Xspray Pharma commences study with improved version of dasatinib

On June 10, 2021 Xspray Pharma reported that a bioequivalence study with the improved version of dasatinib has commenced (Press release, Xspray, JUN 10, 2021, View Source [SID1234650110]). The objective of the study is to demonstrate that a lower dose strength of Xspray Pharma’s improved version of dasatinib is bioequivalent to a higher dose strength of the original drug Sprycel. The study is being conducted with a previously used formulation of Xspray Pharma’s amorphous version of dasatinib. The findings will form the basis of an application for market approval in the US under the 505(b)(2) regulatory pathway. The preliminary findings from this study are expected in the third quarter of 2021.

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"I am pleased that we are initiating this bioequivalence study as planned. This product candidate that has the potential to improve the therapy for a cohort of cancer patients in a high-value field where no new or improved drugs have been registered for many years. In addition, we have tested this formulation A in previous studies and can better predict the findings compared to the studies that have been based on completely new untested formulations," says Per Andersson, CEO of Xspray Pharma.

Xspray Pharma’s improved version of dasatinib for the treatment of acute lymphoblastic leukemia (ALL) and chronic myeloid leukemia (CML) and is designed to enable therapy with proton-pump inhibitors (PPIs) such as omeprazol which should be avoided with the original product. Xspray Pharma’s product will be administered at a lower dose strength compared with Sprycel but with the same availability.

Bioequivalence studies with Xspray Pharma generic product candidate, formulation C, where the objective is to demonstrate bioequivalence with Sprycel, will be initiated this summer. The findings will form the basis of an application for market approval in the US under the ANDA regulatory pathway.

ImmunoPrecise to Present at Antibody Engineering & Therapeutics Europe

On June 10, 2021 ImmunoPrecise Antibodies reported that At this year’s Antibody Engineering & Therapeutics Europe, Dr. Debby Kruijsen will be present the scientific briefing Identification of Unique Antibodies by Parallel Sourcing Chicken and Human B-cell Repertoires Using Innovative Technologies (Press release, ImmunoPrecise Antibodies, JUN 10, 2021, View Source [SID1234583815]). Our team will also be showcasing the scientific poster Successful rabbit mAb CDR-grafting: The first step towards clinically suitable monoclonal antibodies.

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The event will be hosted virtually June 8th-10th, 2021.

CohBar to Present at the BIO 2021 Digital Conference

On June 10, 2021 CohBar, Inc. (NASDAQ: CWBR), a clinical stage biotechnology company developing mitochondria based therapeutics to treat chronic diseases and extend healthy lifespan, reported its Chief Executive Officer Dr. Joseph Sarret will present a corporate overview at the BIO 2021 Digital Conference, to be held on June 14 – 18, 2021 (Press release, CohBar, JUN 10, 2021, View Source [SID1234583833]). This presentation will be available on demand for registered attendees.

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BIO is the world’s largest trade association representing biotechnology companies, academic institutions, state biotechnology centers and related organizations across the United States and in more than 30 other nations. BIO members are involved in the research and development of innovative healthcare, agricultural, industrial and environmental biotechnology products. BIO also produces the BIO International Convention, the world’s largest gathering of the biotechnology industry, along with industry-leading investor and partnering meetings held around the world.

AUM LifeTech, Inc. to Present Preclinical Developments on Lung Cancer, Parkinson’s Disease, and HIV at BIO Digital 2021

On June 10, 2021 AUM LifeTech, Inc., a preclinical stage biotechnology company, reported that it has been selected by the National Institutes of Health (NIH) to present an update on their drug development pipeline at 2021 BIO Digital, the premier biotech event (Press release, AUM Lifetech, JUN 10, 2021, View Source [SID1234583853]). The company has leveraged a self-delivering non-viral RNA targeting technology for therapeutic development in oncology, CNS, and infectious diseases.

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Veenu Aishwarya, Founder and Chief Executive Officer of AUM LifeTech, will present an update on their therapeutic programs. "We are honored to be selected by the NIH to showcase our preclinical developments at BIO 2021. We are very excited about our recent encouraging preclinical data as we move towards the next stages of development," said Aishwarya. "Our therapeutic programs, designed for patients with unmet clinical needs, are now ready for collaborations and strategic alliances to further advance our significantly de-risked preclinical assets," he added.

We are very excited about our recent encouraging preclinical data as we move towards the next stages of development.

AUM LifeTech has developed their preclinical pipeline in cancer immunotherapy with a focus on lung cancer using their proprietary RNA targeting technology. Additionally, their programs in CNS and infectious diseases include therapeutic development for Parkinson’s disease and HIV respectively. AUM LifeTech’s HIV preclinical program is funded by the National Institute of Allergy and Infectious Diseases (NIAID) of the NIH. Their drug development pipeline is based on self-delivering FANA antisense oligonucleotide (FANA ASO) technology.

BIO Digital is scheduled June 10-11 & 14-18, 2021, and AUM LifeTech’s therapeutic developments and insight into their gene silencing technology and preclinical research will be available to registered attendees at 9 am ET on June 10. Attendees at BIO Digital will be able to view the presentation by AUM LifeTech as part of the NIH Innovation Zone before live meetings in the BIO One-on-One Partnering system begin on June 14. To meet with AUM LifeTech at BIO Digital, you can find registration information here.

Innate Pharma Presents New Data on Next-Generation NK Cell Engager Platform at FOCIS 2021 Annual Meeting

On June 10, 2021 Innate Pharma SA (Euronext Paris: IPH – ISIN: FR0010331421; Nasdaq: IPHA) ("Innate" or the "Company") reported it will present the latest preclinical data from its next- generation, proprietary, multi-specific NK cell engager platform known as ANKETTM (Antibody-based NK cell Engager Therapeutics) at the Federation of Clinical Immunology Societies (FOCIS) meeting (Press release, Innate Pharma, JUN 10, 2021, View Source [SID1234583797]). The presentation will take place at 7 pm CEST today.

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Specifically, Innate will share new data from its tetra-specific ANKET molecule, which is the first NK cell engager technology to engage activating receptors (NKp46 and CD16), a tumor antigen and a cytokine (IL-2 variant) in a single molecule. This latest innovation leverages the advantages of harnessing NK cell effector functions against cancer cells and also provides proliferation and activation signals targeted to NK cells. This data set is built on Innate’s existing tri-specific NK cell engager technology, which has demonstrated potent NK cell activation, cytotoxicity and efficient control of tumor growth in preclinical models.

In preclinical studies, tetra-specific ANKET demonstrated in vitro the ability to induce human NK cell proliferation, cytokine production and cytolytic activity against cancer cells expressing the targeted antigen. Tetra-specific ANKET also demonstrated in vivo anti-tumor efficacy in several tumor models, allowing regression of established tumors as well as control of metastasis, associated with increased NK cell infiltration, cytokine and chemokine production at the tumor site. ANKET showed also pharmacodynamic effect, low systemic cytokine release and a manageable safety profile in non-human primates.

"We are excited to introduce the new evolution of our ANKET platform at the FOCIS meeting today," said Pr. Eric Vivier, PhD, DVM, Chief Scientific Officer at Innate Pharma. "NK cells play a critical role in the cancer innate immunity cycle, and engaging them is an exciting path to improve the therapeutic window for cancer treatment compared to T- cell engagers. We believe the new findings obtained with our ANKET technology capture its potential to advance meaningful outcomes for patients. This advancement allows us to create an entirely new class of molecules to induce synthetic immunity against cancer. We look forward to sharing additional detail at our upcoming IR R&D event."

Innate’s lead ANKET asset, IPH6101 (SAR443579), has shown anti-tumor activity in pre-clinical models, including encouraging pharmacokinetic, pharmacodynamic and safety data in preliminary non-human primate studies. In January, Sanofi made the decision to progress this program into investigational new drug (IND)-enabling studies. As part of the previously announced research collaboration, the companies are also currently working on the second research program.

Innate will provide more information on today’s data at an upcoming online R&D presentation for the investor community that is scheduled for 2 p.m. CEST on June 23, 2021.

About ANKETTM

ANKETTM (Antibody-based NK cell Engager Therapeutics) is Innate Pharma’s proprietary platform for developing next-generation, multi-specific NK cell engagers to treat certain types of cancer. The Company’s latest innovation, its tetra-specific ANKET molecule, is the first NK cell engager technology to engage activating receptors (NKp46 and CD16), a tumor antigen and a cytokine (IL-2v) in a single molecule. This leverages the advantages of harnessing NK cell effector functions against cancer cells and also provides proliferation and activation signals targeted to NK cells.

In preclinical studies, Innate’s tri-1 and tetra-specific technology has demonstrated potent NK cell activation, cytotoxicity and efficient control of tumor growth in preclinical models. This versatile fit-for-purpose technology is creating an entirely new class of molecules to induce synthetic immunity against cancer.

About Innate Pharma:

Innate Pharma S.A. is a global, clinical-stage oncology-focused biotech company dedicated to improving treatment and clinical outcomes for patients through therapeutic antibodies that harness the immune system to fight cancer.

Innate Pharma’s broad pipeline of antibodies includes several potentially first-in-class clinical and preclinical candidates in cancers with high unmet medical need.

Innate is a pioneer in the understanding of Natural Killer (NK) cell biology and has expanded its expertise in the tumor microenvironment and tumor antigens, as well as antibody engineering. This innovative approach has resulted in a diversified proprietary portfolio and major alliances with leaders in the biopharmaceutical industry including Bristol-Myers Squibb, Novo Nordisk A/S, Sanofi, and a multi-products collaboration with AstraZeneca.

Headquartered in Marseille, France, with a US office in Rockville, MD, Innate Pharma is listed on Euronext Paris and Nasdaq in the US.