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Hepatitis C VirusPhase 1NCT01288742

TMC435-TiDP16-C108 - A Study in Healthy Volunteers Investigating the Pharmacokinetic Interaction Between TMC435 and Digoxin and Between TMC435 and Rosuvastatin

A Phase 1 study testing Rosuvastatin, TMC435 and Digoxin in people with Hepatitis C Virus, run by Tibotec Pharmaceuticals, Ireland.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

The purpose of this study is to investigate the effect of steady-state concentrations of TMC435 on the single-dose pharmacokinetics of digoxin or rosuvastatin , and the effect of a single dose of digoxin or rosuvastatin on the steady-state pharmacokinetics of TMC435. Read more about this study

Who is it for?
Ages 18 to 55 yearsHealthy volunteers can take part
Conditions the study is for
Hepatitis C Virus
What is being tested?
Rosuvastatin, TMC435 and Digoxin
Type of treatment
Pill or oral medicine
Could I receive a placebo?
No, everyone receives an active treatment
How many people
33 participants
Where
No sites listed yet
Study dates
Jan 2011to May 2011
Phase
Phase 1
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 55 years
  • All sexes
  • Healthy volunteers accepted
  • Adult

Who may be able to join

  • Non-smoker or not having chewed tobacco for at least 6 months
  • Body Mass Index of 18.0 to 30.0 kg/m2
  • Healthy based on a medical evaluation including medical history, physical examination, blood tests, vital signs, and electrocardiogram

Who cannot join

  • Infection with hepatitis A, B or C virus
  • Infection with the human immunodeficiency virus (HIV)
  • History of, or any current medical condition which could impact the safety of the participant in the study
  • Having previously participated in a multiple-dose trial with TMC435
  • Having previously participated in more than 3 single-dose trials with TMC435
  • History of rhabdomyolysis or other muscle abnormalities upon statin intake (Panel 2).

About this study

Official title: A Phase I, 2-panel, Open-label, Randomized, Crossover Trial in Healthy Subjects to Investigate the Pharmacokinetic Interaction Between TMC435 and Transporter Substrates, Digoxin and Rosuvastatin

The purpose of this study is to investigate the effect of steady-state concentrations of TMC435 on the single-dose pharmacokinetics of digoxin or rosuvastatin , and the effect of a single dose of digoxin or rosuvastatin on the steady-state pharmacokinetics of TMC435. Steady state is a term that means that the drug has been given long enough so that the plasma concentrations will remain the same with each subsequent dose. TMC435 is being investigated for the treatment of chronic hepatitis C virus (HCV) infection. Pharmacokinetics (PK) means how the drug is absorbed into the bloodstream, distributed in the body, and eliminated from the body.

Read the detailed description

TMC435 is being investigated for treatment of chronic hepatitis C virus (HCV) infection, in combination with Peg-IFN (pegylated interferon) and RBV (ribavirin). Digoxin and rosuvastatin are expressed in the liver and intestine and mediate the transport of drugs out of the blood circulation. The result of this study will provide dosing recommendations for TMC435 and for digoxin, rosuvastatin, or other substrates using the same drug transporter molecules, when being coadministered. This is a Phase I, open-label (both participant and investigator know the name of the medication given at certain moment), randomized (sequence of treatment with study medications is assigned by chance), crossover trial in 32 healthy volunteers to investigate the pharmacokinetic interaction between TMC435, at steady state, and digoxin or rosuvastatin at a single dose. The volunteers will be allocated to one of two panels. In Panel 1, volunteers will receive two treatments (Trts A and B) in a randomized order. Volunteers will receive digoxin 0.25 mg once daily for 1 day (Trt A) and TMC435 150 mg once daily for 7 days (Trt B) and 0.25 mg digoxin once daily for 1 day (Trt B). In Panel 2, volunteers will receive two treatments (Trts C and D) in a randomized order. Volunteers will receive rosuvastatin 10 mg once daily for 1 day (Trt C) and TMC435 150 mg once daily for 7 days (Trt D) and rosuvastatin 10 mg once daily for 1 day (Trt D). In both panels, there will be a washout period (a period when no study drug will be taken, in order to have all the medication eliminated from the body before starting a new treatment) of at least 14 days between last intake of the study medication in one session and the first intake of study medication in the subsequent session. Pharmacokinetic profiles of all three compounds will be determined through blood samples taken at regular intervals during the study. Safety and tolerability will be assessed during the study period and during follow up. Blood and urine samples, electrocardiogram (ECG) and vital signs (blood pressure and heart rate) will be taken at screening, before medication intake on Day -1 or Day 1 (Trts A, B, C, and D), on Day 2 (Trts A and C), before medication intake and 6 hours postdose (only vital signs and ECG) on Day 7 (Trts B and D), on Day 8 (Trts B and D) and at the 2 follow up visits at 1 week and 4-5 weeks after last dose of study medication in the last session. A physical examination will be performed at screening, on Day -1 (= day before first medication intake in each session for both panels) and on Day 2 in Trts A and C, on Day -1 and on Day 8 of Trts B and D and during the 2 follow-up visits. Each volunteer is part of one panel and follows 2 treatment (Trt) periods, which are a minimum 14 days apart from each other. Trt period for Trts A and C - 5 days; Trt period for Trts B and D - 11 days. Trt A and B = Panel 1, Trt C and D = Panel 2. A single, oral dose of digoxin (0.25 mg) or rosuvastatin (10 mg) to be given in Trt A or Trt C, respectively. Multiple doses of TMC435 (150 mg) for 7 days to be given in TrtB and D, with a single dose of digoxin or rosuvastatin on Day7, respectively.

Being tested
Rosuvastatin, TMC435, Digoxin
Keywords
TMC435-TiDP16-C108, TMC435-C108, TMC435, HPC, HCV, Hepatitis C
Medical subject headings
Hepatitis C

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • RosuvastatinDrug

    One 10-mg tablet for 1 day (Trt C).

  • RosuvastatinDrug

    One 10-mg tablet together with 1 capsule of TMC435 (150 mg) on Day 7 of Trt D.

  • TMC435Drug

    One 150-mg capsule once daily for 7 days (Trts B and D).

  • DigoxinDrug

    One 0.25-mg tablet together with 1 capsule of TMC435 (150 mg) on Day 7 of Trt B.

  • DigoxinDrug

    One 0.25-mg tablet for 1 day (Trt A)

Study groups in NCT01288742
Study groupRoleWhat they receive
001ExperimentalTMC435 One 150-mg capsule once daily for 7 days (Trts B and D).
Receives: Drug: TMC435
002ExperimentalDigoxin One 0.25-mg tablet for 1 day (Trt A)
Receives: Drug: Digoxin
003ExperimentalDigoxin One 0.25-mg tablet together with 1 capsule of TMC435 (150 mg) on Day 7 of Trt B.
Receives: Drug: Digoxin
004ExperimentalRosuvastatin One 10-mg tablet for 1 day (Trt C).
Receives: Drug: Rosuvastatin
005ExperimentalRosuvastatin One 10-mg tablet together with 1 capsule of TMC435 (150 mg) on Day 7 of Trt D.
Receives: Drug: Rosuvastatin

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. Change in absorption of TMC435 following co-administration with Digoxin (Panel 1).

    Measured: Measured on Days 1, 5-11 (Trt B). Reference for TMC435 is from historical data.

  2. Change in absorption of Digoxin following co-administration with TMC435 (Panel 1).

    Measured: Measured on Day 7-11 (Trt B). Reference for Digoxin is on Day 1-5 of Trt A.

  3. Change in absorption of TMC435 following co-administration with rosuvastatin (Panel 2).

    Measured: Measured on Day 1, 5-11 (Trt D). Reference for TMC435 are historical data.

  4. Change in absorption of rosuvastatin following co-administration with TMC435 (Panel 2).

    Measured: Measured on Day 7-11 (Trt D). Reference for rosuvastatin is on Days 1-5 of Trt C.

Secondary outcomes (2)
  1. Number of participants with adverse events as a measure of safety and tolerability - TMC435 and Digoxin

    Measured: 51 to 56 days (until and including last safety follow-up visit) for Panel 1

  2. Number of participants with adverse events as a measure of safety and tolerability - TMC435 and rosuvastatin

    Measured: 51 to 56 days (until and including last safety follow-up visit) for Panel 2

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted2 Feb 2011 (estimated)
  2. Study startJan 2011
  3. Primary completionMay 2011
  4. Study completionMay 2011

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 1
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Crossover
Masking
None (open label)
Enrolment
33 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT01288742
Sponsor's protocol ID
CR017770
Other IDs
TMC435-TiDP16-C108
Status last verified
Nov 2012
First submitted
20 Jan 2011
Last updated
30 Nov 2012
Results posted
No

Questions about this trial

What is this clinical trial studying?

A Phase 1 study testing Rosuvastatin, TMC435 and Digoxin in people with Hepatitis C Virus, run by Tibotec Pharmaceuticals, Ireland.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

The sponsor lists 3 inclusion and 6 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: finished, as of the sponsor's last update on 30 Nov 2012. Status can change between updates, so confirm with the study contact before making plans.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

Change in absorption of TMC435 following co-administration with Digoxin (Panel 1). (time frame: Measured on Days 1, 5-11 (Trt B). Reference for TMC435 is from historical data.). The study lists 4 primary outcomes in all. It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 30 Nov 2012.

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