Drugs / Lopinavir/Ritonavir
last change Feb 2020 re-read 3 minutes ago

Lopinavir/Ritonavir

also known as Kaletra
Developed for
HIV infectious disease
Investigated by
University of Maryland, Baltimore

Trials 1

2006200720082009201020112012201320142015201620172018201920202021202220232024202520262027
PhaseRegistry idDatesIndicationSponsorStatusOutcome
— NCT00344487 Dec 2005 → May 2009 HIV infectious disease University of Maryland, Baltimore Terminated No outcome recorded Stop: Enrollment

News releases announcing trial results or a regulatory action · 1

DateIssuerRelease
2020-02-07 AbbVie Regulatory AbbVie Reports Full-Year and Fourth-Quarter 2019 Financial Results abbvie.com ↗
The application is being reviewed under the FDA's Real-Time Oncology Review pilot program and is based on results from the Phase 3 E1912 study, which showed significantly improved PFS and overall survival (OS) in patients treated with IMBRUVICA plus rituximab compared to those treated with fludarabine, cyclophosphamide and rituximab (FCR).

Evidence & citations 3 cited values

Every value below carries the sentence it was read from. 1 source stands behind the page.

FieldValueCited text
Known as Lopinavir/Ritonavir ClinicalTrials.gov intervention name — accepted as the source's own label NCT00344487 ↗
Known as Kaletra “The dose of lopinavir/ritonavir (Kaletra) for this study will be 400/100mg. BID or 800/200mg. qd.” NCT00344487 ↗
Route Oral “lopinavir/ritonavir (Kaletra)400/100mg tablets by mouth twice a day for 48 weeks.” NCT00344487 ↗