A Randomized, Open-label, Single-dose, Single-center, Crossover Study in Healthy Subjects to Assess the Relative Bioavailability of PT010

PHASE1CompletedINTERVENTIONAL
Enrollment

56

Participants

Timeline

Start Date

October 17, 2017

Primary Completion Date

December 15, 2017

Study Completion Date

December 15, 2017

Conditions
Chronic Obstructive Pulmonary Disease
Interventions
DRUG

Regimen A

2 inhalations BGF MDI; no spacer device; no oral charcoal - reference formulation/total systemic exposure

DRUG

Regimen B

2 inhalations BGF MDI; AeroChamber Plus Flow-Vu spacer device; no oral charcoal - test formulation/total systemic exposure

DRUG

Regimen C

2 inhalations BGF MDI; no spacer device; with oral charcoal - reference formulation/lung exposure

DRUG

Regimen D

2 inhalations BGF MDI; AeroChamber Plus Flow-Vu spacer device; with oral charcoal - test formulation/lung exposure

Trial Locations (1)

21201

Pearl Investigative Site, Baltimore

Sponsors
All Listed Sponsors
lead

Pearl Therapeutics, Inc.

INDUSTRY