(Filing, 10-Q, Champions Oncology, JAN 31, 2013, View Source [SID:1234504159])

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(Filing 10-Q , Lion Biotechnologies, JAN 25, 2013, View Source [SID:1234501579])

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Positive results from the BI-505 phase I study in multiple myeloma

On January 24, 2013 BioInvent reported the first results from the BI-505 phase I study in patients with multiple myeloma (Press release BioInvent, JAN 24, 2013, http://www.bioinvent.com/investors/press-releases/release.aspx?releaseid=736831 [SID:1234500561]). The study has reached a final stage and the preliminary analysis shows that BI-505 has an advantageous safety profile. In cohorts where extended therapy was available, 24 % of the patients had stable disease for at least two months, indicating effect of BI-505. The final conclusions of the study will be available at a later time-point. The optimal dose has been defined according to the study protocol and will be used in the next clinical trial which is approved by the health authorities.
BI-505 is a human antibody selected from the n-CoDeR-library and fully owned by BioInvent. It is directed against the ICAM-1 adhesion protein, which is highly expressed on multiple myeloma cells. BI-505 has demonstrated significant anti-tumor activity in several relevant models of multiple myeloma.
Thirty-five patients with relapsed or refractory disease after at least two previous regimens with other drugs are included in the phase I, dose escalation study. The primary objective is to determine the safety and tolerability of BI-505 in patients with advanced disease. Pharmacokinetics and pharmacodynamic variables including relevant biomarkers for tumor response are also being evaluated in order to determine the optimal dose for further clinical development. The study is being conducted at seven sites in the US and Europe.
Groups of patients are treated with increasing doses of BI-505 (0,0004 – 20 mg/kg; eleven dose levels) every second week over a four-week period, with a possibility of extended therapy every two weeks until disease progression for patients at dose level six and onwards.
The preliminary assessment demonstrates that BI-505 has a favorable safety profile with a low number of reported adverse events. Temporary infusion-related reactions were observed when the first dose was given which is commonly seen. Despite advanced disease, 7 of the 29 patients on extended therapy (at dose level six and onwards) had stable disease for at least two months. A dosing regimen of 10 mg/kg every second week resulted in complete saturation of the ICAM-1 epitopes on the patient´s bone marrow myeloma cells. The 10 mg/kg dose will thus be used in the next clinical trial which has already been approved by the health authorities.

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Alliance of translational research centres established to accelerate global drug development

On January 21, 2013 Six of the world’s top translational health research centres reported that they have come together to form a new Global Alliance of Leading Drug Discovery and Development Centres (Press release, Cancer Research Technology, 21 21, 2013, View Source [SID1234523260]). The aim of this alliance is to strengthen the international academic and/or not-for-profit drug development and commercialization network to ultimately improve the rate at which academic research is translated into new medicines.

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The founding organizations are:

The Centre for Drug Research and Development (CDRD), Canada
Lead Discovery Center (LDC), Germany
The Scripps Research Institute, Scripps Florida, United States
The Centre for Drug Design and Discovery (CD3), KU Leuven R&D, Belgium
Medical Research Council Technology, United Kingdom
Cancer Research Technology, United Kingdom

All member organizations are fully-integrated translational centres capable of professionally advancing drug discovery projects along the value chain from idea to drug candidate with proof-of-concept. Together, they represent close to 400 experienced drug developers collaborating with tens of thousands of academic scientists around the globe on over 165 highly innovative therapeutic projects targeting significant unmet medical needs. For the biopharmaceutical industry, they represent a major source of innovation. Numerous alliances with many of the industry’s leading global companies have been established to develop resulting drug candidates further and ultimately make them available to patients.

Through this Alliance, member organizations will collaborate on mutually-beneficial projects, share best practices, expertise and resources, and develop common standards and performance measurements – ultimately working together to improve the conversion of global early-stage technology into much needed therapies.

Karimah Es Sabar, President and CEO of CDRD commented, "We see a multitude of translational research initiatives around the world, but until now, these have for the most part, worked in isolation of one another. This Alliance will be a powerful vehicle in bringing such organizations together, leveraging one another’s strengths, and ultimately making for a much more effective global translational research environment."

Dr Keith Blundy, Chief Executive Officer of Cancer Research Technology, said: "Cancer Research Technology has historically worked to advance drug discovery opportunities from diverse academic sources including those in the UK, Europe, USA and Australia. This alliance of leading centres fits perfectly with our aim to grow this activity, to share our knowledge and to learn from others with the ultimate goal of providing more and better drugs for cancer patients."

For additional information on the Global Alliance of Leading Drug Discovery and Development Centres, please visit: www.drugdevelopmentalliance.org

Cancer Research UK takes investigational multi-cancer drug from laboratory into unique trial

On January 18, 2013 CANCER RESEARCH UK’s Drug Development Office (DDO) in partnership with AstraZeneca, reported to have opened a unique three-armed study of a new investigational drug called AZD0424 that is being tested for the treatment of a range of cancers (Press release, Cancer Research Technology, 18 18, 2013, View Source [SID1234523261]).

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This first ever phase I trial of the AstraZeneca-owned drug, is led from the Oxford Cancer Research UK Cancer Centre based at the Churchill Hospital*. It will recruit up to 30 patients, initially across all solid tumour types. Later the design of the trial will be adapted, enabling the study to separate into three separate ‘personalised’ arms. Each of these future arms will test AZD0424 in different combinations alongside standard or other experimental treatments in specific patient populations. The Edinburgh and Belfast Cancer Research UK Centres are also involved as clinical sites, carrying out research to guide the drugs to be used in combination with AZD0424 and the specific patient groups involved in the trial.

This is the first time the DDO has undertaken an adaptive design trial of this type – one where the planned combination treatment to be given to patients is modified as the trial progresses.

Study leader, Professor Adrian Harris, Cancer Research UK clinician at the University of Oxford, said: "This unique study design means that for the first time, we’re able to monitor the data we receive in the first phase of the trial and feed this back into the study to adapt it as it’s happening – rather than having to wait until it ends – which could be several years.

"This exciting approach will hopefully accelerate development to give us a better chance of identifying the most effective ways to use the drug either alone or in combination in specific patient groups."

AZD0424 works by blocking two proteins called Src and ABL1 – found in high levels in cancer cells. The proteins have an important role in cell growth and blood vessel development. Laboratory studies have shown that AZD0424 blocks these proteins, preventing delivery of nutrients via blood vessels to cancer cells – stopping their growth.

Cancer Research UK has carried out the preclinical development work of AZD0424 through the charity’s Clinical Development Partnerships (CDP) scheme. CDP is a joint initiative between the DDO and the charity’s commercial arm, Cancer Research Technology, to put drugs that otherwise would not be developed by pharmaceutical companies through early phase clinical trials. The scheme lets companies keep the background rights to their programmes while enabling Cancer Research UK to take on early development work, to see if there is a benefit to cancer patients.

Graham Richmond, AZD0424 project leader at AstraZeneca, said: "Collaborations such as this between AstraZeneca and Cancer Research UK are critical in the fight against cancer. By joining forces and combining our assets with external expertise, it means we can bring forward a wider range of experimental compounds than we could do simply using our own resources and – as a result – patients get access to a trial of a potential new cancer treatment earlier.

"AstraZeneca was the first pharmaceutical company to have a strategic alliance with Cancer Research UK focused on developing novel combinations of experimental cancer drugs through early phase clinical trials."

The trial is also supported by the National Institute for Health Research Oxford Biomedical Research Centre, and the Cancer Research UK and National Institute for Health Research (NIHR) Experimental Cancer Medicine Centre Network.

Dr Vicky John, head of clinical partnerships, at Cancer Research UK’s DDO, said: "We’re delighted that our unique CDP scheme has made it possible to launch the first trial of this promising drug.

"We’re enormously proud of our successes so far from the initiative, which allows us to work alongside industry to take on and develop deprioritised potential cancer treatments – which otherwise may not have reached patients for many years.

"There are now eight drugs in our CDP portfolio – including a multipeptide vaccine, a monoclonal antibody and other molecularly targeted drugs. Four treatments have already successfully entered trials** with others scheduled to open early 2013. This demonstrates how our strong collaborations with international pharmaceutical and biotechnology companies have provided new experimental drugs for patients on trials, for whom existing drugs no longer work.

"We intend to continue to seek future partnerships, to develop more potential drugs and ultimately achieve our goal to save more lives from cancer."