Not exact matches
less
than or equal to lamivudine Acquired Immune Deficiency Syndrome Antiretroviral
therapy, usually means 1 - 2 drugs, used in early studies Antiretroviral zidovudine (also known as ZDV) Breastfeeding Baby Friendly Hospital Initiative Breastfeeding and HIV International Transmission Study Combined antiretroviral therapy Centers for Disease Control and Prevention Deoxyribonucleic Acid Exclusive Breastfeeding Enzyme Linked Immunosorbent Assay Food and Agrigulture Organization Fixed dose combination ART, e.g., lamividine, stavudine, and nevirapine Highly Active Antiretroviral Therapy, 3 or more drugs for more effective treatment used in later studies Human Immunodeficiency virus International Atomic Energy Agency Infant feeding Infant and young child feeding Lopinavir cubic millimetre Mother - to - Child Transmission of HIV Non-governmental organization Nevirapine Polymerase Chain Reaction People Living with HIV Prevention of Mother - to - Child Transmission Replacement Feeding Ritonavir Ribonucleic acid, one of the three major macromolecules (along with DNA and proteins) that are essential for all known forms of life single dose NVP United Nations Agencies Joint United Nations Programme on HIV / AIDS United Nations Population Fund United Nations Commissioner for Refugees United Nations Children's Fund U.S. Agency for International Development World Alliance for Breastfeeding Action United Nations World Food Programme World Health Assembly WHO 2010 Guidelines on HIV and infant feeding World Health Organization Zidovudine (same drug
therapy, usually means 1 - 2 drugs, used in early studies Antiretroviral zidovudine (also known as ZDV) Breastfeeding Baby Friendly Hospital Initiative Breastfeeding and HIV International Transmission Study Combined antiretroviral
therapy Centers for Disease Control and Prevention Deoxyribonucleic Acid Exclusive Breastfeeding Enzyme Linked Immunosorbent Assay Food and Agrigulture Organization Fixed dose combination ART, e.g., lamividine, stavudine, and nevirapine Highly Active Antiretroviral Therapy, 3 or more drugs for more effective treatment used in later studies Human Immunodeficiency virus International Atomic Energy Agency Infant feeding Infant and young child feeding Lopinavir cubic millimetre Mother - to - Child Transmission of HIV Non-governmental organization Nevirapine Polymerase Chain Reaction People Living with HIV Prevention of Mother - to - Child Transmission Replacement Feeding Ritonavir Ribonucleic acid, one of the three major macromolecules (along with DNA and proteins) that are essential for all known forms of life single dose NVP United Nations Agencies Joint United Nations Programme on HIV / AIDS United Nations Population Fund United Nations Commissioner for Refugees United Nations Children's Fund U.S. Agency for International Development World Alliance for Breastfeeding Action United Nations World Food Programme World Health Assembly WHO 2010 Guidelines on HIV and infant feeding World Health Organization Zidovudine (same drug
therapy Centers for
Disease Control and Prevention Deoxyribonucleic Acid Exclusive Breastfeeding Enzyme Linked Immunosorbent Assay Food and Agrigulture Organization Fixed dose combination ART, e.g., lamividine, stavudine, and nevirapine Highly Active Antiretroviral
Therapy, 3 or more drugs for more effective treatment used in later studies Human Immunodeficiency virus International Atomic Energy Agency Infant feeding Infant and young child feeding Lopinavir cubic millimetre Mother - to - Child Transmission of HIV Non-governmental organization Nevirapine Polymerase Chain Reaction People Living with HIV Prevention of Mother - to - Child Transmission Replacement Feeding Ritonavir Ribonucleic acid, one of the three major macromolecules (along with DNA and proteins) that are essential for all known forms of life single dose NVP United Nations Agencies Joint United Nations Programme on HIV / AIDS United Nations Population Fund United Nations Commissioner for Refugees United Nations Children's Fund U.S. Agency for International Development World Alliance for Breastfeeding Action United Nations World Food Programme World Health Assembly WHO 2010 Guidelines on HIV and infant feeding World Health Organization Zidovudine (same drug
Therapy, 3 or more drugs for more effective treatment used in later studies Human Immunodeficiency virus International Atomic Energy Agency Infant feeding Infant and young child feeding Lopinavir cubic millimetre Mother - to - Child Transmission of HIV Non-governmental organization Nevirapine Polymerase Chain Reaction People Living with HIV Prevention of Mother - to - Child Transmission Replacement Feeding Ritonavir Ribonucleic acid, one of the three major macromolecules (along with DNA and proteins) that are essential for all known forms of life single dose NVP United Nations Agencies Joint United Nations Programme on HIV / AIDS United Nations Population Fund United Nations Commissioner for Refugees United Nations Children's Fund U.S. Agency for International Development World Alliance for Breastfeeding Action United Nations World Food Programme World Health Assembly WHO 2010 Guidelines on HIV and infant feeding World Health Organization Zidovudine (same drug as AZT)
The biological complexity of cancer and other
diseases demands a more formidable arsenal of
therapies than currently available.
The fact that TAS - 102 temporarily halted the
disease in many of these patients suggests that it operates through a different biochemical pathway
than 5 - FU, and therefore may serve as an alternative to standard
therapy.
Women, on average, experience coronary artery
disease 10 years later
than men and have lower smoking rates
than men, both of which may partially contribute to the sex disparity in statin
therapy.
Patients who got it lived about 4 months longer, nearly 26 months total,
than those who didn't — but that, say company executives, is still more
than any other
therapy has managed for this
disease in a randomized trial.
In the U.S. alone,
therapy for chronic kidney
disease is likely to exceed $ 48 billion per year, and the end - stage kidney
disease program consumes 6.7 percent of the total Medicare budget to care for less
than 1 percent of the covered population.
«With more
than 1.7 million people dying globally from TB each year and the rise of strains that are resistant to drug treatment, we need a better way to prevent this
disease,» said the study's principal investigator Louis Picker, M.D., who is the associate director of the OHSU Vaccine and Gene
Therapy Institute and a professor of pathology, molecular microbiology, and immunology in the OHSU School of Medicine.
Researchers from Massachusetts Eye and Ear / Harvard Medical School have found that patients who were prescribed corticosteroids as part of treatment for Lyme
disease - associated facial paralysis had worse long - term outcomes of regaining facial function
than those who were prescribed antibiotic
therapy alone.
In addition to providing insights regarding selection of treatment, this blood test may also prove helpful in assessing the presence of residual
disease, recurrence, or relapse and detection of
therapy - resistant cancer cells more quickly
than conventional tissue - based methods.
At a meeting of the Society for Neuroscience in Washington DC last week, Victor Henderson and colleagues from the University of Southern California in Los Angeles, presented findings that suggest women on oestrogen
therapy are 40 per cent less likely to develop the
disease than those who are not.
The same process has been studied as a potential genetic
therapy for more
than a decade, because you can target any
disease gene with matching dsRNA.
While the
disease can take many forms, recent advances have better characterized how lymphoma cells proliferate and interact with other cells and tissues, leading to the development of powerful, targeted
therapies with fewer side effects
than traditional approaches.
In Cohort B — those who received pembrolizumab as first - line
therapy — 12 of 52 patients, or 23 percent, saw tumors shrink by more
than 30 percent, while the
disease was stabilized in nine of them, or 17 percent.
One clinician who has not waited for controlled clinical studies is California osteopath David Steenblock, who offers stem cell
therapy for more
than 20
diseases, including Alzheimer's, traumatic brain injury, Parkinson's, arthritis, stroke, and heart
disease.
The drop in hormone use dates back to July 2002, when the Women's Health Initiative, a 15 - year study tracking the health of more
than 160,000 women, abruptly ended its long - term study of estrogen - progestin hormone replacement
therapy because women taking the drugs faced an elevated risk of invasive breast cancer and heart
disease.
Analyzing more
than 120 million patient records and identifying trends of co-occurrence among hundreds of
diseases, they created a unique genetic map that has the potential to guide researchers and clinicians in diagnosing, identifying risk factors for and someday developing
therapies against complex
diseases.
«Understanding how maternal exposures impact obesity - related
disease such as nonalcoholic fatty liver
disease will allow us to develop lower cost preventative
therapies to utilize up front rather
than awaiting complications down the road.»
Regardless of
disease stage, patients who received surgery lived an average of 57 months, compared to less
than 12 months for patients who received only non-surgical treatment (such as chemotherapy or radiation
therapy), and 1.4 months for patients who received no treatment at all.
«The dog has a retina very similar to ours, much more so
than mice, so when you want to bring a visual
therapy to the clinic, you want to first show that it works in a large animal model of the
disease,» said lead researcher Ehud Isacoff, professor of molecular and cell biology at UC Berkeley.
«Despite having good treatments available, current reports suggest that fewer
than half of individuals who need
therapy are actually getting appropriate HIV medicine to control their virus, leading to more transmission of
disease,» says lead study author Maunank Shah, M.D., Ph.D., an assistant professor of medicine at the Johns Hopkins University School of Medicine.
Although there remains no cure for Alzheimer's, researchers hope that testing potential drugs or
therapies prior to mental decline will prove to be more successful
than previous attempts at finding the most effective treatment in the battle against the debilitating
disease.
There are now more
than 100 gene
therapy clinical trials aimed toward cancer, genetic
diseases (such as ADA deficiency, cystic fibrosis and hemophilia A), infectious
diseases (including AIDS) and autoimmune
diseases (such as rheumatoid arthritis).
Creating a federal initiative to support development of new
therapies for ultra-rare
diseases occurring in fewer
than one in 250,000 births annually.
«It affects many more children
than brittle bone
disease, so we're very hopeful that sclerostin antibody
therapy will be a useful treatment for them as well.
«Sex reassignment surgery may be better for transgender women's health
than hormones only: Study investigates metabolic
disease risk after receiving only hormone
therapy compared to surgery.»
Although the study's approach wasn't a sure bet, the researchers hoped to go further
than any other gene
therapy trial yet for this relatively common inherited
disease that fills people's lungs with sticky mucus that promotes deadly infections.
More
than one - third of those patients, for whom new American College of Cardiology / American Heart Association guidelines would recommend statin
therapy, were reclassified as being at very low risk for cardiovascular
disease.
More
than 10 percent of patients treated with aspirin
therapy for primary cardiovascular
disease prevention were likely inappropriately prescribed medication, according to a new study in the Journal of the American College of Cardiology that examined practice variations in aspirin
therapy.
Given the poor prognosis and limited treatment options in pancreatic cancer, new
therapies to combat the
disease are desperately needed: Earlier this year, the American Cancer Society reported that it is estimated that in 2016, nearly 42,000 people will die from the
disease, surpassing the number of deaths from breast cancer by more
than 1,000.
While a new generation of safer, more effective oral medications to treat hepatitis C patients may cost tens of thousands of dollars for a 12 - week regiment, investing in these new
therapies could generate savings estimated at more
than $ 3.2 billion annually in the U.S. and five European countries, according to a new study (abstract 228) released today at Digestive
Disease Week ® (DDW) 2015.
In the era of personalized cancer
therapy, patients with TNBC remain at considerably higher risk of relapse and death
than patients with other breast cancer subtypes, due to the aggressive nature of TNBC and the lack of newer targeted
therapies for the
disease.
This approach for gene
therapy to treat fatty liver
disease, for example, might prove both safer and more effective
than reengineering cells in the liver itself.
YOKOHAMA, JAPAN — For more
than a decade, stem cell
therapies have been touted as offering hope for those suffering from genetic and degenerative
diseases.
Our approach is to study more
than one or two serial recurrences of the
disease, adding information about the response to
therapy and natural progress of ovarian cancer,» adds J. Brian Szender, MD, MS, senior author and a fellow in Gynecologic Oncology at RPCI.
«Vaccination normally generates protective immunity that prevents the
disease for years in a population at a relatively low cost; whereas, antiviral
therapies can only be treating the
diseases at a higher cost rather
than offer long - term protection.»
Inspired by a grandfather who had Alzheimer's
disease, Dr. Mucke founded Gladstone's neurological research program 15 years ago and today leads more
than 100 students, postdocs, research scientists and principal investigators in the search for new understanding of and
therapies for some of the world's most devastating illnesses — including Alzheimer's, Parkinson's, ALS, and multiple sclerosis.
Included among the numerous recipients of Mr. Sanford's gifts, that total more
than one billion dollars, are: the Edith Sanford Foundation for Breast Cancer that was created in 2012 by a gift of $ 100 million in honor of Mr. Sanford's mother who died of breast cancer when he was four years old; the Sioux Valley Hospitals and Health System, which renamed itself Sanford Health in 2007, in recognition of a $ 400 million gift; a $ 125 million gift in 2014 to establish Sanford Imagenetics, a program that will integrate genomic medicine into primary care for adults; the University of California San Diego which received a $ 100 million gift for the creation of the Sanford Stem Cell Clinical Center in 2013 to accelerate the translation of stem cell research discoveries by advancing clinical trials and patient
therapies; the Burnham Institute for Medical Research that received a $ 50 million gift in 2010, and recognized its appreciation for both this and a 2008 gift of $ 20 million to the Sanford Center for Childhood
Disease research at Burnham by then changing its name to Sanford Burnham Medical Research Institute; a $ 70 million gift to establish a particle physics laboratory named the Sanford Underground Research Facility; and the San Diego Consortium for Regenerative Medicine which received a gift of $ 30 million in 2008 and expressed its gratitude by renaming itself the Sanford Consortium for Regenerative Medicine.
AFM supports each year more
than 400 research programs, among them more
than 30 clinical trials in gene
therapy or cellular
therapy concerning for example muscular, eyes, skin or blood
diseases.
A small, phase 1 trial, published early online in the journal Radiology, found that this approach, designed to treat just the
diseased portion of the prostate rather
than removing or irradiating the entire gland, is safe and can be performed without the troubling complications associated with more aggressive
therapies.
Microscopic models — half living, half not — may prove more reliable
than animals in explaining human
disease and testing
therapies.
According to an international clinical trial led by Sylvia Adams, MD, associate professor of medicine, breast tumors shrank by more
than 30 percent in 12 (23 percent) of 52 patients who received pembrolizumab as first - line
therapy, and the
disease stabilized in 9 additional patients (17 percent).
«C - Path's initiative to identify and position Crohn's
disease - specific biomarkers for regulatory endorsement is a pivotal step in getting improved
therapies into the hands of people living with Crohn's
disease more quickly
than currently possible.»
Novel drug
therapies and novel indications of drug
therapy, e.g. tyrosine kinase inhibitors in lung
disease other
than lung cancer, biological treatments for asthma, COPD, cystic fibrosis and interstitial lung
disease.
As part of our mission, MDA funds research to accelerate treatments and cures for DMD and more
than 40 other neuromuscular
diseases, and we're proud to have supported this work that is sure to help shape DMD
therapies under development today and in the future.»
«The strong evidence that abnormal TDP - 43 protein is involved in the development of ALS, coupled with models that may replicate ALS more faithfully
than other tools, may speed development of
therapies for the thousands of individuals diagnosed with this devastating
disease.»
Inclusion Criteria: • The participant may have no more
than 2 prior lines of systemic
therapies (neoadjuvant and adjuvant
therapies will not be considered as a prior line of
therapy) for advanced or metastatic
disease and is suitable to receive gemcitabine and docetaxel
therapy.
This approach may also be applicable to a number of rare genetic
diseases caused by splicing defects, including ataxia telangiectasia, congenital disorder of glycosylation, and Niemann - Pick
disease type C. Although the three DMD studies referenced here represent a great step forward for CRISPR gene
therapy, it's important to realize that DMD is a simpler case
than other genetic
diseases we'd like to treat with CRISPR.
«Much to our surprise, the trial showed that patients receiving standard
therapy compared to those receiving cetuximab with standard
therapy had no difference in outcomes,» said study author Dr. Steven Alberts, a professor of oncology at the Mayo Clinic College of Medicine in Rochester, Minn. «It also indicates that
disease in earlier stages may be different
than diseases in later stages.»
Reviews of clinical trials on hypnosis have concluded that the evidence of its effectiveness for smoking cessation is insufficient, but other research shows promise: The preliminary results from a small 2007 study of smokers hospitalized with cardiopulmonary
diseases showed that the patients who chose to participate in a hypnotherapy session were more likely to be nonsmokers six months later
than patients who chose nicotinereplacement
therapy (NRT) alone.
Since being designed by Dr. Wilder more
than 90 years ago, ketogenic
therapies have been used to successfully treat headaches, sleep disorders, type 2 diabetes, and Alzheimer's
disease.