On the safety side of things, the car came standard with Bosch ABS and traction control, central carbon fiber
safety cell with a steel and carbon fiber roll bar, and front and rear carbon fiber impact absorbers.
Engine choices include the company's 70 HP (52 kW) plant and the 83 HP (62 kW) unit, and some of the features that make this car a «special edition» include the two - tone colour scheme which combines the red painted tridion
safety cell with the rest of the car's exterior which is painted black, plus the 15 - inch alloy wheels also featuring a brilliant black finish.
New edition # 1 package with design features and Lava Orange Tridon
safety cell with white body panels, plus optional Sport and Lighting packages
Not exact matches
To wit: in recent years, Japanese jails have added
safety bars in
cells and begun offering low - sodium meals to accommodate a surge of criminal senior citizens, shoplifting to cope
with hard times.
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).
Announced a clinical trial collaboration
with Pfizer, Inc. (Pfizer) to evaluate the
safety and efficacy of the investigational combination of Yescarta and Pfizer's utomilumab, a fully humanized 4 - 1BB agonist monoclonal antibody, in patients
with refractory large B -
cell lymphoma.
Examples are 9/11 hijackings, The holding back of stem
cell research that could save countless human lives, Aids being spread due to religious opposition to the use of condoms, Christians legally fighting this year to teach over 1 million young girls in America that they must always be obedient to men, the eroding of child protection laws in America by Christians, for so called faith based healing alternatives that place children's health and
safety at risk, burning of witches, the crusades, The Nazi belief that the Aryans were god's chosen to rule the world, etc... But who cares about evidence in the real world when we have our imaginations and delusions about gods
with no evidence of them existing.
Duly reverential, the panel satisfied itself
with simply listing all the research possibilities, including the improvement and increased
safety of IVF, the creation of
cell lines that might someday be useful for bone marrow transplantation, repair of spinal cord injuries, skin replacement and, naturally, the hint of a greater understanding of cancer.»
The load
cell type SLCAD - ST offers extra
safety in applications
with heavy rollers and increased temperature compensation.
That's a rarity for WWE in the PG era — Hell in a
Cell is a match concept from a much bloodier era
with less regard for
safety.
Some of their
safety features include Safe
Cell Technology, Integrated Steel Bars and Energy Absorbing Versa - Tether and
with the Marathon G4 Britax USA have also incorporated Side Impact Protection.
There is a deluxe parent tray
with a place to store your
cell phone
with a clip for
safety.
The EverTrue Elite Mattress is made
with open
cell, pressure reduction, viscoelastic memory foam for your baby's comfort and
safety.
It is built
with a Safe
Cell Impact Protection that shields your child
with safety precautions that go outside the limitations set by the
safety standards.
Equipped
with a Safe
Cell Impact Protection, this car seat is built
with a number of
safety features including an impact absorbing base, harness and tether as well as an impact stabilizing frame.
Sleep soundly knowing your littlest one is resting on the EverTrue ™ Elite: a crib mattress made
with open
cell, pressure reduction, viscoelastic memory foam for your baby's comfort and
safety.
The clinical trial is designed to assess
safety and activity of escalating doses of the special
cells (AST - OPC1) for individuals
with a complete cervical spinal cord injury.
«The global stem -
cell and regenerative medicine community will be awaiting the results of this
safety trial
with much anticipation.»
A second randomized trial on the use of the sun -
safety mobile app Solar
Cell showed some improvement and was associated
with greater sun protection, according to an article published online by JAMA Dermatology.
However, in the wake of fatalities from gene therapy and other technologies, as well as the potential for cancers associated
with stem
cell transplants, governments are understandably nervous about
safety issues — not to mention the ethical maze of tinkering
with fledgling life.
The finding, published in Nature
Cell Biology, shows that once disrupted, it takes time for the inflammatory loop to reestablish, providing proof - of - principal that intermittent dosing could provide a way to reap the benefits of rapamycin, an FDA - approved drug that extends lifespan and healthspan in mice, while lessening
safety issues associated
with its use.
Along
with improved potency and
safety, the system saves time by providing easy, ready - touse RNA reagents that also reduce
cell toxicity by avoiding activation of cellular innate immune responses.
A clinical trial in the Republic of Korea for patients
with degenerative eye diseases is the first to test the
safety of an embryonic stem
cell therapy for people of Asian descent.
But the summit's organizers concluded that actually trying to produce a human pregnancy from such modified germ
cells or embryos, either through in vitro fertilization (IVF)
with the sperm or eggs or the implantation of an embryo, is currently «irresponsible» because of ongoing
safety concerns and a lack of societal consensus.
A clinical trial investigating a treatment for blindness is under way this winter to evaluate the
safety and efficacy of replacing diseased eye
cells with stem
cells.
Last week, the U.S. Food and Drug Administration gave Geron permission to conduct a
safety test of embryonic stem
cells in a handful of patients
with a recent spinal cord injury.
The Food and Drug Administration approved the trial in January 2009 but put it on hold last September because of
safety concerns after lab animals injected
with stem
cells developed small cysts at the injury site.
As an additional
safety feature, the researchers introduced two mutations that weakened the virus's ability to combat the
cell's defenses against infection, reasoning that the mutated virus still would be able to grow in tumor
cells — which have a poor antiviral defense system — but would be eliminated quickly in healthy
cells with a robust antiviral response.
Unlike for ccr5, there are no known humans
with loss of function cxcr4 mutations that would provide insight into the
safety and viability of cxcr4 disruption in mature CD4 + T
cells.
In contrast, the
safety record of hematopoietic stem
cell gene therapy is less clear,
with a significant frequency of gene - therapy induced oncogenesis or clonal outgrowth reported in several hematopoietic stem
cell trials [56], [57].
The study, conducted in Arizona, was designed to evaluate the
safety of injecting muscle - derived stem
cells directly into the hearts of patients
with congestive heart failure, using a 3 - dimensional guided catheter system.
Several concerns need to be addressed before its use, such as effective delivery and the
safety of tinkering
with DNA in brain
cells.
Under his direction, from 2003 to 2007, the agency brought a new level of commitment to public health,
with special emphasis on emerging issues such as bioterrorism and emergency preparedness, as well as health disparities, patient
safety and creation of the Illinois Regenerative Medicine Institute to support stem
cell research.
An innovative experimental treatment for boosting the effectiveness of stem -
cell transplants
with umbilical cord blood has a favorable
safety profile in long - term animal studies, report scientists from Dana - Farber Cancer Institute, Beth Israel Deaconess Medical Center (BIDMC), and Children's Hospital Boston (CHB).
The Phase I
safety trial, funded
with a pilot grant from The National Institutes of Health and support from the Notsew Orm Sands Foundation, will enroll nine more patients who have suffered a stroke and can be treated
with the stem
cell procedure within 24 to 72 hours of initial symptoms.
Our science and technologies have demonstrated the possibility of highly potent antibody and T
cell responses while maintaining
safety, even
with repeated administrations.
The company had initially submitted its request to begin human trials
with its RPE
cells in November 2009, but has spent the past year addressing the FDA's concerns about the
safety of the embryonic stem from which the RPE
cells are made.
One of the major parameters was the
safety of these agents in the respiratory airways and lung parenchyma, since several of these agents are known to cause adverse effects.23 The main adverse effects observed were cough, transient fever and transient decrease in the respiratory functions after the aerosol administration.8, 19, 20 Moreover; it has been observed that excessive deposition of these agents in one site of the respiratory system can induce non-specific side effects in the form of pulmonary edema as observed
with many other drugs.16 These side effects were milder when a premedication
with bronchodilators and inhaled corticosteroids were administered.8, 19, 20 Until now no long term trial (> 9 months) has been performed since all patients included in previous studies had stage IV non-small
cell lung cancer (NSCLC).
The full paper that this statement is in response to can be found at: Niederberger et al. 2018
Safety and efficacy of immunotherapy
with the recombinant B -
cell epitope — based grass pollen vaccine BM32.
Many of the concerns relate to
safety, in part because the impact of tinkering
with cells at that level may not be completely evident for years or even generations, said Debra Mathews, assistant director for science programs at the Berman Institute of Bioethics at Johns Hopkins University.
Two major
safety concerns of working
with viruses are the potential for generation of replication competent virus, and the potential for oncogenesis (in a host
cell) via insertional mutagenesis.
Safety and immunological effects of mesenchymal stem
cell transplantation in patients
with multiple sclerosis and amyotrophic lateral sclerosis.
AST - VAC1 (antigen - presenting autologous dendritic
cells) is an autologous cancer immunotherapy
with promising efficacy and
safety data from a Phase 2 study in Acute Myeloid Leukemia (AML).
«Human neurons — derived from reengineered skin
cells — could help assess the efficacy and
safety of these drugs, thereby reducing risks and resources associated
with human trials.»
Since 1995, Dr. Maharaj has been applying his academic experience and performing evidence - based chemotherapy treatment and bone marrow stem
cell transplant procedures on a completely outpatient setting,
with the main purpose of improving patients»
safety by minimizing the risks of mortality associated
with hospital - acquired infections and, ultimately, improving quality of life.
With these technologies, we are creating heart cells from skin samples of patients with many cardiovascular diseases, such as heart failure, to test the safety and efficacy of new or existing drugs that treat or prevent the condit
With these technologies, we are creating heart
cells from skin samples of patients
with many cardiovascular diseases, such as heart failure, to test the safety and efficacy of new or existing drugs that treat or prevent the condit
with many cardiovascular diseases, such as heart failure, to test the
safety and efficacy of new or existing drugs that treat or prevent the condition.
A pilot study assessing the
safety and feasibility of the transplantation of autologous iPSC - derived retinal pigment epithelium (RPE)
cell sheets in patients
with exudative (wet - type) age - related macular degeneration was launched in Japan in August 2013.
The routine use of MSC cellular therapy
with would benefit from a uniform
cell source,
with stable phenotype and function as well as providing a solution to potential
safety issues.
Japan has taken some steps in this direction, both in establishing the first centre dedicated entirely to hiPSC research,
with an emphasis on application, and by publishing a draft of what looks to be the world's first governmental regulations specifically focused on hiPSC - derived
cell safety and quality [15].
An additional goal of the partnership is to use patient - derived
cells in Organ - Chips to make progress
with strategies for personalized drug
safety and allow a new approach to augment the prediction of disease or treatment variation between individuals.