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Collaborations Between Biotechnology Companies And Government/Nonprofit Institutions: March 1 - August 17, 2012
cancer patients and holds an option to license the technology 4/17/12 MAY Aeras (Rockville, Md.) Infectious Disease Research Institute Agreement To conduct joint development activities with respect to IDRI's tuberculosis vaccine candidate, ID93/GLA-SE The nonprofit plans to start a Phase I trial later this year 5/10/12 Altor BioScience Corp. (Miramar, Fla.) Melanoma Research Alliance Agreement To jointly sponsor a University of Washington study of Altor's IL-15 superagonist, ALT-803, againstBioWorld Insight | Monday, August 20, 2012 -
Clinic Roundup
Medivation Inc., of San Francisco, and Astellas Pharma Inc., of Tokyo, published Phase III results from the AFFIRM trial of enzalutamide (MDV3100) in metastatic castration-resistant prostate cancer patients previously treated with docetaxel-based chemotherapy in the New England Journal of MedicineBioWorld Today | Friday, August 17, 2012 -
Meta Study: Targeted Cancer Drugs Yield Fewer Side Effects
LONDON – A meta-analysis of cancer patients treated in Phase I studies of targeted drugs has confirmed that there is a much lower risk of the most serious side effects than with traditional chemotherapyBy Nuala Moran | BioWorld International | Wednesday, August 15, 2012 -
Phase I Clinical Trials Update: July 2012
cancers Patient dosing has begun in a Phase I trial 7/13/12 Peregrine Pharmaceuticals Inc. (Tustin, Calif.) Bavituximab Monoclonal antibody Rectal adenocarcinoma The open-label Phase I trial began and will enroll up to 18 patients 7/17/12 Viral Genetics Inc. (San Marino, Calif.) HCQ Hydroxychlor-oquine Drug-resistant ovarian cancer First patient was enrolled in a Phase I trial 7/20/12 CENTRAL NERVOUS SYSTEM Acadia Pharmaceuticals Inc. (San Diego) AM-831 A small molecule that combines muscarinicBioWorld Insight | Monday, August 13, 2012 -
Infinity Pharmaceuticals Aims to Raise $76.85M
For retaspimycin, an inhibitor of heat-shock protein 90 (Hsp90), Infinity is enrolling for a Phase II trial in non-small-cell lung cancer in patients with a history of smokingBy Catherine Shaffer | BioWorld Today | Friday, August 10, 2012 -
Boom in Oncology Research Raises Concerns About Costs
A July 2012 study completed by the Tufts Center for the Study of Drug Development (TCSDD) found that cancer patients in the U.S...It plans to examine potential new models designed to improve the efficiency and effectiveness of cancer prevention, early detection and treatment and maintain the quality of cancer care while reducing the financial burden of cancer for patients, health systems and societyBio Perspectives | Tuesday, August 7, 2012 -
Clinic Roundup
The study showed T-cell responses against one or more of seven cancer-specific antigens in 61 percent (11/18) of evaluable cancer patients, and 89 percent (8/9) of patients with breast or ovarian cancerBioWorld Today | Tuesday, August 7, 2012 -
Boom in Oncology Research Raises Concerns About Costs
A July 2012 study completed by the Tufts Center for the Study of Drug Development (TCSDD) found that cancer patients in the U.S...It plans to examine potential new models designed to improve the efficiency and effectiveness of cancer prevention, early detection and treatment and maintain the quality of cancer care while reducing the financial burden of cancer for patients, health systems and societyBy Peter Winter | BioWorld Insight | Monday, August 6, 2012 -
Clinic Roundup
Diffusion Pharmaceuticals LLC, of Charlottesville, Va., said it completed the first cohort in a Phase I/II trial testing lead compound trans sodium crocetinate (TSC) in newly diagnosed primary brain cancer patientsBioWorld Today | Thursday, August 2, 2012 -
Clinic Roundup
GenSpera Inc., of San Antonio, Texas, said the FDA cleared the firm to start a Phase II trial of lead compound G-202 in prostate cancer patients who have failed prior hormonal therapyBioWorld Today | Wednesday, August 1, 2012 -
Clinic Roundup
One involves a Phase II trial of cabozantinib in non-small-cell lung cancer patients who have tested positive for gene fusions that activate RET, conducted by Naiyer Rizvi, a lung cancer specialist at Memorial Sloan Kettering Cancer CenterBioWorld Today | Friday, July 27, 2012 -
Bench Press: BioWorld Looks at Translational Medicine
Beta Blockers Can Prevent Metastases Stress reduction in cancer patients has the reputation of being a touchy-feely approach...The authors concluded that treating breast cancer patients with either beta blockers or RANKL inhibitors such as Xgeva or Prolia (both denosumab, Amgen Inc.) could "inhibit both the early colonization of bone by metastatic breast cancer cells and the initiation of the 'vicious cycle' of bone destruction induced by these cellsBioWorld Today | Monday, July 23, 2012 -
Genmab, J&J in $175M Per Product DuoBody Deal
The molecule, which gained European approval in 2009 for treating malignant ascites (abdominal fluid) in cancer patients, targets the T-cell antigen CD3 and epithelial cell adhesion molecule (EpCAM; CD326By Cormac Sheridan | BioWorld International | Wednesday, July 18, 2012 -
Genmab, J&J in $175M Per Product DuoBody Deal
The molecule, which gained European approval in 2009 for treating malignant ascites (abdominal fluid) in cancer patients, targets the T-cell antigen CD3 and Epithelial cell adhesion molecule (EpCAM; CD326By Cormac Sheridan | BioWorld Today | Monday, July 16, 2012 -
Other News To Note
Sanofi SA, of Paris, informed the European Medicines Agency that it is withdrawing its application for marketing authorization for Mulsevo (semuloparin sodium) to prevent venous thromboembolism in certain cancer patientsBioWorld International | Wednesday, July 11, 2012 -
Wilex Banks $17.5M Prometheus Payment for Rencarex Milestone
In a trial of HER2-negative breast cancer patients, the drug led to median progression-free survival (PFS) of 8.3 months when administered in combination with capecitabine, vs. 7.5 months for those on capecitabine alone...The company previously reported that in pancreatic cancer patients the drug improved median overall survival to 12.5 months when administered in combination with gemcitabine, vs. 9.9 months for those on gemcitabine onlyBy Cormac Sheridan | BioWorld International | Wednesday, July 11, 2012 -
Pharma: Other News To Note
Sanofi SA, of Paris, informed the European Medicines Agency that it is withdrawing its application for marketing authorization for Mulsevo (semuloparin sodium) to prevent venous thromboembolism in certain cancer patientsBioWorld Today | Tuesday, July 10, 2012 -
Wilex Banks $17.5M Prometheus Payment for Rencarex Milestone
In a trial of HER2-negative breast cancer patients, the drug led to median progression-free survival of 8.3 months when administered in combination with capecitabine, vs. 7.5 months for those on capecitabine alone...The company previously reported that in pancreatic cancer patients the drug improved median overall survival to 12.5 months when administered in combination with gemcitabine, vs. 9.9 months for those on gemcitabine onlyBy Cormac Sheridan | BioWorld Today | Tuesday, July 10, 2012 -
Audeo Files for $60M IPO for Late-Stage Cancer Products
Audeo found in a randomized Phase II trial of HA-Irinotecan (Camptosar, Pfizer Inc.) that progression-free survival was doubled in colon cancer patients receiving the HA-Irinotecan vs...The trial is being carried out at Monash Cancer Centre, Southern Health and Peninsula Oncology Centre in Melbourne, Australia and will enroll 40 first-line small-cell lung cancer patientsBy Catherine Shaffer | BioWorld Today | Tuesday, July 10, 2012 -
American Society of Clinical Oncology Annual Meeting June 1-5, 2012, in Chicago
cancer patients, and 89% of those with breast orBioWorld Insight | Monday, July 9, 2012
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