Thorough QT Study to Evaluate Ampreloxetine in Healthy Subjects

PHASE1CompletedINTERVENTIONAL
Enrollment

72

Participants

Timeline

Start Date

January 18, 2021

Primary Completion Date

March 13, 2021

Study Completion Date

March 26, 2021

Conditions
Symptomatic Neurogenic Orthostatic HypertensionnOH
Interventions
DRUG

Ampreloxetine <Dose A>

Ampreloxetine \<Dose A\> will be administered as 1 tablet of \<Dose A\> and 3 tablets of Ampreloxetine Placebo.

DRUG

Ampreloxetine <Dose B>

Ampreloxetine \<Dose B\> will be administered as 4 tablets of \<Dose A\>

DRUG

Ampreloxetine Placebo

Ampreloxetine Placebo will be administered as 4 tablets of placebo. The placebo tablet will match (in appearance) the ampreloxetine \<Dose A\> tablet.

DRUG

Moxifloxacin

Moxifloxacin will be administered orally as a single tablet.

DRUG

Moxifloxacin Placebo

Moxifloxacin placebo will be administered orally as a single tablet. The placebo tablet will match (in appearance) the moxifloxacin tablet.

Trial Locations (1)

85283

Theravance Biopharma Investigational Site, Tempe

Sponsors
All Listed Sponsors
lead

Theravance Biopharma

INDUSTRY

NCT04688632 - Thorough QT Study to Evaluate Ampreloxetine in Healthy Subjects | Biotech Hunter | Biotech Hunter