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Trials / Completed

CompletedNCT01407003

Safety, Tolerability, Pharmacokinetics (PK) and Pharmacodynamics (PD) Assessment of LIK066 in Healthy Subjects and in Patients With Type 2 Diabetes Mellitus (T2DM)

A Randomized, Double-blind, Placebo-controlled, 4-part, Interwoven Single- and Multiple-ascending Dose Study to Assess Safety, Tolerability, PK and PD of LIK066 in Healthy Subjects and in Patients With T2DM

Status
Completed
Phase
Phase 1 / Phase 2
Study type
Interventional
Enrollment
138 (actual)
Sponsor
Novartis Pharmaceuticals · Industry
Sex
All
Age
18 Years – 65 Years
Healthy volunteers
Accepted

Summary

This study will assess safety, tolerability, and effect of LIK066 on blood glucose in healthy subjects and in patients with T2DM.

Conditions

Interventions

TypeNameDescription
DRUGLIK066Participants will receive a single or multiple doses of LIK066
DRUGPlaceboParticipants will receive a single or multiple doses of a matching placebo

Timeline

Start date
2011-06-01
Primary completion
2013-02-01
Completion
2013-02-01
First posted
2011-08-01
Last updated
2020-12-19

Locations

1 site across 1 country: United States

Source: ClinicalTrials.gov record NCT01407003. Inclusion in this directory is not an endorsement.

Safety, Tolerability, Pharmacokinetics (PK) and Pharmacodynamics (PD) Assessment of LIK066 in Healthy Subjects and in Pa (NCT01407003) · Clinical Trials Directory