NantCell Announces New Celgene Investment

On January 4, 2019 NantCell and it’s founder Dr. Patrick Soon-Shiong reported that Celgene has completed its crossover investment in NantCell (Press release, NantHealth, JAN 4, 2019, View Source;p=RssLanding&cat=news&id=2382455 [SID1234532557]). Dr. Soon-Shiong will be introducing the company at the 37th Annual JP Morgan Healthcare Conference at the Westin St. Francis Hotel, San Francisco on Monday, January 7th at 8:30am.

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NantCell is a privately held immunotherapy company, whose goal is to employ a broad portfolio of biological molecules that will enable it to develop a cancer vaccine to combat multiple tumor types without the use of high-dose chemotherapy. NantCell has one of the most comprehensive late stage clinical pipelines of an integrated platform of immunotherapy technologies addressing both the innate (activated macrophage and natural killer cell) and the adaptive immune system (dendritic, CD4 and CD8 killer T cells). Currently the company is actively enrolling patients for registration trials in 15 indications.

On December 19, 2018, Celgene completed a crossover funding round of $30 million in NantCell at a $4 billion valuation, bringing its overall investment in the company to $105 million with a 2.8% ownership in the company. This follows the May 2015 Celgene initial investment of $75 million in NantCell.

"We have partnered with Dr. Soon-Shiong and his mission to change the course of cancer from the very beginning," said Mark Alles, Chairman and CEO of Celgene. "From his invention of Abraxane, to acquiring his company in 2010, to launching this protein nanoparticle drug as the backbone of immunotherapy to its current blockbuster status, and now to supporting his vision at NantCell of developing a chemo free cancer vaccine utilizing the body’s own immune system. Celgene invested in NantCell since its inception in 2015 and we are excited to extend this partnership today with the significant clinical progress he has made in developing cytokines and bispecific proteins in the ongoing quest to conquer this disease," said Alles. Celgene announced on January 3, 2019 that it would be acquired by Bristol-Myers Squibb for $74 billion.

"To our knowledge" said Soon-Shiong, "there is no other biotech or large pharma company with NantCell’s broad pipeline of bispecific and trispecific fusion cytokine proteins, peptides, mRNA, monoclonal antibodies, neoepitope and tumor associated vaccine delivery and cell therapy products, all in clinical phase of development, across multiple indications, for the treatment of cancer and infectious disease. We are very pleased with Celgene’s continued investment in the company and our shared vision of developing a chemotherapy free cancer vaccine."

"With the clinical advances of the technology platforms across multiple tumor types at NantCell, the company is now poised to integrate the technologies developed at the two early stage immunotherapy public companies, NantHealth and NantKwest," said Dr. Soon-Shiong, founder of all three companies. "The adenovirus and yeast vector delivery systems in NantCell compliments the tumor associated antigen and neoepitope discovery engine (GPS CancerTM) developed by NantHealth, enabling the subcutaneous delivery of the neoepitopes to enable the recruitment of T cells that target only expressed cancer mutations. The bispecific fusion cytokine proteins of NantCell stimulates the patient’s autologous primary NK and T cells, thereby supplementing the off-the-shelf, cryopreserved haNK cells developed by NantKwest. Collectively the immunotherapy platforms in NantCell, NantHealth and NantKwest serve as a comprehensive path to the development of a cancer vaccine," said Soon-Shiong.

Preclinical Pipeline, Technology Platforms and IND Pipeline:

Specifically, NantCell has 28 unique molecules in its preclinical pipeline consisting of fusion proteins, mRNA, cytokines and monoclonal antibodies including checkpoints and novel cytokine fusion proteins, six of which are IND ready with anticipated filings in 2019. The company has developed a novel proprietary library of fully human single chain variable fragment antibodies (ScFv) with a diversity greater than 1012. This library has yielded fully human monoclonal antibodies with high affinity target binding and is being incorporated into chimeric antigen receptor (CAR) in both off-the-shelf NK cell lines as well as autologous primary NK and T cells for the development of novel cell therapy products. To enable intracellular uptake of both DNA and mRNA, NantCell has also developed novel methods of scalable electroporation enabling high viability and high expression of the desired genes in NK92 cell line, and in primary NK and T cells. In addition, NantCell has developed an automated method of a fully closed system for manufacturing targeted NK cell lines, primary NK and T cells (GMP in the box).

Current Phase 1 and Phase 2 Development Program:

In addition to the preclinical pipeline above, currently the company’s activated clinical programs include seven (7) molecules in Phase 1, four (4) molecules in Phase 2, and three (3) molecules in registration clinical trials, across multiple indications. The deep clinical pipeline of 14 unique biomolecules have been tested in over 1,000 patients to date, to evaluate the safety and initial efficacy profiles of these novel molecules as first in human single agent studies.

In 2017 and 2018, the company initiated combination studies of these individual molecules and over 20 Investigational New Drugs (INDs) were authorized by the FDA to enable Phase 1 safety studies using these fusion proteins, monoclonal antibodies, tumor associated adenoviral and yeast delivery systems to evaluate safety and early efficacy of these combinations, termed QUILT Trials . Phase 1 safety and efficacy clinical data for this cancer vaccine of the combined molecules has been completed for multiple tumor types, including metastatic pancreatic cancer, triple negative breast cancer, head and neck cancer, lung cancer and bladder cancer. Preliminary data was presented at the SITC (Free SITC Whitepaper) conference in November 2018.

Registration Trials with NantCell’s Lead Cytokine Fusion Protein:

NantCell has initiated registration trials of its lead cytokine fusion protein in 15 indications. The lead IL15/Fc bispecific fusion protein and cytokine has entered into two registration trials in bladder cancer and obtained Fast Track Designation for the treatment of relapsed non-muscle invasive bladder cancer. The company anticipates completion of accrual in 2019 with a read out of efficacy data by the third quarter.

NantCell has also began enrollment in single arm pivotal trials of this bispecific IL15/Fc cytokine in 12 distinct cancer indications, in which patients have failed checkpoint inhibitors. These single arm pivotal trials include patients in the following indications; non-small cell lung cancer (NSCLC), small cell lung cancer (SCLC), urothelial carcinoma, head and neck squamous cell carcinoma (HNSCC), Merkel cell carcinoma (MCC), melanoma, renal cell carcinoma (RCC), gastric cancer, cervical cancer, hepatocellular carcinoma (HCC), microsatellite instability-high (MSI-H) or mismatch repair deficient (dMMR) solid tumor cancer and colorectal cancer (CRC).

In addition, the company began enrollment in a pivotal randomized trial of patients with non- small cell lung cancer comparing checkpoint therapy alone versus checkpoint therapy in combination with the IL15/Fc fusion protein as a chemotherapy free first line therapy in lung cancer.

Registration Trials at NCI: Two molecules are actively being studied in Phase 3 trials at the NCI for the treatment of patients with Ewing’s sarcoma and Recurrent Chordoma.

Registration Trial in Collaboration with NantKwest: The bispecific IL15/Fc cytokine in combination with NantKwest’s high affinity NK cell (haNK) and a checkpoint inhibitor has been authorized to begin enrollment in patients with relapsed Merkel cell carcinoma.

GMP Manufacturing:

The company has developed and completed GMP manufacturing facilities for its lead bispecific cytokine IL15/Fc fusion protein, for its adenovirus and yeast delivery systems and novel "GMP in a Box" automated manufacturing for its targeted natural killer and T cell therapies.

About the Concept of Chemotherapy Free Cancer Vaccine:

The concept of activating the body’s own immune system evolved during Dr. Soon-Shiong’s studies on developing a micro encapsulated islet cell transplant in the 1990’s. In 1993 he performed the world’s first micro encapsulated islet transplant in a diabetic patient and published a paper entitled "Prevention of CTL and NK Cell-Mediated Cytotoxicity by Microencapsulation," (Hormone and Metabolic Research, 1990, PG. 215-219) demonstrating that the body’s natural killer (NK) cells were responsible for attacking foreign implanted tissue. Inspired by the thought that the cancer cell had discovered a means to trick the body and induce tolerance, Dr. Soon-Shiong began the concept of inventing a nanoparticle to breach the tumor micro environment to activate the innate immune system. By 1998, he invented the first albumin-bound nanoparticle, Abraxane, harnessing the protein pathways (GP60) to enter the tumor micro environment and activate macrophages to attack cancer cells. Abraxane was approved in 2005 and acquired by Celgene in 2010. The drug has since become the backbone for combination therapy with check point inhibitors in multiple tumor types. The theory that Abraxane converts M2 macrophages to activated M1 cells has now been confirmed by independent investigators: "Macropinocytosis of Nab-paclitaxel Drives Macrophage Activation in Pancreatic Cancer."(Cancer Immunology Research, 2017, Pg. OF1-OF9) In October 2010, Celgene acquired Abraxis BioScience and by 2017 achieved blockbuster status for Abraxane in the treatment of breast, lung, and pancreatic cancer.

To continue the quest of chemotherapy as immune-modulatory agents Dr. Soon-Shiong published and patented the use of Abraxane in a low dose metronomic form in 2010. The efficacy of Abraxane in this low dose metronomic form combined with checkpoint inhibitors was validated in the New England Journal of Medicine publications in 2018 in studies on patients with triple negative breast cancer "Atezolizumab and Nab-Paclitaxel in Advanced Triple-Negative Breast Cancer."(The New England Journal of Medicine, 2018, Pg. 1-14) and in patients with lung cancer "Pembrolizumab plus Chemotherapy for Squamous Non–Small-Cell Lung Cancer."(The New England Journal of Medicine, 2018, Pg. 1-12)

With the sale of APP and Abraxis in 2011, Dr. Soon-Shiong was free to pursue the concept of a cancer memory vaccine and founded NantWorks to bring this concept to the clinic. He developed the whole genome DNA–RNA next generation sequencing test (GPS Cancer) in order to elucidate the tumor associated antigens and neoepitopes, unique to each individual patient. This test received CLIA/CAP in 2015. Five seminal patents were issued covering the discovery of neoepitopes using the GPS Cancer test (US 9,646,134; US 9,652,587; US 9,721,062; US 9,824,181; US 9,262,719). In 2016, NantHealth (Nasdaq: NH) completed its IPO to launch GPS Cancer.

Next was the development of an off-the-shelf Natural Killer cell in order to establish a universal activated and targeted NK cell. With the discovery of a natural killer cell line (NK92) Dr. Soon-Shiong developed a GMP method to produce a cryopreserved, high affinity CD16 natural killer cell (haNK), forming the bases for the second element of the cancer vaccine and launched NantKwest (Nasdaq:NK).

Finally, to deliver the antigens identified by GPS Cancer at NantHealth and to supplement the off-the-shelf haNK cells at NantKwest with the patient’s own CD4, CD8 T cells and NK cells, Dr. Soon-Shiong founded an immunotherapy company beyond checkpoints, NantCell. In 2015, NantCell was launched and developed immunotherapy platforms including the adenovirus virus and yeast delivery systems, cytokine fusion proteins, monoclonal libraries and novel methods to manufacture of primary NK and T cell on a personalized basis for a single patient utilizing an automated "GMP in the box." These technology platforms form the basis of NantCell, the immunotherapy company current enrolling patients in registration trials for 15 indications in cancer.

With the clinical advances across multiple tumor types accomplished at NantCell, the company is now poised to harness the technologies developed at the public entities, NantHealth and NantKwest. The adenovirus and yeast vector delivery systems in NantCell complements the tumor associated antigen and neoepitope discovery engine (GPS Cancer) developed by NantHealth, enabling the subcutaneous delivery of the neoepitopes in the cancer vaccine. The bispecific fusion cytokine proteins of NantCell stimulates the patient’s autologous NK and T cells, thereby supplementing the off-the-shelf cryopreserved haNK cells developed by NantKwest. Collectively the immunotherapy platforms in NantCell, NantHealth and NantKwest serve as a comprehensive path to the development of a cancer vaccine.

About the Evolution and Financial History of NantCell:

In the early 1990s, Dr. Soon-Shiong invented the drug Abraxane, the nation’s first human protein (albumin) nanoparticle to activate a specific receptor on the blood vessels supplying the tumor and began the journey of seeking to transform the tumor microenvironment and activating the immune system. Abraxane was approved by the FDA for metastatic breast cancer in 2005, lung cancer in 2012 and pancreatic cancer in 2013. Abraxane is now approved in many countries across the globe with annual sales of approximately $1.0 billion.

From 1997 to 2010, Dr. Soon-Shiong served as founder, Chairman and Chief Executive Officer of two public pharmaceutical companies, American Pharmaceutical Partners, Inc. (NASDAQ: APPX) and Abraxis BioScience, Inc. (NASDAQ: ABII). In June 1998, APPX acquired Fujisawa USA, Inc.’s generic injectable pharmaceutical business to invent manufacturing processes for the first human albumin nanoparticle delivery system. In December 2001, Dr. Soon-Shiong successfully completed an IPO of APPX at a valuation of approximately $769 million. In November 2005, following the approval of Abraxane, APPX announced an approximately $2.4 billion all-stock merger with the privately-held American Bioscience, Inc. to create Abraxis BioScience, combining the strengths of a commercial-stage biotechnology company with a growing injectable pharmaceutical business. In 2007, ABII spun off as a separate entity, with stockholders receiving one share of ABII for every four shares of APPX.

In 2008, Fresenius SE acquired APPX for approximately $5.6 billion inclusive of the full value of a CVR. Each stockholder received $29.00 per share inclusive of the full value of a CVR. In 2010, ABII was acquired by Celgene for approximately $3.6 billion. Each stockholder received, for each share of ABII common stock, a total value of approximately $73.23 per share and one CVR. When the full value of the CVRs are included, the investors in APPX at the time of the Fujisawa acquisition in 1998 would have received a total return of approximately 2,070% and an IRR of approximately 32.4%.

In 2011, Dr. Soon-Shiong founded NantWorks to pursue the concept of a cancer vaccine for all tumor types. He founded NantHealth in 2016 to develop the genomic discovery engine for tumor associated antigens and neoepitopes and announced Cancer Breakthrough 2020 vision.

In 2015 Dr. Soon-Shiong launched NantKwest to establish the world’s first off-the-shelf cryopreserved universal NK cell line.

In May 2015 he founded NantCell, with an initial investment from Celgene, whose goal is to employ a broad portfolio of biological molecules that will enable it to develop a cancer vaccine to combat multiple tumor types without the use of chemotherapy. NantCell has one of the most comprehensive late stage clinical pipelines of an integrated platform of technologies addressing both the innate (activated macrophage and natural killer cells) and the adaptive immune system (dendritic, CD4 and CD8 killer T cells). Currently, NantCell is actively enrolling patients for registration trials in 15 indications. In December 2018, Celgene completed a crossover funding round of $30 million at a $4 billion valuation, bringing its overall investment in the company since its inception in 2015 to $105 million and 2.8% ownership in the Company. On January 3, 2019, Celgene announced that it will be acquired by Bristol-Myers Squibb for $74 billion.

Lamellar to conduct Business Development Meetings about LAMELLASOME™ technology at Biotech Showcase in San Francisco

On January 4, 2019 Lamellar Biomedical Limited (Lamellar), an innovative biotechnology company, pioneering new approaches for the safe and effective transfer of functional nucleic acids, reported that Dr Alec McLean, CEO; Steven Porteous, Head of Clinical and Regulatory and Dr Lynsey Howard, Head of Pre-clinical Development will be attending Biotech Showcase in San Francisco on 7-9 January 2019 (Press release, Lamellar Biomedical, JAN 4, 2019, View Source [SID1234532438]).

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During the event the Lamellar team will conduct multiple business development meetings with potential partners and investors to highlight the potential of its cutting-edge LAMELLASOME technology for the delivery of nucleic acid therapeutics (NAT). These meetings will build on the very positive reaction to its LAMELLASOME platform, when it was introduced at BIO-Europe 2018 in Copenhagen in November 2018.

Alec McLean, CEO of Lamellar Biomedical, said, "We were very pleased with the reaction from potential partners and investors when we introduced our LAMELLASOME platform for the safe and effective delivery of nucleic acid therapeutics at BIO-Europe late last year. We are now looking forward to multiple new and follow up meetings in San Francisco reflecting the explosion in the number of novel nucleic-acid based therapeutics being developed for a broad range of diseases. Two key factors limiting their progress, from preclinical promise to clinical reality, are safe and effective delivery. Based on our work to-date, Lamellar is confident that it is in an unique position to unlock this enormous potential of nucleic acid based therapeutics using its LAMELLASOME technology."

Lamellar believes that its LAMELLASOME technology will play a key role in realising the potential of many of the nucleic acids in development, including mRNAs, siRNAs, miRNAs and plasmids, potentially revolutionising the treatment of numerous rare and intractable diseases.

In October 2018, Lamellar filed a patent detailing that it had demonstrated functional target downregulation by a transfected nucleic acid delivered via its LAMELLASOME technology. Lamellar has also shown that LAMELLASOME formulations have been effective in delivering functional nucleic acids to a range of cell types including macrophages, human pulmonary fibroblasts and human dendritic cells.

Crucially, all transfected cells types have exhibited very high cell viability and maintenance of cell phenotype/function. Lamellar’s LAMELLASOME technology is entirely novel and does not utilise viral vectors or cationic or divalent ion-associated liposomal systems.

Lamellar is also developing its own pipeline of nucleic-acid based therapeutics, the most advanced of which target two areas of unmet clinical need: Idiopathic Pulmonary Fibrosis and Cystic Fibrosis.

Lamellar is currently completing in-vivo models to demonstrate safe and effective pulmonary delivery and transfection of microRNA(s) prior to executing the final proof of concept efficacy study for its Idiopathic Pulmonary Fibrosis microRNA product in Q1 2019. These studies will be designed to show the performance of LAMELLASOME IPF-NA product in-vivo as well as to demonstrate the unique capabilities of LAMELLASOME nucleic acid transfer technology platform.

The Lamellar team will be available to present the proprietary LAMELLASOME technology to any companies attending Biotech Showcase who see enhanced delivery of their novel nucleic-acid based therapeutics as crucial to their future success.

MabVax Therapeutics and Oncotelic Enter into Merger Discussions

On January 4, 2019 MabVax Therapeutics Holdings, Inc. (OTC Pink: MBVX), a clinical-stage immuno-oncology drug development company with a fully human antibody discovery platform focused on the clinical development of products to address unmet medical needs in the treatment of cancer and pancreatitis, reported that it has entered into discussions to merge with Oncotelic, Inc., a privately held cancer immunotherapy company (Press release, MabVax, JAN 4, 2019, View Source [SID1234532459]). Oncotelic is developing a unique TGF-b antisense therapy which has demonstrated the ability to break immune tolerance in mid-stage clinical trials for the treatment of glioblastoma and pancreatic cancer.

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Based on terms of a non-binding letter of intent signed by both companies on January 3, 2019, MabVax and Oncotelic are entering discussions to combine the companies to form a publicly traded company focused on the development of proprietary immunotherapy-based products of both companies to diagnose and treat cancer. Under the terms of the letter of intent, Oncotelic will merge with a wholly-owned subsidiary of MabVax in an all-stock transaction and will become a wholly-owned subsidiary of MabVax. The merger is subject to the approval of the MabVax board of directors and achieving certain financing objectives and other customary conditions. Upon closing of the transaction, MabVax will be re-named Oncotelic, Inc. and will operate under the leadership of the combined Oncotelic and MabVax management teams, with Vuong Trieu, founder of Oncotelic, an experienced and successful biotechnology entrepreneur, as executive chairman. Certain current senior management team members at MabVax will remain with the merged companies to fill key operational roles.

On a pro forma basis, calculated at the close of the merger, the current MabVax stockholders will own 25% and Oncotelic stockholders will own 75% of the combined company, respectively. The merger agreement contemplates securing financing of at least $10 million simultaneous with execution of the merger to support the clinical development of Trabedersen, Oncotelic’s TGF-b antisense therapy, in both glioblastoma and pancreatic cancer trials.

Vuong Trieu, Ph.D., who will be executive chairman of the company post-merger, said, "Our goal has been to grow a strong RNA therapeutic company that leverages innate immunity to achieve durable and effective immunotherapies for solid tumors and the merger with MabVax will allow us to complement that effort with key programs and capabilities from MabVax that will significantly strengthen the effort."

David Hansen, President and CEO of MabVax, said, "Through this transaction we hope to leverage our clinical and operational expertise in the post-merger company to advance the clinical development of Trabedersen while also integrating the development of key assets discovered by MabVax. This will allow us to continue the process of realizing the maximum value of assets we have developed through a process already initiated with Objective Capital while simultaneously maximizing the value of our lead technologies for stockholders."

On December 13, 2018, MabVax announced that it had engaged Objective Capital Partners, LLC to serve as a financial advisor to assist MabVax in exploring the sale of clinical and preclinical assets of the Company with the goal of maximizing the value of these assets within the near term. MabVax’s lead monoclonal antibody product, 5B1 for the treatment of pancreatic cancer, could be one of the assets that potentially could be developed into later stage clinical trials by the combined company.

KalGene Appoints James E. Callaway, Ph.D. as Chief Executive Officer

On January 4, 2019 KalGene Pharmaceuticals Inc., a biotechnology company developing therapeutics to slow the progression of Alzheimer’s disease, reported the appointment of James Callaway, Ph.D. as chief executive officer, effective immediately (Press release, KalGene Pharma, JAN 4, 2019, View Source [SID1234532493]).

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"This has been a very important transition year as we have confirmed our initial thesis with respect to validating the company’s lead KG207, which in pre-clinical studies was shown to successfully cross the blood brain barrier and safely reduce plaque load. The company has successfully completed early toxicology studies and has carried out all the requisite steps to manufacture product," said Dr. Jacki Jenuth, Chairperson of the Kalgene’s board of directors. "We are very pleased to have executed on the next key step of our strategy in attracting an accomplished new CEO to the company as we leverage this foundation and address significant inbound interest for the company and its lead program. Jim brings an ideal set of leadership skills and domain expertise to guide the team through the transition from a pre-clinical to a clinical stage company."

"KG207 has shown exceptional potential in pre-clinical studies, and I am excited about the prospect of bringing such a promising compound into the clinic," Dr. Callaway commented. "I look forward to working with the savvy and talented team at KalGene as we strive to make a difference in the lives of individuals affected by Alzheimer’s disease."

Dr. Callaway has over three decades of biopharmaceutical development experience, primarily targeting CNS therapeutics, and has served most recently as CEO for two privately-held biotech companies. As the CEO of ArmaGen, he brought its products from the laboratory to the clinic, helping the company emerge as the first to demonstrate the ability of engineered biologics to cross the blood-brain barrier. In addition, Dr. Callaway led the Alzheimer’s immunotherapy program at Elan Pharmaceuticals, which became the first company to introduce disease-modifying biologics (e.g., AN1792, bapinuzumab, ACC001) into clinical studies. Dr. Callaway has filed and defended numerous NDAs and INDs during his career, including shepherding the approval of MyoBloc and the production of Tysabri. He previously served in senior development roles at Bayer Pharmaceuticals, SmithKline Beecham (GSK), and InGene (since acquired by Xoma Corporation). He holds a Ph.D. in Biological Chemistry from UCLA, with a focus on peptide chemistry

BerGenBio Announces Start of Phase II Investigator Initiated Trial Evaluating Selective AXL Inhibitor Bemcentinib in high-risk MDS

On January 4, 2019 BerGenBio ASA (OSE: BGBIO), reported that the first patient has been dosed in an investigator-initiated phase II trial of bemcentinib, a selective, potent and orally bio-available AXL inhibitor, in patients with high-risk myelodysplastic syndrome (MDS) who have failed first-line treatment with hypomethylating agents (Press release, BerGenBio, JAN 4, 2019, View Source [SID1234532440]). The trial may also enrol a proportion of patients with acute myeloid leukaemia (AML). The study is being sponsored by GWT-TUD GmbH (a specialist cancer clinical research institution associated with the University of Dresden, Germany) with the support of BerGenBio.

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The trial (BGBIL009 / BERGAMO) aims to confirm the efficacy of bemcentinib monotherapy in patients with high-risk MDS and AML and will enrol up to 43 patients at 8 hospitals in Germany, France, the Netherlands and Italy. The study will allow for the evaluation of potential predictive and pharmacodynamic biomarkers for MDS in bone marrow and blood, including those associated with patient benefit from bemcentinib.

Prof. Uwe Platzbecker, lead investigator of the trial and director of the Medical Clinic and Policlinic 1, Hematology and Cell Therapy at the University Hospital in Leipzig, Germany, commented: "As treatment of MDS and AML has not changed significantly over the past decades, novel therapies are urgently needed. The survival is still dismal, especially in elderly patients who are not eligible for allogeneic stem cell transplantation and who have failed first line treatment with hypomethylating agents. AXL, a member of the Tyro3, AXL, Mer (TAM) receptor family, mediates proliferation and survival of leukemic cells and is upregulated upon cytostatic treatment. Pre-clinical studies with the inhibitor bemcentinib demonstrated in vitro and in mouse models that leukaemic proliferation was blocked by interference with AXL signalling. Hence, AXL represents a promising new target for the patient population investigated in the BERGAMO trial."

Richard Godfrey, Chief Executive Officer of BerGenBio, added: "We are very pleased that Prof. Platzbecker and GWT-TUD are initiating this study, which if positive will add valuable information on bemcentinib’s monotherapy use in a larger leukaemia population and provide support for our broader development plans for bemcentinib in these indications. We look forward to reporting results as the trial progresses."

END

About MDS
Myelodysplastic syndromes (MDS) are stem cell disorders characterised by a decreased ability of the bone marrow to produce normal blood cells and platelets. MDS is associated with increased risk of developing AML and immune dysfunctions are seen in patients both with lower and higher-risk MDS. Drugs that modify immunological responses can improve blood values and prolong survival in some patients. Thus far, however, the only curative treatment for MDS remains stem cell transplantation. Hence, there is an urgent need for novel therapies to treat MDS.

About AXL
AXL kinase is a cell membrane receptor and an essential mediator of the biological mechanisms underlying aggressive and life-threatening diseases. In cancer, AXL drives tumour survival, treatment resistance and spread, as well as suppressing the body’s immune response to tumours. AXL expression has been established as a negative prognostic factor in many cancers. AXL inhibitors, therefore, have potential value at the centre of cancer combination therapy, addressing significant unmet medical needs and multiple high-value market opportunities.

About Investigator-sponsored trials
Investigator-sponsored clinical trials are clinical trials proposed by front-line patient-facing physicians who act as the regulatory sponsor and are supported by industry in bespoke clinical development partnerships. The industry partner does not assume the role of sponsor according to European or US regulatory guidelines but may offer support in a variety of different ways, such as providing investigational medicinal product at no cost