RayzeBio to Present at J.P. Morgan Healthcare Virtual Conference on Tuesday, January 11, 2022

On January 6, 2022 RayzeBio, Inc., a targeted radiopharmaceutical company developing an innovative pipeline against validated solid tumor targets, reported that Ken Song, M.D., President and CEO of the Company, will be presenting at the 40th Annual J.P. Morgan Healthcare Conference being held virtually on Tuesday, January 11, 2022 (Press release, RayzeBio, JAN 6, 2022, View Source [SID1234598372]).

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J.P. Morgan Healthcare Conference
Date: Tuesday, January 11, 2022
Time: 11:00 a.m. – 11:25 a.m. EST
Please click on the below link to find additional details about the J.P. Morgan Healthcare Conference
View Source

Paula and Rodger Riney Foundation Makes $40 Million Transformative Grant to Further Multiple Myeloma Research at Dana-Farber Cancer Institute

On January 6, 2022 Paula and Rodger Riney of St. Louis, MO, through the Paula and Rodger Riney Foundation, reported a $40 million grant to support multiple myeloma research at Dana-Farber Cancer Institute (Press release, Dana-Farber Cancer Institute, JAN 6, 2022, View Source [SID1234598389]). The grant represents the largest single award supporting multiple myeloma research in Dana-Farber’s history. The Paula and Rodger Riney Foundation has been a strong supporter of Dana-Farber and with this grant has cumulatively donated nearly $60 million to the Institute.

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Multiple myeloma is a challenging cancer that forms in a type of white blood cell called a plasma cell. Dana-Farber has been at the forefront of multiple myeloma therapies over the past two decades, helping to convert myeloma from a fatal disease to a chronic condition for many patients. However, therapeutic resistance and drug-related toxicities continue to take a toll on many patients, underscoring the need for innovative treatments.

"The path to developing new treatments for multiple myeloma is through rigorous research. The most effective way to spur that research is in supporting the scientists doing the complex work. The Riney Family are generous and stalwart supporters, and through this grant and their previous support they continue to make a profound impact on scientific discovery and clinical care. Their leadership will help patients at Dana-Farber and around the world," said Laurie H. Glimcher, MD, President and CEO of Dana-Farber and the Richard and Susan Smith Professor of Medicine at Harvard Medical School.

"My own journey as a myeloma patient—and knowing how many others are also living with this disease—has led us to seek out the individuals, teams, and organizations that are on the leading edge of research," said Rodger Riney. "There is no time to waste in the pursuit of better understanding, treatment, and cures. My family and I feel grateful to be able to support Ken, Paul, and Nikhil and their teams at Dana-Farber who are making incredible inroads. We are humbled by the lifelong dedication that Ken, Paul, and Nikhil bring to myeloma patients suffering from this terrible disease. We hope this gift will inspire others to also support the tremendous work happening every day in Dana-Farber’s labs and clinics."

This new $40 million grant builds upon ongoing work and will deepen and expand approaches for addressing the most complex challenges in myeloma research and improving patient care. Specifically, this grant will:

Renew support for preclinical experiments to identify novel targets and develop new medicines and immune-based therapies for patients;
Fund clinical research designed to test novel myeloma therapies, alone and in combination with standard and experimental treatments, to improve patient outcomes; and,
Support to co-locate myeloma labs at Dana-Farber to facilitate greater cohesion and collaboration among members of the research team.
"I extend my heartfelt thanks to Paula and Rodger Riney for their unprecedented support of our research to develop novel treatments for multiple myeloma. This very generous grant will fast-forward our translation of basic discoveries to clinical trials, ultimately providing innovative treatments for patients and their families," said Ken Anderson, MD, program director at Dana-Farber’s Jerome Lipper Multiple Myeloma Center and LeBow Institute for Myeloma Therapeutics and Kraft Family Professor of Medicine at Harvard Medical School. Anderson will lead the research efforts supported by this grant in close partnership with Nikhil Munshi, MD, director of Basic and Correlative Science at the Jerome Lipper Multiple Myeloma Center and Kraft Family Chair at Dana-Farber. The grant will also provide support for clinical work led by Paul Richardson, MD, clinical program leader and director of clinical research at the Jerome Lipper Multiple Myeloma Center and RJ Corman Professor of Medicine at Harvard Medical School.

The Rineys have a strong legacy of supporting multiple myeloma research at Dana-Farber and in 2019 gave a $16.5 million gift to establish the Riney Family Multiple Myeloma Initiative, which has driven groundbreaking research in record time. Examples of recent discoveries by Dana-Farber investigators include:

Bringing therapeutic antibodies, which help immune cells find and attack tumors, to patients with multiple myeloma.
Leading clinical studies demonstrating the remarkable therapeutic effects of CAR T-cells that have been engineered to target multiple myeloma.
Setting the stage for the development of innovative therapies that exploit the unique vulnerabilities of multiple myeloma cells.
Over the past two years, the Paula and Rodger Riney Foundation also made gifts totaling $2.6 million to establish the Riney Family Fund for COVID-19 and Multiple Myeloma Research at Dana-Farber, under Richardson’s direction.

These commitments provide powerful momentum for The Dana-Farber Campaign, an ambitious multi-year $2 billion fundraising effort to prevent, treat, and defy cancer by accelerating revolutionary science, extraordinary care, exceptional expertise, and essential opportunities.

ONK Therapeutics Announces $21.5M Series A Financing to Advance Pipeline of Next-Generation Optimally Engineered Off-the-Shelf NK Cell Therapies

On January 6 2022 ONK Therapeutics, an innovative NK cell therapy platform company, reported the closing of its $21.5 million Series A financing, led by current investors Acorn Bioventures and ALSHC, who were joined by Cormorant Asset Management (Press release, ONK Therapeutics, JAN 6, 2022, View Source [SID1234598318]).

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The financing will enable ONK to maintain its strong momentum as it advances pre-clinical programs through comprehensive IND-enabling studies, including in-vivo proof-of-concept models across multiple programs. ONK will also continue progress towards a GMP manufacturing capability, as it optimizes both its proprietary cell engineering platform and process development.

ONK’s pipeline currently has three programs in pre-clinical development across both hematological malignancies and solid tumors. The Company is pioneering optimally engineered natural killer (NK) cell therapies, utilising a suite of engineering strategies to optimize cytotoxic potential, metabolic health and persistence of NK cells, while reducing the potential for their exhaustion in the tumor microenvironment. This is made possible through the Company’s ability to achieve unique proprietary gene edits.

ONK’s comprehensive owned and exclusively licensed patent estate covers CISH knockout (KO) in the field of human NK cells for the treatment of cancer, irrespective of the NK cell source; the expression of high affinity, membrane bound,TNF-related apoptosis-inducing ligand variants (TRAILv); and the deletion of checkpoint receptors in NK cells, including extracellular proteins CD96, TIGIT, Siglec-7 and PD-1.

These different strategies are being employed across the ONK pre-clinical product portfolio, including:

ONKT102, the Company’s lead program, an optimized affinity CD38 CAR (chimeric antigen receptor) NK cell therapy being developed for the treatment of patients with relapsed refractory multiple myeloma
ONKT104, a CLL-1 CAR-NK program targeting AML stem cells, which is advancing through later stages of its pre-clinical evaluation
ONKT103, which is being optimized to treat solid tumors such as Ovarian, Breast and Non-Small Cell Lung Cancer (NSCLC) and is based on tumor associated MUC-1 targeting CAR NK cells
In addition, these programs will explore incorporating further novel gene edits, such as CISH KO and TRAIL variants targeting DR5 or DR4.

ONK has also recently started two programs focused on the potential of highly functional CISH KO NK cells, namely:

ONKT105, exploring CISH KO cord blood derived NK cells
ONKT106, exploring CISH KO iPSC derived NK cells
The Company also continues to make significant progress on the manufacturing front, optimizing its process development, gene editing capability, efficient expansion techniques and its cryopreservation capability. In combination, these will support manufacturing as part of ONK’s progress towards GMP manufacturing of large numbers of NK cell therapy batches from a single cord.

Chris Nowers, ONK Therapeutics’ CEO said, "We thank our existing investors for their continued support and are pleased to welcome Cormorant Asset Management as a new investor and Andy Phillips to our Board, as we continue against our goal to optimally engineer, off-the-shelf, NK cell therapies to potentially cure patients with cancer. This financing will allow us to continue to deliver against our focused strategy, funding significant program progression, organizational development, and company growth. Within the next 18 months, we have the potential for multiple IND approvals to enable our evolution into a clinical-stage company."

Commenting on the investment, Isaac Manke, Ph.D., Partner at Acorn Bioventures said, "Over the 12 months of our investment, ONK Therapeutics has made excellent progress in advancing both its innovative next-generation NK cell therapy platform and across its exciting portfolio of pre-clinical assets. We are pleased to continue our support and to have introduced Cormorant Asset Management as a new investor to join with ourselves and founding investor ALSHC."

Andy Phillips, Ph.D., Managing Director at Cormorant Asset Management said, "We are impressed by the Company’s potential to make a highly innovative contribution to the quickly evolving field of NK cell therapies, which we believe have the opportunity to improve the lives of patients in need of new treatments for their disease. We are pleased to join the current investor groups in financing ONK as it looks forward to important proof of principle in vivo data and additional value catalyzing milestones."

Ultragenyx to Present at H.C. Wainwright BioConnect Healthcare Conference

On January 6, 2022 Ultragenyx Pharmaceutical Inc. (NASDAQ: RARE), a biopharmaceutical company focused on the development and commercialization of novel therapies for serious rare and ultra-rare genetic diseases, reported that Emil D. Kakkis, M.D., Ph.D., the company’s Chief Executive Officer and President, will present at the H.C. Wainwright BioConnect Conference on Thursday, January 13, 2022 at 7:00 AM ET (Press release, Ultragenyx Pharmaceutical, JAN 6, 2022, View Source [SID1234598335]).

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The live and archived webcast of the presentation will be accessible from the company’s website at View Source The replay of the webcast will be available for 90 days.

ImCheck to Present at 40th Annual J.P. Morgan Healthcare Conference

On January 6, 2022 ImCheck Therapeutics reported that its Chief Executive Officer, Pierre d’Epenoux, will present a corporate overview on Monday, January 10th at 7:30 am Eastern Time/13:30 Central European Time during the 40th Annual J. P. Morgan Healthcare Conference being held virtually from January 10-13, 2022 (Press release, ImCheck Therapeutics, JAN 6, 2022, View Source [SID1234598355])

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