Embryonic stem (ES) cells are important tools in the study of gene function and may also become important
in cell therapy applications.
Not exact matches
These risks and uncertainties include: Gilead's ability to achieve its anticipated full year 2018 financial results; Gilead's ability to sustain growth
in revenues for its antiviral and other programs; the risk that private and public payers may be reluctant to provide, or continue to provide, coverage or reimbursement for new products, including Vosevi, Yescarta, Epclusa, Harvoni, Genvoya, Odefsey, Descovy, Biktarvy and Vemlidy ®; austerity measures
in European countries that may increase the amount of discount required on Gilead's products; an increase
in discounts, chargebacks and rebates due to ongoing contracts and future negotiations with commercial and government payers; a larger than anticipated shift
in payer mix to more highly discounted payer segments and geographic regions and decreases
in treatment duration; availability of funding for state AIDS Drug Assistance Programs (ADAPs); continued fluctuations
in ADAP purchases driven by federal and state grant cycles which may not mirror patient demand and may cause fluctuations
in Gilead's earnings; market share and price erosion caused by the introduction of generic versions of Viread and Truvada, an uncertain global macroeconomic environment; and potential amendments to the Affordable Care Act or other government action that could have the effect of lowering prices or reducing the number of insured patients; the possibility of unfavorable results from clinical trials involving investigational compounds; Gilead's ability to initiate clinical trials
in its currently anticipated timeframes; the levels of inventory held by wholesalers and retailers which may cause fluctuations
in Gilead's earnings; Kite's ability to develop and commercialize
cell therapies utilizing the zinc finger nuclease technology platform and realize the benefits of the Sangamo partnership; Gilead's ability to submit new drug
applications for new product candidates
in the timelines currently anticipated; Gilead's ability to receive regulatory approvals
in a timely manner or at all, for new and current products, including Biktarvy; Gilead's ability to successfully commercialize its products, including Biktarvy; the risk that physicians and patients may not see advantages of these products over other
therapies and may therefore be reluctant to prescribe the products; Gilead's ability to successfully develop its hematology / oncology and inflammation / respiratory programs; safety and efficacy data from clinical studies may not warrant further development of Gilead's product candidates, including GS - 9620 and Yescarta
in combination with Pfizer's utomilumab; Gilead's ability to pay dividends or complete its share repurchase program due to changes
in its stock price, corporate or other market conditions; fluctuations
in the foreign exchange rate of the U.S. dollar that may cause an unfavorable foreign currency exchange impact on Gilead's future revenues and pre-tax earnings; and other risks identified from time to time
in Gilead's reports filed with the U.S. Securities and Exchange Commission (the SEC).
Cambridge, MA — February 6, 2017 — Aura Biosciences, a biotechnology company developing a new class of
therapies to target and selectively destroy cancer
cells using viral nanoparticle conjugates, announced today that the U.S. Food and Drug Administration (FDA) has cleared the investigational new drug
application (IND) for the company's lead program, light - activated AU - 011
in ocular melanoma (OM).
Even more
applications for
cell therapies beyond cancer could become reality
in the coming years.
Investigations aimed at determining the downstream targets of LIF would help to clarify the functional importance of LIF
in muscle regeneration, and further its potential
application in cell transplantation
therapy.»
The present and potential clinical
applications of mesenchymal stem
cell therapy in cats are explored
in a state - of - the - art review article published this month
in the Journal of Feline Medicine and Surgery.
«For the broad
application of stem
cell - derived pituitary
cells in the future,
cell replacement
therapy may need to be customized to the specific needs of a given patient population,» Zimmer says.
For these
cells to be as useful as embryonic stem
cells, «we have to find a way to avoid retroviruses before
application in cell therapy», Yamanaka says, as they could result
in tumours.
To the Editor:
In their Clinical Review, Dr Burt and colleagues1 assessed clinical
applications of adult stem
cell therapies for nonmalignant diseases.
Furthermore, this study also encourages the
application of iPSC - MSCs as an exciting new therapeutic option for a range of immunological disorders and suggests that further study of the secreted factors may allow the construction of efficient
cell - free
therapies in the near future.
Intellia is developing human gene and
cell therapies for both ex vivo and
in vivo
applications using CRISPR - Cas9 gene editing technology.
In parallel to this
cell therapy application, keratynocytes and melanocytes derived from pluripotent stem
cells will be used for pathological modelling of genodermatoses allowing identification of new disease - specific pharmacological treatments
The symposium brings together leaders
in biology, medicine, and industry to present on the latest advances
in technology development, mechanistic understanding, and therapeutic
application of stem
cells for both drug development and
cell - based
therapy.
San Diego, California, October 29, 2013 — ViaCyte, Inc., a leading regenerative medicine company focused on developing new approaches to treat major diseases through the
application of a stem
cell - derived
cell therapy, announced today that the Company was granted over 20 patents worldwide
in 2013 thus far, three U.S. and twenty foreign.
Zernicka - Goetz's research could also lead to important advancements
in the study of embryonic stem
cell therapy applications.
This spotlight on
cell therapy regulation will aim to provide insight into challenges, trends, developments and debates
in the regulation of
cell therapies aimed at regenerative medicine
applications.
The long - term vision is to apply these technologies to other genetic diseases, such as sickle
cell disease, and to explore
applications in developing effective immune
therapies for cancer.
«I highly respect Novocell technologies and am pleased to collaborate with Novocell and explore the potential of their hES
cell to islet
cell advances
in combination with our iPS
cells as a potential new sources for the generation of cellular models and
therapies for diabetes,» said Dr. Yamanaka, Director of Center for iPS Research and
Application at Kyoto University.
That has been
in part a result of how much response efficacy that has been achieved with some patients
in addition to work with different types of gene
therapy applications and coupling those with
cell therapy advancements.
The Bulte Lab has developed methods to label
cells magnetically using tiny superparamagnetic iron oxide nanoparticles
in order to make them visible by magnetic resonance imaging; this technology has now been introduced
in the clinic for several
cell therapy applications.
«Having a very efficient and practical way of generating patient - specific stem
cells, which unlike human embryonic stem
cells, wouldn't be rejected by the patient's immune system after transplantation brings us a step closer to the clinical
application of stem
cell therapy,» says Belmonte, PhD., a professor
in the Gene Expression Laboratory and director of the Center of Regenerative Medicine
in Barcelona, Spain.
A promising clinical
application for stem and progenitor
cell transplantation is
in rescue
therapy for degenerative diseases.
«Finding this population of stem
cells in a human source represents a major breakthrough for us because it brings us much closer to a clinical
application of this
therapy,» said Dr. Huard, the Henry J. Mankin Professor and vice chair for Research
in the Department of Orthopaedic Surgery at the University of Pittsburgh School of Medicine.
It is conceivable the techniques being developed might have some
application in future stem
cell therapies in humans where a cloning process was used to generate particular tissues for transplantation.
The advent of human induced pluripotent stem
cells has been heralded as a major breakthrough
in the study of pluripotent stem
cells, for these
cells have yielded fundamental insights into the reprogrammability of somatic
cell fates, but also because of their seemingly great promise
in applications, including potential uses
in cell therapy.
Initially founded
in 2011 as a Heart Institute, our treatment protocols were later expanded to include adult stem
cell therapy for patients with severe and chronic medical needs that, per scientific research, clinical trials and
application, can be safely and potentially efficaciously treated with patients» own stem and regenerative
cells.
Given our extensive experiences
in neuronal differentiation of hESCs [6], [7], [8] and the potential
application of hESC - derived neurons
in cell replacement
therapies for neurodegenerative diseases, we designed a set of experiments aimed at developing a hESC - based automated assay for screening small molecules that have differential toxicity to hESC - derived NSCs and their differentiated neural progenies.
Importantly, because it is already approved for clinical use, amiodarone HCL may have clinical
applications in cell replacement
therapies by selectively removing only the unwanted undifferentiated NSCs during the pre-transplant period.
«The proposed experiments, if successful, will address an important unmet need
in bringing stem
cell therapies to clinical use and provide the foundation for a wide range of additional
applications,» Clegg said.
In a review published in the Journal of Feline Medicine and Surgery, Jessica M. Quimby, DVM, Ph.D., DACVIM, Department of Veterinary Clinical Sciences at The Ohio State University, and Dori L. Borjesson, DVM, MPVM, Ph.D., Veterinary Institute for Regenerative Cures at the University of California, Davis, consider both the current and potential clinical applications of mesenchymal stem cell therapy in cat
In a review published
in the Journal of Feline Medicine and Surgery, Jessica M. Quimby, DVM, Ph.D., DACVIM, Department of Veterinary Clinical Sciences at The Ohio State University, and Dori L. Borjesson, DVM, MPVM, Ph.D., Veterinary Institute for Regenerative Cures at the University of California, Davis, consider both the current and potential clinical applications of mesenchymal stem cell therapy in cat
in the Journal of Feline Medicine and Surgery, Jessica M. Quimby, DVM, Ph.D., DACVIM, Department of Veterinary Clinical Sciences at The Ohio State University, and Dori L. Borjesson, DVM, MPVM, Ph.D., Veterinary Institute for Regenerative Cures at the University of California, Davis, consider both the current and potential clinical
applications of mesenchymal stem
cell therapy in cat
in cats.