Search Results for:
-
Gilead Data Suggest Targeted Cancer Drugs Coming of Age
Gilead Science Inc.'s oral targeted cancer drug, idelalisib (GS-1101), made a splash last week when the American Society of Clinical Oncology (ASCO) unveiled thousands of abstracts scheduled for presentation at next week's annual meeting in Chicago...As a cancer drug, ABT-199 interferes with anti-apoptotic proteins but – unlike precursor navitoclax – not platelet functionBy Marie Powers | BioWorld Insight | Monday, May 20, 2013 -
MedImmune: Phase III Begins, IMTC Poised as Cancer Key
MP looked promising in Phase I, with a manageable safety profile, which led London-based AstraZeneca to make the compound one of three cancer drugs moving into Phase III trials soonBy Randy Osborne | BioWorld Today | Friday, May 17, 2013 -
Tokai Adds $35.5M in Series E, Preps for Phase III CRPC Trials
Development of Tokai Pharmaceuticals Inc.'s triple-acting prostate cancer drug galeterone got a $35.5 million boost, with the Cambridge, Mass.-based biotech closing a Series E round with current investors Apple Tree Partners and Novartis Venture Funds, as well as undisclosed angel investors...ARMOR2, the second study in Tokai's ARMOR (Androgen Receptor Modulation Optimized for Response) program, is testing a new oral formulation of galeterone in CRPC patients, including those with either metastaticBy Jennifer Boggs | BioWorld Today | Thursday, May 16, 2013 -
Astellas Axes OSI, Perseid Units, Cuts Jobs in Japan
Inc., of Whitehouse Station, N.J. (See BioWorld Today, Feb. 3, 2012.) In all, pharmaceutical companies collectively jettisoned 150,000 jobs worldwide over the past three years, according to a report earlier this year by PwC's Health Research Institute. (See BioWorld Today, Feb. 8, 2013.) Founded in 1983 as Oncogene Science Inc., OSI developed cancer drug Tarceva (erlotinib) in partnership with Genentech Inc., now a unit of Roche AG, of Basel, SwitzerlandBy Marie Powers | BioWorld Today | Wednesday, May 15, 2013 -
Diagnostics Rapidly Evolving, Ideal Companions in Drug R&D
In its pipeline is cancer drug EC145 (vintafolide), which delivers a potent vinca chemotherapy directly to cancer cells by targeting the folate receptor expressed on cancer cells, but not on most normal cellsBy Peter Winter | BioWorld Insight | Monday, May 13, 2013 -
Array Expanding Capabilities, Runs First Phase III Trial
That experience should help Array as it develops its own cancer drugsBy Brian Orelli | BioWorld Insight | Monday, May 13, 2013 -
Word on the Street
Patients don't benefit from this type of approach." – Carlo Toniatti, head of research at the Institute for Applied Cancer Science and the Center for Co-Clinical Trials at the University of Texas MD Anderson Cancer Center, discussing improved clinical success rates for cancer drugs identified by the Tufts Center for the Study of Drug Development "It's been a long time since we did a public financing – 12 or 13 years – and we've managed through by being cautious in how we spend our cash and byBioWorld Insight | Monday, May 13, 2013 -
Bench Press: BioWorld Looks at Translational Medicine
The findings appeared in the May 8, 2013, issue of Cell Metabolism. (See BioWorld Today, March 27, 2013.) Cancer Drug Fights Neurodegeneration Very low doses of chronic myelogenous leukemia (CML) drug Tasigna (nilotinib, Novartis AG) may be a way to treat neurodegenerative disorders that are characterized by toxic protein accumulations, scientists from Georgetown University have discoveredBioWorld Today | Monday, May 13, 2013 -
Extending the Runway: $54M Cash Infusion for Symphogen
Tolcher has been involved in running Phase I studies for a number of marketed cancer drugs, including the recently approved antibody-drug conjugate Kadcyla (trastuzumab emtansine, Roche AG), and Drejer said his appointment "brings a wealth of cancer knowledge to the company."By Nuala Moran | BioWorld International | Wednesday, May 8, 2013 -
Earnings Roundup
Ariad Pharmaceuticals Inc., of Cambridge, Mass., reported its first revenue from cancer drug Iclusig (ponatinib), which was approved in December for use in adults with chronic myelogenous leukemia or Philadelphia chromosome-positive acute lymphoblastic leukemia that is resistant or intolerant to prior tyrosine kinase inhibitor therapyBioWorld Today | Wednesday, May 8, 2013 -
Tufts Study: More Cancer Drugs Succeeding in the Clinic
Success rates doubled for cancer drugs that entered clinical trials in the early 1990s and those that entered the clinic a decade later, even as the number of such compounds increased by 50 percent over the period, according to a new analysis by the Tufts Center for the Study of Drug Development (CSDD...However, cancer drugs that filed for regulatory approval mostly succeeded, with 92 percent that submitted a new drug application or biologics license application gaining the FDA's endorsementBy Marie Powers | BioWorld Today | Wednesday, May 8, 2013 -
Changing Face of Partnering in a Milieu of Risk Sharing
with its cancer drug EC145 (vintafolide) attracting a potential $1 billion based on the achievement of development, regulatory and commercialization goals for EC145 in six cancer indications. (See BioWorld Today, April 17, 2012.) The upfront $120 million was notable because it represented one of the largest upfront payments to a U.S biotechnology company in 2012, bucking a trend that had seen these payments decline in value during the past five yearsBio Perspectives | Tuesday, May 7, 2013 -
Other News To Note
BIO said it shares many of the USTR's concerns over the decision by India's Supreme Court to deny patent protection for for the cancer drug Gleevec/Glivec, developed by Novartis AG, of Basel, Switzerland, on the grounds that the compound did not demonstrate "enhanced efficacyBioWorld Today | Monday, May 6, 2013 -
Changing Face of Partnering in a Milieu of Risk Sharing
with its cancer drug EC145 (vintafolide) attracting a potential $1 billion based on the achievement of development, regulatory and commercialization goals for EC145 in six cancer indications. (See BioWorld Today, April 17, 2012.) The upfront $120 million was notable because it represented one of the largest upfront payments to a U.S biotechnology company in 2012, bucking a trend that had seen these payments decline in value during the past five yearsBy Peter Winter | BioWorld Insight | Monday, May 6, 2013 -
Arena Yanks MAA, Falls on Belviq Launch Delay in U.S.
Allergan licensed rights to the Darpin technology from Molecular Partners AG for development in AMD and other eye diseases. (See BioWorld Today, Aug. 22, 2012.) And Eylea has fared well so far against Roche AG's Lucentis (ranibizumab), due to its lower cost and a label that calls for less frequent dosing, and even to cancer drug Avastin (bevacizumab), a cheaper, off-label alternativeBy Jennifer Boggs | BioWorld Today | Monday, May 6, 2013 -
ODAC Takes AVEO to Task over Single Phase III Trial
AVEO's confidence in the drug was shared by RBC Capital Markets analyst Adnan Butt, who said he believes tivozanib "could be a differentiated agent that could demonstrate better efficacy than existing kidney cancer drugs...patients, due to differences in standard of care and access to other cancer drugsBy Mari Serebrov | BioWorld Today | Friday, May 3, 2013 -
Capital Royalty's $805M Fund: Sifting Through Surplus of Deals
Cancer is 50 percent of the market, and so you have to always be looking at cancer drugs," Düster said...One of our earlier investments, which is undisclosed, is in a leading cancer drug, so it's an area of expertise for us and an area of interest to usBy Randy Osborne | BioWorld Today | Friday, May 3, 2013 -
Extending the Runway: $54M Cash Infusion for Symphogen
Tolcher has been involved in running Phase I studies for a number of marketed cancer drugs, including the recently approved antibody-drug conjugate Kadcyla (trastuzumab emtansine, Roche AG), and Drejer said his appointment "brings a wealth of cancer knowledge to the companyBy Nuala Moran | BioWorld Today | Friday, May 3, 2013 -
Oncology Dominates Biotech Deals in 2012; Changes Loom
Cancer drug pricing seems to follow a fairly basic formula, however, with new drugs being priced about 10 percent to 20 percent higher than the most recent similar drug on the market...Although much of the discussion is happening outside the U.S., it's not unreasonable to assume that pushback on cancer drug pricing will gain momentum within the U.SBy Catherine Shaffer | BioWorld Today | Wednesday, May 1, 2013 -
Bench Press: BioWorld Looks at Translational Medicine
Inhibiting nucleolin in cells that are resistant to the breast cancer drug Faslodex (fulvestrant, AstraZeneca plc) restored sensitivity to the drug both in cell culture and in animal studiesBioWorld Today | Monday, April 29, 2013
Category
Current Filters
- xcancer drug
Related Keywords
Categories
- x BioWorld Today (2134)
- x BioWorld Insight (436)
- x BioWorld International (296)
- x Bio Perspectives (82)
- x State of the Industry Report (78)
- x BioWorld Snapshots (28)
- x BioWorld Genomics Review (13)
- x Top 25 Drug Report (12)
- x Biotech Innovations (4)
- x Market-Leading Biotech Drugs (3)
- x BioWorld Phase III Report (1)
- x RNAi Report (1)
BioWorld | 3525 Piedmont Road
Building 6, Suite 400 | Atlanta, Georgia 30305, USA
Building 6, Suite 400 | Atlanta, Georgia 30305, USA
Part of Thompson Media Group LLC
Free Ezine
Sign up for Perspectives FREE e-mail newsletter.
Customer Service: In the U.S. and Canada: 1-800-477-6307
Outside the U.S.: 1-404-262-5476
customerservice@bioworld.com
Hours: Monday - Thursday, 8:30 am - 6:00 pm EST
Friday, 8:30am - 4:30 pm EST
Outside the U.S.: 1-404-262-5476
customerservice@bioworld.com
Hours: Monday - Thursday, 8:30 am - 6:00 pm EST
Friday, 8:30am - 4:30 pm EST
Copyright @ 2013 AHC Media. Reproduction, reposting content is strictly prohibited.