Clinical Trials Directory

Trials / Completed

CompletedNCT01243151

Safety And Tolerability Of Multiple Doses Of PF-04950615 (RN316) In Subjects With Hypercholesterolemia

A Phase 1, Placebo-controlled, Randomized Study To Assess The Safety, Tolerability, Pharmacokinetics, And Pharmacodynamics Following Multiple Intravenous Doses Of Pf-04950615 In Healthy Adult Subjects With Hypercholesterolemia

Status
Completed
Phase
Phase 1
Study type
Interventional
Enrollment
68 (actual)
Sponsor
Pfizer · Industry
Sex
All
Age
18 Years – 80 Years
Healthy volunteers
Accepted

Summary

The primary objective of this study is to evaluate the safety and tolerability of repeated doses of PF-04950615 (RN316) in study volunteers with hypercholesterolemia. PF-04950615 is an investigational drug that is currently being studied as a lipid lowering agent.

Conditions

Interventions

TypeNameDescription
BIOLOGICALPF-04950615 (RN316)Infusion every week
BIOLOGICALPF-04950615 (RN316)Infusion every week
BIOLOGICALPF-04950615 (RN316)Infusion every week
BIOLOGICALPF-04950615 (RN316)Infusion every week
BIOLOGICALPF-04950615 (RN316)Infusion every week

Timeline

Start date
2011-02-01
Primary completion
2011-10-01
Completion
2011-10-01
First posted
2010-11-18
Last updated
2019-01-22
Results posted
2019-01-22

Locations

9 sites across 1 country: United States

Source: ClinicalTrials.gov record NCT01243151. Inclusion in this directory is not an endorsement.

Safety And Tolerability Of Multiple Doses Of PF-04950615 (RN316) In Subjects With Hypercholesterolemia (NCT01243151) · Clinical Trials Directory