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Myovant Sciences and Pfizer Receive U S FDA Approval of MYFEMBREE, Once-Daily Treatment for Management of Moderate to Severe Pain

Myovant Sciences and Pfizer Receive U S FDA Approval of MYFEMBREE, Once-Daily Treatment for Management of Moderate to Severe Pain
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United statesSan franciscoJames rusnakLinda giudiceJuan camilo arjona ferreiraUniversity of californiaMyovant sciencesDrug administrationGlobal product development at pfizerPfizer incMyovant sciences incProgram steering committeeChief medical officerSenior vice presidentChief development officerInternal medicine

Myovant Sciences and Pfizer Announce Publication in Lancet of Phase 3 SPIRIT 1 and SPIRIT 2 Studies of Once-Daily Relugolix

Myovant Sciences and Pfizer Announce Publication in Lancet of Phase 3 SPIRIT 1 and SPIRIT 2 Studies of Once-Daily Relugolix
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United statesJames rusnakJuan camilo arjona ferreiraEffect on other laboratoryEndometriosis healthDrug administrationMyovant sciencesGlobal product development at pfizerPfizer incMyovant sciences incChief medical officerSenior vice presidentChief development officerInternal medicineGlobal product developmentNew drug application

HTG to Sponsor Keynote Presentation Featuring Customer Use of its HTG EdgeSeq Technology in Clinical Trials

HTG to Sponsor Keynote Presentation Featuring Customer Use of its HTG EdgeSeq Technology in Clinical Trials
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San diegoUnited statesChetan deshpandeAshley robinsonMarketsandmarkets biomarkerGlobal product development at pfizerMolecular diagnostics incAnnual marketsandmarkets biomarkerCompanion diagnostics conferenceBiomarker strategyBiomarker clinical assay leadGlobal product developmentKeynote presentation

Myovant Sciences (MYOV), Pfizer (PFE) Announce FDA Acceptance of sNDA for MYFEMBREE®

Myovant Sciences (MYOV), Pfizer (PFE) Announce FDA Acceptance of sNDA for MYFEMBREE®
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United statesJames rusnakJuan camilo arjona ferreiraPfizer incMyovant sciences incMyovant sciencesDrug administrationGlobal product development at pfizerNew drug applicationStates prescribing informationPrescription drug user fee actChief medical officerSenior vice presidentChief development officerInternal medicineGlobal product development

Myovant Sciences and Pfizer Announce FDA Acceptance of Supplemental New Drug Application for MYFEMBREE

Myovant Sciences and Pfizer Announce FDA Acceptance of Supplemental New Drug Application for MYFEMBREE
miragenews.com - get the latest breaking news, showbiz & celebrity photos, sport news & rumours, viral videos and top stories from miragenews.com Daily Mail and Mail on Sunday newspapers.

United statesJames rusnakJuan camilo arjona ferreiraProgram in uterine fibroidsEffect on other laboratoryPfizer incMyovant sciences incMyovant sciencesDrug administrationGlobal product development at pfizerNew drug applicationStates prescribing informationPrescription drug user fee actChief medical officerSenior vice presidentChief development officer