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Cabenuva approved for use every eight weeks to treat HIV

Cabenuva approved for use every eight weeks to treat HIV
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Lynn baxterTurner overtonDrug administrationDepartment of medicineUniversity of alabama at birminghamViiv healthcareNorth americaIntent to treat exposedPrimary investigator

GlaxoSmithKline : ViiV Healthcare announces US FDA approval of Cabenuva (cabotegravir, rilpivirine) for use every two months, expanding the label of the first and only complete long-acting HIV treatment

For media and investors only Issued: London UK Cabenuva is now approved for administration as few as six times a year for virologically suppressed adults living. | February 1, 2022

United statesUnited kingdomSouth africaSouth koreaLynn baxterTurner overtonDrug administrationJanssen pharmaceutical companies of johnsonUniversity of alabama at birminghamCompany annual report on formShionogi limitedPfizer incViiv healthcare patient assistance programDepartment of medicineJanssen sciences ireland unlimited companyLondon united

ViiV Healthcare Announces US FDA Approval of Cabenuva (cabotegravir, rilpivirine) for Use Every Two Months, Expanding the Label of the First and Only Complete Long-Acting HIV Treatment

Cabenuva is now approved for administration as few as six times a year for virologically suppressed adults living with HIV without prior treatment failure or resistance to cabotegravir or rilpivirine ViiV

United statesNorth carolinaSouth africaCity ofUnited kingdomUnited kingdom generalSouth koreaLynn baxterJosh williamsJeff mclaughlinMick readeyCatherine hartleyLyndsay meyerTim foleyMadeleine breckonEvan berland

PharmaTher Announces FDA Approval of Investigational New Drug (IND) Application for Ketamine to Treat ALS

TORONTO, Jan. 12, 2022 (GLOBE NEWSWIRE) PharmaTher Holdings Ltd. (the “Company” or “PharmaTher”) (OTCQB: PHRRF) (CSE: PHRM), a company focused on the…

United statesRichard barohnLou gehrigFabio chianelliUniversity of kansasHuman servicesCompany or pharmatherRisk factors in companyDrug administrationUniversity of missouriHealth affairsPharmather holdings ltdNeither the canadian securities exchangeNextgen precision healthPostmedia network incDepartment of health

PharmaTher Announces FDA Approval of Investigational New Drug (IND) Application for Ketamine to Treat ALS

PharmaTher Holdings announced that the U.S. FDA has accepted IND application to proceed with a Phase 2 clinical trial evaluating ketamine in the treatment of ALS

United statesRichard barohnLou gehrigUniversity of kansasHuman servicesDrug administrationUniversity of missouriHealth affairsPharmather holdings ltdNextgen precision healthDepartment of healthMu health careAssociation of american physiciansAmyotrophic lateral sclerosisPrimary investigatorPresident biden