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ASCO Abstracts Shine Light on Cancer Immunotherapy
Nivolumab Wows as Companion to Yervoy Jedd Wolchok, medical oncologist at the Memorial Sloan-Kettering Cancer Center and the study lead on clinical trials that led to the approval of Yervoy (ipilimumab, Bristol-Myers Squibb Co.), provided the overview of a second ASCO abstract focusing on cancer immunotherapy, sponsored by BMS...Wolchok and colleagues studied the clinical activity and safety of nivolumab, an anti-PD-1 currently in clinical trials, in combination with the anti-CTLA-4 ipilimumab, inBy Marie Powers | BioWorld Today | Thursday, May 16, 2013 -
Tokai Adds $35.5M in Series E, Preps for Phase III CRPC Trials
Proceeds will be used to fund ongoing and new clinical trials and development and commercialization efforts for pimavanserin, as well as activities for other product candidates and for general corporate purposes...Gross proceeds totaled about $35 million, with net proceeds of $32.8 million to fund SFP clinical trials and for other general corporate purposesBy Jennifer Boggs | BioWorld Today | Thursday, May 16, 2013 -
Committee Looks for the Bright Line in Compounding
There may be value in discussing the benefit-risk framework at end-of-Phase II meetings, in order to ensure alignment on identified and potential risks and benefits, critical efficacy and safety assessments, and risk mitigation strategies in Phase III clinical trials," PhRMA notedBio Perspectives | Wednesday, May 15, 2013 -
Washington Roundup
With an eye on streamlining the review of clinical trials with low biosafety risks, the National Institutes of Health's Office of Biotechnology Activities is proposing a revision to its guidelines for research involving recombinant or synthetic nucleic acid moleculesBioWorld Today | Wednesday, May 15, 2013 -
Financings Roundup
Funds will be used for general corporate purposes, including expenses related to the potential commercialization of OMS302 for intraocular lens replacement, as well as for R&D expenses such as funding planned clinical trials for its OMS103HP, PDE10, MASP-2 and PDE7 programsBioWorld Today | Wednesday, May 15, 2013 -
Clinic Roundup
Mirna Therapeutics Inc., of Austin, Texas, has initiated a Phase I study of MRX34, the first miRNA to advance to a clinical trial for cancerBioWorld Today | Tuesday, May 14, 2013 -
Phase II Clinical Trials Update: April 2013
Company (Location) Product Description Indication Status Date AUTOIMMUNE Biogen Idec Inc. (Weston, Mass.) DAC HYP A daclizumab high-yield process Multiple sclerosis Phase IIb data showed it reduced the annualized relapsed rate by 54%, meeting the study's primary endpoint 4/5/13 Fibrocell Science Inc. (Exton, Pa.) LaViv Autologous fibroblast injection azficel-T Moderate-to-severe acne scars Phase II study demonstrated that azficel-T treatment was associated with clinically meaningful improvementBioWorld Insight | Monday, May 13, 2013 -
Diagnostics Rapidly Evolving, Ideal Companions in Drug R&D
Moving Quickly While most drugs languish in clinical trials for upwards of a decade, Zelboraf and Xalkori were able to move quickly, largely due to the fact that both were paired with companion diagnostics very early in their clinical development, allowing them to find the right patient population, establish efficacy and present a convincing case to regulators. (See BioWorld Insight, Sept. 6, 2011.) "Early development of these tests also potentially enables clinical trials to be smaller and moreBy Peter Winter | BioWorld Insight | Monday, May 13, 2013 -
Phase I Clinical Trials Update: April 2013
Company (Location) Product Description Indication Status Date AUTOIMMUNE Acorda Therapeutics Inc. (Ardsley, N.Y.) rHIgM22 A remyelinating antibody Multiple sclerosis Enrollment began in the first trial 4/24/13 Arena Pharmaceuticals Inc. (San Diego) APD334 An oral drug targeting the sphingosine 1-phosphate subtype 1 receptor Autoimmune diseases Initiated dosing in a Phase I trial 4/8/13 Idera Pharmaceuticals Inc. (Cambridge, Mass.) IMO-8400 An agonist of Toll-like receptors 7, 8 and 9 PsoriasisBioWorld Insight | Monday, May 13, 2013 -
Short-lived Stem Cells Fight Brain Tumors, for a Time
The first such cells are now in clinical trials, and corresponding author Aboody and her colleagues published preclinical studies that formed a key part of the investigational new drug (IND) application for them in the May 9, 2013, issue of Science Translational Medicine...In a clinical trial approved partly on the basis of the data now published in Science Translational Medicine, 15 patients with recurrent gliomas have now been treated with single injections of low doses of neural stem cellsBy Anette Breindl | BioWorld Today | Monday, May 13, 2013 -
Phase III Clinical Trials Update: April 2013
Company (Location) Product Description Indication Status Date AUTOIMMUNE Rigel Pharmaceuticals Inc. (South San Francisco) and AstraZeneca plc (London) Fostamatinib Oral spleen tyrosine kinase inhibitor Rheumatoid arthritis Missed the X-ray endpoint of modified Total Sharp score, but hit statistical significance in ACR20 scoring, although the Phase III still fell short of those achieved by Pfizer Inc.'s approved Xeljanz 4/8/13 CANCER Array BioPharma Inc. (Boulder, Colo.) ARRY-520 A selective KSPBioWorld Insight | Monday, May 13, 2013 -
Array Expanding Capabilities, Runs First Phase III Trial
The agreement is that Array will be entitled to run a clinical trial with 162...Running the MILO trial could benefit Array financially because some overhead will be included in the clinical trial costs, but that isn't the main impetus for facilitating the trialBy Brian Orelli | BioWorld Insight | Monday, May 13, 2013 -
Non-U.S. Clinical Trials & Regulatory Actions: April 2013
Company (Location) Product Description Indication Status Date AUTOIMMUNE Genzyme Corp. (Cambridge, Mass.) Aubagio Teriflunomide; once-daily Multiple sclerosis Was approved in Argentina in a 14 mg formulation for patients with relapsing forms 4/9/13 CANCER Celgene Corp. (Summit, N.J.) Revlimid Lenalidomide Transfusion-dependent anemia CHMP adopted a positive opinion for Revlimid 4/29/13 Curis Inc. (Lexington, Mass.) Erivedge Vismodegib Symptomatic metastatic basal cell carcinoma CHMP recommendedBioWorld 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 -
Financings Roundup
Net proceeds are expected to total about $16.1 million and will be used for general corporate purposes, including expenses related to the potential commercialization of OMS302 for intraocular lens replacement, as well as for R&D expenses such as clinical trials of its OMS103HP, PDE10, MASP-2 and PDE7 programsBioWorld Today | Monday, May 13, 2013 -
Committee Looks for the Bright Line in Compounding
There may be value in discussing the benefit-risk framework at end-of-Phase II meetings, in order to ensure alignment on identified and potential risks and benefits, critical efficacy and safety assessments, and risk mitigation strategies in Phase III clinical trials," PhRMA notedBy Mari Serebrov | BioWorld Today | Friday, May 10, 2013 -
Alexza Banking $40M Up Front in U.S. Adasuve Deal with Teva
The biotech also will earn revenue for supplying the drug to Teva for sale and for clinical trialsBy Jennifer Boggs | BioWorld Today | Thursday, May 9, 2013 -
Lumena Large: $23M Series A Funds Phase II Cholestatic Bid
The drug has gone through 12 clinical trials in more than 1,400 subjects already, showing that it knocks down serum bile acid levels safelyBy Randy Osborne | BioWorld Today | Thursday, May 9, 2013 -
Increased Demand for Pediatric Trials Leads to BIO Initiative
Eventually, it could be used to find research centers, staffing talent and other resources needed to conduct a pediatric clinical trial in a specific region...To get FDA authorization to charge for an investigative drug or for an unapproved use of an approved drug in a clinical trial, a sponsor must demonstrate that the drug has a potential clinical benefit that would be a significant advantage over available therapiesBy Mari Serebrov | BioWorld Today | Thursday, May 9, 2013 -
Galapagos Lands $71M from Stoked U.S. Investors
The first clinical trials of the drug, GLPG1790, are expected to start within the next year.By Nuala Moran | BioWorld International | Wednesday, May 8, 2013
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