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Vertex Pharma (VRTX) Advances Inaxaplin into Phase 3 Portion of Adaptive Phase 2/3 Trial

Vertex Pharma (VRTX) Advances Inaxaplin into Phase 3 Portion of Adaptive Phase 2/3 Trial
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Carmen bozicGlennm chertowData monitoring committeeStanford university school of medicineVertex pharmaceuticals incorporated nasdaqProgram steering committeeDrug administrationEuropean medicines agencyGlobal medicines developmentVertex pharmaceuticals incorporatedExecutive vice presidentMedical affairsChief medical officerStanford university schoolIndependent data monitoring committeeRare pediatric disease designation

Vertex Pharmaceuticals Incorporated: Vertex Advances Inaxaplin (VX-147) into Phase 3 Portion of Adaptive Phase 2/3 Clinical Trial for the Treatment of APOL1-Mediated Kidney Disease

Vertex Pharmaceuticals Incorporated: Vertex Advances Inaxaplin (VX-147) into Phase 3 Portion of Adaptive Phase 2/3 Clinical Trial for the Treatment of APOL1-Mediated Kidney Disease
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United statesCity ofUnited kingdomGlenn chertowHeather nicholsGlennm chertowMiroslava minkovaSusie lisaManisha paiCarmen bozicDennis riedlEuropean medicines agencyGlobal medicines developmentProgram steering committeeCompanies to workExchange commission

Vertex Advances Inaxaplin (VX-147) into Phase 3 Portion of Adaptive Phase 2/3 Clinical Trial for the Treatment of APOL1-Mediated Kidney Disease

Vertex Pharmaceuticals Incorporated today announced that inaxaplin (VX-147) has advanced into the Phase 3 portion of the global Phase 2/3 pivotal clinical trial in APOL1-mediated kidney disease (AMKD), where a 45 mg once daily oral dose will be.

City ofUnited kingdomUnited statesCarmen bozicGlenn chertowGlennm chertowVertex pharmaceuticals incorporated nasdaqExchange commissionProduct serviceProgram steering committeeStanford university school of medicineData monitoring committeeDrug administrationGlobal medicines developmentEuropean medicines agencyCompanies to work

Akebia Receives FDA Approval of Vafseo® (vadadustat) Tablets for the Treatment of Anemia due to Chronic Kidney Disease in Adult Patients on Dialysis

Akebia Receives FDA Approval of Vafseo® (vadadustat) Tablets for the Treatment of Anemia due to Chronic Kidney Disease in Adult Patients on Dialysis
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United statesUnited kingdomGlennm chertowLori hartwellJohnp butlerClin nephrolDivision of nephrology at stanford universityRenal support networkDrug administrationNational institutes of healthNational institute of diabetesExchange commissionAkebia therapeutics incClin lab haematolSteering committeeCompany to host conference call on

Akebia Receives FDA Approval Of Vafseo® (Vadadustat) Tablets For The Treatment Of Anemia Due To Chronic Kidney Disease In Adult Patients On Dialysis

Akebia Receives FDA Approval Of Vafseo® (Vadadustat) Tablets For The Treatment Of Anemia Due To Chronic Kidney Disease In Adult Patients On Dialysis
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United statesUnited kingdomLori hartwellJohnp butlerGlennm chertowDivision of nephrology at stanford universityDrug administrationAkebia therapeutics incRenal support networkSteering committeeCompany to host conference call onOnce daily oralActivates physiologic responseLaunch strategy developedDrive towardPotential new oral standard