Drugs / Mavyret

Regulatory milestones approvals, filings & regulatory actions · 1 recorded

MilestoneJurisdictionBrandIndicationDateSentence it was read from
Approved US (FDA) MAVYRET — 2017-08-03 fda.gov ↗

Trials 7

PhaseRegistry idDatesIndicationSponsorStatusOutcome
Phase 1/21 trial · 1 met primary
Phase 1/2 NCT02743897 May 2016 → Mar 2022 end stage renal failure University of Pennsylvania Completed Met primary
Phase 21 trial
Phase 2 NCT03523871 May 2018 → Sep 2020 hepatitis C virus infection NYU Langone Health Completed No outcome recorded
Phase 44 trials
Phase 4 NCT04508907 Sep 2020 → Nov 2025 overdue disease related to solid organ transplantation, hepatitis C virus infection Mayo Clinic Active not recruiting No outcome recorded
Phase 4 NCT03625687 Feb 2019 → Apr 2022 hepatitis C virus infection, respiratory failure Massachusetts General Hospital Terminated No outcome recorded Stop: Business
Phase 4 NCT03382847 Jan 2018 → May 2020 heart failure NYU Langone Health Completed No outcome recorded
Phase 4 NCT02946034 Feb 2017 → Sep 2020 chronic hepatitis C virus infection, chronic kidney disease Massachusetts General Hospital Completed No outcome recorded
Phase not applicable1 trial
— NCT05108935 Feb 2022 → Mar 2023 HIV infectious disease, hepatitis C virus infection, opiate dependence Duke University Completed No outcome recorded

Evidence & citations 3 cited values

Every value below carries the sentence it was read from. 7 sources stand behind the page.

FieldValueCited text
Known as Mavyret “Patients who develop HCV viremia post-transplant will be treated with an FDA-approved, pan-genotypic direct acting antiviral drug, Mavyret.” NCT03382847 ↗
6

NCT02946034 ↗

NCT02743897 ↗

NCT03625687 ↗

NCT05108935 ↗

NCT03523871 ↗

NCT04508907 ↗

Modality Other / unclassified “Direct-acting antiviral treatment for HCV” NCT02743897 ↗
Route Oral “is taken by mouth” NCT02743897 ↗