. EDT
Webcast link: https://protect-us.mimecast.com/s/ZywXCrkNz7tw9D5fLtfAM

A live and archived webcast of the presentation will be available in the Investors and Media section of the Company’s website at www.cuebiopharma.com. The webcast will be archived for 30 days.