Category Archives: Stem Cell Treatment


Immunotherapy After Chemotherapy Improves Outcomes in Metastatic Bladder Cancer – Curetoday.com

Using immunotherapy earlier, immediately after the conclusion of chemotherapy to treat metastatic bladder cancer, can delay the time until disease progression.

After completing chemotherapy, patients in the phase 2 study who took Keytruda (pembrolizumab) experienced no disease progression for 5.4 months versus 3 months for those who took placebo. In addition, the patients in the Keytruda group survived for a median 22 months compared with a median 18.7 months in the placebo group.Serious and severe side effects were more common in the immunotherapy group.

The study was published April 9, 2020 in the Journal of Clinical Oncology by Dr. Matthew Galsky, director of genitourinary medical oncology at Mount Sinai, in New York, and his colleagues at institutions across the country.

Bladder cancer becomes metastatic when it spreads to parts of the body that are far from where it developed, such as the lungs, liver, bones or other organs. For decades, the standard treatment for bladder cancer at this stage has been platinum-based chemotherapy followed by observation until the disease progresses. Since immunotherapy has proven effective in treating recurrences of metastatic bladder cancer, researchers wanted to establish whether using it immediately after chemotherapy would improve outcomes both in those who later took immunotherapy again to treat recurrence and in patients who never took another therapy. Giving immunotherapy under these circumstances is a strategy known as switch maintenance.

Between 2015 and 2018, the researchers treated 53 adults who had urothelial carcinoma the most common type of bladder cancer with placebo after they completed chemotherapy, mimicking the current standard of care. Meanwhile, 55 other adults with the disease received Keytruda starting two to six weeks after they finished chemotherapy.

Keytruda is part of a class of drugs called checkpoint inhibitors that interfere with the activity of proteins whose job is to keep the immune system in check. This frees up the immune system to better recognize and fight cancer.

During the study, participants were not told whether they were receiving Keytruda or a placebo in IV treatments every three weeks for 24 months, but those whose disease progressed while taking placebo were invited to switch to the Keytruda group. All the patients were checked for disease progression with imaging after every four cycles.Patients eligible to participate had a disease that was either stable or improved after chemotherapy. They were not eligible if cancer had spread to their brains or if they had used immunosuppressive drugs long-term or had previously been treated with a checkpoint inhibitor. The median age of participants was mid- to late 60s, and the majority were men and white.

The researchers findings of the length of time until disease progression were statistically significant, meaning that they were unlikely to be due to chance, but their results demonstrating lengthened life did not meet that standard. However, the researchers called both trends favorable.

The researchers found that 9% of the patients taking Keytruda experienced a complete response to therapy, meaning they had no remaining detectable cancer. No patients taking placebo had a complete response.

The researchers also reported that the objective response rate (the proportion of patients who experienced a prespecified amount of tumor reduction) was 23% with Keytruda versus 10% with placebo. Patients who were cancer-free after chemotherapy were not included in objective response rate calculations.

While tumors that express a lot of the protein programmed death ligand-1, more commonly referred to as PD-L1, often respond especially well to checkpoint inhibitors, that characteristic did not make a difference in patients outcomes in this study.

Serious and severe side effects that emerged during treatment affected 59% of the patients receiving Keytruda and 38% of the patients receiving placebo, the researchers reported. In the Keytruda group, there was one death from a treatment-related side effect, hepatitis, and 20% of patients initially assigned to that group experienced immune system-related side effects that required treatment with steroids. The largest proportion of side effects experienced during the study were serious, and they included anemia, hypertension, fatigue, difficulty breathing, urinary tract infection and liver problems.

Other recent research supports the finding that switch maintenance with a checkpoint inhibitor can be beneficial to patients in this population, the authors noted. They pointed out that a recent phase 3 trial found a survival benefit with this strategy, and that other trials are investigating even earlier use of immunotherapy in these patients, giving it along with chemotherapy and then continuing it afterward.

Ultimately, the outcomes of the several pending randomized trials will together shape the near-term landscape of first-line treatment for metastatic urothelial cancer, a disease state characterized by a paucity of advances in decades, the researchers wrote.

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Immunotherapy After Chemotherapy Improves Outcomes in Metastatic Bladder Cancer - Curetoday.com

Celularity Expands Strategic Collaboration with United Therapeutics Corporation to COVID-19 Infection and Acute Respiratory Distress Syndrome – Yahoo…

- The expanded strategic collaboration includes the use of Celularity's proprietary CYNK-001 for treatment of SARS-CoV-2 virus, which causes COVID-19 and Acute Respiratory Distress Syndrome

WARREN, N.J., April 9, 2020 /PRNewswire/ --Celularity Inc. ("Celularity" or the "Company"), a clinical-stage company developing allogeneic cellular therapies from human placentas, today announced the expansion of its existing collaborative license agreement with United Therapeutics Corporation's (Nasdaq: UTHR) wholly-owned subsidiary, Lung Biotechnology PBC, to include the treatment of COVID-19 and Acute Respiratory Distress Syndrome (ARDS).

(PRNewsfoto/Celularity, Inc.)

This announcement builds on recent pioneering work by Celularity for the use of its proprietary CYNK-001 for the treatment of the SARS-CoV-2 virus that causes the coronavirus disease, COVID-19, and extends this application of the technology to ARDS. The U.S. Food and Drug Administration recently cleared Celularity's investigational new drug application (IND 019650) to evaluate CYNK-001's safety, tolerability, and efficacy for the treatment of COVID-19.

ARDS, the most devastating complication of COVID-19, is a serious inflammatory lung injury that causes hypoxemia, or below-normal oxygen level in the blood. Hypoxemia can lead to multi-organ system failure and death. Recent findings indicate that ARDS may develop in as many as 17-29% of COVID-19 patients who are hospitalized with pneumonia.

Celularity founder and Chief Executive Officer, Dr. Robert Hariri, said, "This promising, novel approach to treating COVID-19 and the pulmonary complications associated with this infection may unlock a powerful new therapeutic option for patients. The exceptional expertise in pulmonary disease, cellular medicine, and manufacturing makes this strategic collaboration particularly well suited to tackle this urgent, global medical crisis."

Under the amended collaborative agreement, Celularity will seek regulatory approval for CYNK-001 in COVID-19, and Lung Biotechnology will seek regulatory approval for CYNK-001 in ARDS. Lung Biotechnology has global rights under the amended collaborative agreement to commercialize CYNK-001 in COVID-19 and ARDS. The collaboration will be governed by a Joint Steering Committee to oversee development and commercialization activities. Financial terms were not disclosed.

Celularity's CYNK-001 is the only cryopreserved allogeneic, off-the-shelf Natural Killer (NK) cell therapy being developed from placental hematopoietic stem cells and is being investigated as a potential treatment option for various hematologic cancers and solid tumors, and is the first cell therapy granted an IND to treat COVID-19. NK cells are a unique class of immune cells, innately capable of targeting cancer cells and virally infected cells and interacting with adaptive immunity. CYNK-001 cells derived from the postpartum placenta have been shown to be well-tolerated in early clinical trials and are currently being investigated as a treatment for acute myeloid leukemia (AML), multiple myeloma (MM), and glioblastoma multiforme (GBM).

Media and Investor RelationsMedia Contact:Factory PRcelularity@factorypr.com

Investor Relations Contact:John R. Haines, Executive Vice Presidentjohn.haines@celularity.com

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About Celularity: Celularity, headquartered in Warren, N.J., is a clinical-stage cell therapeutics company delivering transformative allogeneic cellular therapies derived from the postpartum human placenta. Using proprietary technology in combination with its IMPACT platform, Celularity is the only company harnessing the purity and versatility of placental-derived cells to develop and manufacture innovative and highly scalable off-the-shelf treatments for patients with cancer, inflammatory, infectious, and age-related diseases. To learn more, please visit http://www.celularity.com.

Forward-Looking Statements: This press release contains forward-looking statements. These forward-looking statements are based on expectations and are subject to certain factors, risks, and uncertainties that may cause actual results, the outcome of events, timing and performance to differ materially from those expressed or implied by such statements. The information contained in this press release is believed to be current as of the date of the original issue. Celularity expressly disclaims any obligation or undertaking to release publicly any updates or revisions to any forward-looking statements contained herein to reflect any change in our expectations with regard thereto or any change in events, conditions or circumstances on which any such statements are based.

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Celularity Expands Strategic Collaboration with United Therapeutics Corporation to COVID-19 Infection and Acute Respiratory Distress Syndrome - Yahoo...

UCSD To Advance Stem Cell Therapies in New Space Station Lab – Technology Networks

A three-year, nearly $5 million award from NASA will allow researchers at the Sanford Stem Cell Clinical Center at UC San Diego Health, Sanford Consortium for Regenerative Medicine and their partners at Space Tango to develop a new integrated space stem cell orbital research laboratory within the International Space Station (ISS) and launch three collaborative research projects within it.Stem cells self-renew, generating more stem cells, and specialize into tissue-specific cells, such as blood, brain and liver cells, making them ideal for biological studies far from Earths resources. The goal of the new effort is to leverage microgravity and these unique properties of stem cells to better understand how space flight affects the human body. The studies will also inform how aging, degenerative diseases, cancers and other conditions develop in a setting with increased exposure to ionizing radiation and pro-inflammatory factors. The findings from these studies may speed the development of new therapeutics for a broad array of degenerative diseases on Earth.

We envision that the next thriving ecosystem of commercial stem cell companies, the next nexus for biotechnology, could be created 250 miles overhead by the establishment of these capabilities on the ISS, said Catriona Jamieson, MD, PhD, co-principal investigator of the award and Koman Family Presidential Endowed Chair in Cancer Research, deputy director of Moores Cancer Center, director of the Sanford Stem Cell Clinical Center and director of the CIRM Alpha Stem Cell Clinic at UC San Diego Health.

The projects first flight to the ISS is planned for mid-2021. The ISS stem cell lab is expected to be fully operational and self-sustaining by 2025.

With hardware designed by Space Tango, a developer of fully automated, remote-controlled systems for research and manufacturing on orbit, initial projects in the new lab will include investigations of:Blood cancers and immune reactivation syndromes, led by Jamieson, who is also a member of the Sanford Consortium for Regenerative Medicine, and Sheldon Morris, MD, MPH, clinical professor of family medicine and public health and infectious diseases at UC San Diego School of Medicine.In whats known as the NASA Twins Study, investigators around the nation assessed identical twin astronauts Scott and Mark Kelly. Scott flew aboard the ISS for 342 days in 2015 and 2016, while his identical twin brother, Mark, remained on Earth. In a paper published in Science in early 2019, researchers, including UC San Diego School of Medicines Brinda Rana, PhD, described the many ways Scotts body differed from Marks due to his time spent in microgravity, including signs of pre-cancer.

In the new ISS lab, Jamieson and Morris will use stem cell-derived blood and immune cells to look for biomarkers tell-tale molecular changes as cancer develops and immune cells malfunction in microgravity. They will also work with experts in the Jacobs School of Engineering at UC San Diego and Space Tango to build special microscopes and bioreactors that fit the ISS lab space and transmit images to Earth in near real-time.

If we can find early predictors of cancer progression on the ISS, we are ideally positioned to rapidly translate them into clinical trials in our Sanford Stem Cell Clinical Center back on Earth, Jamieson said.Brain stem cell regeneration and repair, led by Alysson R. Muotri, PhD, professor of pediatrics and cellular and molecular medicine and director of the Stem Cell Program at UC San Diego School of Medicine and a member of the Sanford Consortium for Regenerative Medicine, and Erik Viirre, MD, PhD, professor of neurosciences and director of the Arthur C. Clarke Center for Human Imagination.This project will build on a previous proof-of concept flight that sent a payload of stem cell-derived human brain organoids to the ISS in 2019. Brain organoids also called mini-brains are 3D cellular models that represent aspects of the human brain in the laboratory. Brain organoids help researchers track human development, unravel the molecular events that lead to disease and test new treatments.

Since their last trip to space, the UC San Diego team has significantly advanced the brain organoids levels of neural network activity electrical impulses that can be recorded by multi-electrode arrays.

All the research models we currently use to study aging in a laboratory dish rely on artificial things, such as increasing oxidative stress or manipulating genes associated with aging, said Muotri, who is also co-principal investigator on the award. Here, were taking a different approach to speed up the aging process and study how it plays a role in developmental diseases and neurodegenerative conditions such as Alzheimers.Liver cell injury and repair, led by David A. Brenner, MD, vice chancellor of health sciences at UC San Diego, and Tatiana Kisseleva, MD, PhD, associate professor of surgery at UC San Diego School of Medicine.On Earth, Brenner and Kisseleva study ailments of the liver, such as liver fibrosis and steatohepatitis, a type of fatty liver disease. Liver diseases can be caused by alcohol use, obesity, viral infection and a number of other factors. They are interested in determining the impact microgravity may have on liver function, which could provide insights into diseases on Earth, as well as potential effects during space travel. In the future, the team may test therapies for steatohepatitis in the new ISS lab, where microgravity mimics aging and can lead to liver cell injury.

These insights may allow us to develop new ways to stop the progression of liver disease and cirrhosis conditions that affect approximately 4.5 million people in the U.S., Brenner said.

Once the ISS stem cell lab is validated, the team said it will replicate the Earth-based Sanford Consortium for Regenerative Medicine, a collaboratory in La Jolla, Calif. that brings together experts from five research institutions: UC San Diego, Scripps Research, Salk Institute for Biological Studies, Sanford Burnham Prebys Medical Discovery Institute and La Jolla Institute for Immunology.

This article has been republished from the following materials. Note: material may have been edited for length and content. For further information, please contact the cited source.

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UCSD To Advance Stem Cell Therapies in New Space Station Lab - Technology Networks

Convalescent plasma therapy useful in treating COVID-19 – Anadolu Ajans

ANKARA

Apheresis therapy can be widely beneficial in treating patients with the novel coronavirus, the president of the World Apheresis Association said Wednesday.

Speaking on convalescent plasma therapy, Fevzi Altuntas said this therapy is being successfully applied in many scientific areas of therapeutic apheresis in Turkey.

What is apheresis?

Apheresis is a science that deals with the processing of blood outside of the body to cure a disease and obtaining the desired blood component or stem cell or cellular therapy products, Altuntas said.

Apheresis is a treatment method that has been successfully applied in treating a wide range of diseases that concern a lot of disciplines such as blood diseases, nephrology, neurology, intensive care, emergency medicine, microbiology and clinical infection, he said.

Stressing that apheresis therapy is not applied only for plasma production in patients with the coronavirus, he said in the pandemic, apheresis is also applied for removal of the virus, the released cytokines and chemicals, replacing the coagulation proteins consumed and the collection of plasma of people who have recovered from COVID-19 disease for transfer.

Turkey started applying convalescent plasma therapy faster than many developed countries, he said.

"This situation sums up the success that our country has reached in the field of apheresis science."

What is convalescent plasma therapy?

This passive antibody therapy is aimed at transferring antibodies to a person for the purpose of protecting and treating against disease, Altuntas underlined.

The aim of the therapy is to take antibodies from the blood of a person who has recovered from a virus and transfer them to a sick person, he said.

In this way, the virus in the patient is expected to be deactivated.

Process of therapy

Commenting on the process of therapy, Altuntas said all donors must be diagnosed with COVID-19.

Donors should have no complaints and feel good for at least 14 days after recovery, he said, stressing that legally, people between the ages of 18-60 can be donors.

He went on to say that immunized plasmas are collected from individuals who meet these criteria and stored in blood banks.

Product collection in apheresis center

Speaking on how to collect products at an apheresis center, Altuntas said the apheresis process will take an average of 60-80 minutes. Approximately 200-600 cc of plasma will be collected with apheresis devices.

Also, the donor will be kept under surveillance for 15 minutes after the transaction is completed, he said, adding an appointment for a new plasma donation will be made again with the consent of the donor.

What will happen to collected products?

Touching on the process after collecting the products, Altuntas said barcoding will be done by the Turkish Red Crescent, also known as Kizilay, for the collected products.

Barcoded products will be stored at minus 18-25 degrees or below in a separate storage cabinet, he said, adding convalescent plasma will be transplanted to severe and critical COVID-19 patients.

Finally, 200-400 ml of convalescent plasma will be transplanted to selected patients, he said.

"I invite everyone recovering from this disease to become a volunteer plasma donor. This is not only a social responsibility but a national duty.

Our examples of social solidarity such as plasma donation are crucial to overcoming this fight together healthfully," he added.

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Convalescent plasma therapy useful in treating COVID-19 - Anadolu Ajans

Stempeutics partners with Global Consortium of cell therapy companies – BSI bureau

Stempeutics will test its stem cell product Stempeucel for Acute Respiratory Disease Syndrome (ARDS) caused by COVID-19 Pneumonia

Bengaluru based Stempeutics Research, a group company of Manipal Education and Medical Group (MEMG), announced that it has partnered with Global Consortium of cell therapy companies seeking European Commission Funding to Fight Against Corona! (FAC!).

Under this partnership, Stempeutics will export its stem cell product Stempeucel (subject to regulatory approvals) for treating critically ill COVID-19 patients with lung disease. First the product will be clinically tested and upon successful outcomes, it intends to export the product on a regular basis. In this connection it is signing up an alliance with Educell Ltd, Slovenia.

Stempeucel is an allogeneic, off the shelf, pooled mesenchymal stromal cells having antiinflammatory and immune-modulatory properties which prevents the over activation of the immune system. Stempeucel product exhibits a wide range of potent therapeutic properties.

The product exhibits potent immunomodulatory and anti-inflammatory properties which could help in reducing the inflammation caused due to the cytokine storm elicited by the bodys immune cells in response to SARS-CoV-2 (COVID-19) related infection in the lungs. Also, the growth factor, Angiopoietin-1 (Ang-1) is effective in reducing alveolar epithelium permeability in the lung. Hence it is envisaged, Stempeucel will reduce the fatal symptoms of COVID 19 induced pneumonia and its progression to ARDS.

BN Manohar, CEO of Stempeutics said, From the clinical data using Stempeucel in different clinical trialsin other indications it may be postulated that Stempeucel has the potential capability for treating COVID 19 infection. Together with the safety profile observed from DCGI approved clinical trials involving more than 350 patients injected with Stempeucel by different routes of injection, this therapy may help in mitigating the lung tissue damaging effects of COVID 19 infection.

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Stempeutics partners with Global Consortium of cell therapy companies - BSI bureau

DNA Repair Gene-Related CHIP Is a Marker for Worse Outcomes in Patients With Lymphoma – Cancer Therapy Advisor

In contrast to findings from previously conducted retrospective single-centerstudies, results of a study of a large population-based cohort of patients withlymphoma undergoing autologous hematopoietic stem cell (HSC) harvesting showedno independent association between the general presence of clonal hematopoiesisof indeterminate origin (CHIP) and overall survival. These findings werepublished in Leukemia.1

In normal hematopoiesis, a single type of HSC accounts for only a verylow percentage of the overall HSCs present. However, in the case of CHIP, asingle HSC clone can expand to comprise 10% or more of the overall HSCpopulation.2 Specifically, CHIP has often been defined as thepresence of somatic mutations in HSCs at a variant gene frequency of 2% orhigher.3

Although CHIP can occur in individuals without a known hematologicmalignancy, previous retrospective studies of patients with cancer conducted atsingle centers with varying amounts of follow-up have shown worse clinicaloutcomes in those with CHIP compared with patients without this condition.

This large population-based study included data for 565 adult patientsfrom 5 independent national stem cell harvest registries from Denmark whounderwent autologous HSC harvesting between January 1, 2000, and July 1, 2012,followed by high-throughput DNA sequencing of HSC specimens.

Although this was a retrospective analysis, specimen collection andclinical follow-up were performed prospectively. The main aims of this studywas to evaluate the impact of CHIP on survival, as well as the tolerability ofautologous-HSC transplantation (ASCT).

Immediate HSCT was planned for 440 ofthese patients, and only this subgroup was included in the survival analysis. Thepercentages of lymphoma subtypes represented in this subgroup were as follows:diffuse large B-cell lymphoma (DLBCL; 37%), follicular lymphoma (8%), Hodgkinlymphoma (15%), mantle cell lymphoma (19%), peripheral T-cell lymphoma (PTCL;17%) and other lymphoma subtypes (4%).

In the patient subgroup for which immediateHSCT was planned, at least 1 CHIP mutation of any type or DNA repair pathway-relatedCHIP mutation was present in 112 (26%) and 40 patients (9.1%), respectively. Specifically,of the 143 total CHIP mutations identified, 48 (34%) encoded for a regulator ofDNA repair (ie, PPM1D, TP53, RAD21,BRCC3). Other types of CHIP mutations were mostcommonly identified in DNMT3Aand TET2.

At a median follow-up of 9.1 years, the overall group had a 15-yearoverall survival of 40.2%. Although OS was worse in the subgroup with CHIP,these patients were significantly older than thosewithout this condition (P <.0001).No significant difference in OS was found following multivariate analysesadjusting for age and aggressiveness of lymphoma subtype.

Incontrast, median OS was 2.2 years and 9.0 years in inthe subgroup of patients with CHIP mutations in DNA pathway-associated genescompared with those without these CHIP mutations. Multivariateanalyses showed significantly worse late but not early OS for those with these typesof CHIP mutations versus not (P =.00067). However, OS was not significantly different for thosewith common CHIP mutation in nonDNA repair-associated genes compared withthose without CHIP mutations.

Anotherinteresting finding of this study was that patients with CHIP mutations in DNArepair genes had a significantly higher risk of being admitted to an intensivecare unit compared with those without these mutations (P =.035 on multivariate analysis). Furthermore, this finding wasnot observed when the overall subgroups of those with and without any CHIPmutations were compared.

In their concluding remarks, the study authors commented that this information could aid [in] the identification of patients with lymphoma who are susceptible to adverse outcomes after ASCT.

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DNA Repair Gene-Related CHIP Is a Marker for Worse Outcomes in Patients With Lymphoma - Cancer Therapy Advisor

Canadian Company STEMCELL Technologies Is an Essential Industry Partner for COVID-19 Research and Vaccine Development – Financial Post

VANCOUVER, British Columbia Products made by Vancouvers STEMCELL Technologies are now being used in over 30 COVID-19 studies worldwide. These studies are focusing on areas ranging from diagnostics and treatments to vaccine development and future prevention. STEMCELL is playing a crucial role in COVID-19 research by providing cutting-edge laboratory tools and reagents as well as through close collaborations with scientists. This will ultimately accelerate the pace of discovery and hopefully lead to a rapid resolution to the global pandemic.

At STEMCELL, we have a team of world-class scientists who have dedicated their careers to developing superior cell culture and cell isolation systems required to study devastating diseases, said Dr. Allen Eaves, STEMCELLs Founder, President, and CEO. It is always incredibly rewarding to see their hard work and expertise put to use. Every day were learning about new ways our customers are using our products to research solutions for the COVID-19 pandemic, and were actively working to support these researchers in any way we can.

STEMCELL is the global industry expert in developing systems for culturing human organoids, which are three-dimensional clusters of cells that closely resemble the biology of human organs. STEMCELL has partnered with an international team including Dr. Josef Penninger at the University of British Columbia, along with Nuria Montserrat in Spain, Drs. Haibo Zhang and Art Slutsky from Toronto, and Ali Mirazimis infectious biology team in Sweden. The group used STEMCELLs organoid systems in a study that examined how SARS-CoV-2 infects patients. Their findings, recently published in the top scientific journal Cell, provide insight into a potential treatment capable of stopping early infection of the novel coronavirus.

Human organoids enable us to better understand the pathology of this disease and to rapidly reach a therapeutic breakthrough. This work stems from an amazing collaboration among academic researchers and companies, including Dr. Ryan Conders gastrointestinal group at STEMCELL Technologies, who have all been working tirelessly day and night for weeks, said Dr. Penninger.

Life science researchers and clinical labs also depend on STEMCELLs specialized cell isolation tools and instruments to extract the white blood cells responsible for immune responses from blood samples. Dr. James Crowe at the Vanderbilt Vaccine Center in Nashville, Tennessee is using a custom version of STEMCELLs EasySep system to isolate specific immune cells from the blood of COVID-19 survivors. Their goal is to rapidly develop antibody treatments and vaccines. This research group has used the same system to identify potential treatments for other viruses, including Ebola, chikungunya, HIV, dengue, norovirus, and respiratory syncytial virus.

STEMCELL listened to us when we came to them asking for custom tools to isolate the specific immune cells were working with from COVID-19 patients, said Dr. Crowe. We were able to integrate the new products and protocols into our research. In turn, we hand information about these products back to STEMCELL so that they can make it available to other labs. Its been a productive collaboration.

STEMCELL recently reported that researchers at Chinas Centre for Disease Control (CDC) successfully used STEMCELLs lung cell culture product, PneumaCultTM, to grow human lung airway cells and quickly obtain the viruss gene sequence, drastically shortening the path to vaccine development. Additionally, an international team including long-time STEMCELL collaborator Dr. Franois Jean at the University of British Columbia, an expert in antiviral drug discovery and emerging human viruses, is using STEMCELLs lung tissue culture system in a recently-funded study to develop and evaluate candidate therapeutics for COVID-19.

Solving medical challenges requires experts in science and medicine to work together with efficiency and accuracy, says Dr. Eaves. STEMCELL is proud to be a crucial component of this network by providing innovative tools, services, and expertise needed by our colleagues in research labs and clinical settings globally.

In addition to supporting rapid and groundbreaking developments for COVID-19 research, STEMCELLs products have been used successfully to study many other devastating viruses. This includes the use of PneumaCult to study respiratory viruses such as various coronaviruses, parvovirus, rhinovirus, respiratory syncytial virus, and influenza. Scientists have also successfully modeled microcephaly caused by Zika virus and cytomegalovirus using STEMCELLs BrainPhys and other products for neuroscience research. Similarly, STEMCELLs IntestiCult was used to study viruses targeting the intestinal system, including enteric coronavirus and norovirus. Finally, STEMCELLs EasySep reagents and RoboSep instrument have been central to studies of the immune response to viruses including HIV, Ebola, and dengue viruses.

About STEMCELL Technologies

STEMCELL Technologies is Canadas largest biotechnology company, with over 1,500 employees and year-on-year growth of approximately 20% for the last 26 years. Based in Vancouver, STEMCELL supports life sciences research around the world with more than 2,500 specialized reagents, tools, and services. STEMCELL offers high-quality cell culture media, cell separation technologies, instruments, accessory products, and educational resources that are used by scientists advancing the stem cell, immunology, cancer, regenerative medicine, microbiology, and cellular therapy fields. Find more information at http://www.stemcell.com.

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Contacts

Nicole Quinn, PhD Associate Director, Scientific Communications public.relations@stemcell.com

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Canadian Company STEMCELL Technologies Is an Essential Industry Partner for COVID-19 Research and Vaccine Development - Financial Post

SNUH team finds causal gene of inherited retinal disorder – Korea Biomedical Review

A group of Korean researchers said they have confirmed a gene responsible for inherited retinal disorders (IRD) among Koreans.

IRD is a combination of several rare diseases that usually develops at a young age and progresses slowly over the lifetime. The patients gradually lose their sight, and most of them eventually lose their vision entirely due to continuous retinal cell degeneration.

The Seoul National University Bundang Hospital (SNUBH) Department of Ophthalmology and Seoul National University Hospital (SNUH) Department of Laboratory Medicine jointly conducted the study.

Currently, antioxidant therapy, artificial retinal transplantation, and stem cell therapy are being used to treat the disorder regardless of mutations, but the only viable treatment is gene therapy. Even when gene therapy is possible, only less than 1 percent of all IRD patients can be treated with it.

In the West, genetic abnormalities of these retinal diseases have been studied and known well. However, researches on Korean cases are still lacking, and the joint research team tackled the subject to find the causative gene for IRDs with 86 domestic patients, the team said in a news release on Wednesday.

The team studied and identified the gene responsible for the disorders by using the latest technique of gene analysis with the most number of patients who have been reported so far.

The study revealed that only 44 percent of the patients, 38 out of 86, possessed the causal gene for IRDs. Even among the patients with retinitis pigmentosa, the most common disorder among the IRDs, only 41 percent had the causative gene.

The causative genes could be quite diverse even in the same disorder. The patients can find a responsible gene only when they receive genetic counseling very actively and can receive gene counseling, too, the research team explained.

Differences were found in the type and frequency of causal gene mutations between Korean and Western cases. However, there were similarities between those of Korean and other Asian nations, including Japan.

The research and diagnosis environment for IRDs has been very poor until now, and our study has significance as a basic data for diagnosis and treatment for Korean patients with IRDs, SNUH Department of Ophthalmology Professor Woo Se-joon said.

Patients need to receive causal gene tests actively to provide the domestic medical communities with sufficient data, and a list of patients who can be treated. By doing so, clinical trials and new drug development in gene therapy will progress smoothly, he added.

Previously, only a few hospitals could diagnose the causative gene for IRDs and afford to test and treat IRD patients due to the high cost of genetic testing. Recently, however, the chance of diagnosis has increased as more hospitals are conducting genetic tests amid the lowered cost thanks to insurance benefits.

Also, the therapeutic opportunity for IRD patients is likely to get broadened, as the retinal pigment epithelium 65 gene (RPE65) therapy won approval from the U.S. Food and Drug Administration for the first time in the world.

Although we do not have a clear way to prevent IRDs at the moment, the prediction of risk and their early detection are developing through the discovery of family history and causative genes, Professor Woo said. Early diagnosis can prevent impaired vision by gene therapy and vision correction, and the patients will be able to choose appropriate jobs with social activities.

Also taking part in the research team were Professors Joo Kwang-sic and Park Kyu-hyung of SNUBH and Professors Seong Moon-woo and Park Sung-sup of SNUH.

The results of this study were published in the Journal of Korean Medical Science.

shim531@docdocdoc.co.kr

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SNUH team finds causal gene of inherited retinal disorder - Korea Biomedical Review

FDA Accepts IND for NK Cell Therapy CYNK-001 to Treat Patients with COVID-19 – Cancer Network

The FDA cleared the investigational new drug (IND) application for the use of CYNK-001 in adults with coronavirus disease 2019 (COVID-19), according to Celularity, the agents manufacturer.1

The company also announced that it will immediately begin a phase I/II clinical study of CYNK-001 in collaboration with Sorrento Therapeutics, which will include up to 86 patients with COVID-19.

We are confident that our strategic relationship with Sorrento will help assure our ability to meet the scale requirements for our efforts in COVID-19, Robert Hariri, MD, PhD, CEO for Celularity, said in a press release.

Individuals who are enrolled in the trial will receive infusions of natural killer (NK) cells, which the company believes could kill cells infected with the virus and address the resulting inflammation caused by the immune system.

Infectious Disease Research Institute (IDRI), a nonprofit based in Seattle, says it is coordinating the trial, which will take place at medical centers in the US.2

To date, efforts to treat COVID-19 cases have been primarily focused on antiviral medications, Corey Casper, MD, MPH, clinical professor of global health and medicine at the University of Washington and interim president and CEO at IDRI, said in a press release. While these are important, patients with serious disease may not respond completely to antiviral medications because they are experiencing damage already inflicted on the bodys vital organs.

CYNK-001 is the only cryopreserved allogeneic, off-the-shelf NK cell therapy being developed from placental hematopoietic stem cells. The company suggests that using such cells eliminates the risk of an immune system reaction that other kinds of donor cells can cause.

The therapy is already being tested in patients with acute myeloid leukemia and multiple myeloma in early-stage studies, and as a potential treatment option for various solid tumors.

In January, the FDA cleared Celularitys investigational new drug (IND) application for CYNK-001 in patients with glioblastoma multiforme (GBM).3The clinical trial is anticipated to be the first clinical trial in the US to investigate intratumoral administration of an allogeneic NK cell therapy.

The FDA clearance of our IND validates the versatility of our allogeneic, off-the-shelf, placental-derived NK cell therapy platform to generate novel clinical candidates against a broad range of devastating cancers, Hariri said in a press release. This IND represents a significant step toward a potential immunotherapy option that is more accessible and tolerable to patients with glioblastoma multiforme.

According to the company, they expect to initiate first-in-human clinical testing of CYNK-001 administered either intravenously or intratumorally. The study is anticipated to evaluate the safety, feasibility, and tolerability of multiple doses of CYNK-001 in patients with relapsed GBM.

Nonclinical safety and efficacy data were presented at the 2019 Society for Neuro-Oncology (SNO) Annual meeting, demonstrating that a single administration of CYNK-001 was well-tolerated and showed enhancedin vivoanti-tumor activity against GBM.

References:

1. Sorrento to Provide Manufacturing Support to Celularity as CYNK-001 NK Cell Trial for COVID-19 Begins Enrolling Patients [news release]. San Diego, CA. Published April 2, 2020. globenewswire.com/news-release/2020/04/02/2010998/0/en/SORRENTO-TO-PROVIDE-MANUFACTURING-SUPPORT-TO-CELULARITY-AS-CYNK-001-NK-CELL-TRIAL-FOR-COVID-19-BEGINS-ENROLLING-PATIENTS.html. Accessed April 2, 2020.

2. Xconomy National. Celularity to Test Natural Killer Cell Therapy for Cancer Against COVID. Xconomy National website. Published April 2, 2020. xconomy.com/national/2020/04/02/celularity-to-test-natural-killer-cell-therapy-for-cancer-against-covid/. Accessed April 2, 2020.

3. Celularity Announces FDA Clearance of Landmark IND for CYNK-001, an Allogeneic, Off-the-Shelf Cyropreserved NK Cell Therapy [news release]. Warren, NJ. Published January 22, 2020. businesswire.com/news/home/20200122005061/en/Celularity-Announces-FDA-Clearance-Landmark-IND-CYNK-001. Accessed April 2, 2020.

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FDA Accepts IND for NK Cell Therapy CYNK-001 to Treat Patients with COVID-19 - Cancer Network

Fate Therapeutics Strikes Multi-Billion Dollar Cell Therapy Deal with Janssen – BioSpace

Shares of Fate Therapeutics were up more than 21% in premarket trading after the company announced a multi-billion dollar deal with Janssen Biotech to develop cell therapies for the treatment of cancer.

The partnership will leverage San Diego-based Fate Therapeutics induced pluripotent stem cell (iPSC) product platform and Janssens proprietary tumor-targeting antigen binders to create novel CAR NK and CAR T-Cell product candidates that will be developed against up to four tumor-associated antigens for hematologic malignancies and solid tumors. Fate will advance the different candidates through preclinical studies to the point of the filing of an Investigational New Drug Application with the U.S. Food and Drug Administration. When that time comes, Janssen will have the right to exercise its option for an exclusive license for the development and commercialization of collaboration candidates targeting the tumor-associated antigens.

Fates iPSC platform enables mass production of off-the-shelf, engineered, homogeneous cell products that can be administered with multiple doses, according to the company. The companys approach involves engineering human iPSCs in a one-time genetic modification event and selecting a single engineered iPSC for maintenance as a clonal master iPSC line. Analogous to master cell lines used to manufacture biopharmaceutical drug products such as monoclonal antibodies, clonal master iPSC lines are a renewable source for manufacturing cell therapy products which are well-defined and uniform in composition, can be mass-produced at significant scale in a cost-effective manner, and can be delivered off-the-shelf for patient treatment, the company said.

Under terms of the agreement, Fate will receive $50 million in upfront cash, as well as a $50 million equity investment by Janssen. Janssen will also cover the funding costs of the R&D of the collaboration candidates. Once Janssen takes over the program, Fate will then be eligible to receive payments of up to $1.8 billion upon the achievement of development and regulatory milestones and up to $1.2 billion upon the achievement of commercial milestones. Fate will also be eligible to receive double-digit royalties on worldwide commercial sales of products targeting the antigens. Additionally, Fate has the right to co-commercialize the candidates should they be approved and share equally in profits and losses, the company said in its announcement.

Scott Wolchko, president and chief executive officer of Fate Therapeutics, touted the partnership with Janssen. He said the collaboration combines Janssens deep domain expertise in oncology, along with their proprietary technologies for targeting and binding certain tumors with Fates iPSC product platform to develop novel off-the-shelf CAR NK and T-cell cancer immunotherapies.

The collaboration strengthens our financial and operating position through a focused effort of developing cell-based cancer immunotherapies utilizing Janssens proprietary antigen-binding domains while enabling us to continue to exploit our deep pipeline of wholly-owned product candidates and further develop our off-the-shelf, iPSC-derived cell-based immunotherapies, Wolchko said in a statement.

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Fate Therapeutics Strikes Multi-Billion Dollar Cell Therapy Deal with Janssen - BioSpace