Brooklyn ImmunoTherapeutics CEO Howard J. Federoff Provides Roadmap for the Company’s Future During May 25, 2021 Shareholder Update Call

On May 26, 2021 -Brooklyn ImmunoTherapeutics, Inc. (NYSE American: BTX) ("Brooklyn"), a biopharmaceutical company currently focused on exploring the role that cytokine and gene editing/cell therapy can have in treating patients with cancer and blood disorders, reported that investors to review the Company’s shareholder update conference call presentation via its website, which can be found here (Press release, Brooklyn ImmunoTherapeutics, MAY 26, 2021, View Source [SID1234580642]).

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

                  Schedule Your 30 min Free Demo!

Highlights include:

A review of the company’s multiple programs, including its unique Phase 2 mixed cytokine asset, IRX-2, being developed for head and neck cancer
A discussion of its recently acquired license for mRNA cell reprogramming technology, mRNA-based gene editing, proprietary gene editing protein and proprietary lipid delivery system, which the company believes may provide a completely different approach to treating certain solid tumors, liquid tumors, sickle cell disease and a host of other inherited monogenic disorders that may have no currently available therapy
An overview of the company’s current financial position and future financial plans

GM-CSF Gene-Edited CAR-T Data to be Presented at International Society for Cell & Gene Therapy Annual Meeting 2021

On May 26, 2021 Humanigen, Inc. (Nasdaq: HGEN), a clinical-stage biopharmaceutical company focused on preventing and treating an immune hyper-response called ‘cytokine storm’ with its lead drug candidate, lenzilumab, reported that granulocyte macrophage-colony stimulating factor (GM-CSF) gene-edited CAR-T data will be presented at the International Society for Cell & Gene Therapy (ISCT) 2021 Annual Meeting which will be held in New Orleans from May 26- 28, 2021 (Press release, Humanigen, MAY 26, 2021, View Source [SID1234580641]).

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

                  Schedule Your 30 min Free Demo!

Researchers at the Mayo Clinic, Rochester, MN have demonstrated that CRISPR/Cas9 GM-CSF knock-out in CAR-T cells (GM-CSFKO CAR-T) dampens CAR-T cell early activation and reduces activation-induced cell death (AICD), resulting in enhanced antigen-specific T-cell expansion in vivo. The modulation of intrinsic pathways is not due to an off-target effect and provides additional mechanistic rationale for the improved anti-tumor activity observed with GM-CSFKO CAR-T.

"These findings highlight the intrinsic value of GM-CSFKO CAR-T as a novel, potentially more effective and less toxic platform to enhance current CAR-T cell therapies," said Cameron Durrant, MD, MBA, chief executive officer of Humanigen.

Mayo Clinic researchers will present their research entitled, "GM-CSF disruption in CAR-T cells ameliorates CAR-T cell activation and reduces activation-induced cell death," on May 28, 2021 from 11:30 AM to 1:00 PM ET as part of the session titled "Novel Allo-Engineering Approaches and Progress in Off-the-Shelf Products."

"Mayo Clinic is enthusiastic about these findings, and they provide us with valuable information to enhance our current CAR-T cell therapies," said Saad S. Kenderian, MD, Division of Hematology, Mayo Clinic.

Details for the upcoming event are below:

ISCT 2021 New Orleans VIRTUAL Meeting

Novel Allo-Engineering Approaches and Progress in Off-the-Shelf Products Session
Date: Friday, May 28, 2021
Time: 11:30 AM ET

Aptorum Group CEO Subscribed Shares In The Company

On May 26, 2021 Aptorum Group Limited (NASDAQ: APM, Euronext Paris: APM) ("Aptorum Group", the "Company"), a clinical-stage biopharmaceutical company focused on the development of novel therapeutics to address global unmet medical needs, reported that Mr. Ian Huen, Founder, Chief Executive Officer and Executive Director of the Company, through his wholly owned investment company Jurchen Investments Limited, has purchased an aggregate of 1,387,925 Class A Ordinary Shares in the Company at $2.882 per share, representing a 10% premium to the last closing price (Press release, Aptorum, MAY 26, 2021, View Source [SID1234580640]).

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

                  Schedule Your 30 min Free Demo!

"Further to our ALS-4 and SACT-1 updates early this week, I am pleased to say that our leading programs are remaining on track with positive progress," said Mr. Huen. "I believe that my latest subscription demonstrates my steadfast confidence in the Company and I look forward for the Company to continue to deliver the exciting catalysts in 2021 and beyond."

Verseau Therapeutics Appoints John Edwards as Chief Executive Officer

On May 26, 2021 Verseau Therapeutics, Inc. reported the appointment of John Edwards as Chief Executive Officer (Press release, Verseau Therapeutics, MAY 26, 2021, View Source [SID1234580639]). John brings over 30 years of biopharmaceutical leadership experience and has been involved in the discovery, development or global commercialization of 10 FDA-approved biologics and eight biotech companies with successful exits .

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

                  Schedule Your 30 min Free Demo!

"John has a proven track record of guiding biotech companies through pivotal growth points during all stages of development, including taking companies from discovery to clinical stage and through newly marketed therapies reaching patients," said Verseau Board member Robert Langer, who co-founded Verseau in 2017 with Tatiana Novobrantseva, Igor Feldman, and Dan Anderson. "We welcome John to the Verseau team and look forward to benefitting from his experience as the company pursues its mission to develop an important new class of cancer immunotherapies based on macrophage repolarization."

"Repolarizing macrophages not only leads to a direct attack on tumor cells, but also sets in motion a coordinated immune response to attract and turn on other important cancer-fighting immune cells in the tumor microenvironment," said John. "This breakthrough approach could expand the potential of immunotherapy across more tumor indications and benefit a greater number of patients compared to current T-cell-targeting therapies. I am honored to join Verseau and to help guide the company’s trajectory as it rapidly progresses toward clinical trials later this year."

John previously served as Executive Chair at Tilos Therapeutics, where in less than two years he helped advance the company from its formation to its acquisition by Merck. John has also served as Executive Chair of F-star, where he helped grow the company from discovery-stage to a leading developer of clinical-stage bispecific antibodies, which included bringing over $200M in revenue from business development deals. John has also played a key role in building Siamab and Exonics, both having successful M&A exits in 2019. During his tenure as Chief Operating Officer at Adnexus, he took the company from start-up through a $450M acquisition by Bristol Myers Squibb. Following the acquisition, he served as President of Adnexus and worked within BMS during the early days of immuno-oncology. John also previously held the role of Vice President of Sales, Marketing, and Medical Affairs at Transkaryotic Therapies and served a 15-year tenure with Genetics Institute/Wyeth, where he was responsible for leading the company’s first product from research to FDA and EMA approvals. John started his career as one of the first employees at Genzyme. In addition to his role at Verseau, John is Executive Chair at Abcuro. John received his MBA from Boston University and his B.S. in chemical engineering from the University of Massachusetts, Amherst.

Engine Biosciences Announces $43 Million Series A Round to Decipher Genetic Codes for New Medicines Through Machine Learning and Next-Generation Combinatorial Genetics

On May 26, 2021 Engine Biosciences ("Engine") reported the successful completion of an oversubscribed $43 million Series A funding round (Press release, Engine Biosciences, MAY 26, 2021, View Source [SID1234580638]). Engine identifies errors in the complex genetic codes of diseases, fixing them with precise therapeutic solutions. This round was led by Polaris Partners and also included new investors Invus and one of the world’s premier institutional investors, based in Singapore. Existing investors also participated in the Series A, which included 6 Dimensions Capital, WuXi AppTec, DHVC, EDBI, Baidu Ventures, Vectr Ventures, Goodman Capital, WI Harper, and Nest.Bio. Amy Schulman, Managing Partner at Polaris Partners, has joined the Engine Biosciences Board of Directors. Engine has now raised $53 million to date, including $10 million in a 2018 seed round.

Schedule your 30 min Free 1stOncology Demo!
Discover why more than 1,500 members use 1stOncology™ to excel in:

Early/Late Stage Pipeline Development - Target Scouting - Clinical Biomarkers - Indication Selection & Expansion - BD&L Contacts - Conference Reports - Combinatorial Drug Settings - Companion Diagnostics - Drug Repositioning - First-in-class Analysis - Competitive Analysis - Deals & Licensing

                  Schedule Your 30 min Free Demo!

"The past year has reinforced the importance of rapid innovation and adaptation"

Located in Singapore and Silicon Valley, Engine has been operating at the intersection of data science, machine learning, high-throughput biology experimentation, combinatorial genetics, chemistry, and drug discovery. Engine’s technologies enable researchers and drug developers to uncover the gene interactions and biological networks underlying diseases orders-of-magnitude faster and more cost-effectively than conventional methods. Additionally, the company generates important insights for precision medicine applications.

"Many breakthrough tools to edit, program, and modulate biology have emerged and matured in recent years. The fundamental question continues to be whether we know the disease-driving errors in the genetic code of biology to direct these tools, including therapeutics," said Jeffrey Lu, Engine Biosciences’ Co-Founder and CEO. "We are honored that this preeminent group of life science and technology investors has recognized the progress our team has made and is supporting our mission to unleash new medicines by deciphering biology."

Engine has already been progressing its novel biology findings into drug discovery programs and proprietary small molecule inhibitors. It will utilize the new funds to expand its portfolio of precision oncology therapeutics, prepare for its first clinical programs, and scale its proprietary technology platform.

"The past year has reinforced the importance of rapid innovation and adaptation," said Polaris Partners’ Amy Schulman. "Engine’s distinct combination of biology, technology, and drug discovery, as well as its global perspective, may well enable the company to be particularly capable of realizing the promise of artificial intelligence in drug discovery and tackling a wide variety of diseases. We are excited to be part of this next step with the team."

Initial Disease Targets

Engine has performed several large-scale computational and experimental cycles with respect to genetic interactions and their relevance to multiple cancers, yielding new and subsequently validated discoveries. Engine’s growing and advancing pipeline of targeted therapies for genetically-defined patient populations has shown promise in treating liver, ovarian, colorectal, and breast cancers, representing major areas of unmet medical need and, in total, approximately 2.5 million deaths every year.

Through collaborations, Engine has also demonstrated its platform’s applicability in other disease areas and will continue to enable new therapeutics for more patients.

"We believe Engine’s AI-enabled technology platform has the potential to discover new biology targets and disease-causing links amongst known targets," said Leon Chen, CEO and Founding Partner of 6 Dimensions Capital. "Considering the field’s tremendous needs for the right drug targets for the right patients and Engine’s unique capabilities in finding those, we continue to be excited by Engine’s potential to power new medicines."

How It Works: NetMAPPR and CombiGEM

Two scientific innovations lie at the heart of Engine Biosciences: NetMAPPR and CombiGEM. NetMAPPR is Engine’s searchable biology platform, revealing gene combinations and drug targets integral to diseases. Employing combinatorial CRISPR, CombiGEM enables experimental confirmation of how genes and gene combinations relate to disease in supercharged fashion.

Engine has engineered NetMAPPR to operate in predict-test-learn cycles and scale for many research and drug discovery programs. Advanced computational tools leverage large patient and disease datasets and analyze the vast universe of millions-to-billions of gene interactions, making predictions on the most critical biologies for medicines. Engine uses its patented CombiGEM technology to test hundreds of thousands of gene interactions experimentally in diseased cells, thus breaking through bottlenecks in validation and data generation. The resulting data from well-controlled experiments improves Engine’s machine learning algorithms, while high-ranking genes are prioritized for drug discovery and development.

Compared to conventional approaches that are challenged by human limitations and less efficient and less precise experimental systems and hence cover tiny slices of biology, NetMAPPR searches much wider expanses of the complex architecture of biology at greater speeds, unleashing more new therapeutic opportunities.