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European Commission Approves KIMMTRAK® (tebentafusp) for

PRESS RELEASE European Commission Approves KIMMTRAK® (tebentafusp) for the treatment of unresectable or metastatic uveal melanoma KIMMTRAK is the first.

United statesUnited kingdomWestern australiaSophie piperno neumannJessica hasselImmunocore immBahija jallalDebra nielsenClayton robertsonExchange commission onInstitute curie asEuropean unionCommittee for medicinal products human useHead of communicationsEuropean commission approvesDrug administration

Mundipharma and Cidara Therapeutics, Inc : Rezafungin Awarded Promising Innovation Medicine (PIM) Designation by the UK s Medicines and Healthcare Products Regulatory Agency (MHRA) for the Treatment of Invasive Candidiasis

For Trade and Medical Media Only Rezafungin is a next-generation once-weekly echinocandin being developed for both the treatment and prevention of serious fungal infections, such as invasive candidiasis

United statesSan diegoUnited kingdomTaylor sandisonPatrick burseyBrian sheehanJan milton edwardsAsia pacificBrian ritchieCommunity registerCidara therapeutics incEuropean commissionDrug administrationExchange commissionUs food drug administrationLifesci communications

Immunocore receives positive CHMP opinion for KIMMTRAK® (tebentafusp) for the treatment of unresectable or metastatic uveal melanoma

PRESS RELEASE Immunocore receives positive CHMP opinion for KIMMTRAK® for the treatment of unresectable or metastatic uveal melanoma If approved by the European Medicines Agency, KIMMTRAK will. | February 25, 2022

United kingdomUnited statesWestern australiaImmunocore immBahija jallalDebra nielsenClayton robertsonPaul nathanChris welshJessica hodgsonMary jane elliottHead of communicationsEuropean commissionMedicines agencyDrug administrationEuropean organisation for research

In review: the life sciences regulatory regime in United Kingdom

This article reviews the essential regulatory considerations surrounding medicines and medical devices in United Kingdom, including clinical trials and marketing authorisations.

United kingdomNorthern irelandGreat britainAssociation of the british pharmaceutical industryUn convention on psychotropic substancesOrganisation for economicUn single convention on narcotic drugsEuropean commissionPrescription medicines code of practice authorityAssociation of british healthcare industriesEuropean federation of pharmaceutical industriesNational health serviceHome officeProperty officeEnforcement divisionEuropean union

Global Blood Therapeutics : GBT Reports Fourth Quarter and Full Year 2021 Financial Results - Form 8-K

GBT Reports Fourth Quarter and Full Year 2021 Financial Results Achieved Oxbryta® net revenues of $56.1 million in the fourth quarter and $194.7 million for full year 2021,. | February 23, 2022

United statesMinistry of healthUnited arab emiratesUnited kingdomGreat britainSteven immergutCourtney robertsAlain romeroSickle cell disease researchResearch collaborative data hubGalien foundationAmerican society of hematologyEuropean unionBlood instituteNational heartCenters for disease

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