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Synairgen plc: Synairgen announces commencement of dosing in its international Phase III study of inhaled interferon beta in hospitalised COVID-19 patients


Synairgen plc: Synairgen announces commencement of dosing in its international Phase III study of inhaled interferon beta in hospitalised COVID-19 patients
( Synairgen or the Company )
Synairgen announces commencement of dosing in its international Phase III study of inhaled interferon beta in hospitalised COVID-19 patients
Southampton, UK - 13 January 2021: Synairgen plc (LSE: SNG), the respiratory drug discovery and development company, today announces that the first patient has been dosed in the UK as part of its global Phase III trial (SG018) evaluating Synairgen s inhaled formulation of interferon beta-1a (SNG001), for the treatment of hospitalised COVID-19 patients.
As previously announced, Synairgen has appointed Parexel Biotech, a division of the leading global clinical research organisation, Parexel, to help conduct the Phase III trial and several UK sites have now been initiated, with further sites in the US and the EU expected to follow. The trial is ....

United Kingdom , Olivia Manser , Carina Jurs , Geoff Nash , Richard Marsden , John Ward , Donna Davies , Duncan Monteith , James Black , Mary Jane Elliott , Ratko Djukanovic , Kate Bannatyne , Freddie Barnfield , Numis Securities Limited Joint Broker , United Kingdom National Institute For Health Research , University Of Southampton Professors Sir Stephen Holgate , Urgent Public Health , Drug Administration , Consilium Strategic Communications Financial Media , Parexel Biotech , National Institute , Health Research , Fast Track , Market Abuse Regulation , Chief Executive , Charlie Beeson ,

Blue Earth Diagnostics Announces Dosing of Initial Patient in Phase 3 REVELATE Clinical Trial of 18F-Fluciclovine PET Imaging for Detection of Recurrent Brain Metastases


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- Clinical utility of Axumin (fluciclovine F 18) being investigated in expanded areas of cancer imaging -
Blue Earth Diagnostics, a Bracco company and recognized leader in the development and commercialization of innovative PET radiopharmaceuticals, today announced that the first patient has been dosed in its Phase 3 REVELATE clinical trial of
18F-fluciclovine, a positron emission tomography (PET) imaging radiopharmaceutical being studied for potential use in detecting recurrent brain metastases. The REVELATE study is a Phase 3, multi-center, single-arm imaging study being conducted in the United States. Its purpose is to assess the diagnostic performance of
18F-fluciclovine PET in detecting recurrent brain metastases in patients previously treated with radiation therapy. The first patient dosed in the study was at Yale University, New Haven, Conn., under the auspices of Dr. Mariam Aboian, Assistant Professor of Radiology. ....

United States , United Kingdom , Samuelt Chao , Mariam Aboian , Peter Gardiner , Priscilla Harlan , Jonathan Allis , Kostenloser Wertpapierhandel , Clare Gidley , Mike Beyer , Yale University , Emory University , Drug Administration , Emory University Department Of Radiology , Sam Brown Inc , Bracco Group , Nuclear Medicine , Corporate Communications , European Union , Imaging Sciences , Department Of Radiation Oncology , Ge Healthcare , Earth Diagnostics , New Haven , Assistant Professor , Blue Earth Diagnostics ,