Dose Adaptation to Offset the Interaction Between Ticagrelor and Ritonavir by Population-based PK Modeling

Healthy Clinical Trial

Official title:

Dose Adaptation to Offset the Pharmacokinetic Interaction Between Ticagrelor and Ritonavir in Healthy Volunteers by Population-based PK Modeling (Simcyp®)

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT02435563
• Other study ID #: 13-182
• Status: Completed
• Phase: Phase 2
• First received: September 15, 2014
• Last updated: February 6, 2017
• Start date: August 2014
• Est. completion date: April 2015

Study information

• Verified date: February 2017
• Source: University Hospital, Geneva
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

Ticagrelor is a new generation antiplatelet agent with higher efficacy as compared to clopidogrel and prasugrel in treatment of patients with moderate and high ischemic risks. Ticagrelor is active as such and its hepatic metabolism by CYP3A generates also an active metabolite. Because of the remarkable progress in HIV therapies the number of older age patients is on the rise, requiring adequate cardiovascular treatment. Since frontline HIV therapies include ritonavir, a strong inhibitor of CYP3A enzyme, ticagrelor is contraindicated in these patients because of the expected interaction and bleeding risk. A lower efficacy of clopidogrel and prasugrel, which are both pro-drugs, in the presence of ritonavir has been already demonstrated. Therefore, administration of a lower dose of ticagrelor may be a good alternative in HIV patients in order to lessen the impact of this pharmacokinetic interaction. The aim of this study is to adjust the dose of ticagrelor in case of co-treatment with ritonavir to achieve the same pharmacokinetic profile as administered alone using a physiologically-based pharmacokinetic (PBPK) model.

As the first step, a pharmacokinetic (PK) model for ticagrelor and its active metabolite will be created based on available in vitro and in vivo parameters in healthy volunteers.

An open-label, 2 sessions cross over study will be conducted with 20 healthy male volunteers at Clinical Research Center (CRC) of Geneva University Hospitals (HUG). During the first session of the clinical trial, a single dose 180 mg ticagrelor will be administered to the volunteers and obtained pharmacokinetic data will be fitted into the model for optimization. Thereafter a simulated trial by the Simcyp® simulator in presence of a single dose 100 mg ritonavir will allow evaluating the impact of CYP3A inhibition on the concentration-time profile of ticagrelor and its active metabolite. The necessary dose of ticagrelor to minimize the magnitude of this interaction will be calculated. This new dose will be co-administered with ritonavir in the same volunteers during the second session of the clinical trial. The purpose is to obtain the same PK profile with single dose of 180 mg ticagrelor administered alone and with an adapted dose of ticagrelor co-administered with a single dose 100 mg ritonavir. Moreover, the pharmacodynamic effect of ticagrelor will be measured in both sessions of the clinical trial using two specific platelet function tests: the VAsodilator-Stimulated Phosphoprotein assay (VASP) and VerifyNow® P2Y12. With the same PK profile, the same pharmacodynamic activity is expected. The modulation of activity of CYP3A and P-gp by ritonavir will be also monitored using micro dose midazolam and fexofenadine as probe substrates.

The purpose of this study is to use the Simcyp® Simulator mechanistic PBPK modeling to broaden the application field of ticagrelor, especially in HIV patients. Since PK models are often created after clinical observations, the prospective aspect of this study is of particular value as the model will be first created and then applied to an unknown clinical scenario.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 22
• Est. completion date: April 2015
• Est. primary completion date: April 2015
• Accepts healthy volunteers: Accepts Healthy Volunteers
• Gender: Male
• Age group: 18 Years to 60 Years

Eligibility

Inclusion Criteria:

• Healthy male volunteers

• Aged between 18 and 60 years

• BMI between 18 and 27

• Understanding of French language and able to give an inform consent.

Exclusion Criteria:

• Hypersensitivity to ticagrelor or ritonavir or any constituents of the tablets

• Concomitant diseases

• Smokers (> 20 cigarettes per day)

• Intake of any drug or food (grapefruit) that is metabolized by or can affect CYP3A or P-glycoprotein activity within the last 10 days

• Pathologies or drugs associated with an increased bleeding risk such as aspirin, non-steroidal anti-inflammatory drugs, steroids and serotonin reuptake inhibitors

• Bleeding familial history or antecedent or hemorrhagic disease

• Previous or active gastro-intestinal ulcer

• Alteration of hepatic tests (ASAT>100 U/l, ALAT >100 U/l, GGT >80 U/l, BILI > 50 µmol/l)

Related Conditions & MeSH terms

• Healthy

Intervention

Drug:
• ticagrelor 180 mg administrated alone

• Ticagrelor adjusted dose + ritonavir 100mg

Locations

Country	Name	City	State
Switzerland	Centre de Recherche Clinique, HUG, Rue Gabrielle Perret-Gentil 4	Genève

Sponsors (1)

Lead Sponsor	Collaborator
University Hospital, Geneva

Country where clinical trial is conducted

Switzerland, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Change in AUC of ticagrelor and its metabolite from baseline	Venous blood samples will be taken to assess the baseline pharmacokinetic parameters of ticagrelor and its metabolite, prior to ticagrelor administration (time zero) and at the following post dosage times: 0.5, 1, 2, 3, 4, 6, 8, and 24 hours	30 min 1hr 2hr 3hr 4hr 6hr 8hr 24hr
Secondary	Measure of the pharmacodynamic response to ticagrelor by two platelet reactivity tests VASP and VerifyNow® P2Y12	4 hours after administration of ticagrelor the pharmacodynamic, response of ticagrelor will be assessed by the VAsodilator-Stimulated Phosphoprotein Assay (VASP) and VerifyNow® P2Y12 tests	4hr
Secondary	Change in P-gp phenotyping from baseline (0 min)	Venous blood samples will be taken to assess the P-gp phenotyping, prior to fexofenadine administration (time zero) and at the following post dosage times: 0.5, 1, 2, 3, 4, 6, 8, and 24 hours	30 min 1hr 2hr 3hr 4hr 6hr 8hr 24hr
Secondary	Change in CYP3A4 phenotyping from baseline (0 min)	Venous blood samples will be taken to assess the CYP3A4 phenotyping, prior to midazolam administration (time zero) and at the following post dosage time: 1 hour	1hr