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NCT01756404

Study to Assess the Pharmacokinetics, Pharmacodynamics, and Safety of Canagliflozin (JNJ-28431754) in Otherwise Healthy Obese Volunteers

Completed Phase 1 Last updated 13 December 2018
What this trial tests

Phase 1 trial testing Canagliflozin (JNJ-28431754) in Healthy in 80 participants. Completed in 5 December 2007.

Timeline
14 June 2007
Primary endpoint
5 December 2007
5 December 2007

Quick facts

Lead sponsorJohnson & Johnson Pharmaceutical Research & Development, L.L.C.
PhasePhase 1
StatusCompleted
Study typeINTERVENTIONAL
Allocationrandomized
Designsingle group
Maskingdouble
Primary purposetreatment
Enrollment80
Start date14 June 2007
Primary completion5 December 2007
Estimated completion5 December 2007
Sites1 location across United States

Drugs / interventions tested

Conditions studied

Sponsor

Johnson & Johnson Pharmaceutical Research & Development, L.L.C. — full company profile →

Who can join

Adults 18 to 60, any sex, with Healthy. Patients with the condition only — healthy volunteers not accepted.

Sponsor's own description

The purpose of this study is to assess the pharmacokinetics (ie, how the body affects the drug) and pharmacodynamics (ie, how the drug affects the body) of increasing doses of canagliflozin (JNJ-28431754) in healthy obese volunteers.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Emerging Role of SGLT-2 Inhibitors for the Treatment of Obesity.
    Pereira MJ, Eriksson JW. · · 2019 · cited 231× · PMID 30701480 · DOI 10.1007/s40265-019-1057-0

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Other recruiting trials for Healthy

Currently open trials in the same condition.

Other Johnson & Johnson Pharmaceutical Research & Development, L.L.C. trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT01756404.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing