Search Results for: Clinical Roundup
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Clinic Roundup
The goal of the trial will be first to find optimum dosing of the drug, and second to assess safety, pharmacokinetics, pharmacodynamics and clinical activity in disease-specific cohorts of at least 12 patients eachBioWorld Today | Friday, February 1, 2013 -
Antibody Firm KaloBios Prices $70M IPO in Lukewarm Debut
30, will support clinical trials of KaloBios' Humaneered antibody pipeline, as well as general corporate purposes...Should Sanofi opt in for the CF program, the small biotech would retain co-promotion rights in the U.S. (See BioWorld Today, Jan. 12, 2010.) On its own, KaloBios has two other clinical-stage programs: KB003, a Humaneered recombinant anti-granulocyte macrophage colony-stimulating factor monoclonal antibody in Phase II testing is severe asthma patients inadequately controlled byBy Jennifer Boggs | BioWorld Today | Friday, February 1, 2013 -
Newlink Adds $42.5M in Public Offering for Immunotherapies
The company has an extensive pipeline of products in clinical development, including HyperAcute Pancreas (algenpantucel-L), HyperAcute Lung (tergenpumatucel-L), HyperAcute Melanoma, HyperAcute Renal and others...Total gross proceeds from the offering will be $38.2 million. (See BioWorld Today, Jan. 30, 2013.)By Catherine Shaffer | BioWorld Today | Thursday, January 31, 2013 -
Clinic Roundup
Medivir AB, of Stockholm, Sweden, said it entered a nonexclusive collaboration between Janssen Pharmaceuticals Inc., part of Johnson & Johnson, of New Brunswick, N.J., and Idenix Pharmaceuticals Inc., of Cambridge, Mass., for the clinical development of an all-oral (interferon-free) direct-acting antiviral (DAA) hepatitis C (HCV) combination therapy...Repros Therapeutics Inc., of The Woodlands, Texas, provided a revised date for expected clinical results from the first pivotal trial, ZA-301, ofBioWorld Today | Tuesday, January 29, 2013 -
Bone Therapeutics Gets $10M For Cell Therapy Development
Bone Therapeutics will also move an allogeneic version of the product into a clinical trial in patients with delayed union fractures later this year...If the clinical data are good, it will be able to marshal strong pharmacoeconomic arguments...KAHR will receive NIS4.95 million to assist in developing its SCP (signal converter proteins) platform technology that enables the creation of protein-based drugs with two active sites.By Cormac Sheridan | BioWorld Today | Tuesday, January 29, 2013 -
Clinic Roundup
Data were presented at the American Society of Clinical Oncology's Gastrointestinal Cancers Symposium in San FranciscoBioWorld Today | Monday, January 28, 2013 -
Anthera Approaches Phase III, Prices $40M Public Offering
Anthera's Phase IIb study, PEARL-SC, missed its primary efficacy endpoint of clinical improvement at 24 weeks in the Systemic Lupus Erythematosus Responder Index...The primary efficacy endpoint will be clinical improvement in the Systemic Lupus Erythematosus Responder Index (SRI-8...Net proceeds are expected to support general corporate purposes, including working capital, R&D, clinical trials and capital expendituresBy Catherine Shaffer | BioWorld Today | Monday, January 28, 2013 -
GAO: Agencies Earn Poor Grades in Transparency
Thus, "Clinical Pharmacogenomics: Premarket Evaluation in Early-Phase Clinical Studies and Recommendations for Labeling" is specifically for use in exploratory and observational studies that are intended to generate genomic hypotheses that will be tested in later confirmatory trials...identifying the basis for pharmacokinetic outliers and intersubject variability in clinical responseBy Mari Serebrov | BioWorld Today | Monday, January 28, 2013 -
Clinic Roundup
Sirtex Medical Ltd., of New South Wales, Australia, reported results from an analysis of 548 patients in a clinical study testing Selective Internal Radiation Therapy (SIRT) with SIR-Spheres microspheres in patients with metastatic colorectal cancer...Those data were presented at the American Society of Clinical Oncology's 2013 Gastrointestinal Cancers Symposium in San FranciscoBioWorld Today | Friday, January 25, 2013 -
Ariad Pads Cash with $300M For Iclusig Launch, Clinic Work
The infusion of an additional $300 million, however, will "go a long way for us to support the global launch of Iclusig," as well as advancing additional clinical programs, said Maria Cantor, Ariad's senior vice president of corporate affairs...A full readout from the pivotal PACE study was presented at the American Society of Clinical Oncology meeting in June, with data showing that 54 percent of chronic-phase CML patients showed a response, besting what had been reported previously in top-lineBy Jennifer Boggs | BioWorld Today | Friday, January 25, 2013 -
Clinic Roundup
Tasimelteon-treated patients maintained their clinical benefits while placebo-treated patients showed significant deterioration in measures of nighttime sleep, daytime naps and timing of sleepBioWorld Today | Thursday, January 24, 2013 -
House Vote Has Makers of MCMs Breathing a Little Easier
NIH Clinical Trial News...The trial will test multiple doses of cyclodextrin in nine patients to identify a safe dose for a Phase II multicenter trial.By Mari Serebrov | BioWorld Today | Thursday, January 24, 2013 -
Gene Signal Raises New Cash for Its Antisense Drug Trials
Gross proceeds totaled about $34.1 million and will be used for general corporate purposes, including clinical trial, preclinical and other R&D expenses, capital expenditures, working capital and general and administrative costs...Citigroup and Leerink Swann acted as joint book-running managers, while Baird acted as co-lead manager. (See BioWorld Today, Jan. 22, 2013.)By Cormac Sheridan | BioWorld Today | Thursday, January 24, 2013 -
Clinic Roundup
Ampio plans to start enrolling in a 450-patient clinical trial this quarter...Those data completed the pivotal pharmacokinetic and clinical program for BNX, which BDSI said will enable a new drug application submission in mid-2013...Sihuan Pharmaceutical Holdings Group Ltd., of Hong Kong, said it received approval for clinical studies from Chinese regulators to test Benapenem, a carbapenem drug in the class of broad-spectrum beta-lactam antibiotics, with a Phase I program set to start in the firstBioWorld Today | Wednesday, January 23, 2013 -
Back in 'Control': Tivo Data Explained; AVEO Bags $50M
Specifically, OS showed somewhat greater in the control arm than in the tivozanib arm. (See BioWorld Today, Jan. 4, 2012, and Aug. 6, 2012.) The OS glitch is "something that we have addressed with the FDA," Johnston said, and AVEO will be presenting more OS data at the American Society of Clinical Oncology's Genitourinary Cancers Symposium in Orlando, Fla., next month, along with some data from subpopulations...Clinical Cancer Research included a paper that suggested the compound, ENMD-2076, actsBy Randy Osborne | BioWorld Today | Friday, January 18, 2013 -
Clinic Roundup
Cytos Biotechnology Ltd., of Zurich, Switzerland, said a technical issue was identified with the rubber stoppers used to close the injection vials containing clinical trial material for its Phase IIb study testing lead candidate CYT003 in allergic asthma...Cytos will replace that material with new material available at clinical sites in the second quarterBioWorld Today | Thursday, January 17, 2013 -
Versartis' $25M Series C to Fund HGH Trial in Children
Versartis Inc., of Redwood City, Calif., closed a $25 million Series C financing round through Aisling Capital, Index Ventures, New Leaf Venture Partners and Advent Venture Partners to support clinical trials of VRS-317 for growth hormone deficiency in children...Proceeds will be used for general corporate purposes, ultimately focused on advancing the firm's clinical pipeline...Goldman, Sachs and Co., and J.P. Morgan Securities LLC are joint book-running managers for the offerings, which will be filedBy Catherine Shaffer | BioWorld Today | Wednesday, January 16, 2013 -
FDA Begins Blazing Narrow Trail for Approval Shortcut
The proposed trail is intended to cut through the undergrowth of current clinical trial requirements by allowing for smaller, more targeted studies that wouldn't take as long to complete...Clinical trials represent an aggregate expense of about $31.3 billion, or nearly 40 percent of the R&D budget of major drug developers – much of that due to systemic inefficiency, according to the report...It's hoped that the results will help guide decisions in the future on whether a drug warrants further clinicalBy Mari Serebrov | BioWorld Today | Tuesday, January 15, 2013 -
Aileron $12M Raise to Propel Stapled Peptide into Clinic
Together, the three collaborated in the seminal discovery of the first biologically active stapled peptide and translation into a potential clinical application...Proceeds from any offering are expected to support general corporate purposes, including to R&D costs, payment obligations and capital expenditures.By Marie Powers | BioWorld Today | Tuesday, January 15, 2013 -
Clinic Roundup
BioTime Inc., of Alameda, Calif., said it submitted a clinical investigation protocol to European regulatory authorities for approval to initiate studies for its Renevia stem cell delivery platformBioWorld Today | Friday, January 11, 2013
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