ClinicalTrials.Veeva

Menu

To Explore The Potential For PF-04531083 To Effect The Blood Concentrations Of Simvastatin And Its Main Acid Metabolite Following Co-Administration Of Both Medications

Pfizer logo

Pfizer

Status and phase

Completed
Phase 1

Conditions

Chronic Pain

Treatments

Drug: simvastatin
Drug: PF-04531083

Study type

Interventional

Funder types

Industry

Identifiers

NCT01103739
B1351007

Details and patient eligibility

About

The purpose of this study is to quantify the effect of multiple doses of PF-04531083 on the pharmacokinetics (PK) of co-administered single dose simvastatin.

Full description

observational- quantify any effects of PF_04531083 on the PK of Simvastatin

Enrollment

24 patients

Sex

All

Ages

18 to 45 years old

Volunteers

Accepts Healthy Volunteers

Inclusion criteria

  • young
  • healthy
  • male and female volunteers

Exclusion criteria

  • Elderly
  • Patients

Trial design

24 participants in 2 patient groups

cohort 1
Experimental group
Treatment:
Drug: simvastatin
Drug: PF-04531083
Drug: PF-04531083
Drug: simvastatin
cohort 2
Experimental group
Treatment:
Drug: simvastatin
Drug: PF-04531083
Drug: PF-04531083
Drug: simvastatin

Trial contacts and locations

1

Loading...

Data sourced from clinicaltrials.gov

Clinical trials

Find clinical trialsTrials by location
© Copyright 2026 Veeva Systems