Category Archives: Cell Therapy

Chimeric antigen receptor (CAR) T-cell therapy is a type of immunotherapy that uses a patients own genetically modified T cells to find and kill cancer. UPMC Hillman Cancer Center currently offers two types of FDA-approved CAR T-cell therapy.

UPMC Hillman Cancer Center was one of the first in the United States certified to provide ABECMA (idecabtagene vicleucel) for 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 antidCD38 monoclonal antibody.

Hillman was the first of 10 centers in the United States to offer BREYANZI (lisocabtagene maraleucel), an FDA-approved CAR T-cell therapy for adult patients with relapsed or refractory large B-cell lymphoma after two or more lines of systemic therapy, including:

UPMC Hillman Cancer Center is the first in western Pennsylvania to provide TECARTUSTM (brexucabtagene autoleucel), an FDA-approved CAR T-cell therapy for patients with relapsed or refractory mantle cell lymphoma.

UPMC Hillman Cancer Center is part of the network of certified treatment centers providing KYMRIAHTM(tisagenlecleucel), an FDA-approved CAR T-cell therapy for:

UPMC Hillman Cancer Center is the first center in western Pennsylvania providing YESCARTATM (axicabtagene ciloleucel), the first FDA-approved CAR T-cell therapy for adult patients with certain types of B-cell lymphoma.

The FDA has approved this treatment for patients with the following conditions that have either not responded to or have relapsed following two or more lines of systemic therapy:

Patients will undergo an extensive evaluation to determine their eligibility for this highly specialized treatment. To learn more, please call 1-833-UPMC-CART.

Patients who are approved for CAR T-cell therapy will undergo the following treatment process:

To refer a patient for evaluation for one of these clinical trials, please call 1-833-876-2227 (1-833-UPMC-CART).

If you think you might be a candidate for one of these clinical trials, please call 1-833-876-2227 (1-833-UPMC-CART).

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FDA-approved CAR T-cell Therapies | UPMC Hillman

Duchenne muscular dystrophy (DMD) is the most common and serious form of muscular dystrophy. One out of every 3500 boys is born with the disorder, and it is invariably fatal. Until recently, there was little hope that the widespread muscle degeneration that accompanies this disease could be combated.

However, stem cell therapy now offers that hope. Like other degenerative disorders, DMD is the result of loss of cells that are needed for correct functioning of the body. In the case of DMD, a vital muscle protein is mutated, and its absence leads to progressive degeneration of essentially all the muscles in the body.

To begin to approach a therapy for this condition, we must provide a new supply of stem cells that carry the missing protein that is lacking in DMD. These cells must be delivered to the body in such a way that they will engraft in the muscles and produce new, healthy muscle tissue on an ongoing basis.

We now possess methods whereby we can generate stem cells that can become muscle cells out of adult cells from skin or fat by a process known as reprogramming. Reprogramming is the addition of genes to a cell that can dial the cell back to becoming a stem cell. By reprogramming adult cells, together with addition to them of a correct copy of the gene that is missing in DMD, we can potentially create stem cells that have the ability to create new, healthy muscle cells in the body of a DMD patient. This is essentially the strategy that we are developing in this proposal.

We start with mice that have a mutation in the same gene that is affected in DMD, so they have a disease similar to DMD. We reprogram some of their adult cells, add the correct gene, and grow the cells in incubators in a manner that will produce muscle stem cells. The muscle stem cells can be identified and purified by using an instrument that detects characteristic proteins that muscles make.

The corrected muscle stem cells are transplanted into mice with DMD, and the ability of the cells to generate healthy new muscle tissue is evaluated. Using the mouse results as a guide, a similar strategy will then be pursued with human cells, utilizing cells from patients with DMD. The cells will be reprogrammed, the correct gene added, and the cells grown into muscle stem cells. The ability of these cells to make healthy muscle will be tested by injection into mice with DMD that are immune-deficient, so they will accept a graft of human cells.

In order to make this process into something that could be used in the clinic, we will develop standard procedures for making and testing the cells, to ensure that they are effective and safe. In this way, this project could lead to a new stem cell therapy that could improve the clinical condition of DMD patients. If we have success with DMD, similar methods could be used to treat other degenerative disorders, and perhaps even some of the degeneration that occurs during normal aging

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Stem Cell Therapy for Duchenne Muscular Dystrophy ...

DUBLIN, October 05, 2021--(BUSINESS WIRE)--The "Global Gene and Cell Therapy (GCT) Market - Analysis By Vector, Application, By Region, By Country (2021 Edition): Market Insights, Pipeline, Forecast with Impact of COVID-19 (2021-2026)" report has been added to ResearchAndMarkets.com's offering.

The Global Gene and Cell Therapy (GCT) Market is estimated at USD 2504.2 Million in the year 2020.

Growth in the historic period in the cell and gene therapy market resulted from increase in investments in cell and gene therapies, growth in research and development, advances in cancer drug discovery, rise in public-private partnerships, strong economic growth in emerging markets, increased healthcare expenditure, and rising in pharmaceutical R&D expenditure.

Companies in the gene and cell therapy for oncology market are increasing their product innovation through strategic collaborations. To sustain in the increasingly competitive market, organizations are developing innovative products as well as sharing skills and expertise with other such enterprises.

While oncology drug companies have long collaborated with each other as well as with academic and research institutions in this market by way of partnerships, in or out licensing deals, this trend has been increasing over the recent years.

Further, the market was restrained by inadequate reimbursements, challenges due to regulatory changes, low healthcare access, and limited number of treatment centers.

Going forward increasing prevalence of cancer and chronic diseases, rising geriatric population, rising geriatric population, rising focus on cell and gene therapy, and rise in healthcare expenditure will drive the growth in the gene and cell therapy market.

Factors that could hinder the growth of the market in the future include high costs of therapy, stringent regulations, reimbursement challenges, and coronavirus pandemic.

The report tracks competitive developments, strategies, mergers and acquisitions and new product development. The companies analysed in the report include F. Hoffman-La Roche Ltd., Novartis, Sanofi, Alnylam Pharmaceuticals Inc., Pfizer, BlueBird Inc., Sarepta Therapeutics, Voyager Therapeutics, Orchard Therapeutics Plc, AnGes Inc.

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Key Topics Covered:

1. Report Scope and Methodology

1.1 Scope of the Report

1.2 Research Methodology

1.3 Executive Summary

2. Strategic Recommendations

3. Gene and Cell Therapy Market: Product Outlook

4. Global Gene and Cell Therapy Market: Sizing and Forecast

4.1 Global Gene and Cell Therapy Market Size, By Value, Year 2016-2026

5. Global Gene and Cell Therapy Market Segmentation - By Vector, By Application

5.1 Competitive Scenario of Global Gene and Cell Therapy Market: By Vector

5.1.1 Lentivirus - Market Size and Forecast (2016-2026)

5.1.2 AAV - Market Size and Forecast (2016-2026)

5.1.3 Retrovirus & Gammaretrovirus - Market Size and Forecast (2016-2026)

5.1.4 Others - Market Size and Forecast (2016-2026)

5.2 Competitive Scenario of Global Gene and Cell Therapy Market: By Application

5.2.1 Oncology - Market Size and Forecast (2016-2026)

5.2.2 Neurological Disorders - Market Size and Forecast (2016-2026)

5.2.3 Cardiovascular disorders - Market Size and Forecast (2016-2026)

5.2.4 Others - Market Size and Forecast (2016-2026)

6. Global Gene and Cell Therapy Market: Regional Analysis

6.1 Competitive Scenario of Global Gene and Cell Therapy Market: By Region

7. North America Gene and Cell Therapy Market: An Analysis (2016-2026)

7.1 North America Gene and Cell Therapy Market: Size and Forecast (2016-2026), By Value

7.2 North America Gene and Cell Therapy Market - Prominent Companies

7.3 Market Segmentation By Vector (Lentivirus, AAV, Retrovirus & Gammaretrovirus and Others)

7.4 Market Segmentation By Application (Oncology, Neurological Disorders, cardiovascular disorders and Others)

7.5 North America Gene and Cell Therapy Market: Country Analysis

7.6 Market Opportunity Chart of North America Gene and Cell Therapy Market - By Country, By Value, 2026

7.7 Competitive Scenario of North America Gene and Cell Therapy Market: By Country

7.8 United States Gene and Cell Therapy Market: Size and Forecast (2016-2026), By Value

7.9 United States Gene and Cell Therapy Market Segmentation - By Vector, By Application (2016-2026)

7.10 Canada Gene and Cell Therapy Market: Size and Forecast (2016-2026), By Value

7.11 Canada Gene and Cell Therapy Market Segmentation - By Vector, By Application (2016-2026)

8. Europe Gene and Cell Therapy Market: Segmentation: An Analysis (2016-2026)

9. Asia Pacific Gene and Cell Therapy Market:: An Analysis (2016-2026)

10. Global Gene and Cell Therapy Market Dynamics

10.1 Drivers

10.2 Restraints

10.3 Trends

11. Market Attractiveness

11.2 Market Attractiveness Chart of Global Gene and Cell Therapy Market - By Vector, 2026

11.3 Market Attractiveness Chart of Global Gene and Cell Therapy Market - Application, 2026

11.4 Market Attractiveness Chart of Global Gene and Cell Therapy Market - By Region, 2026

12. Competitive Landscape

12.1 Major Technological Innovations, Mergers & Acquisitions and Role of Manufacturers

12.2 Product Pipeline of Leading Gene Therapy Companies

12.3 Market Share Analysis

13. Company Analysis

13.1 F. Hoffman-La Roche Ltd.

13.2 Novartis

13.3 Sanofi

13.4 Alnylam Pharmaceuticals Inc.

13.5 Pfizer

13.6 BlueBird Inc.

13.7 Sarepta Therapeutics

13.8 Voyager Therapeutics

13.9 Orchard Therapeutics Plc

13.10 AnGes Inc.

For more information about this report visit https://www.researchandmarkets.com/r/mw6ql7

View source version on businesswire.com: https://www.businesswire.com/news/home/20211005005880/en/

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Global Gene and Cell Therapy (GCT) Market 2021-2026: Insights, Pipeline, Forecast with Impact of COVID-19 - ResearchAndMarkets.com - Yahoo Finance

The $85 million Iovance Cell Therapy Center (ICTC) has opened its doors at the Philadelphia Navy Yard with capacity to supply thousands of patients per year.

Iovance celebrated the opening of its 136,000 square-foot commercial-scale production facility, commissioned in 2018 at a cost of around $85 million, this week.

Since Iovance was founded, we have been dedicated to advancing novel cell therapies for patients with solid tumor cancers, Iovance CEO Frederick Vogt said.

Image: Stock Photo Secrets

A little over two years after breaking ground, iCTC is now one of the largest cell therapy manufacturing facilities in the world and may ultimately house hundreds of employees.

He added: We now have the capacity to supply broad access to TIL therapies for patients.

Iovance is developing several tumor infiltrating lymphocyte (TIL) cell therapies for various cancers. Lead product lifileucel has US FDA regenerative medicine advanced therapy (RMAT) designation and is in pivotal trials for both melanoma and cervical cancer.

Its program LN-145 is looking at using lifileucel in patients with metastatic non-small cell lung cancer, and the first clinical batch has been successfully manufactured and delivered from the new facility, the firm said.

Moving forward, we are diversifying between internal and external TIL manufacturing for clinical studies, and iCTC remains on track to provide commercial supply upon potential product approval, COO Igor Bilinsky said. Establishing our internal manufacturing capabilities is a top priority at Iovance to ensure broad access to and reduce the costs of Iovance TIL cell therapy.

Iovance has previously inked deals with contract development and manufacturing organizations (CDMOs) for clinical supply of its TILs, specifically WuXI Apptec which produces TILs from its Commerce Center 3 facility within WuXi Advanced Therapies cell and gene therapy site in the Philadelphia Navy Yard.

TILs are based on a 22-day process. This involves the isolation of TIL cells from a patients tumor and then expanding them by stimulating them ex vivo. The cells are fragmented in a minimalized cell culture system for the first 11 days before rapid expansion begins. On day 16 the cells are split into multiple flasks, and day 22 they are harvested.

However, the firm has looked to the opening of the Philadelphia, Pennsylvania plant as an opportunity to improve the process further and reduce costs.

In January 2020, Michelle Simpson-Abelson, then principal scientist at Iovance, said: The thought process of having our own manufacturing facility and being able to tweak the process is to allow it to be as accessible to as many patients as we can.

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Iovance opens cell therapy plant; makes first batch ...

CARLSBAD, Calif., Oct. 5, 2021 /PRNewswire/ -- Thermo Fisher Scientific today announced the launch of Gibco Cell Therapy Systems (CTS) NK-Xpander Medium, a GMP-manufactured cell culture medium that supports large-scale growth and culture of functional natural killer (NK) cells with or without the use of feeder cells. This is the first medium from Thermo Fisher specifically designed to support expansion of NK cells for cell therapy applications and is supported by raw material traceability and regulatory documentation.

"Cell therapy developers are increasingly turning to NK cells because they do not elicit the kinds of active immune responses that trigger conditions such as graft versus host disease," said Mark Powers, vice president, research and development at Thermo Fisher Scientific. "With NK-Xpander Medium, manufacturers can reach the necessary scale they need for NK cell therapies while minimizing regulatory burden and risk."

NK cells grown in NK-Xpander Medium exhibit a greater rate of expansion when compared to NK cells grown in other media and demonstrate cell killing in in vitro and in vivo models. In addition to their low immunogenicity, the ease of availability and sourcing of NK cells, coupled with efficient in vitro expansion, make them ideally suited for the development of allogeneic cell therapies. Unlike autologous therapies, which are produced using a patient's own cells, allogeneic cell therapies are derived from healthy donor tissue, and are more conducive to cost-effective scale-up of cell therapy manufacturing.

"NK cell therapies hold promising applications in treating solid tumors, which haven't been well served by therapies derived from other cell types," said Richard Eckert, professor and chairman at University of Maryland School of Medicine. "To capitalize on the promise of these therapies, our lab used human NK cells grown in Gibco CTS NK-Xpander Medium to study their impact on solid tumor-derived cancer cells. The NK cells cultured in NK-Xpander Medium displayed robust and potent cancer cell killing activity."

NK-Xpander Medium is part of Thermo Fisher's CTS product line, a comprehensive portfolio of GMP-manufactured products backed by regulatory documentation and designed to work synergistically, from cell isolation/activation to gene transfer and cell expansion, to address cell therapy developers' manufacturing workflow needs.

To learn more about Thermo Fisher's cell and gene therapy solutions, please visit http://www.thermofisher.com/CGT. To learn more about Gibco CTS NK-Xpander Medium, please visit http://www.thermofisher.com/nkcelltherapy.

* For Research Use or Manufacturing of Cell, Gene, or Tissue-Based Products. This product is not intended for direct administration into humans or animals.

About Thermo Fisher Scientific Thermo Fisher Scientific Inc. is the world leader in serving science, with annual revenue of approximately $35 billion. Our Mission is to enable our customers to make the world healthier, cleaner and safer. Whether our customers are accelerating life sciences research, solving complex analytical challenges, improving patient diagnostics and therapies or increasing productivity in their laboratories, we are here to support them. Our global team of more than 90,000 colleagues delivers an unrivaled combination of innovative technologies, purchasing convenience and pharmaceutical services through our industry-leading brands, including Thermo Scientific, Applied Biosystems, Invitrogen, Fisher Scientific, Unity Lab Services and Patheon. For more information, please visitwww.thermofisher.com.

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Media Contact Information:

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New Culture Medium Supports Expansion of Natural Killer Cells for Cell and Gene Therapies - PRNewswire

Research and development of stem cell-based therapies, where a patients own cells, or those from a donor, are used to fight injury and disease, is one of the fastest growing areas in the biotech space. Longeveron Inc. (NASDAQ: LGVN), a clinical-stage biotechnology company in the thick of clinical development, continues to advance its investigational therapeutic, Lomecel-B, for chronic, aging-related and life-threatening conditions.

The company recently announced the results of its randomized, blinded and placebo-controlled Phase 2 trial to evaluate the safety and efficacy of its proprietary Lomecel-B infusion in frail, older patients between 70 and 85 years old. The trial, which was partially funded by the National Institute on Aging, evaluated a single intravenous infusion of 4 different doses of Lomecel-B cell therapy compared to placebo on the change in the distance a person could walk in 6 minutes (a test known as the 6-minute walk test). Results showed that a single infusion of Lomecel-B resulted in an increase in walk distance of approximately 50 meters (164 feet) at 6 and 9 months after infusion, while the placebo-treated subjects showed minimal improvement at 6 months and a deterioration by 9 months.

Lomecel-B is a proprietary allogeneic product comprised of medicinal signaling cells (MSCs) from the bone marrow of adult donors, which are culture-expanded in Longeverons current good manufacturing practice cell-processing facility. According to trial results so far, Lomecel-B, and MSCs in general, may be injected or infused into an unrelated recipient without triggering a harmful reaction (rejection) due to the biochemical properties of these specialized cells. This is in part what makes this class of biologic so intriguing for use as a regenerative therapeutic.

A growing global trend is for biotech companies to direct their services to the cell and gene therapy industry and moving to expand into a new branch of the pharmaceutical contract development and manufacturing organization world.

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The U.S. Food and Drug Administration (FDA) has approved a small number of cell and gene therapy drugs. Still, a new product pipeline is fighting for the agencys attention with approximately 1,200 experimental therapies more than half in Phase 2 clinical trials. The annual sales growth estimates for cell therapies are projected to reach 15%.

Longeveron has also initiated a Phase 2 trial evaluating the safety and efficacy of Lomecel-B injection into the heart of children born with hypoplastic left heart syndrome (HLHS), a rare and often fatal congenital heart defect.

Longeveron believes that using the same cells that promote tissue repair, organ maintenance and immune system function can develop safe and effective therapies for some of the most challenging diseases and conditions associated with aging.

We continue to make steady progress advancing our Lomecel-B clinical research programs forward, Longeveron CEO Geoff Green said. We have encouraging top-line results from our Aging Frailty program, and anticipate initiating a Phase 2 trial in Alzheimers disease later this year.

Longeveron shared their review of the Aging Frailty trial data with independent frailty experts, with the objective of planning the next steps for the program. The company presented clinical data at the 2021 International Conference on Frailty & Sarcopenia Research on Sept. 29 during a round-table presentation.

Learn more about Longeveron at http://www.longeveron.com.

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Longeveron Successfully Advancing its Cell-Based Therapy Studies in a Growing Industry Segment - Yahoo Finance

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With a compound annual growth rate (CAGR) of 34.2%, the global CAR-T cell therapy market is projected to hit $15.4 billion by 2028. This hypergrowth is largely driven by the incredible promise of CAR-T cell therapy as an effective, lasting way to fight cancer. Historically, however, that growth has been hindered by obstacles to developing a fast, affordable and low side-effect version of the treatment.

Avalon GloboCare (NASDAQ: AVCO), a clinical-stage biotech company focused on immunotherapy, diagnostics and therapeutics, may have found the breakthrough researchers have been looking for the past decade with its leading drug candidate, AVA-011, an mRNA CAR-T platform that solves the key obstacles blocking the revolutionary cell therapy from becoming more widely available.

Heres why CAR-T therapy has taken the biotech industry by storm, and why Avalon is optimistic that AVA-011 could finally offer a safe, affordable version of the treatment to patients around the world.

What Is CAR-T Cell Therapy?

CAR-T cell therapy is an exciting cancer treatment thats made huge waves in the biotech community over the last 10 years. Using a blood sample from a patient, developers can isolate the patients T cells, reengineer them with chimeric antigen receptors (CAR) and then reintroduce those cells into the patients bloodstream through an infusion.

T cells are the workhorses of our immune system. They systematically destroy foreign substances that could cause harm. The reengineered CAR-T cells offer two benefits on top of what T cells already do. First, the CAR molecule acts as a kind of molecular GPS guiding the T cell to the tumor site. Second, the CAR molecule itself is an added weapon that can bind to the signature tumor it was engineered to target and trigger an immune-driven cancer killing effect.

When the infusion is made it acts as a living drug, multiplying and remaining in the body to suppress any recurrence of the cancer it was engineered to target.

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In human trials of various versions of CAR-T cell therapy, more than 80% of patients saw a complete remission or a partial response for their cancer. While long-term studies are scarce because the treatment is still so new, one 5-year study found that every single patient who showed a full or partial response to the CAR-T cell therapy maintained that response five years later meaning that those with a complete response were still cancer-free and those with a partial response saw no progression of the disease to worse stages.

While the results of CAR-T cell therapy are nothing short of impressive, key challenges have prevented it from becoming more widespread. Above all, theres a high risk of adverse reactions. Cytokine Release Syndrome (CRS) is the most common reaction, causing fever and hypotension in 13% to 49% of patients, depending on which treatment was used.

Moreover, designer CAR-T cells like those used in this powerful new treatment are difficult and expensive to produce. The conventional protocol takes 14 days from vein to vein that is, from the time its extracted from the patient to the time its reengineered and delivered to the patient again via infusion. It also requires a disarmed viral vector to deliver the CAR molecule to the T cell. This adds additional cost and time to the manufacturing of the treatment. On average, a single infusion produced using this conventional protocol costs $500,000 for the patient.

Avalons FLASH-CAR Platform Addresses Key Challenges in CAR-T Cell Therapy

To overcome these obstacles, Avalon developed its proprietary FLASH-CAR platform. Using messenger RNA (mRNA), the platform is able to bypass the need for a viral vector to introduce the CAR molecule to the T cell. That bypassing shortens the vein to vein time to just 1 to 2 days and significantly reduces the cost of manufacturing.

Moreover, the mRNA used is modified to come with a safety switch. If a patient experiences CRS or another adverse reaction, Avalon has developed an FDA-approved antidote that can target those CAR-T cells and deactivate them, stopping the adverse reaction. This built-in safety switch is a game changer that gives patients and their healthcare providers more control over their cancer treatments.

The mRNA also enhances the living drug-effect by signaling a more rapid proliferation of CAR-T cells. This could potentially make the treatment more effective and offer even more long-term protection for patients.

Finally, mRNA contains functional units that allow manufacturers to activate other immune systems cell types as well, including natural killer cells and dendritic cells. This ability to engineer more than just T cells expands the potential of the cell therapy beyond the domain of blood cancers the only kinds of cancers the T cell-based infusions have currently been able to target successfully.

AVA-011 Prepares for First Human Clinical Trials

Avalons leading FLASH-CAR drug candidate is AVA-011, which is indicated to treat B-cell acute lymphoblastic leukemia and non-Hodgkin lymphoma (both blood cancers). With the potential of the FLASH-CAR platform to engineer other immune cell types, Avalon is working to develop other drug candidates that could target solid tumors. The promising new treatment has completed preclinical testing and slated to begin its first human clinical trials in 2022.

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Avalon GloboCare Aims to Revolutionize Cell Therapy Market with a Faster, Safer CAR-T Treatment - Yahoo Finance

Oral presentation to discuss new data updates from the high- and low-dose cohorts from the ongoing Phase 1/2 trial of AXO-AAV-GM1 for the treatment of GM1 gangliosidosis

NEW YORK and DURHAM, N.C., Oct. 04, 2021 (GLOBE NEWSWIRE) -- Sio Gene Therapies Inc. (NASDAQ: SIOX), a clinical-stage company focused on developing gene therapies to radically transform the lives of patients with neurodegenerative diseases, today announced that it will present new clinical and preclinical data in two oral presentations and one poster presentation at the upcoming European Society of Gene & Cell Therapy (ESGCT) Virtual Congress 2021, to be held virtually from October 19-22, 2021.

Oral presentations will include an update on the Phase 1/2 trial of AXO-AAV-GM1, the companys adeno-associated viral vector (AAV)9-based gene therapy for the treatment of Type I (early infantile onset) and Type II (late infantile and juvenile onset) GM1 gangliosidosis. Presentation will include new data from the low- and high-dose cohorts. The Company will also present a poster review of patient-level data up to 24 months from the Phase 1/2 study of AXO-Lenti-PD gene therapy for the treatment of Parkinsons disease.

Oral Presentation Details:

Presentation Title: Phase 1/2 Trial of AXO-AAV-GM1 Gene Therapy for the Treatment of Infantile- and Juvenile-onset GM1 GangliosidosisPresentation Number: OR28Session: Session 4a: CNS & Sensory IIPresenting Author: Erica De Boever, Ph.D., DDS, MPH, Vice President of Clinical Development at Sio Gene TherapiesPresentation Date and Time: Thursday October 21, 2021; 9:00-11:00 AM CEST

Presentation Title: Bicistronic AAV Gene Therapy for Tay-Sachs and Sandhoff Diseases in a Sheep ModelPresentation Number: OR30Session: Session 4a: CNS & Sensory IIPresenting Author: Toloo Taghian, Ph.D., University of MassachusettsPresentation Date and Time: Thursday, October 21, 2021; 9:00-11:00 AM CEST

Poster Presentation Details:

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Presentation Title: Phase 1/2 Open-label Dose Evaluation Study of AXO-Lenti-PD Gene Therapy for Parkinsons Disease: Efficacy, Safety, and Tolerability Data up to 24 MonthsPoster Number: P254Presenting Author: Gavin Corcoran, MD, Chief R&D Officer of Sio Gene Therapies

Copies of the presentation materials will be made available under the Events and Presentations section of Sios website.

About AXO-AAV-GM1AXO-AAV-GM1 delivers a functional copy of the GLB1 gene via an adeno-associated viral (AAV) vector, with the goal of restoring -galactosidase enzyme activity for the treatment of GM1 gangliosidosis. The gene therapy is delivered intravenously, which has the potential to broadly transduce the central nervous system and treat peripheral manifestations of the disease as well. Preclinical studies in murine and a naturally-occurring feline model of GM1 gangliosidosis have supported AXO-AAV-GM1s ability to improve -galactosidase enzyme activity, reduce GM1 ganglioside accumulation, improve neuromuscular function, and extend survival.

AXO-AAV-GM1 has received both Orphan Drug Designation and Rare Pediatric Disease Designation from the Food and Drug Administration and is the only gene therapy in clinical development for all pediatric forms of GM1 gangliosidosis. In 2018, Sio licensed exclusive worldwide rights from the University of Massachusetts Medical School for the development and commercialization of gene therapy programs for GM1 gangliosidosis and GM2 gangliosidosis, including Tay-Sachs and Sandhoff diseases.

About AXO-AAV-GM2AXO-AAV-GM2 is an investigational gene therapy for GM2 gangliosidosis (also known as Tay-Sachs and Sandhoff diseases), a set of rare and fatal pediatric neurodegenerative genetic disorders caused by defects in the HEXA (leading to Tay-Sachs disease) or HEXB (leading to Sandhoff disease) genes that encode the two subunits of the -hexosaminidase A (HexA) enzyme. These genetic defects lead to progressive neurodegeneration and shortened life expectancy. AXO-AAV-GM2 aims to restore HexA function by introducing a functional copy of the HEXA and HEXB genes via delivery of two co-administered AAVrh8 vectors.

About AXO-Lenti-PDAXO-Lenti-PD is an investigational gene therapy for the treatment of Parkinsons disease that is designed to deliver three genes (tyrosine hydroxylase, cyclohydrolase 1, and aromatic L-amino acid decarboxylase) via a single lentiviral vector to encode a set of critical enzymes required for dopamine synthesis, with the goal of reducing variability and restoring steady levels of dopamine in the brain. The investigational gene therapy aims to provide patient benefit for years following a single administration. Axovant expects to dose the first patient in EXPLORE-PD, a randomized, sham controlled study in 2021.

About Sio Gene TherapiesSio Gene Therapies combines cutting-edge science with bold imagination to develop genetic medicines that aim to radically improve the lives of patients. Our current pipeline of clinical-stage candidates includes the first potentially curative AAV-based gene therapies for GM1 gangliosidosis and Tay-Sachs/Sandhoff diseases, which are rare and uniformly fatal pediatric conditions caused by single gene deficiencies. We are also expanding the reach of gene therapy to highly prevalent conditions such as Parkinsons disease, which affects millions of patients globally. Led by an experienced team of gene therapy development experts, and supported by collaborations with premier academic, industry and patient advocacy organizations, Sio is focused on accelerating its candidates through clinical trials to liberate patients with debilitating diseases through the transformational power of gene therapies. For more information, visit http://www.siogtx.com.

Forward-Looking Statements

This press release contains forward-looking statements for the purposes of the safe harbor provisions under The Private Securities Litigation Reform Act of 1995 and other federal securities laws. The use of words such as "expect," "estimate," "may" and other similar expressions are intended to identify forward-looking statements. For example, all statements Sio makes regarding costs associated with its operating activities, funding requirements and/or runway to meet its upcoming clinical milestones, and timing and outcome of its upcoming clinical and manufacturing milestones are forward-looking. All forward-looking statements are based on estimates and assumptions by Sios management that, although Sio believes to be reasonable, are inherently uncertain. All forward-looking statements are subject to risks and uncertainties that may cause actual results to differ materially from those that Sio expected. Such risks and uncertainties include, among others, the impact of the Covid-19 pandemic on our operations; the actual funds and/or runway required for our clinical and product development activities and anticipated upcoming milestones; actual costs related to our clinical and product development activities and our need to access additional capital resources prior to achieving any upcoming milestones; the initiation and conduct of preclinical studies and clinical trials; the availability of data from clinical trials; the development of a suspension-based manufacturing process for AXO-Lenti-PD; the scaling up of manufacturing; the expectations for regulatory submissions and approvals; the continued development of our gene therapy product candidates and platforms; Sios scientific approach and general development progress; and the availability or commercial potential of Sios product candidates. These statements are also subject to a number of material risks and uncertainties that are described in Sios most recent Quarterly Report on Form 10-Q filed with the Securities and Exchange Commission on August 12, 2021, as updated by its subsequent filings with the Securities and Exchange Commission. Any forward-looking statement speaks only as of the date on which it was made. Sio undertakes no obligation to publicly update or revise any forward-looking statement, whether as a result of new information, future events or otherwise, except as required by law.

Contacts:

Media Josephine Belluardo, Ph.D. LifeSci Communications(646) 751-4361jo@lifescicomms.cominfo@siogtx.com

Investors and AnalystsParag V. Meswani, Pharm.D.Sio Gene Therapies Inc.Chief Commercial Officer investors@siogtx.com

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Sio Gene Therapies to Present New Data at the European Society of Gene and Cell Therapy Virtual Congress 2021 - Yahoo Finance

The updated report on the Personalized Cell Therapy market gives a precise analysis of the value chain assessment for the review period of 2021 to 2027. The research includes an exhaustive evaluation of the administration of the key market companies and their revenue-generating business strategies adopted by them to drive sustainable business. The Service industry report further enlists the market shortcomings, stability, growth drivers, restraining factors, opportunities for the projected timeframe.

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The top companies in this report include: Novartis AG, Vericel Corporation, Bellicum Pharmaceuticals, MolMed SpA, Cytori Therapeutics Inc, Gilead Sciences, Inc, Celgene Corporation, Bluebird Bio, Aurora Biopharma Inc, Saneron CCEL TherapeuticsInc, Kuur Therapeutics, MediGene AG, Sangamo Therapeutics.

The Global Personalized Cell Therapy market is expected to register a notable market expansion of XX% during the review period owing to the largest market value in 2019. The market study provides a measure of the effectiveness of the product, real-time Personalized Cell Therapy market scenario, along custom ease. The study further offers market analysis, strategies and planning, R & D landscape, target audience management, market potential, due diligence, and competitive landscape.

Scope of the report:

A thorough analysis of statistics about the current as well as emerging trends offers clarity regarding the Personalized Cell Therapy market dynamics. The report includes Porters Five Forces to analyze the prominence of various features such as the understanding of both the suppliers and customers, risks posed by various agents, the strength of competition, and promising emerging businesspersons to understand a valuable resource. Also, the report spans the Personalized Cell Therapy research data of various companies, benefits, gross margin, strategic decisions of the worldwide market, and more through tables, charts, and infographics.

The Personalized Cell Therapy report highlights an all-inclusive assessment of the revenue generated by the various segments across different regions for the forecast period, 2021 to 2027. To leverage business owners, gain a thorough understanding of the current momentum, the Personalized Cell Therapy research taps hard to find data on aspects including but not limited to demand and supply, distribution channel, and technology upgrades. Principally, the determination of strict government policies and regulations and government initiatives building the growth of the Personalized Cell Therapy market offers knowledge of what is in store for the business owners in the upcoming years.

Global Personalized Cell Therapy Market Segmentation:

Market Segmentation: By Type

Cardiovascular DiseasesNeurological DisordersInflammatory DiseasesDiabetesCancerOthers

Market Segmentation: By Application

Cardiovascular DiseasesNeurological DisordersInflammatory DiseasesDiabetesCancerOthers

Geographic analysis:

The global Personalized Cell Therapy market has been spread across North America, Europe, Asia-Pacific, the Middle East and Africa, and the rest of the world.

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COVID-19 Impact Analysis

The pandemic of COVID-19 has emerged in lockdown across regions, line limitations, and breakdown of transportation organizations. Furthermore, the financial vulnerability Personalized Cell Therapy Market is a lot higher than past flare-ups like the extreme intense respiratory condition (SARS), avian influenza, pig influenza, bird influenza, and Ebola, inferable from the rising number of contaminated individuals and the vulnerability about the finish of the crisis. With the rapid rising cases, the worldwide Personalized Cell Therapy refreshments market is getting influenced from multiple points of view.

The accessibility of the labor force is by all accounts disturbing the inventory network of the worldwide Personalized Cell Therapy market as the lockdown and the spread of the infection are pushing individuals to remain inside. The presentation of the Personalized Cell Therapy makers and the transportation of the products are associated. If the assembling movement is stopped, transportation and, likewise, the store network additionally stops. The stacking and dumping of the items, i.e., crude materials and results (fixings), which require a ton of labor, is likewise vigorously affected because of the pandemic. From the assembling plant entryway to the stockroom or from the distribution center to the end clients, i.e., application ventures, the whole Personalized Cell Therapy inventory network is seriously compromised because of the episode.

The research provides answers to the following key questions:

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Excerpt from:
Increasing Demand of Personalized Cell Therapy Market by 2028 with Top Key Players Novartis AG, Vericel Corporation, Bellicum Pharmaceuticals ...

Oral Presentation of Clinical Data for TIL in Combination with Pembrolizumab in Immune Checkpoint Inhibitor-Nave Patients with Advanced Cancers

Poster for LN-145 Monotherapy in Advanced, Immune Checkpoint Inhibitor-Treated Non-Small Cell Lung Cancer (NSCLC)

Additional Posters Highlight Potential to Expand TIL into New Indications and Further Optimize TIL Manufacturing

SAN CARLOS, Calif., Oct. 01, 2021 (GLOBE NEWSWIRE) -- Iovance Biotherapeutics, Inc. (NASDAQ: IOVA), a late-stage biotechnology company developing novel T cell-based cancer immunotherapies, today announced oral and poster presentations of clinical and non-clinical data for tumor infiltrating lymphocyte (TIL) cell therapies in multiple solid tumors will be presented at the 36th Annual Meeting of the Society for Immunotherapy of Cancer (SITC). The SITC 36th Annual Meeting will be held from November 12-14, 2021 in Washington, D.C. and virtually. Details of the oral presentation and posters are as follows:

Title: Phase 2 efficacy and safety of autologous tumor-infiltrating lymphocyte (TIL) cell therapy in combination with pembrolizumab in immune checkpoint inhibitor-nave patients with advanced cancers

Authors: D OMalley, et al.

Presentation Type: Oral Presentation

Date and Time: Saturday, November 13, 2021

Abstract ID: 492

Title: First phase 2 results of autologous tumor-infiltrating lymphocyte (TIL; LN-145) monotherapy in patients with advanced, immune checkpoint inhibitor-treated, non-small cell lung cancer (NSCLC)

Authors: A Schoenfeld, et al.

Presentation Type: Poster (available beginning on Friday, November 12, 2021 at 7 a.m. ET)

Abstract ID: 458

Title: Successful generation of tumor-infiltrating lymphocyte (TIL) product from renal cell carcinoma (RCC) tumors for adoptive cell therapy

Authors: B Halbert, et al.

Presentation Type: Poster (available beginning on Friday, November 12, 2021 at 7 a.m. ET)

Abstract ID: 176

Title: Expansion of tumor-infiltrating lymphocytes (TIL) using static bag for the clinical manufacturing rapid expansion protocol (REP) process

Authors: K Onimus, et al.

Presentation Type: Poster (available beginning on Friday, November 12, 2021 at 7 a.m. ET)

Abstract ID: 101

About Iovance Biotherapeutics

Story continues

Iovance Biotherapeutics aims to be the global leader in innovating, developing and delivering tumor infiltrating lymphocyte (TIL) cell therapies for patients with cancer. We are pioneering a transformational approach to cure cancer by harnessing the human immune systems ability to recognize and destroy diverse cancer cells in each patient. Our lead late-stage TIL product candidate, lifileucel for metastatic melanoma, has the potential to become the first approved one-time cell therapy for a solid tumor cancer. The Iovance TIL platform has demonstrated promising clinical data across multiple solid tumors. We are committed to continuous innovation in cell therapy, including gene-edited cell therapy, that may extend and improve life for patients with cancer.

Forward-Looking Statements

Certain matters discussed in this press release are forward-looking statements of Iovance Biotherapeutics, Inc. (hereinafter referred to as the Company, we, us, or our) within the meaning of the Private Securities Litigation Reform Act of 1995 (the PSLRA). All such written or oral statements made in this press release, other than statements of historical fact, are forward-looking statements and are intended to be covered by the safe harbor for forward-looking statements provided by the PSLRA. Without limiting the foregoing, we may, in some cases, use terms such as predicts, believes, potential, promising, pioneering, continue, estimates, anticipates, expects, plans, intends, forecast, guidance, outlook, may, could, might, will, should or other words that convey uncertainty of future events or outcomes and are intended to identify forward-looking statements. Forward-looking statements are based on assumptions and assessments made in light of managements experience and perception of historical trends, current conditions, expected future developments and other factors believed to be appropriate. Forward-looking statements in this press release are made as of the date of this press release, and we undertake no duty to update or revise any such statements, whether as a result of new information, future events or otherwise. Forward-looking statements are not guarantees of future performance and are subject to risks, uncertainties and other factors, many of which are outside of our control, that may cause actual results, levels of activity, performance, achievements and developments to be materially different from those expressed in or implied by these forward-looking statements. Important factors that could cause actual results, developments and business decisions to differ materially from forward-looking statements are described in the sections titled "Risk Factors" in our filings with the Securities and Exchange Commission, including our most recent Annual Report on Form 10-K and Quarterly Reports on Form 10-Q, and include, but are not limited to, the following substantial known and unknown risks and uncertainties inherent in our business: the effects of the COVID-19 pandemic; risks related to the timing of and our ability to successfully develop, submit, obtain and maintain U.S. Food and Drug Administration (FDA) or other regulatory authority approval of, or other action with respect to, our product candidates, and our ability to successfully commercialize any product candidates for which we obtain FDA approval; preliminary and interim clinical results, which may include efficacy and safety results, from ongoing clinical trials or cohorts may not be reflected in the final analyses of our ongoing clinical trials or subgroups within these trials or in other prior trials or cohorts; the risk that enrollment may need to be adjusted for our trials and cohorts within those trials based on FDA and other regulatory agency input; the new version of the protocol which further defines the patient population to include more advanced patients in our cervical cancer trial may have an adverse effect on the results reported to date; the risk that we may be required to conduct additional clinical trials or modify ongoing or future clinical trials based on feedback from the FDA or other regulatory authorities; the risk that our interpretation of the results of our clinical trials or communications with the FDA may differ from the interpretation of such results or communications by the FDA; the acceptance by the market of our product candidates and their potential reimbursement by payors, if approved; our ability or inability to manufacture our therapies using third party manufacturers or our own facility may adversely affect our potential commercial launch; the results of clinical trials with collaborators using different manufacturing processes may not be reflected in our sponsored trials; the risk that unanticipated expenses may decrease our estimated cash balances and forecasts and increase our estimated capital requirements; and other factors, including general economic conditions and regulatory developments, not within our control.

CONTACTS

Iovance Biotherapeutics, Inc:Sara Pellegrino, IRCVice President, Investor Relations & Public Relations650-260-7120 ext. 264Sara.Pellegrino@iovance.com

Solebury Trout:Zara Lockshin646.378.2960zlockshin@soleburytrout.com

Excerpt from:
Iovance Biotherapeutics to Present Clinical Data for Tumor Infiltrating Lymphocyte (TIL) Cell Therapies Across Multiple Solid Tumors and Treatment...