Search Results for: Pharma: Clinical Roundup
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Clinic Roundup
Acasti Pharma Inc., of Laval, Quebec, a subsidiary of Neptune Technologies & Bioressources Inc., reported preliminary data from a randomized, open-label, dose-ranging, multicenter trial assessing the safety and efficacy of NKPL66, or CaPre, in mild-to-high hypertriglyceridemia...The NX03-0040 prostate cancer clinical study of 150 men is testing low (2.5 mg) and high (15 mg) single doses of NX-1207 for the effect to eradicate or shrink low-grade localized prostate cancer tumorsBioWorld Today | Wednesday, March 20, 2013 -
Clinic Roundup
Secondary objectives of the trial include clinical activity by serum TTR levels...For the Uceris 9-mg group, 17.4 percent of patients achieved clinical and endoscopic remission, compared to 4.5 percent of the placebo group (p = 0.0047...Virobay Inc., of Menlo Park, Calif., and Leo Pharma A/S, of Ballerup, Denmark, achieved a milestone in their collaboration on development of an oral therapy for psoriasis upon initiation of a Phase I trial of VBY-891 by VirobayBioWorld Today | Tuesday, March 19, 2013 -
Pharma: Clinic Roundup
The study design calls for the collection of 5,250 clinical endpoints, and Merck remains blinded to the actual results of the analysis and to other safety and efficacy dataBioWorld Today | Wednesday, March 13, 2013 -
Pharma: Clinic Roundup
Inc., of Whitehouse Station, N.J., said researchers from the Clinical Trial Service Unit at Oxford University presented results from the HPS2-THRIVE (Heart Protection Study 2-Treatment of HDL to Reduce the Incidence of Vascular Events) study of Tredaptive (extended-release niacin/laropiprant) during the late-breaking clinical trial session at the American College of Cardiology 62nd Annual Scientific Session in San Francisco...Findings were presented during the late-breaking clinical trial sessionBioWorld Today | Tuesday, March 12, 2013 -
Pharma: Clinic Roundup
Janssen and partner Bayer AG, of Leverkusen, Germany, will enroll patients into five global clinical trials, which will involve a total of 28,850 patientsBioWorld Today | Monday, March 11, 2013 -
Clinic Roundup
Zealand Pharma A/S, of Copenhagen, Denmark, disclosed in a pipeline update that it plans to advance danegaptide into a single site clinical efficacy study to further profile the peptide drug in cardio protectionBioWorld Today | Monday, March 11, 2013 -
Following Ravicti Win in UCD, Hyperion Seeks $59.7M for HE
The company plans to use proceeds from the offering to complete clinical development of Ravicti in hepatic encephalopathy (HE) and to fund post-approval studies in UCD...Hyperion gained rights to Ravicti from Ucyclyd Pharma Inc., a subsidiary of Scottsdale, Ariz.-based Medicis Pharmaceutical Corp...at the same unit price.By Marie Powers | BioWorld Today | Monday, March 11, 2013 -
Pharma: Clinic Roundup
Boehringer Ingelheim Pharmaceuticals Inc., of Ridgefield, Conn., part of Boehringer Ingelheim GmbH, reported the first interim results in HCV/HIV co-infected patients from the company's ongoing hepatitis C (HCV) clinical trial program, HCVerso...Polyphor Ltd., of Allschwil, Switzerland, completed a Phase I trial demonstrating the clinical safety and tolerability of its Pseudomonas-specific antibiotic POL7080...The study compared the efficacy and safety of once-weekly Milprosa to daily 8 percentBioWorld Today | Tuesday, March 5, 2013 -
Clinic Roundup
Targeted Medical Pharma Inc., of Los Angeles, said results from an open-label study of oral amino acid-based erythrocyte stimulating system (ESS) for the treatment of chronic anemia showed that hemoglobin increased an average of 11.39 percent from baseline measurement to 45 days...Vertex Pharmaceuticals Inc., of Cambridge, Mass., said VX-787 in a Phase II influenza challenge study resulted in statistically significant improvements in viral and clinical measurements of infection...Also, 93 percent ofBioWorld Today | Tuesday, March 5, 2013 -
Pharma: Clinic Roundup
The volasertib clinical development program is the company's most advanced in cell cycle inhibitionBioWorld Today | Friday, March 1, 2013 -
Financings Roundup
Dezima Pharma BV, of Naarden, the Netherlands, said it raised €14.2 million (US$18.6 million) for the clinical development of its cholesteryl ester transfer protein (CETP) inhibitor, DEZ-001 (previously TA-8995), and to develop additional earlier-stage dyslipidemia assets...It will use the proceeds to advance its opthalmic programs through clinical proof of conceptBioWorld Today | Friday, March 1, 2013 -
Clinic Roundup
Antisense Pharma GmbH, of Regensburg, Germany, revised its business objectives related to the advancement of its next-generation TGF-beta inhibitor oligonucleotide program...In conjunction with the changes in its clinical program, the company said it reduced its work force by 50 percent and outsourced noncritical research and development functions...Kiadis Pharma BV, of Amsterdam, the Netherlands, said it received a No Objection Letter from Canadian regulators to proceed with a Phase II study testingBioWorld Today | Wednesday, February 27, 2013 -
$7M Series B Puts Investor Skin in Game for Brickell
Competitors in atopic dermatitis include Anacor Pharmaceuticals Inc., Oculus Innovtive Sciences and LEO Pharma A/S...Atopic dermatitis was also part of a recent set of collaborations between LEO Pharma A/S and institutions in Australia, France, Germany and the U.S., including the International Institute of Dermatology and Allergy with Charité University of Medicine in Berlin...The company is planning to begin clinical studies in the first half of 2014By Catherine Shaffer | BioWorld Today | Wednesday, February 27, 2013 -
Pharma: Clinic Roundup
Sihuan Pharmaceutical Holdings Group Ltd., of Hong Kong, said pinoxacin hydrochloride received approval for clinical studies from the State Food and Drug AdministrationBioWorld Today | Monday, February 25, 2013 -
Clinic Roundup
Amicus Therapeutics Inc., of Cranbury, N.J., reported positive results from clinical and preclinical studies of the pharmacological chaperone AT2220 (duvoglustat HCl) in combination with ERT for Pompe disease at the Lysosomal Disease Network World Symposium...Based on those results, the company plans to initiate a repeat-dose clinical study in the third quarter of 2013 to evaluate an intravenous formulation of AT2220 co-administered with Myozyme/Lumizyme...BioAlliance Pharma SA, of Paris, said the FDABioWorld Today | Friday, February 15, 2013 -
Pharma: Clinic Roundup
The data, from the latest pre-specified interim analysis of the study, were presented at the annual American Society of Clinical Oncology Genitourinary Cancers Symposium in Orlando, FlaBioWorld Today | Thursday, February 14, 2013 -
Clinic Roundup
Two posters feature clinical data of PROSTVAC evaluated as monotherapy or in combination with a radiopharmaceutical...The preliminary results from the studies supported the further clinical investigation in patients suffering from advanced prostate cancer, the company said...BHR Pharma LLC, of Herndon, Va., said the European Medicines Agency (EMA) granted an orphan medicinal product designation for treating moderate and severe traumatic brain injury (TBI) to its intravenous progesterone infusion agentBioWorld Today | Thursday, February 14, 2013 -
e-Therapeutics Raises $63M to Fund Solid Tumor Drug
As this money is dispensed through its clinical development programs, the company expects to receive £12 million in government R&D tax credits, bringing the total pot to £60 million...Pharma doesn't want more questions than answers, so you can't do development on a shoestring or cut corners...The total amount raised in the private placement is $7.9 million.By Nuala Moran | BioWorld Today | Tuesday, February 12, 2013 -
Clinic Roundup
Acceleron Pharma Inc., of Cambridge, Mass., said it started a Phase II study testing dalantercept (ACE-041), an angiogenesis inhibitor designed to target the activin receptor-like kinase pathway, in combination with Inlyta (axitinib, Pfizer Inc.), a vascular endothelial growth factor receptor tyrosine kinase inhibitor, in patients with metastatic renal cell carcinoma...Portola Pharmaceuticals Inc., of South San Francisco, inked a clinical collaboration with Janssen Pharmaceuticals Inc., a unit ofBioWorld Today | Wednesday, February 6, 2013 -
Clinic Roundup
Cerulean Pharma Inc., of Cambridge, Mass., said the first patient was dosed in a Phase II study of CRLX101, a nanopharmaceutical designed to inhibit both topoisomerase 1 and hypoxia-inducible factor-1 alpha, in extensive-stage small-cell lung cancer sensitive to first-line platinum-based chemotherapy...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 leastBioWorld Today | Friday, February 1, 2013
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