Calidi Biotherapeutics Announces Dr. Maciej S. Lesniak Presentation at 13th International Oncolytic Virotherapy Conference

On November 5, 2021 Calidi Biotherapeutics, Inc., a clinical-stage biotechnology company at the forefront of stem cell-based delivery of oncolytic viruses, reported that its physician advisor, Maciej S. Lesniak, MD, Department Chair of Neurological Surgery, Feinberg School of Medicine, Northwestern University, will present at the upcoming International Oncolytic Virotherapy Conference (IOVC), which will be held in hybrid format November 5 through November 7, 2021, as both a virtual event and an in-person meeting in Sedona, AZ (Press release, Calidi Biotherapeutics, NOV 5, 2021, View Source [SID1234594661]).

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Dr. Lesniak’s presentation: "Neural Stem Cell Delivery of Oncolytic Virotherapy for Glioma," will focus on the use of stem cells for virotherapy of cancer, featuring clinical findings from a first-in-human, open-label, Phase 1, dose-escalation trial demonstrating strong safety and efficacy signals for the NSC-CRAd-S-pk7 product, which Calidi refers to as NeuroNova (NNV), in patients with newly diagnosed high-grade glioma. Results from the clinical trial are published in The Lancet Oncology (June 29, 2021).

"Malignant glioma has been historically associated with dismal survival rates due to a lack of effective treatment," said Maciej S. Lesniak, MD, Department Chair of Neurological Surgery, Feinberg School of Medicine, Northwestern University. "I’m eager to share the promising results of our recently completed Phase 1 trial examining the safety and activity of NeuroNova in patients with advanced glioma."

In June 2021, Calidi reached an exclusive license agreement with Dr. Lesniak’s team at Feinberg School of Medicine, Northwestern University—designating exclusive commercialization rights to Northwestern’s investigational new drug (IND) application and data generated from the clinical trial, as well as commercial development rights for stem-cell based products loaded with adenovirus. NNV is composed of an immortalized neural stem cell (NSC) line loaded with an engineered oncolytic adenovirus.

"Calidi’s continued collaboration with Dr. Lesniak has been critical to the development and clinical success of our NeuroNova platform," said Allan J. Camaisa, Chairman and CEO of Calidi Biotherapeutics.

Scheduled for Sunday, November 7, Dr. Lesniak’s presentation will occur during Scientific Session 9: Clinical Trials 3 of the IOVC. Hosted by the American Society of Gene & Cell Therapy (ASGCT) (Free ASGCT Whitepaper), the conference spans three days, with presentations from credentialed professionals in the following categories: Novel Payloads and Mechanisms of Action, Novel Combinations and Mechanisms of Action, Novel Platforms, and Clinical Trials. A full program schedule and complete list of invited speakers are available at asgct.org/events/iovc.

Jaime Leandro Foundation treats first cancer patient with personalized neoantigen peptide vaccine under expanded access through xCures

On November 5, 2021 The Jaime Leandro Foundation for Therapeutic Cancer Vaccines (JLF) and partners reorted the treatment of the first cancer patient with a personalized neoantigen vaccine through a self-pay compassionate use program (Press release, xCures, NOV 5, 2021, View Source [SID1234594659]).

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JLF is a 501(c)3 non-profit organization whose mission is to make personalized anticancer vaccines available to patients with limited or no treatment options. Although neoantigen vaccines are not currently FDA approved, preliminary data is supportive of their use via compassionate access.

Personalized neoantigen vaccines are directed at tumor-specific mutation targets called neoantigens and leverage vaccine technology approaches to boost immune responses to a patient’s tumor. Although personalized neoantigen vaccines are very promising and have shown a favorable safety profile, their development and administration are hampered by regulatory, intellectual property, and clinical science obstacles. JLF has therefore partnered with multiple companies and institutions to bring these promising neoantigen vaccines directly to patients and their physicians.

By accelerating progress, informing patients, and enabling treatment, JLF and partners have worked diligently to help cancer patients and their clinicians overcome limited access to cancer vaccines through traditional trials. JLF has partnered with Washington University School of Medicine in St. Louis to use their pVAC-Seq algorithm, an important technology for the selection of neoantigens in the design of the vaccines. Of the many instrumental partners, key steps of vaccine design, manufacture, and patient treatment are provided by ennov1, CSBio, and xCures.

"We are delighted that xCures’ backend technology, regulatory know-how, and partnerships, enable cancer patients to access novel treatments while providing important real-world data," said Mika Newton, CEO of xCures. "By partnering with JLF we enabled the use of a personalized neoantigen vaccine under compassionate use/expanded access."

"We are thrilled to collaborate with JLF, and partners to ensure efficient analysis, optimal vaccine design and secure storage through our cloud-based platform and genomic technology," said James Inglis-Jones, Chairperson of ennov1.

"It’s exciting to contribute with CSBio’s peptide and instrumentation manufacturing technology towards manufacturing a fully personalized anticancer peptide vaccine," stated the CEO of CSBio, Jason Chang.

After a long process starting in fall 2020, the FDA approved treatment for the first two patients in the Spring of 2021. "We are very pleased to announce the initiation of treatment of the first cancer patient at Providence Saint John’s Health Center in Santa Monica, CA under the care of Dr. Santosh Kesari," stated JLF President, William Hoos.

The patient’s husband praised this new pathway to treatment. "JLF and partners allowed us the option to pursue a treatment we wanted, a cancer therapy based on current research, trials, and science." said Brad C. Through cancer vaccines, we now have hope for more time, better chance for survival, and hopefully a roadmap for others to follow as well."

Zealand Pharma and DEKA Research & Development Corp. Announce Collaboration Agreement to Advance Development of Infusion Pump to Be Used with Dasiglucagon for Treatment of Congenital Hyperinsulinism (CHI)

On November 5, 2021 Zealand Pharma A/S (Nasdaq: ZEAL) (CVR-no. 20045078,) a biotechnology company focused on the discovery, development and commercialization of innovative peptide-based medicines, reported that it has entered into definitive collaboration agreements with DEKA Research & Development Corp., to develop a continuous infusion pump to be used in combination with dasiglucagon, an investigational agent currently in phase 3 trials in patients with congenital hyperinsulinism (Press release, Zealand Pharmaceuticals, NOV 5, 2021, View Source [SID1234594658]). The agreement covers the technical development of the pump system as well as associated manufacturing and commercialization activities.

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"As we progress toward completion of our pivotal clinical trials for dasiglucagon as a potential treatment option for CHI, we are thrilled to announce this collaboration agreement with DEKA," said Emmanuel Dulac, President and Chief Executive Officer of Zealand Pharma. "DEKA’s innovative drug infusion pump has been FDA cleared in other uses and it represents an attractive potential solution for dasiglucagon administration in CHI, taking us one step closer to achieving our goal of improving the lives of CHI patients and their families."

"We are very pleased to be working with Zealand, leveraging our long experience with infusion pumps to aid in their development of a new treatment option for CHI," said Dean Kamen, Founder of DEKA. "Our mission at DEKA is to develop technology that can solve problems and improve people’s lives – this collaboration is a great example of how we work to fulfill that mission."

Under the terms of the agreement, DEKA and Zealand will develop a medical pump system that is suitable for use in combination with dasiglucagon. DEKA and its affiliates will be responsible for pump development and pump manufacturing activities. Zealand will be solely responsible for clinical development around the drug-device combination as well as for distribution and commercialization in all territories.

About CHI

CHI is a rare pediatric disease that affects mainly newborns, infants and toddlers. Due to a genetic defect in the insulin producing cells, these children have increased insulin levels, resulting in persistent and recurrent hypoglycemia throughout childhood. Current treatment options are limited, complex and may be insufficient to adequately control hypoglycemia.

About dasiglucagon

Invented by Zealand Pharma, dasiglucagon is a glucagon analog that is stable in aqueous solution and is thus suitable for chronic pump use. In 2017, both the U.S. Food and Drug Administration (FDA) and the European Commission granted orphan drug designation for dasiglucagon for the treatment of CHI.

2seventy bio Completes Spin Transaction and Launches Innovative Immuno-oncology Cell Therapy Company

On November 4, 2021 2seventy bio, Inc., (NASDAQ: TSVT), an emerging immuno-oncology company reported its official launch as an independent, publicly traded company. 2seventy bio will trade on the Nasdaq Global Select Market, commencing tomorrow, November 5 under the ticker symbol "TSVT (Press release, bluebird bio, NOV 4, 2021, View Source [SID1234594629])."

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"We’ve done the intense work to reach the start line and we are extremely excited to officially introduce 2seventy bio. 2seventy was created from an unrelenting desire to find new ways to outmaneuver cancer and give more time to the people we serve," said Nick Leschly, chief kairos* officer, 2seventy bio. "Our organization is ready: from our bold and seasoned team to our deep scientific expertise and our strong financial foundation. Our commitment is to sustain the energy, passion and rigor that we have today as we establish the leading immuno-oncology cell therapy company with an aim to deliver transformative treatment options to people living with a range of difficult to treat cancers."

The company officially separates today from bluebird bio, Inc. and launches with a robust cell therapy pipeline across a range of hematologic and solid tumors including two candidates that are planned to enter the clinic in the first half of 2022. The portfolio also includes a development and 50/50 U.S. commercialization partnership with Bristol Myers Squibb (BMS) for ABECMA, a first-in-class, BCMA-directed CAR T cell immunotherapy for multiple myeloma approved in the U.S.

Unique Scientific Approach to Cell Therapy

"Our differentiated cell therapy platform is built around the goal of delivering therapies that provide significant benefit to people living with cancer," said Philip Gregory, chief scientific officer, 2seventy bio. "We begin with the foundational understanding that autologous CAR T cell therapy works, yet there’s room to build and improve. We identify the unmet medical need, and we strive to understand where there are unique opportunities to change the path of disease. We then undertake a deliberate process to devise an engineered solution that relies on the robust toolbox of targeting, signaling, and enhancement technologies that we have established through our extensive experience and partnerships across industry and academia. Importantly, we are uniquely positioned to deliver these therapies to patients through a development strategy that is designed to efficiently test our hypotheses and quickly deliver answers not only for a given program, but across the technologies. By taking this approach, we’re able to apply learnings across the platform in rapid succession."

2seventy bio’s cell therapy pipeline includes approaches to hematologic malignancies and solid tumors, including two clinical studies expected to be initiated in the first half of 2022:

Multiple Myeloma (MM):
ABECMA (idecabtagene vicleucel; ide-cel): ABECMA, a first-in-class, B-cell maturation antigen (BCMA)-directed CAR T cell immunotherapy approved in the U.S. for the treatment of adult patients with relapsed or refractory multiple myeloma after four or more prior lines of therapy, including an immunomodulatory agent, a proteasome inhibitor, and an anti-CD38 monoclonal antibody, is being jointly developed and commercialized with BMS in the U.S.1 ABECMA generated $67 million in U.S. sales in 3Q21, its first full quarter of launch and 2seventy bio and BMS are pursuing additional clinical studies in earlier lines of treatment for patients with MM.
bb21217: Data from the ongoing Phase 1 study of bb21217, a BCMA-directed CAR T cell therapy in patients with relapsed and refractory MM that uses the ide-cel CAR molecule and is cultured with a PI3 kinase inhibitor (bb007) to enrich for T cells displaying a memory-like phenotype with the intention to increase the in vivo persistence of CAR T cells, to be presented by the end of 2021.
Next-generation: In addition, the company is exploring a next-generation approach that utilizes the experience applying the first commercial CAR T cell in MM to aid the design of a novel autologous T cell approach.
Acute Myeloid Leukemia (AML)/SC-DARIC33: The initiation of an upcoming Phase 1 study of SC-DARIC33 in relapsed/refractory pediatric and young adult AML in collaboration with Seattle Children’s Therapeutics will be a first-in-human investigation of 2seventy bio’s proprietary Dimerizing Agent Regulated Immunoreceptor Complex (DARIC) T cell platform.
B-cell non-Hodgkins Lymphoma (bNHL)/bbT369: The initiation of an upcoming Phase 1 dose-escalation study in patients with relapsed and refractory bNHL will be a proof-of-concept study of 2seventy bio’s proprietary gene editing platform, dual-targeting strategies and split co-stimulation signaling technology.
Solid Tumors: Pre-clinical studies are underway utilizing 2seventy bio’s diversified and innovative toolbox, including a program targeting MAGEA4, a surface antigen that is highly expressed across multiple solid tumors.
Blend of Strategic Collaboration and In-House Approach to Manufacturing

Integral to the delivery of 2seventy bio’s platform of cell therapies is the company’s manufacturing network, including best-in-class partnerships with academic centers and industry, purpose-built for messenger RNA (mRNA) and lentiviral vector (LVV) production. This network also includes a planned build for an internal clinical cell therapy manufacturing capability at the company’s headquarters in Cambridge, Massachusetts. This facility is designed to enable deep integration of Chemistry, Manufacturing and Controls (CMC) with research, correlative science, and clinical development, and enable the flexibility to rapidly innovate and learn as programs advance.

Launching with a Strong Financial Foundation and Leadership

2seventy bio is launching with a clear and differentiated strategy and is well-funded to deliver:

ABECMA – In 3Q21, BMS reported total U.S. revenues of $67 million for ABECMA. 2seventy bio will continue to share equally in the costs and revenue for ABECMA in the U.S. The companies continue to experience robust demand for ABECMA and are working to improve manufacturing capacity and supply.
Board – 2seventy bio is launching with an experienced leadership team and Board of Directors, including:
Daniel S. Lynch (chairman – independent), Sarah Glickman (Audit Committee chair – Criteo), Denice Torres, J.D. (formerly of Johnson & Johnson), Ramy Ibrahim, M.D. (Broad Institute of MIT and Harvard), Marcela Maus, Ph.D. (Mass General Cancer Center), William Sellers, M.D. (Core Institute Member, Broad Institute of MIT, and Harvard) and Nick Leschly (2seventy bio)
Financial Position – 2seventy bio is launching with approximately $442 million in cash, which the company anticipates is sufficient to fund operations into 2023.

Glycostem announces initial clinical data to be presented at 2021 ASH Annual Meeting

On November 5, 2021Glycostem Therapeutics B.V., a leading clinical-stage company focused on the development of therapeutic allogeneic off-the-shelf Natural Killer (NK) cells, reported that the abstract on the initial findings of the first two patients treated in its phase I/IIa WiNK trial have been accepted and will be presented at the 63rd American Society of Hematology (ASH) (Free ASH Whitepaper) Annual Meeting and Exposition (ASH 2021), which will take place 11th – 14th December 2021 in Atlanta, GA, USA (Press release, Glycostem Therapeutics, NOV 5, 2021, View Source [SID1234594626]). oNKord is the company’s first-generation off-the-shelf allogeneic NK cell therapy under clinical development. Glycostem is furthermore developing a range of CAR-NK, combination therapy and TCR-NK products in-house.

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The accepted abstract is published today and available on the ASH (Free ASH Whitepaper) website: www.hematology.org.

Title: Allogeneic, CD34+, Umbilical Cordblood-Derived NK Cell Adoptive
Immunotherapy for the Treatment of Acute Myeloid Leukemia Patients With
Measurable Residual Disease
Abstract #: 1745
Session Name: 704. Cellular Immunotherapies: Clinical: Poster I
Date: Saturday, 11th December 2021
Presentation Time: 5:30 PM – 7:30 PM (EST)
Location: Georgia World Congress Center, Hall B5, Atlanta, GA, USA

"We are very excited to share the first clinical data from our WiNK phase I/IIa trial of oNKord in patients with Acute Myeloid Leukemia. We are very pleased to see that these first positive results with a single dose infusion with our off-the shelf and allogeneic NK cell product, are confirming our observations from our past clinical trial," said Kai Pinkernell, MD, Chief Medical Officer of Glycostem.

The first patient converted to measurable residual disease (MRD) negativity (<0.1%) as assessed by multiparametric flowcytometry (MFC) on bone marrow on day 0, which was sustained at 1, 2, 3 and 6 months. NPM1 MRD, which was detectable by next generation sequencing (MRD-NGS) up to month 1 in peripheral blood (PB), became undetectable by month 2, 3 and 6 in PB (<0.01%VAF). Results in BM showed that NPM1 MRD was detectable at month 1 but was cleared at months 3 and 6.
The second patient showed MRD positivity in BM by MFC at screening and on day 0, which turned to MRD negativity at month 1, turning positive again at month 2 and 3. Assessments in PB and BM by MRD-NGS showed that a IDH2 and a SRSF2 clone persisted after preconditioning and GTA002 infusion, but that a PTPN11 clone became undetectable in PB by Day 0 and in BM by month 2 and month 3.
The most recent available follow up will be presented at time of presentation.