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Tag Archives: Clinical Trials

GlycoMimetics’ GMI-1271 Receives EU Orphan Drug Designation for Acute Myeloid Leukemia

Thursday, May 25th 2017 at 1:25pm UTC ROCKVILLE, Md.–(BUSINESS WIRE)– GlycoMimetics, Inc. (NASDAQ: GLYC) today announced that the European Commission, based on a favorable recommendation from the European Medicines Agency (EMA) Committee for Orphan Medicinal Products, has granted orphan designation for the company’s drug candidate GMI-1271 for the treatment of …

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Neural Analytics Announces Data that Demonstrates its Portable Transcranial Doppler Technology Can Assess Early Strokes With More than 95 Percent Accuracy

Wednesday, May 24th 2017 at 3:30pm UTC Data Presented at 26th European Stroke Conference LOS ANGELES–(BUSINESS WIRE)– Neural Analytics Inc., a medical device company developing and commercializing technology to measure, diagnose and track brain health, today announced initial results of the EXPEDITE clinical study showing its Transcranial Doppler Technology Platform …

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Origenis Announces Patent Grants for Lead Small Molecule LRRK2 Inhibitors for Treatment of Neurodegenerative and Inflammatory Diseases

Tuesday, May 23rd 2017 at 12:30pm UTC Strengthens IP position in the US, complements grants in other key markets and protects further development of small molecule drugs capable of penetrating the blood-brain barrier MARTINSRIED, Germany–(BUSINESS WIRE)– Origenis GmbH, a privately held biopharmaceutical company developing novel therapeutics to fight neurodegenerative and …

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Debiopharm International SA Enters the Field of Antibody-Drug Conjugates Through Acquisition of Phase II Asset from ImmunoGen

Tuesday, May 23rd 2017 at 8:01pm UTC Transaction adds innovative clinical-stage program to expanding Debiopharm portfolio and broadens its clinical development expertise Divestiture aligns with ImmunoGen’s focus on strategic growth initiatives and generates near-term value LAUSANNE, Switzerland & WALTHAM, Mass.–(BUSINESS WIRE)– Debiopharm International SA (Debiopharm –, part of Debiopharm Group™, a Switzerland-based …

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Octapharma réaffirme son engagement fort envers les patients atteints d’hémophile A avec la publication de nouvelles données cliniques sur la prophylaxie personnalisée avec nuwiq® basée sur l’analyse PK, suivant l’approche NuPreviq

Wednesday, May 24th 2017 at 1:30pm UTC LACHEN, Suisse–(BUSINESS WIRE)– Octapharma annonce de nouvelles données cliniques positives chez 66 patients préalablement traités (PPT) pour hémophilie A sévère (HA) ayant bénéficié d’une prophylaxie personnalisée basée sur une analyse pharmacinetique (PK) avec Nuwiq®, suivant l’approche NuPreviq. Les données de l’étude NuPreviq (GENA-21, …

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Clinical Ink and endpoint Announce Industry-First Alliance

Tuesday, May 23rd 2017 at 12:00pm UTC eSource and IRT Integration Simplifies the Site Experience SAN FRANCISCO & PHILADELPHIA–(BUSINESS WIRE)– endpoint Clinical, the leading global interactive response technology (IRT®) company, and Clinical Ink, the pioneering provider of eSource and patient engagement technologies, have teamed up to integrate IRT and eSource …

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PureTech Health to Present at Jefferies 2017 Global Healthcare Conference

Thursday, May 25th 2017 at 6:00am UTC BOSTON–(BUSINESS WIRE)– PureTech Health plc (« PureTech », LSE: PRTC), an advanced, clinical-stage biopharmaceutical company, today announced that Bharatt Chowrira, President and Chief of Business and Strategy at PureTech Health, will present at the Jefferies 2017 Global Healthcare Conference in New York City on Thursday, …

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Sunovion Announces Utibron™ Neohaler® (indacaterol/glycopyrrolate) Inhalation Powder Data Showing Lung Function and Health-Related Quality of Life Improvement in Patients with Moderate-to-Severe Chronic Obstructive Pulmonary Disease

Tuesday, May 23rd 2017 at 1:18pm UTC – Presentations at the American Thoracic Society 2017 International Conference (ATS 2017) also included long-term safety data and pooled analyses of pivotal studies – MARLBOROUGH, Mass.–(BUSINESS WIRE)– Sunovion Pharmaceuticals Inc. (Sunovion) announced that multiple data analyses from two Phase 3 studies demonstrating that …

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FDA Approves Merck’s KEYTRUDA® (pembrolizumab) for Adult and Pediatric Patients with Unresectable or Metastatic, Microsatellite Instability-High (MSI-H) or Mismatch Repair Deficient Cancer

Tuesday, May 23rd 2017 at 8:34pm UTC KEYTRUDA Now Approved for Patients with MSI-H or Mismatch Repair Deficient Solid Tumors That Have Progressed Following Prior Treatment and Who Have No Satisfactory Alternative Treatment Options, Which Includes MSI-H or Mismatch Repair Deficient Colorectal Cancer That Has Progressed Following Treatment with a …

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