KEYNOTE-006

GPTKB entity

Statements (53)
Predicate Object
gptkbp:instance_of gptkb:legal_case
gptkbp:bfsLayer 6
gptkbp:bfsParent gptkb:pembrolizumab
gptkbp:analysis statistical methods
gptkbp:analyzes gptkb:pembrolizumab
gptkbp:business_model gptkb:board_game
gptkbp:class immune checkpoint inhibitor
gptkbp:clinical_trial gptkb:Clinical_Trials.gov
gptkb:KEYNOTE-001
gptkb:KEYNOTE-002
KEYNOTE-005
gptkbp:collaborations various institutions
gptkbp:collection clinical assessments
gptkbp:committee gptkb:battle
gptkbp:criteria previous anti-PD-1 therapy
unresectable stage III or IV melanoma
gptkbp:duration up to 24 months
gptkbp:finale_date overall survival
progression-free survival
gptkbp:followed_by up to 5 years
gptkbp:future_plans further research needed
https://www.w3.org/2000/01/rdf-schema#label KEYNOTE-006
gptkbp:impact changed treatment guidelines
gptkbp:is_compared_to gptkb:ipilimumab
gptkbp:is_studied_in multicenter
gptkbp:is_tested_for Phase 3
gptkbp:issue_number NC T01866319
gptkbp:location multiple countries
gptkbp:members placebo
gptkbp:notable_work pembrolizumab showed superior efficacy
gptkbp:outcome assessed
improved survival rates
gptkbp:population diverse population
gptkbp:primary_source Dr. Jeffrey S. Weber
gptkbp:published_year gptkb:2016
gptkbp:publishes gptkb:New_England_Journal_of_Medicine
peer-reviewed
gptkbp:recorded_by gptkb:battle
gptkbp:regulatory_compliance FDA approved
gptkbp:result gptkb:2016
gptkbp:safety_features acceptable
gptkbp:side_effect immune-related adverse events
improved in treatment group
gptkbp:sponsor gptkb:Merck_&_Co.
gptkbp:status completed
gptkbp:student_enrollment approximately 690 patients
gptkbp:targets gptkb:healthcare_organization
gptkbp:treatment two
monotherapy
gptkbp:vision double-blind
gptkbp:warranty ongoing
gptkbp:year gptkb:2015
gptkbp:year_created gptkb:2013