Clinical Study to Investigate the Effect of Macitentan on the Concentrations of Rosuvastatin in the Blood of Healthy Male Subjects
Study Details
Study Description
Brief Summary
The aim of this Phase 1 trial is to study a potential drug-drug interaction between macitentan and rosuvastatin, a model substrate of various transporter proteins (e.g. in the gut).
| Condition or Disease | Intervention/Treatment | Phase |
|---|---|---|
| Phase 1 |
Detailed Description
Rosuvastatin is a substrate of various transporter proteins including breast cancer resistance protein (BCRP) and organic anion-transporting polypeptides (OATP). It is unknown to which extent macitentan has an effect, if any, on BCRP transporters, especially intestinal BCRP. The primary purpose of this Phase 1 study is to investigate the effect of macitentan on the pharmacokinetics of rosuvastatin, a model BCRP substrate.
Study Design
Arms and Interventions
| Arm | Intervention/Treatment |
|---|---|
| Experimental: Sequence AB Subjects participate in two study periods: During the first period (treatment A), they receive a single oral dose of rosuvastatin on Day 1. During the second period (treatment B), they receive a single oral loading dose of macitentan on Day 5 and oral doses of macitentan from Day 6 to Day 16 (i.e., 11 doses). Subjects receive a single oral dose of 10 mg rosuvastatin concomitantly with macitentan in the morning of Day 10. |
Drug: Rosuvastatin
Single oral dose of 10 mg rosuvastatin (film-coated tablet) on Day 1 and Day 10
Drug: Macitentan
Single oral dose of 30 mg macitentan (film-coated tablet) on Day 5 and 10 mg macitentan administered orally from Day 6 to Day 16
Other Names:
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Outcome Measures
Primary Outcome Measures
- AUC(0-inf) of rosuvastatin following administration of rosuvastatin alone (treatment A) and in combination with macitentan (treatment B) [From Day1 to Day17 (treatment A: from Day1-Day5 and treatment B: from Day10-Day17)]
AUC(0-inf) is the area under the plasma concentration-time curves of rosuvastatin, calculated from time zero to the extrapolated infinite time
- Cmax of rosuvastatin following administration of rosuvastatin alone (treatment A) and in combination with macitentan (treatment B) [From Day1 to Day17 (treatment A: from Day1-Day5 and treatment B: from Day10-Day17)]
Cmax is the maximum observed plasma concentration and is directly derived from the individual plasma concentration time curves of rosuvastatin
Secondary Outcome Measures
- tmax of rosuvastatin following administration of rosuvastatin alone (treatment A) and in combination with macitentan (treatment B) [From Day1 to Day17 (treatment A: from Day1-Day5 and treatment B: from Day10-Day17)]
The time to reach maximum plasma concentration (tmax) of rosuvastatin
- t½ of rosuvastatin following administration of rosuvastatin alone (treatment A) and in combination with macitentan (treatment B) [From Day1 to Day17 (treatment A: from Day1-Day5 and treatment B: from Day10-Day17)]
t½ is the terminal half-life of rosuvastatin and corresponds to the period of time required for the concentration levels of rosuvastatin to be reduced by one-half
- AUC(0-t) of rosuvastatin following administration of rosuvastatin alone (treatment A) and in combination with macitentan (treatment B) [From Day1 to Day17 (treatment A: from Day1-Day5 and treatment B: from Day10-Day17)]
AUC(0-t) is the area under the plasma concentration-time curve from time zero to time t of the last measured concentration above the limit of quantification of rosuvastatin
- Trough plasma concentrations of macitentan and its metabolite ACT-132577 [From Day5 to Day17]
Trough concentrations of macitentan and ACT-132577 are measured before oral administration of macitentan
- Change from baseline in supine blood pressure [From Day1 to end-of-study visit (Day 26-28)]
Change from baseline to each time point of measurement during study period
- Change from baseline in pulse rate [From Day1 to end-of-study visit (Day 26-28)]
Change from baseline to each time point of measurement during study period
- Change from baseline in heart rate (HR) [From Day1 to end-of-study visit (Day 26-28)]
Change from baseline to each time point of measurement during study period
- Change from baseline in ECG variables [From Day1 to end-of-study visit (Day 26-28)]
Change from baseline to each time point of measurement during study period in ECG variables: PR, QRS, QT, RR, and QT corrected for Bazett's and Fridericia's formulae (QTcB and QTcF, respectively)
- Change from baseline to end-of-study (EOS) in body weight [From Day1 to end-of-study visit (Day 26-28)]
Change in body weight measured in kg during study period
- Change from baseline in clinical laboratory tests [From Day1 to end-of-study visit (Day 26-28)]
Change from baseline to each time point of measurement during study period for clinical laboratory tests (hematology, clinical chemistry, serology)
- Incidence rate of treatment-emergent treatment-emergent adverse events (AEs) and serious adverse events (SAEs) [From Day1 to follow-up period (Day46-48)]
Incidence rates of treatment-emergent AEs including abnormalities in ECG variables during each treatment as well as AEs leading to the discontinuation of study treatment. A treatment-emergent AE is any AE temporally associated with the use of a study treatment, whether or not considered related to the study treatment.
Eligibility Criteria
Criteria
Principal Inclusion Criteria:
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Signed informed consent in the local language prior to any study-mandated procedure.
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Healthy male subjects aged between 18 and 55 years (inclusive) at screening.
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No clinically significant findings on the physical examination at screening.
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Body mass index of 18.0 to 30.0 kg/m2 (inclusive) at screening.
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Systolic blood pressure 100-140 mmHg, diastolic blood pressure 60-90 mmHg, and pulse rate 50-90 beats per minute (inclusive), measured on the dominant arm, after 5 min in the supine position at screening.
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12-lead electrocardiogram (ECG) without clinically relevant abnormalities, measured after 5 min in the supine position at screening.
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Hematology and clinical chemistry test results not deviating from the normal range to a clinically relevant extent at screening.
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Negative results from urine drug screen and alcohol breath test at screening and Day -1.
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Ability to communicate well with the investigator, in the local language, and to understand and comply with the requirements of the study.
Principal Exclusion Criteria:
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Known allergic reactions or hypersensitivity to macitentan, rosuvastatin, any drug of the same classes, or any of their excipients.
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Any contraindication for rosuvastatin treatment.
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History or clinical evidence of myopathy.
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Subjects of Asian race.
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Known hypersensitivity or allergy to natural rubber latex.
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Values of hepatic aminotransferase (alanine aminotransferase and aspartate aminotransferase) outside of the normal range at screening.
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Hemoglobin or hematocrit outside of the normal range at screening.
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History or clinical evidence of any disease and/or existence of any surgical or medical condition, which might interfere with the absorption, distribution, metabolism or excretion of the study treatment(s) (appendectomy and herniotomy allowed, cholecystectomy not allowed).
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Previous history of fainting, collapse, syncope, orthostatic hypotension, or vasovagal reactions.
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Veins unsuitable for intravenous puncture on either arm (e.g., veins that are difficult to locate, access or puncture, veins with a tendency to rupture during or after puncture).
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Previous exposure to macitentan.
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Previous exposure to rosuvastatin.
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Treatment with another investigational drug within 3 months prior to screening or participation in more than 3 investigational drug studies within 1 year prior to screening.
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History or clinical evidence of alcoholism or drug abuse within the 3-year period prior to screening.
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Excessive caffeine consumption, defined as ≥ 800 mg per day at screening.
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Nicotine intake (e.g., smoking, nicotine patch, nicotine chewing gum or electronic cigarettes) within 3 months prior to screening and inability to refrain from nicotine intake from screening until End-Of-Study (EOS).
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Previous treatment with any prescribed medications (including vaccines) or over-the-counter (OTC) medications (including herbal medicines such as St John's Wort, homeopathic preparations, vitamins, and minerals) within 3 weeks prior to first study treatment administration.
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Loss of 250 mL or more of blood within 3 months prior to screening.
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Positive results from the hepatitis serology, except for vaccinated subjects or subjects with past but resolved hepatitis, at screening.
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Positive results from the HIV serology at screening.
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Any circumstances or conditions, which, in the opinion of the investigator, may affect full participation in the study or compliance with the protocol.
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Legal incapacity or limited legal capacity at screening.
Contacts and Locations
Locations
| Site | City | State | Country | Postal Code | |
|---|---|---|---|---|---|
| 1 | CRS Clinical Research Services Mannheim | Mannheim | Germany | 68167 |
Sponsors and Collaborators
- Actelion
Investigators
- Study Director: Shirin Bruderer, PhD, Actelion
Study Documents (Full-Text)
None provided.More Information
Publications
None provided.- AC-055-122