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Job Seekers With Disabilities Face Discrimination At Application Stage, UK
In a snapshot survey published by Terrence Higgins Trust today, two thirds of top organisations were found to ask irrelevant health related questions on job application forms. A coalition of charities wants these questions banned to reduce the discrimination faced by people with "invisible" conditions such as mental illness or HIV.
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Spectranetics Announces First Human Uses Of Turbo-Tandem™ System
Spectranetics Corporation (Nasdaq: SPNC) reported the first human procedures using its Turbo-Tandem™ System, which had earlier received FDA clearance and CE mark approval for marketing in the US and the EU. The Turbo-Tandem System is a single-use, disposable device indicated for atherectomy of infrainguinal arteries. It is comprised of two integrated catheters, a 7 French laser guide catheter in combination with a 2.0mm excimer laser ablation catheter, and is designed to perform atherectomy and ablation of plaque in arterial lesions above the knee, primarily within the superficial femoral and popliteal arteries.
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Countries Address Financial Crisis, Burden On Developing Nations At U.N. Financial Summit
At the opening of a three-day U.N. financial summit on Wednesday, developing countries joined U.N. officials in "calling for more money and a greater role in regulating the world economy in the wake of the worst global financial crisis since the Great Depression, which has taken a disproportionate toll on poor nations," AP/Google.com reports (Astor, AP/Google.com, 6/25).
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PharmaMar Announces The Initiation Of Phase I Clinical Trials With PM1183, A New Antitumor Compound

PharmaMar SA (Grupo Zeltia, ZEL.MC) announces the initiation of Phase I clinical trials with PM1183, a new antitumor compound developed by PharmaMar"s internal research program. The first patient enrolled in the trial has already started treatment with the compound. PM1183 is a new synthetic alkaloid which binds to the minor groove of DNA, generates DNA double strand breaks and caused cell cycle perturbation that finally results in a specific type of cell death calles apoptosis. Results from preclinical studies indicate a pattern of activity of PM1183 different from that of conventional alkylating agents. In preclinical studies PM1183 demonstrated strong in vitro and in vivo antitumoural activity in a wide variety of tumour cell lines and human transplantable xenografted tumours. PM11883 also demonstrated a manageable and reversible preclinical toxicology profile. As a single agent, PM1183 significantly reduced tumor proliferation in vivo, with the strongest effect observed on the xenografts of the breast cancer cell line MX1. PM1183 was also evaluated for in vivo activity using M5076 sarcoma model that spontaneously metastasizes in the liver of the C57Bl/6 female tumor bearing mice. The compound statistically reduced the number of liver metastasis compared to placebo-treated animal. In vitro studies show cell lines with mutant p53 or lacking P53 are more sensitive with PM1183. Further studies are on going in human ovarian cancer and human sarcoma xenografts. PharmaMar"s clinical portfolio currently includes five new, first-in-class compounds: Yondelis®, Aplidin®, Zalypsis®, Irvalec® and PM1183. The PharmaMar patent portfolio is composed of over 1,800 files and it has a continous flow of new compound into the clinic (1 new compound every 24 months). About PM1183 PM1183 is a new synthetic alkaloid compound developed by PharmaMar"s internal research program. It binds to the minor groove of DNA, generates DNA double strand brakes and caused cell cycle perturpation mainly consisting in a delayed progression of S phase and cycle arrest in G2M. Results from preclinical studies indicate a pattern of activity of PM1183 different from that of conventionaol alkylating agents. PharmaMar PharmaMar is the world leader biopharmaceutical company of the Zeltia Group, committed to advancing the treatment of cancer through the discovery and development of new marine-derived medicines. PharmaMar"s first product, Yondelis®, received marketing authorisation from the European Commission for the treatment of advanced or metastatic soft tissue sarcoma in September 2007. In 2008 a registration dossier was submitted to the European Medicines Agency (EMEA) and Food and Drug Administration (FDA, USA) for Yondelis® when administered in combination with DOXIL®/Caelyx™ (pegylated liposomal doxorubicin) for the treatment of women with relapsed ovarian cancer. It is also in phase II clinical trials for prostate, breast, and lung cancers. Three other PharmaMar compounds, Aplidin®, Irvalec®, and Zalypsis® are in various stages of clinical development. PharmaMar


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