Statements (60)
Predicate | Object |
---|---|
gptkbp:instanceOf |
clinical trial
|
gptkbp:analyzes |
multiple hospitals
venetoclax intention-to-treat |
gptkbp:built |
2018
|
gptkbp:clinicalTrials |
yes
high two Phase III obtained NCT02005471 |
gptkbp:collaborations |
gptkb:Roche
|
gptkbp:collection |
clinical assessments
|
gptkbp:contraindication |
reported side effects
|
gptkbp:controls |
bendamustine_plus_rituximab
|
gptkbp:courseRating |
multicenter
|
gptkbp:dataUsage |
yes
available upon request |
gptkbp:distribution |
yes
|
gptkbp:enrollment |
389 participants
|
gptkbp:focusesOn |
chronic lymphocytic leukemia
|
gptkbp:followedBy |
24 months
|
gptkbp:funding |
pharmaceutical industry
|
gptkbp:future_plans |
Phase 3
|
gptkbp:hasPopulation |
relapsed_or_refractory_CLL
|
gptkbp:healthcare |
diverse population
completed successfully |
gptkbp:historicalResearch |
long-term effects of treatment
|
https://www.w3.org/2000/01/rdf-schema#label |
MURANO trial
|
gptkbp:impact |
influenced treatment protocols
|
gptkbp:includes |
previous treatment with BCL-2 inhibitors
adults_with_CLL |
gptkbp:is_studied_in |
yes
positive completed highly regarded in the field short follow-up period significant improvement in PFS |
gptkbp:isPublishedIn |
gptkb:The_New_England_Journal_of_Medicine
|
gptkbp:launchDate |
2014
|
gptkbp:leads |
gptkb:Dr._John_C._Byrd
|
gptkbp:location |
multiple countries
|
gptkbp:moral |
yes
|
gptkbp:outcome |
safety and efficacy
|
gptkbp:primaryMission |
treatment
progression-free survival |
gptkbp:regulatoryCompliance |
supported by trial results
|
gptkbp:relatedModel |
parallel assignment
|
gptkbp:relatedTo |
bendamustine_plus_rituximab
venetoclax_plus_rituximab |
gptkbp:releaseYear |
2019
|
gptkbp:research |
venetoclax
provided_by_AbbVie |
gptkbp:research_areas |
hematology
|
gptkbp:researchField |
oncology
|
gptkbp:researchInterest |
adhered to guidelines
|
gptkbp:result |
venetoclax plus rituximab improved outcomes
|
gptkbp:secondaryMission |
overall survival
|
gptkbp:sponsor |
AbbVie
|
gptkbp:vision |
no
|