A Phase 1, Fixed-Sequence, Open-Label Drug-Drug Interaction Study to Assess the Effect of Fluvoxamine (CYP1A2 Inhibitor), Cigarette Smoking (CYP1A2 Inducer) and Itraconazole (CYP3A4 Inhibitor) on the Pharmacokinetics of TD-9855 in Healthy Subjects

Theravance Biopharma1 site in 1 country41 target enrollmentFebruary 28, 2018

ConditionsDrug Drug Interaction (DDI)

InterventionsTD-9855 Fluvoxamine Caffeine Itraconazole

DrugsTD-9855 Fluvoxamine Itraconazole Caffeine

Overview

Phase: Phase 1
Intervention: TD-9855
Conditions: Drug Drug Interaction (DDI)
Sponsor: Theravance Biopharma
Enrollment: 41
Locations: 1
Primary Endpoint: Change in TD-9855 plasma exposure when administered with itraconazole or fluvoxamine
Status: Completed
Last Updated: 5 years ago

Overview Investigators Eligibility Criteria Arms & Interventions Outcomes Sites Similar Trials

Overview

Brief Summary

This study is designed to assess the effect of fluvoxamine, itraconazole and smoking on the PK disposition of multiple doses TD-9855 in healthy male subjects. The study will also assess the relationship between caffeine PK and TD-9855 PK disposition in healthy male smokers and non-smokers.

Registry

clinicaltrials.gov

Start Date

February 28, 2018

End Date

April 21, 2018

Last Updated

5 years ago

Study Type

Interventional

Study Design

Parallel

Sex

Male

Investigators

Sponsor

Theravance Biopharma

Responsible Party

Sponsor

Eligibility Criteria

Inclusion Criteria

•Willing and able to give written, signed informed consent
•Male subjects 19 to 55 years of age (inclusive)
•Body mass index 19 to 32 kg/m2 (inclusive), and weigh at least 55 kg
•No clinically important abnormal physical findings as determined by the Principal Investigator (PI) at the screening and Day -1 examinations
•Negative for hepatitis B virus (HBV), hepatitis C virus (HCV), and human immunodeficiency virus (HIV) antibody at screening.
•No clinically important laboratory abnormalities as determined by the PI
•Ability to communicate effectively with the Investigator and to comply with all study requirements, restrictions, and direction of the clinic staff
•Male subjects must abstain from sexual intercourse or use a highly effective method of birth control
•Male smokers: Subjects who self-report to have smoked \> 9 cigarettes per day for at least 6 month prior to screening as confirmed by urine cotinine test at screening and Day -
•Male smokers: Subjects must be willing to continue consistent use of their tobacco products throughout the study.

Exclusion Criteria

•Positive for hepatitis B virus (HBV), hepatitis C virus (HCV), and human immunodeficiency virus (HIV) antibody at screening.
•History or presence of clinically significant respiratory, gastrointestinal, renal, hepatic, hematologic, neurologic (including history of seizure and insomnia), cardiovascular (including postural orthostatic hypotension or tachycardia), psychiatric (including depression and known addictive disorders), musculoskeletal, genitourinary (including urinary retention), immunologic, or dermatologic disorder.
•Any other condition that, in the opinion of the PI, would confound or interfere with study participation; evaluation of safety, tolerability, or PK of the investigational drug; or prevent compliance with the study protocol
•Any history of suicide attempts/ideation or current suicidal ideation.
•Have participated in another clinical trial of an investigational drug (or medical device) within 30 days (or 5 half-lives of the investigational drug if longer than 30 days) prior to Screening, or are currently participating in another trial of an investigational drug (or medical device), or intending to participate in another trial of an investigational drug (or medical device) before completion of all scheduled safety evaluations in this trial
•Additional inclusion criteria apply