Healthcare in 2022: what you need to know
With the Covid-19 pandemic sending shockwaves in the hospital sector, healthcare providers will continue looking for ways to slowly rebuild …
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Lilly reports Phase III BRUIN CLL-322 trial results for Jaypirca combo
Eli Lilly and Company has reported results from the BRUIN CLL-322 Phase III trial, assessing Jaypirca (pirtobrutinib), a non-covalent bruton …
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FDA clears MSD’s Keytruda combo plus Welireg for ccRCC treatment
Merck & Co (MSD) has received approval from the US Food and Drug Administration (FDA) for both Keytruda (pembrolizumab) and …
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Fleming Initiative and Cepheid begin TRACE-CPE study on rapid CPE testing
The Fleming Initiative, a partnership between Imperial College London and Imperial College Healthcare National Health Service (NHS) Trust, and Cepheid, …
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First patient treated in Airiver Medical’s RESTORE-2 trial for CRS
Airiver Medical has treated the first patient in its RESTORE-2 pivotal clinical trial assessing the ESSpand Sinus drug-coated balloon (DCB) …
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Novo Nordisk identifies unauthorised data access from trials
Novo Nordisk has identified that certain patient information from some of its clinical trials was accessed and copied externally in …
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Healthcare in 2022: what you need to know
With the Covid-19 pandemic sending shockwaves in the hospital sector, healthcare providers will continue looking for ways to slowly rebuild …
-
Fleming Initiative and Cepheid begin TRACE-CPE study on rapid CPE testing
The Fleming Initiative, a partnership between Imperial College London and Imperial College Healthcare National Health Service (NHS) Trust, and Cepheid, …
-
First patient treated in Airiver Medical’s RESTORE-2 trial for CRS
Airiver Medical has treated the first patient in its RESTORE-2 pivotal clinical trial assessing the ESSpand Sinus drug-coated balloon (DCB) …
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Novo Nordisk identifies unauthorised data access from trials
Novo Nordisk has identified that certain patient information from some of its clinical trials was accessed and copied externally in …
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FDA grants priority review for Roche’s Tecentriq combo sBLA
Roche has received the US Food and Drug Administration (FDA) priority review for its supplemental biologics licence application (sBLA) for …
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Sibel Health’s ANNE One platform secures EU MDR CE mark
Sibel Health has received CE mark certification under the EU Medical Device Regulation (EU MDR 2017/745) for its ANNE One …
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CONNECTA Therapeutics begins Phase IIa trial of CTH120 for FXS
CONNECTA Therapeutics has commenced a Phase IIa trial to assess its lead programme, CTH120, a neuroplasticity modulator, in male adults …
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EMA validates Bayer’s asundexian application for ischaemic stroke
The European Medicines Agency (EMA) has validated Bayer's marketing authorisation application for asundexian, an oral Factor XIa inhibitor, to prevent …
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MHRA to roll out new AI sandbox for medicines development
The UK’s Medicines and Healthcare products Regulatory Agency (MHRA) has announced plans to launch a new AI sandbox to expedite …
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Windward Bio doses first patients in Phase II SIRIUS COPD trial
Harbour BioMed’s partner Windward Bio has dosed the first patients in the Phase II SIRIUS trial with HBM9378/WIN378 (SKB378), a fully …
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Gore secures CE Mark for venous stent to treat inferior vena cava
W L Gore & Associates Medical Products (Gore) has secured CE Mark approval under the EU's Medical Device Regulation (MDR) for …
