A Study to Investigate the Effect of CYP3A Inhibition on the Pharmacokinetics of RO7017773 in Healthy Participants
NCT03774576 · Status: COMPLETED · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 14
Last updated 2020-05-07
Summary
The purpose of this study is to investigate the effect of multiple oral doses of itraconazole on the pharmacokinetics of RO7017773 in healthy volunteers.
Conditions
- Healthy Volunteers
Interventions
- DRUG
-
RO7017773
Single doses of RO7017773
- DRUG
-
Itraconazole
Multiple doses of Itraconazole
Sponsors & Collaborators
- lead INDUSTRY
Principal Investigators
-
Clinical Trials · Hoffmann-La Roche
Study Design
- Allocation
- NON_RANDOMIZED
- Purpose
- TREATMENT
- Masking
- NONE
- Model
- SINGLE_GROUP
Eligibility
- Min Age
- 18 Years
- Max Age
- 55 Years
- Sex
- ALL
- Healthy Volunteers
- Yes
Timeline & Regulatory
- Start
- 2018-12-17
- Primary Completion
- 2019-03-14
- Completion
- 2019-03-14
Countries
- France
Study Locations
More Related Trials
-
Effect Of Itraconazole On The Pharmacokinetics Of Palbociclib
NCT02131298 ·Status: COMPLETED ·Phase: PHASE1
-
Relative Bioavailability, Safety, Tolerability, Pharmacokinetics (PK) and Food Effect Study of GSK2140944 in Healthy Subjects
NCT02045849 ·Status: COMPLETED ·Phase: PHASE1
-
A Study of RO4995819 to Assess Bioavailability and Safety in Healthy Volunteers
NCT01901159 ·Status: COMPLETED ·Phase: PHASE1
-
A Pharmacokinetic Study to Assess the Influence of Simultaneous CYP3A4 and P-glycoprotein Inhibition on E7080 Pharmacokinetics Following Single Dose Oral Administration of 5 mg E7080 to Healthy Volunteers
NCT02198170 ·Status: COMPLETED ·Phase: PHASE1
-
A Fixed-Sequence, Two-Period, Open-Label Drug-Drug Interaction Study to Assess the Effect of an Inhibitor of Cytochrome P450 Isoenzyme 3A4 and Permeability Glycoprotein 1 on the Pharmacokinetics of TD-1211
NCT01568411 ·Status: COMPLETED ·Phase: PHASE1
-
Study of BIIB091 Formulations in Healthy Participants
NCT04564612 ·Status: COMPLETED ·Phase: PHASE1
-
Study in Postmenopausal Women to Investigate the Drug-drug Interaction (DDI) Between Itraconazole(ITZ) and Orally Administered Vilaprisan; Absolute Bioavailability Using Intravenous Microtracer Dose of [14C]Vilaprisan
NCT02456129 ·Status: COMPLETED ·Phase: PHASE1
-
Study to Evaluate the Effect of SCY-078 (Ibrexafungerp) on the PK of Pravastatin in Healthy Subjects
NCT04092751 ·Status: COMPLETED ·Phase: PHASE1
-
Effect of GSK376501 on CYP450 Activity in Healthy Adult Subjects
NCT00615212 ·Status: COMPLETED ·Phase: PHASE1
-
A Bioavailability and Pharmacokinetic Study of Subcutaneous and Intravenous RO6811135 in Healthy Volunteers
NCT01802853 ·Status: COMPLETED ·Phase: PHASE1
-
A 2 Part Study to Assess the Relative Bioavailability of Tablet Formulation Compared to Capsule Formulation and the Effect of Food and Taste Assessment on the Tablet Formulation in Healthy Participants
NCT03847987 ·Status: COMPLETED ·Phase: PHASE1
-
Effect of Ketoconazole on Regorafenib (BAY73-4506) Pharmacokinetics
NCT01318265 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Assess the Relative Bioavailability of Roxadustat Following a Single Dose of Pediatric Azo Dye-free Tablet Formulation and Pediatric Azo Dye-free Mini-tablet Formulation Compared to a Single Dose of Azo Dye-containing Tablet Formulation in Healthy Adult Subjects
NCT03960489 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Investigate the Recovery, Excretion and Pharmacokinetics of [14C]-GSK2140944 Administered as a Single Intravenous and Single Oral Dose to Healthy Adult Male Subjects
NCT02000765 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Evaluate the Pharmacokinetics and Safety of IN-M00007 and IN-R00007 in Healthy Adult Volunteers
NCT07311811 ·Status: NOT_YET_RECRUITING ·Phase: PHASE1
-
To Assess Safety, Tolerability and Pharmacokinetics of BI 416970 in Healthy Male Volunteers
NCT02093819 ·Status: COMPLETED ·Phase: PHASE1
-
Effects of Altered Formulation on the Bioequivalence of Tacrolimus in Healthy Female and Male Volunteeers
NCT02341274 ·Status: COMPLETED ·Phase: PHASE1
-
Pharmacokinetic and Tolerability of Alirocumab SAR236553 (REGN727) in Patients With Hepatic Impairment and in Healthy Subjects
NCT01670734 ·Status: COMPLETED ·Phase: PHASE1
-
Safety Tolerability and Pharmacokinetic of BI 411034
NCT01581684 ·Status: COMPLETED ·Phase: PHASE1
-
A Study to Evaluate the Relative Bioavailability of New Formulations of INCB057643 Tablets Administered Orally in Healthy Participants
NCT06941077 ·Status: COMPLETED ·Phase: PHASE1
-
A Study of the Relative Bioavailability of Single Dose RO4917838 and the Effect of Food in Healthy Volunteers
NCT01665976 ·Status: COMPLETED ·Phase: PHASE1
-
Relative Bioavailability and Food Effect of SYHA1813 Oral Solution in Healthy Participants
NCT06157918 ·Status: COMPLETED ·Phase: PHASE1
-
A Study of Bitopertin (RO4917838) in Healthy Male Volunteers
NCT01636492 ·Status: COMPLETED ·Phase: PHASE1
-
Safety of Single Rising Doses and Relative Bioavailability of BI 691751
NCT01843972 ·Status: COMPLETED ·Phase: PHASE1
-
Study to Investigate Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of Single Rising Doses of BI 187004 CL
NCT01587417 ·Status: COMPLETED ·Phase: PHASE1