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Merus N.V.: Petosemtamab granted Breakthrough Therapy Designation by the U.S. FDA

Merus N.V.: Petosemtamab granted Breakthrough Therapy Designation by the U.S. FDA
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United Kingdom , Ashley Pereira , Drug Administration , Exchange Commission , Regulatory Affairs At Merus , Breakthrough Therapy Designation , Fast Track Designation , Biologics License Application , Regulatory Affairs , Rev Dis Primers , Private Securities Litigation Reform Act , Middle East , Quarterly Report , Chance Des ,

Immutep Announces Positive Preliminary Topline Results From TACTI-003 Cohort B

Immutep Announces Positive Preliminary Topline Results From TACTI-003 Cohort B
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United States , New South Wales , Chris Basta , Immutep Limited , Merck Sharp Dohme , Merck Co Inc , International Agency For Research On Cancer , Drug Administration , Corporate Communications , Media Release , Combined Positive Score , Merck Sharp , Overall Response Rate , Overall Survival , Progression Free Survival , Eftilagimod Alpha , Fast Track , United States Food , Lymphocyte Activation , Investor Relations , Cancer Observatory , International Agency , Death Dis , Rev Dis Primers ,

Mundipharma acquires all assets and rights related to REZZAYO® (rezafungin), reinforcing continued commitment to management of infectious diseases and specialty care therapeutic area

Mundipharma acquires all assets and rights related to REZZAYO® (rezafungin), reinforcing continued commitment to management of infectious diseases and specialty care therapeutic area
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United Kingdom , United States , Marc Princen , Asia Pacific , Antimicrob Chemother , Drug Administration , European Commission , Healthcare Products Regulatory Agency , European Medicines Agency , Napp Pharmaceutical Group , Vp Communications Corporate Affairs , Ministry Of Health , Chief Executive Officer , United Kingdom Medicines , Orphan Drug Designation , Napp Pharmaceutical Group Limited , Latin America , Rev Dis Primers , Englj Med , Database Syst Rev , Medicines Agency , Kingdom Medicines , Corporate Affairs ,

Mundipharma acquires all assets and rights related to REZZAYO (rezafungin), reinforcing continued commitment to management of infectious diseases and specialty care therapeutic area

Mundipharma acquires all assets and rights related to REZZAYO (rezafungin), reinforcing continued commitment to management of infectious diseases and specialty care therapeutic area
finanznachrichten.de - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from finanznachrichten.de Daily Mail and Mail on Sunday newspapers.

United Kingdom , United States , Asia Pacific , Antimicrob Chemother , Dennis Riedl , Marc Princen , Healthcare Products Regulatory Agency , European Medicines Agency , European Commission , Vp Communications Corporate Affairs , Napp Pharmaceutical Group , Drug Administration , Ministry Of Health , Chief Executive Officer , United Kingdom Medicines , Orphan Drug Designation , Napp Pharmaceutical Group Limited , Latin America , Rev Dis Primers , Englj Med , Database Syst Rev , Medicines Agency , Kingdom Medicines , Del Medico , Corporate Affairs , Aktien Sie ,

Mundipharma: Napp announces authorisation of REZZAYO (rezafungin) in Great Britain by the UK Medicines and Healthcare Products Regulatory Agency for the treatment of invasive candidiasis in adults1

Mundipharma: Napp announces authorisation of REZZAYO (rezafungin) in Great Britain by the UK Medicines and Healthcare Products Regulatory Agency for the treatment of invasive candidiasis in adults1
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United Kingdom , United States , Great Britain , Ben David , P Lewis White , Antimicrob Chemother , Stefan Klotter , Asia Pacific , Napp Pharmaceuticals , Mycology Reference Laboratory , Napp Pharmaceuticals Limited , Trademark Of Cidara Therapeutics Inc , Cardiff University Centre For Trials Research , Healthcare Products Regulatory Agency , Data Review Committee , Medical Media , Pharmaceuticals Limited , White Phd , Consultant Clinical Scientist , Reference Laboratory , Honorary Professor , Cardiff University Centre , Trials Research , Medical Director , Northern Europe , Orphan Drug Designation ,