Our team of experienced trial and appellate lawyers craft and execute comprehensive intellectual property strategies from initial
drug development through trial and appeal.
To assist
drug development through the identification of essential genes and pathways, we have measured competitive growth rates in mice of 2,578 barcoded Plasmodium berghei knockout mutants, representing > 50 % of the genome, and created a phenotype database.
The investigations include research on protein crystal growth, which may lead to
drug development through protein mapping, and plant biology.
Not exact matches
Zymeworks, meanwhile, went
through a number of lean years; investors in Canada were still more comfortable with a
development model that produced widely applicable chemical
drugs.
Alnylam $ ALNY may be going solo on the
development of rare disease
drug lumasiran after Sanofi took a pass on its option, but the FDA has come
through with a major assist.
Sierra Oncology, Inc., a clinical stage
drug development company focused on advancing next - generation DNA damage response therapeutics for the treatment of patients with cancer, went public near $ 29 in July 2015, then began a downtrend that continued
through a June 2017 all - time low of $ 1.10.
UCSD's renowned Cancer Therapeutics Training Program, also known as CT2, addresses the shortage of professionals qualified to oversee the
development of innovative, new cancer
drugs through its two - year intensive post-doctoral student training at National Cancer Institute - designated Comprehensive Cancer Centers.
Educational Session # 1: When: June 3rd, Wednesday, 3:15 PM — 4:00 PM Where: Institute 2015 Pre-conference Cybersecurity, Technology and Infrastructure Advancements Forum What: Optimize PBM Value Proposition to Payers
through Disruptive Innovation by Terry Ramey, EVP, Business
Development and Client Engagement Session Details: PBMs that manage over $ 300 billion of pharmacy benefits for plan sponsors have historically been challenged to support plan sponsors» goals to reduce avoidable
drug - impacted medical costs and optimize overall pharmacy costs.
A spinoff or sale could benefit Pfizer
through additional cash that it could use to acquire new high - growth products that are already approved or are late in the
drug development process.
By accelerating promising
drug candidates
through the
drug discovery and
development pipeline and spearheading innovative public - private partnerships, we increase the chance of finding an effective treatment, and a cure, for Alzheimer's disease.
Smoking and
drug use — smoking
through pregnancy can affect your baby's
development in a number of ways and increases your chances of having a premature baby
The funding is provided
through the State's Public Housing Modernization
Drug Elimination program, part of a modernization program that provides grants to public housing
developments where rental income is insufficient and funds are unavailable from other sources for needed repairs and improvements.
«When the AIDS crisis burned and ravaged its way
through this community and thousands of gay men were literally dying, every day New Yorkers stood up... they organized, they put their bodies on the line... they forced the
development of antiretroviral
drugs and that's why me and many people are alive today.»
Although these postdocs are active in research, the talk largely centered on moving scientific advances
through the complex
drug -
development process to the marketplace and the clinic — and on the skills and strategies needed to build a career in industry.
The Cent - 1 molecule kills cancer cells
through a mechanism similar to that of the template
drug Rigosertib that is currently under commercial
development.
What I especially like about working for UKHTB is that it offers a new challenge and is pioneering in an area that has the potential to benefit human health
through the enhanced
development of new
drugs and diagnostic tools.
Written by 25 authors, it described the collaboration between government, academic researchers, and disease advocacy groups that led to the ICV trial as a model of the teamwork that can speed
drugs through early
development, boosting their chances of being commercialized.
«To the EC and EFPIA, it was clear that the only way to restore European competitiveness in
drug development was
through collaboration.»
The three Ras genes found in humans — H - Ras, K - Ras and N - Ras — were among the first to be linked to cancer
development, and a new study led by VCU Massey Cancer Center researcher Paul Dent, Ph.D., has shown the recently approved breast cancer
drug neratinib can block the function of Ras as well as several other oncogenes
through an unexpected process.
«Our preliminary results suggest that TREML4 - regulated signaling
through TLR7 may be a potential
drug target to limit inflammation and the
development of autoimmunity.»
«This study is the first step in a potential
drug development for a new class of
drugs for osteoarthritis, although there are a number of hurdles we have to go
through — necessarily so — before it gets nearer patients.
As early as 1969, these collaborations led to important products - directly, as with the
development of diagnostics for
drugs of abuse, Abuscreen; or indirectly,
through the
development of technologies, which later played a key role in the first isolation and characterization of the a-interferons and to Roche's patents for Roferon.
These «nanoswimmers» cross the blood — brain barrier highly efficiently, and could lead to the
development of
drug delivery systems that navigate
through tissues and organs to target specific sites precisely.
Results show that coping with a stressful event
through behavioral disengagement — giving up on dealing with the stress — or by using alcohol or
drugs each significantly mediated the relationship between stress exposure and insomnia
development.
Only one out of ten
drugs in
development makes it successfully
through clinical trials, he adds.
In his current role, he combines population research and functional genomics strategies to inform
drug development from preclinical
through phase 3 trials.
Through these images, the team will discover exactly how the immune system molecules bind to the Ebola virus and stop it from functioning, a critical step in
drug development.
Two new tuberculosis
drugs are in the final stages of
development, and could also help to replace those being rendered less useful
through resistance, he adds.
The expert group was convened
through the Alzheimer's Association Research Roundtable — an ongoing effort that brings together experts in the field from academia, industry, and government to address ways to overcome barriers to
drug development.
Robotized «high - throughput screens» like this are a growing trend in
drug development as they can work
through massive libraries of candidate
drugs quickly and accurately in a day, as opposed to the months required by manual methods.
Pharmaceutical companies, by contrast, focus most of their efforts at the other end of the
drug development pipeline, moving potential
drug compounds
through human clinical trials into the market.
There are many stages in the
drug discovery /
development process from target identification, assay design, and screening
through to compound optimization, pharmacology, and testing in animal models.
Pending approval
through an Investigative New
Drug Application, the aerosolized form of the vaccine will be evaluated for replication, safety and immunity
development in a study in adults.
Founded in 2003, the Spinal Muscular Atrophy Foundation is a nonprofit organization dedicated to accelerating progress towards a treatment and cure for Spinal Muscular Atrophy
through targeted funding of clinical research and novel
drug development efforts.
This is especially the case with
drugs for developing - world diseases, where the financial investment, both in launching and maintaining research programs and ultimately bringing a candidate
drug through clinical
development and to market, is very limited.
Under the agreement, Biotecnol and Cancer Research UK's Centre for
Drug Development will collaborate to take forward Tb535H through a Biotecnol - sponsored first - in - man Phase I clinical trial, using Cancer Research UK's drug development expertise in return for shareholdings in Biotec
Drug Development will collaborate to take forward Tb535H through a Biotecnol - sponsored first - in - man Phase I clinical trial, using Cancer Research UK's drug development expertise in return for shareholdings in
Development will collaborate to take forward Tb535H
through a Biotecnol - sponsored first - in - man Phase I clinical trial, using Cancer Research UK's
drug development expertise in return for shareholdings in Biotec
drug development expertise in return for shareholdings in
development expertise in return for shareholdings in Biotecnol.
The Learning Collaborative will engage a for - profit partner to advance auranofin
through late stage
drug development, registration and commercialization.
About the SMA Foundation Founded in 2003, the Spinal Muscular Atrophy Foundation is a nonprofit organization dedicated to accelerating progress towards a treatment for Spinal Muscular Atrophy
through targeted funding of clinical research and novel
drug development efforts.
We start with a compelling scientific idea or promising
drug candidate from collaborators in academia and / or industry, and then efficiently advance the therapy
through pre-clinical research to enable the establishment of an independent company to progress
drug candidates
through clinical and regulatory
development to commercialization.
The Spinal Muscular Atrophy Foundation is a nonprofit organization dedicated to accelerating progress towards a treatment and cure for spinal muscular atrophy
through targeted funding of clinical research and novel
drug development efforts.
Anna Huttenlocher, University of Wisconsin, USA Neutrophils in the Tumor Microenvironment Neutrophils, Wounds, and Cancer Progression Stefan Kaufmann, Max Planck Institute, Germany Pathology and immune reactivity: understanding multidimensionality in pulmonary tuberculosis Constitutive BAK activation as a determinant of
drug sensitivity in malignant lymphohematopoietic cells Kathryn Moore, New York University, USA MicroRNA -33-dependent regulation of macrophage metabolism directs immune cell polarization in atherosclerosis Lalita Ramakrishnan, University of Cambridge, UK Myeloid Growth Factors Promote Resistance to Mycobacterial Infection by Curtailing Granuloma Necrosis
through Macrophage Replenishment Beth Stevens, Harvard University, USA Microglia: Dynamic Mediators of Synapse
Development and Plasticity Do glia drive synaptic and cognitive impairment in disease?
By working in an integrated fashion, the Research Engine enables us to rapidly move our mRNA medicines
through the
drug discovery phase — from initial concept to
development candidate (DC) nomination.
It helps us understand the genetic basis of diversity and evolutions in organisms, leading to the insight understanding into how living things evolved
through stressed environments to the pathogenesis of pathogens, including identification novel
drug targets and
development of novel
drug candidates.
He is responsible for further developing Hookipa's groundbreaking science
through the
development of promising product candidates — from the initial research to manufacturing of the final
drug.
«We can infuse very small amounts of multiple
drugs compared to what we can do intravenously or orally, and also manipulate behavioral changes
through drug infusion,» says Canan Dagdeviren, the LG Electronics Career
Development Assistant Professor of Media Arts and Sciences and the lead author of the paper, which appears in the Jan. 24 issue of Science Translational Medicine.
Chemotype Evolution, Carmot's proprietary technology, enables the rapid identification of novel
drugs through an evolutionary discovery paradigm and has produced a pipeline of breakthrough therapeutics currently in pre-clinical
development.
About the Spinal Muscular Atrophy Foundation Founded in 2003, the Spinal Muscular Atrophy Foundation is a nonprofit organization dedicated to accelerating progress towards a treatment for Spinal Muscular Atrophy
through targeted funding of clinical research and novel
drug development efforts.
We believe that leveraging human intuition
through creation of a scientific game for
drug discovery can not only provide a new avenue to discover therapeutic
drugs for protein targets, but can also contribute to the
development of new sophisticated algorithms to use in computer aided
drug design.
BridgeBio has committed $ 30 million and a team of senior business managers to the company, while MD Anderson,
through its Institute for Applied Cancer Sciences (IACS), provides intellectual property and an oncology
drug development team to advance SHP2 inhibitors toward clinical studies.
An open - source content management system then would search
through upwards of a billion
drug combinations to find those with the greatest potential to inhibit a given tumor, or a billion hypothetical compounds to identify candidates for new
drug development.