Not exact matches
On Wednesday, Swiss pharmaceutical giant Novartis made history
as the first company to win Food and
Drug Administration (FDA) approval
for a groundbreaking new type of
cancer treatment known
as CAR - T.
Along with the introduction of other new
drugs such
as psoriasis
treatment Cosentyx, Novartis is hoping that Kymriah will help turn things around after the patent protections expired
for its Gleevec
cancer drug and Gilenya multiple sclerosis
treatment, opening the door to cheaper competitors.
When the results are announced, they indicate that Medico's
drug candidate works better than expected
as a
treatment for skin
cancer.
As an example, consider a hypothetical biotech company, Medico, that has a drug candidate in advanced clinical trials as a treatment for skin cance
As an example, consider a hypothetical biotech company, Medico, that has a
drug candidate in advanced clinical trials
as a treatment for skin cance
as a
treatment for skin
cancer.
Besides, many of the so - called abortion
drugs are used
for cancer and auto - immune disease
treatment, so it is not
as simple
as just not covering a specific
drug.
This was before Mackey had won a single Iditarod, let alone four straight; before he used what he calls his marathon style — catnapping
as his sled moves and covering 100 - mile chunks at a moderate pace without prolonged rest, instead of sprinting from rest stop to rest stop like most other racers — to win an unprecedented double (the Yukon Quest, the world's other 1,000 - mile dogsled race, and just weeks later the Iditarod) not once but twice; before he became so dominant that slower competitors complained they had no chance to finish within five days of him (the requirement
for an official place and a commemorative belt buckle); and before a rival pushed
for drug testing at the 2010 Iditarod, suspecting that Mackey's secret was his prescription
for medical marijuana to alleviate the side effects of
cancer treatment.
«The extensive overlap in risk genes
for autism and
cancer, many of which are chromatin remodeling factors, supports the idea of repurposing epigenetic
drugs used in
cancer treatment as targeted
treatments for autism,» said Yan.
A dozen human studies of MDMA, LSD, a powerful African
drug called ibogaine and psilocybin, from so - called «magic mushrooms,» are now under way, testing the once - stigmatized
drugs as treatments for not only PTSD, but also cluster headaches and addiction,
as well
as anxiety and depression in
cancer patients.
As a result, P - gp causes resistance of the diseased cells to a majority of drugs currently available for the treatment of cancer, as well as drugs used for treatment of infectious diseases like HIV / AID
As a result, P - gp causes resistance of the diseased cells to a majority of
drugs currently available
for the
treatment of
cancer,
as well as drugs used for treatment of infectious diseases like HIV / AID
as well
as drugs used for treatment of infectious diseases like HIV / AID
as drugs used
for treatment of infectious diseases like HIV / AIDS.
With the release and aggressive marketing of the long - acting narcotic OxyContin in 1996, a class of
drugs that had largely been reserved
for cancer patients was becoming a go - to
treatment for conditions such
as lower back pain.
«This research is highly significant
as it implies that a commercially available
drug, amphotericin B, which has never been used before
for patients with gliomas, may be a novel
treatment to consider in future trials of patients with this frequently lethal
cancer,» says Dr. Rutka.
«Our preclinical data suggest that combining low doses of these inhibitors will enhance the clinical effects of both
drugs as a potential
treatment for patients with AML,» says the senior author, Feyruz V. Rassool, PhD, associate professor of radiation oncology at the University of Maryland School of Medicine (UM SOM) and a researcher at the University of Maryland Marlene and Stewart Greenebaum Comprehensive
Cancer Center (UMGCCC).
These include the ability to bring new, innovative products to the market; progress in oncology, such
as the approval of Genentech's
drug Avastin
for breast
cancer and advances in the use of gene therapy, despite some setbacks; continuing progress in research on stem cells; the emergence of
treatments for previously untreated diseases; and solutions
for food and fuel shortages, such
as biocrops and biofuels.
«These findings are important
for cancer treatments,
as currently there are no
drug therapies
for enchondromas and there are no universally effective chemotherapies
for chondrosarcomas,» said senior author Benjamin Alman, M.D., chair of the Orthopaedic Surgery Department at Duke University Medical Center.
In preliminary
drug - mutation matching studies, they found that JAK1 - mutated SS cells were sensitive to JAK inhibitors,
drugs that are currently approved
for treatment of other hematologic
cancers such
as polycythemia vera and myelofibrosis.
Often such trials include genetic markers
for drugs that target particular pathways, such
as a kinase inhibitor
for cancer treatment.
A genetic analysis led by Dr. Erik Knudsen (left) and Dr. Agnieszka Witkiewicz suggests that most pancreatic
cancers harbor genetic alterations that could be targeted by existing
drugs, using their genetic features
as a roadmap
for treatment.
Current chemotherapy
treatments cure the disease in fewer than 10 % of patients who have a FLT3 mutation — partly because toxic chemotherapy
drugs can be used
for only a few days at a time, not killing
as many
cancer cells
as they might.
The
drug was approved by the FDA
as a combination first - line therapy
for postmenopausal women with ER + / HER2 - breast
cancer,
as initial endocrine - based
treatment for their metastatic disease.
A genetic analysis led by UT Southwestern Medical Center researchers suggests that most pancreatic
cancers harbor genetic alterations that could be targeted by existing
drugs, using their genetic features
as a roadmap
for treatment.
Epigenetic therapies are rapidly being developed
as cancer treatments, opening the possibility to also test these
drugs for antiviral activity.
P: We found discodermolide [a
drug from Discodermia, a sponge found in the Caribbean, the Bahamas, and the Gulf of Mexico], and it's gone through phase I clinical trials
for treatment of solid tumors such
as ovarian, pancreatic, breast, colon, or lung
cancers.
This small molecule is in clinical trials against
cancer and has high specificity and good pharmacological properties, which could warrant its further development
as antiviral
drug for treatment of pH1N1 virus infection,» Dr. Oxana Denisova says.
Small molecule
drugs can be screened or designed to increase telomerase activity exclusively within stem cells
for disease
treatment as well
as anti-aging therapies without increasing the risk of
cancer.
Geschwind, a professor in the Russell H. Morgan Department of Radiology and Radiological Science at the Johns Hopkins University School of Medicine and its Kimmel
Cancer Center, and others at Johns Hopkins have been studying the experimental drug as a cancer treatment for over a decade because of its ability to block a key metabolic pathway of cancer
Cancer Center, and others at Johns Hopkins have been studying the experimental
drug as a
cancer treatment for over a decade because of its ability to block a key metabolic pathway of cancer
cancer treatment for over a decade because of its ability to block a key metabolic pathway of
cancer cancer cells.
Finding ways to use CaSR - directed
drugs also
for the
treatment of diseases such
as diabetes, Alzheimer's disease and various types of
cancer, would be a breakthrough.
It also showed that the public cost of expanding public coverage
for high - cost
drugs — such
as treatments for cancer and rheumatoid arthritis — would be modest and, under most plausible scenarios, would be offset by savings achieved in relatively common
drug classes — like
treatments for high cholesterol and high blood pressure.
Torres notes that it will be important to screen
for HCV because
treatment with antiviral
drugs may possibly prevent
cancer from ever developing,
as reported
for liver
cancers and non-Hodgkin's lymphoma.
Two existing
drugs — one the active ingredient in an anti-fungal medication and the other now used to control iron levels in the blood — both show promise
as potential
treatments for cervical
cancer, according to newly published research by scientists at Rutgers New Jersey Medical School.
The researchers studied a class of anti-cancer
drugs called BET inhibitors, which are considered promising new
drugs for the
treatment of blood
cancers such
as leukemias and lymphomas.
«If successful, I envisage it can be a good alternative
treatment in the future, one which is low cost and yet effective
for the
treatment of
cancers involving solid tumours,
as it might minimise the side effects of
drugs.»
Buoyed by these results, Dana - Farber researchers are working to create a derivative of dBET1 that can be used
as a
drug in human patients — and to extend the conjugate strategy
for the
treatment of other
cancers and other genetically - caused diseases.
The New EPOC study, published in The Lancet Oncology and funded by
Cancer Research UK, evaluated whether the drug cetuximab and chemotherapy together worked better than chemotherapy alone as a treatment in addition to surgery for people with bowel cancer that had spread to the liver but could be surgically re
Cancer Research UK, evaluated whether the
drug cetuximab and chemotherapy together worked better than chemotherapy alone
as a
treatment in addition to surgery
for people with bowel
cancer that had spread to the liver but could be surgically re
cancer that had spread to the liver but could be surgically removed.
The
drugs are already approved
for treatment of patients with advanced breast
cancer as well
as ovarian, pancreatic and certain lung
cancers.
While this limits the clinical implications of using a 24p3 inhibitor
as a sole
treatment for leukemia, adding it to a
cancer drug such
as Gleevec might prove effective, he says.
Nell Barrie, senior science information manager at
Cancer Research UK, said: «Finding new uses
for existing
drugs is a great way to speed up improvements in
treatment,
as these
drugs will have previously been through safety tests.
«The work has implications
for the future
treatment or prevention of LFS - associated osteosarcoma, and possibly
for all forms of bone
cancer driven by p53 mutations, with H19 and p53 established now
as potential targets
for future
drugs.»
«RNAi therapies are a unique approach to
cancer treatment as they have the potential to «turn off» the genes» coding for proteins involved in cancer cell division,» said Ramesh K. Ramanathan, M.D., medical director of the Virginia G. Piper Cancer Center Clinical Trials Program at Scottsdale Healthcare and deputy director of the Clinical Translational Research Division of the Translational Genomics Research Institute (TGen) in Phoenix, Ariz. «Using a lipid nanoparticle, the RNAi drug can be delivered to a cancer cell to block the expression of specific proteins involved in tumor growth.&
cancer treatment as they have the potential to «turn off» the genes» coding
for proteins involved in
cancer cell division,» said Ramesh K. Ramanathan, M.D., medical director of the Virginia G. Piper Cancer Center Clinical Trials Program at Scottsdale Healthcare and deputy director of the Clinical Translational Research Division of the Translational Genomics Research Institute (TGen) in Phoenix, Ariz. «Using a lipid nanoparticle, the RNAi drug can be delivered to a cancer cell to block the expression of specific proteins involved in tumor growth.&
cancer cell division,» said Ramesh K. Ramanathan, M.D., medical director of the Virginia G. Piper
Cancer Center Clinical Trials Program at Scottsdale Healthcare and deputy director of the Clinical Translational Research Division of the Translational Genomics Research Institute (TGen) in Phoenix, Ariz. «Using a lipid nanoparticle, the RNAi drug can be delivered to a cancer cell to block the expression of specific proteins involved in tumor growth.&
Cancer Center Clinical Trials Program at Scottsdale Healthcare and deputy director of the Clinical Translational Research Division of the Translational Genomics Research Institute (TGen) in Phoenix, Ariz. «Using a lipid nanoparticle, the RNAi
drug can be delivered to a
cancer cell to block the expression of specific proteins involved in tumor growth.&
cancer cell to block the expression of specific proteins involved in tumor growth.»
Men with newly diagnosed metastatic, hormone - sensitive prostate
cancer lived more than a year longer when they received a chemotherapy drug as initial treatment instead of waiting to for the disease to become resistant to hormone - blockers, report scientists from Dana - Farber Cancer Institute and the Eastern Co-operative Oncology
cancer lived more than a year longer when they received a chemotherapy
drug as initial
treatment instead of waiting to
for the disease to become resistant to hormone - blockers, report scientists from Dana - Farber
Cancer Institute and the Eastern Co-operative Oncology
Cancer Institute and the Eastern Co-operative Oncology Group.
Drugs used to block copper absorption
for a rare genetic condition may find an additional use
as a
treatment for certain types of
cancer, researchers at Duke Medicine report.
In a 1988 paper summarizing his findings, Fiebig concluded that xenograft mice were wonderful models
for broadly testing new
drugs against human tumors, but they «can not be used
as a clinical routine method»
for predicting patient
treatment.1 The idea of using xenograft mice
as personal avatars
for cancer patients was discarded.
Paclitaxel, the first of a class of
drugs known
as taxanes, is approved by the FDA
for the
treatment of advanced ovarian
cancer.
On October 2, 2015, the FDA approved the immunotherapy
drug pembrolizumab (Keytruda ®), made by Merck,
as second - line
treatment for patients with lung
cancer, the leading cause of
cancer - related death in the U.S. and the world.
For more information regarding Bristol - Myers Squibb Clinical Trial participation, please visit www.BMSStudyConnect.com Inclusion Criteria: • Early stage IB - IIIA, operable non-small cell lung
cancer, confirmed in tissue • Lung function capacity capable of tolerating the proposed lung surgery • Eastern Cooperative Oncology Group (ECOG) Performance Status of 0 - 1 • Available tissue of primary lung tumor Exclusion Criteria: • Presence of locally advanced, inoperable or metastatic disease • Participants with active, known or suspected autoimmune disease • Prior
treatment with any
drug that targets T cell co-stimulations pathways (such
as checkpoint inhibitors) Other protocol defined inclusion / exclusion criteria could apply
This new work provides a target
for future
cancer drugs as well
as autoimmune
treatments.
To cite a few instances, polymerase chain reaction (PCR), a molecular method developed over three decades ago, has been widely applied in disease diagnosis, disease mechanism deciphering, and prognosis prediction; the elucidation of tyrosine kinase activity in
cancer cells has led to the development of novel
drugs for cancer treatment; and the identification of proteins and genetic molecules by molecular methods
as biomarkers
for disease diagnosis and prognosis has been drawing great interest.
Antimitotic
drugs, such
as the microtubule poisons taxanes and vinca alkaloids, are widely used
as chemotherapeutics
for cancer treatment.
Berkeley Lab researchers have developed a new family of nanocarriers, called «3HM,» that meets all the size and stability requirements
for effectively delivering therapeutic
drugs to the brain
for the
treatment of a deadly form of
cancer known
as glioblastoma multiforme.
This framework will be built upon available open - source deep learning platforms that can be adapted to address different aspects of the
cancer process
as represented by JDACS4C's challenge topics: 1) understand the molecular basis of key protein interactions; 2) develop predictive models
for drug response; and 3) automate the extraction and analysis of information from millions of
cancer patient records to determine optimal
cancer treatment strategies.
Autistic people and carers of children with autism should not consider using the
drug other than
for its approved use
as a
cancer treatment.»