Study To Determine The Effects Of Doses Of Relacatib On The Metabolism Of Acetaminophen, Ibuprofen And Atorvastatin

Osteoarthritis Clinical Trial

Official title:

A Study to Evaluate the Potential for Pharmacokinetic Interaction Between SB 462795 and SSRIs in Healthy Subjects [3A]

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT00411190
• Other study ID #: SB-462795/008
• Status: Completed
• Phase: Phase 1
• First received: December 11, 2006
• Last updated: October 2, 2017
• Start date: October 19, 2006
• Est. completion date: December 15, 2006

Study information

• Verified date: October 2017
• Source: GlaxoSmithKline
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Relacatib is being developed for the treatment of osteoporosis, osteoarthritis and possibly other bone disorders. Recent results suggest that relacatib interacts with the way our bodies metabolise drugs and so some drugs which are commonly prescribed to the intended target patient population could be affected by giving relacatib at the same time. The purpose of this study is to evaluate the effect of repeat dose administration of relacatib on the way subjects bodies metabolise three commonly prescribed medications in the osteoarthritis population: ibuprofen, acetaminophen, and atorvastatin.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 32
• Est. completion date: December 15, 2006
• Est. primary completion date: December 15, 2006
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Female
• Age group: 18 Years to 70 Years

Eligibility

Inclusion Criteria:

• Healthy

• Postmenopausal

• Body weight > 50 kg

• Body mass index (BMI) between 19 and 30

• The subject is willing and able to give a signed and dated written informed consent prior to admission to the study

• The subject is able to understand and comply with protocol requirements, instructions and protocol-stated restrictions.

Exclusion Criteria:

• Subjects with known morphea or sclerodermia

• Subjects with a history of myocardial infarction.

• Subjects with a history of renal/or hepatic disease unless the disease has been successfully treated and is no longer active; subjects with any evidence of renal/ or hepatic impairment on the screening physical and laboratory examination.

• Subjects with history of hypertension or systolic blood pressure

• Subjects with history of diabetes

• History of regular alcohol consumption exceeding 7 drinks/week (1 drink = 5 ounces of wine or 12 ounces of beer or 1.5 ounces of hard liquor) within 6 months of screening.

• History of use of tobacco- or nicotine-containing products within 6 months of screening, or a positive urine cotinine indicative of smoking at screening.

• Positive urine drug screen including alcohol (or alcohol breath test) at screening.

• Positive for HIV, hepatitis B virus or hepatitis C virus.

• Donation of blood in excess of 500 mL within 56 days prior to dosing

• History of sensitivity or contraindications to any of the study medications (i.e., relacatib, paracetamol, ibuprofen or atorvastatin) or components thereof.

• Treatment with an investigational drug within 30 days or 5 half-lives (whichever is longer) preceding the first dose of study medication.

• Subjects whom are judged by the investigator to be at risk for acute angle closure glaucoma.

Related Conditions & MeSH terms

• Osteoarthritis

Intervention

Drug:
• Relacatib
Subjects will administer 60 or 120 mg tablets in Session 2
• Acetaminophen
Acetaminophen will be administered orally
• Ibuprofen
Ibuprofen will be administered orally
• Atorvastatin
Atorvastatin will be administered orally

Locations

Country	Name	City	State
Belgium	GSK Investigational Site	Antwerpen
Belgium	GSK Investigational Site	Liège

Sponsors (1)

Lead Sponsor	Collaborator
GlaxoSmithKline

Country where clinical trial is conducted

Belgium, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	The primary objective of this study is to characterize the effect of relacatib at steady-state on the pharmacokinetics of a single oral dose of acetaminophen, ibuprofen and atorvastatin in healthy postmenopausal females.		Up to Day 17
Secondary	To assess the safety and tolerability of the concomitant administration of oral doses of relacatib and acetaminophen, ibuprofen and atorvastatin. To describe the changes from baseline in serum CTXI levels for each relacatib dose tested.		Up to Day 17

External Links

•   Results for study SB-462795/008 can be found on the GSK Clinical Study Register.