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A team of US researchers have become the first to completely suppress a gene that is crucial to HIV infection, paving the way to a protective gene therapy.
Aptuit Laurus, the newly formed joint venture between Aptuit and Laurus Labs in India, will focus on an expected rise in the demand for preclinical and Phase I research and development services as part of its growth plan in India.
Waters has combined its award winning Synapt MS with a MALDI ionisation source to broaden the number of applications the instrument can be used in - including MALDI imaging.
The worlds of biochemistry and electronics have collided after scientists successfully developed a biosensor that can measure a drug's effectiveness without killing the cells it is trying to analyse.
Teva Pharmaceuticals has licensed a drug that could offer new hope for both treating and preventing allergic reactions, according to its award-winning developers.
Six months after a couple of failed Phase III trials, Nuvelo has reinstated clinical development for its blood clot dissolving drug, but it will have to go it alone after Bayer decided enough is enough and pulled out of the collaboration.
US microfluidics company CellASIC has developed a device that enables the effects of anticancer drugs to be studied in an environment that mimics a real cancerous growth.
The latest in a series of periodic roundups of drugs that have moved from preclinical research into clinical testing via the announcement of a Phase I trial or an application for a trial to industry regulators.
Asterand said it is to slash 10 per cent of its total workforce in a cost-cutting strategy although it is not a knock-on effect of the recent ban on export of human samples from Russia.
A new class of diabetes drugs is showing promising clinical results, with the big players in the field all scrapping it out for a slice of the potential rewards.
Research into new tools that will remove the need to use animals in medical research has received a £240,000 (€356,000) boost at the University of Nottingham.
Pharma giant Roche has gone public in its fight to acquire tissue-analysis instrument and reagent expert Ventana Medical Systems for $3bn (€2.2bn).
In this week's review of recent activity within the preclinical research services arena, news has emerged involving Gendata, Achaogen, NiKem Research and Verona Pharma.
A virtual version of the microbe that causes tuberculosis could help 'revolutionise' TB treatment by unlocking the key to how a few cells remain resistant to drugs.
Researchers have discovered three potential microRNA (miRNA) tumour suppressor genes using real-time PCR (polymerase chain reaction) techniques.
An unusual drug that contains a crucial boron atom can effectively treat fungal infections, and could also prove invaluable in the effort to counter antibacterial drug resistance.
Roche has committed hundreds of millions of dollars to an early-phase rheumatoid arthritis drug, a move that is indicative of big pharma's increasing tendency to license earlier phase compounds.
Parexel talks to Outsourcing-Pharma about Phase I trials, touching on trends and growth opportunities, future plans for India and lessons learned from Tegenero.
Genzyme has put pen to paper on a licensing deal for Ceregene's Parkinson's drug, as a rival gene therapy for the same disease shows promise in initial clinical trials.
The latest in a series of periodic roundups of drugs that have moved from preclinical research into clinical testing via the announcement of a Phase I trial or an application for a trial to industry regulators.
Finnish CRO Technical Research Center (VTT) has spun-off Zora Biosciences, which becomes the only company in the Nordic region to provide metabolomics services to pharma companies - a market with high potential.
Scientists have developed a faster means of searching non-gene DNA for mutations that cause disease, paving the way for faster and cheaper drug development.
Thermo Fisher Scientific has opened a new RNAi Discovery and Therapeutics Services Laboratory to help pharmaceutical companies in their quest for new drugs.
US-microfluidics expert Fluidigm has launched a new dynamic array for its BioMark instrument that increases the efficiency of PCR (polymerase chain reaction) genotyping while reducing the amount of costly equipment and reagents needed.
European and US regulatory bodies have revamped their relationship to ease administrative burdens and improve communication, as well as implementing new measures directed specifically at paediatric drug products.
Despite a lift of the ban on biological sample transportation out of Russia, the country's clinical research industry is still in the dark on the new rules to control export of such materials.
Farfield Scientific has teamed up with Monash University, Australia to create biosensor chips that will enable researchers to unravel how membrane proteins function and interact with drug molecules.
A team of Canadian scientists have identified which genes help decide a stem cell's fate; a discovery that one day could lead to drugs that invoke their regenerative power.
Experts from around the world have gathered this week to discuss the best emerging therapies for a number of neurological disorders such as multiple sclerosis and stroke.
Teva Pharmaceuticals has licensed some protein kinase B technology, including preclinical drug candidates, adding to the buzz around this up-and-coming cancer target.
In the inevitable reshuffle that comes after a major acquisition, Bayer's healthcare division has today announced plans to cut 30 per cent of its drug pipeline.
Diamyd Medical will continue with a clinical trial of its gene therapy designed to protect insulin-producing cells in diabetes patients, despite major errors invalidating the study.
Swedish researchers have developed a method of separating a continuous flow of (bio)particles based on their size and density using acoustic forces.
US researchers have developed a three part screening process to find new cancer genes and used it to identify a new gene associated with about a third of all breast cancers.
GlaxoSmithKline's (GSK) new drug to treat a rare form of bleeding disorder has shown good results in trials so far, but while experts remain mystified as to why it works, a true cure will remain elusive.
GlaxoSmithKline's (GSK) new drug to treat a rare form of bleeding disorder has shown good results in trials so far, but while experts remain mystified as to why it works, a true cure will remain elusive.
ThalesNano Nanotechnology has launched a new version of its H-Cube flow reactor for use in higher education laboratories - the H-Cube Tutor.
The latest in a series of periodic roundups of drugs that have moved from preclinical research into clinical testing via the announcement of a Phase I trial or an application for a trial to industry regulators.
Nicholas Piramal India (NPIL) has opened its second clinical research facility and is eyeing the growing area of biopharmaceutical testing.
The former director of the country's State Food and Drug Administration (SFDA) has lodged an appeal against the death penalty slapped on him after a corruption conviction.
Pfizer is to plough $300m (€226m) into South Korean research and development over the next five years, while it's CEO is planning to visit North Korea tomorrow.
German researchers have developed a microfluidic device that greatly increases the efficiency of measuring the melting temperature of DNA double strands.
A drug that provides the brain with an alternative energy source to glucose is helping to roll back the symptoms of Alzheimer's disease.
Researchers have used a protein lysate array to profile and classify multiple components of aberrant cell signalling pathways in 90 cancer cell lines.
Asterand has announced a restructure and changes to its operational model in a bid to grasp hold of profitability.
GlaxoSmithKline (GSK) outlined more details on the mechanism of its anticancer drug ofatumumab - an antibody that was the subject of the biggest ever pharma licensing deal.
Pharmaceutical companies are actually set to benefit from reduced testing requirements now that the new European chemicals regulation is in place, however, some bulk manufacturers and ingredients suppliers could face increased burdens.
BioFocus DPI has released a new informatics system that can combine chemical and biological data from various sources to optimise protein kinase inhibitor candidate selection.
Diverse manufacturer 3M has agreed to sell off another chunk of its pharmaceuticals business, fourteen months after it decided to give up on the 'very competitive' industry.
A drug that is popularly used to treat high blood pressure and stroke could also be used to rejuvenate dopamine neurons in the brain, according to US scientists.
Histological evidence of tumour destruction has confirmed the promise of Epeius Biotechnologies' Rexin-G as an effective targeted gene therapy platform for metastatic cancer.
While traditional cancer treatments currently have the lion's share of the market, a new wave of immunological and biotherapy treatments are set to take the industry by storm, predicts new market research.
This year's American Society for Clinical Oncology (ASCO) conference is over and as 45,000 scientists head home, DrugResearcher.com looks at some of the most innovative drugs that were on show.
Agilent has launched a new tool that removes the 14 most abundant proteins found in blood plasma and serum to speed up the discovery and identification of low-abundance proteins and biomarkers.
A molecule that links spontaneous physical activity such as fidgeting and food intake could be a promising new target for drugs to control diet-induced obesity, researchers from Europe and the US suggest.
Just as the clinical trials sector in Russia is starting to take off, the industry has been dealt a severe blow with the sudden and indefinite banning of biological sample exports.
IDBS look to speed up laboratory research by enabling more efficient knowledge transfer with its latest electronic lab notebook (ELN) suite, E-WorkBook 7.0.
Amsterdam Molecular Therapeutics (AMT) lead candidate AMT 011, a Lipoprotein Lipase (LPL) Deficiency treatment has received Orphan Drug Designation from the US Food and Drug Administration (FDA).
A new drug from Merck KGaA could be the first in a new type of anticancer therapy that works by starving the tumour of its blood supply.
The seventeenth in a series of periodic roundups of drugs that have moved from preclinical research into clinical testing via the announcement of a Phase I trial or an application for a trial to industry regulators.
The number of clinical trial registries that drug companies and researchers can use if they want to have their results later published in prominent medical journals has been increased. Meanwhile, as of July next year, Phase I trials will also have to comply with the registration requirements.
Oxigene's potentially first-in-class cancer drug is showing promising clinical results and could rival a drug Novartis' recently spent nearly a billion dollars on.
Scientists have successfully used ribozymes - considered by some to be the 'living fossils' of a time when life was based on RNA - to prevent the spread of HIV in the body.
Japanese researchers have developed a way to increase protein sequence coverage by removing the need for organic matrices that can mask low weight analytes during MALDI-MS experiments.
DeltaDOT has been given a government grant to commercially develop a new tool to allow researchers to reduce dramatically the time it takes to weed out unsuitable drug candidates.
Phase 0 studies have a great potential in selecting drug candidates early in the drug development but the pharma industry will stay sceptical until more research has been done, said Prof. Colin Garner, CEO of microdosing service firm Xceleron.
Newly-formed Brane Discovery has licensed a Parkinson's research programme to become the third company in three years to own the potentially first-in-class drug candidates.
Thermo Fisher Scientific has introduced a range of powerful new mass spectroscopy products at the 55th ASMS Conference on Mass Spectrometry currently being held in Indianapolis, US.
A new approach to Phase I clinical trials could revolutionise drug development, enabling innovative drugs to get to market faster and cheaper.
In a groundbreaking decision, Janssen-Cilag has offered to give the UK government their money back if its expensive new bone cancer treatment does not work on patients.
Japanese researchers have developed a high throughput method for screening the activity of beta-amyloid protein aggregation inhibitors that should speed up the discovery of new Alzheimer's therapies.
Analysing the images from protein separation experiments, such as 2D gel electrophoresis (2DGE), is not only time consuming but can often miss 'hits' and give false positives. But it doesn't have to be that way, according to Swedish company Ludesi.
Wyeth has presented more clinical data for its first-in-class cancer drug, which was approved for use in the US last week.
The world's biggest cancer conference kicked off this weekend with drug companies from around the world keen to showcase their new therapies.
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