A 42-day Parallel Group Safety Study of Revefenacin and Formoterol, Administered in Sequence and as a Combination, in Participants With COPD

PHASE3CompletedINTERVENTIONAL
Enrollment

122

Participants

Timeline

Start Date

May 31, 2018

Primary Completion Date

September 25, 2018

Study Completion Date

September 25, 2018

Conditions
Chronic Obstructive Pulmonary Disease (COPD)
Interventions
DRUG

Revefenacin

Revefenacin is administered via a nebulizer.

DRUG

Placebo

Placebo version of Revefenacin is administered via a nebulizer.

DRUG

Formoterol

Administered sequentially in both revefenacin and placebo arms using a nebulizer.

Trial Locations (12)

16508

Theravance Biopharma Investigational Site, Erie

28112

Theravance Biopharma Investigational Site, Monroe

29303

Theravance Biopharma Investigational Site, Spartanburg

29341

Theravance Biopharma Investigational Site, Gaffney

29615

Theravance Biopharma Investigational Site, Greenville

32825

Theravance Biopharma Investigational Site, Orlando

33155

Theravance Biopharma Investigational Site, Miami

33603

Theravance Biopharma Investigational Site, Tampa

34239

Theravance Biopharma Investigational Site, Sarasota

43213

Theravance Biopharma Investigational Site, Columbus

63301

Theravance Biopharma Investigational Site, Saint Charles

97504

Theravance Biopharma Investigational Site, Medford

Sponsors

Lead Sponsor

Collaborators (1)

All Listed Sponsors
collaborator

Theravance Biopharma

INDUSTRY

lead

Mylan Inc.

INDUSTRY