Independent directory Public ClinicalTrials.gov records United States
ClinicalTrials.gov record
Completed Phase 3 Interventional Results available

Co-administration of Olodaterol Respimat® and Tiotropium Handihaler®

ClinicalTrials.gov ID: NCT01696058

Public ClinicalTrials.gov record NCT01696058. Field values are reproduced from the official study page; the official ClinicalTrials.gov record remains the source of truth for eligibility, enrollment, and contact information.

ClinicalTrials.gov public records Last synced Oct 16, 2026, 9:34 PM EDT

Data is sourced from official ClinicalTrials.gov public API records. Always review the official ClinicalTrials.gov record for the latest information.

Official title

A Randomised, Double Blind, Parallel Group Study to Assess the Efficacy and Safety of 12 Weeks of Once Daily, Orally Inhaled, Co-administration of Olodaterol 5µg (Delivered by the Respimat® Inhaler) and Tiotropium 18µg (Delivered by the HandiHaler®) Compared to Once Daily, Orally Inhaled, Co-administration of Placebo (Delivered by the Respimat® Inhaler) and Tiotropium 18µg (Delivered by the HandiHaler®) in Patients With Chronic Obstructive Pulmonary Disease (COPD)[ANHELTO TM 2]

Brief summary

Reproduced verbatim from the official ClinicalTrials.gov record. Not medical advice.

The overall objective of this study is to assess efficacy and safety of 12 weeks, once daily, orally inhaled co-administration of olodaterol 5 µg (delivered by the Respimat® Inhaler) and tiotropium (delivered by the Handihaler® as Spiriva Handihaler®), compared to tiotropium (Spiriva Handihaler®) monotherapy on lung function in patients with COPD.

Study identification

NCT ID
NCT01696058
Recruitment status
Completed
Study type
Interventional
Phase
Phase 3
Lead sponsor
Boehringer Ingelheim
Industry
Enrollment
1,137 participants

Conditions and interventions

Eligibility (public fields only)

Age range
40 Years and older
Sex
All
Healthy volunteers
Healthy volunteers not accepted

This page does not interpret eligibility. Detailed inclusion and exclusion criteria are on the official ClinicalTrials.gov record.

Study timeline

Start date
Sep 2012 (Type not available)
Primary completion
Oct 2013 (Actual)
Completion
Oct 2013 (Actual)
Last update posted
Nov 25, 2014

2012 – 2013

United States locations

U.S. sites
94
U.S. states
34
U.S. cities
85
Facility City State ZIP Site status
1222.52.02090 Boehringer Ingelheim Investigational Site Anniston Alabama — —
1222.52.02046 Boehringer Ingelheim Investigational Site Birmingham Alabama — —
1222.52.02014 Boehringer Ingelheim Investigational Site Mobile Alabama — —
1222.52.02017 Boehringer Ingelheim Investigational Site Montgomery Alabama — —
1222.52.02092 Boehringer Ingelheim Investigational Site Anchorage Alaska — —
1222.52.02072 Boehringer Ingelheim Investigational Site Chandler Arizona — —
1222.52.02063 Boehringer Ingelheim Investigational Site Glendale Arizona — —
1222.52.02088 Boehringer Ingelheim Investigational Site Peoria Arizona — —
1222.52.02012 Boehringer Ingelheim Investigational Site Phoenix Arizona — —
1222.52.02006 Boehringer Ingelheim Investigational Site Huntington Beach California — —
1222.52.02031 Boehringer Ingelheim Investigational Site San Jose California — —
1222.52.02011 Boehringer Ingelheim Investigational Site Torrance California — —
1222.52.02061 Boehringer Ingelheim Investigational Site Boulder Colorado — —
1222.52.02054 Boehringer Ingelheim Investigational Site Fort Collins Colorado — —
1222.52.02001 Boehringer Ingelheim Investigational Site Hartford Connecticut — —
1222.52.02037 Boehringer Ingelheim Investigational Site Norwalk Connecticut — —
1222.52.02055 Boehringer Ingelheim Investigational Site Waterbury Connecticut — —
1222.52.02094 Boehringer Ingelheim Investigational Site Clearwater Florida — —
1222.52.02022 Boehringer Ingelheim Investigational Site Fort Lauderdale Florida — —
1222.52.02074 Boehringer Ingelheim Investigational Site Orlando Florida — —
1222.52.02016 Boehringer Ingelheim Investigational Site Ponte Verda Florida — —
1222.52.02084 Boehringer Ingelheim Investigational Site Saint Petersberg Florida — —
1222.52.02043 Boehringer Ingelheim Investigational Site Tampa Florida — —
1222.52.02009 Boehringer Ingelheim Investigational Site Blue Ridge Georgia — —
1222.52.02048 Boehringer Ingelheim Investigational Site Duluth Georgia — —
1222.52.02077 Boehringer Ingelheim Investigational Site Gainsville Georgia — —
1222.52.02040 Boehringer Ingelheim Investigational Site Rincon Georgia — —
1222.52.02024 Boehringer Ingelheim Investigational Site O'Fallon Illinois — —
1222.52.02002 Boehringer Ingelheim Investigational Site Muncie Indiana — —
1222.52.02008 Boehringer Ingelheim Investigational Site Fort Mitchell Kentucky — —
1222.52.02025 Boehringer Ingelheim Investigational Site Louisville Kentucky — —
1222.52.02089 Boehringer Ingelheim Investigational Site New Orleans Louisiana — —
1222.52.02005 Boehringer Ingelheim Investigational Site Baltimore Maryland — —
1222.52.02029 Boehringer Ingelheim Investigational Site Columbia Maryland — —
1222.52.02036 Boehringer Ingelheim Investigational Site Hollywood Maryland — —
1222.52.02015 Boehringer Ingelheim Investigational Site Townson Maryland — —
1222.52.02034 Boehringer Ingelheim Investigational Site North Dartmouth Massachusetts — —
1222.52.02003 Boehringer Ingelheim Investigational Site Chelsea Michigan — —
1222.52.02020 Boehringer Ingelheim Investigational Site Kalamazoo Michigan — —
1222.52.02047 Boehringer Ingelheim Investigational Site Minneapolis Minnesota — —
1222.52.02049 Boehringer Ingelheim Investigational Site Minneapolis Minnesota — —
1222.52.02079 Boehringer Ingelheim Investigational Site Plymouth Minnesota — —
1222.52.02068 Boehringer Ingelheim Investigational Site Chesterfield Missouri — —
1222.52.02028 Boehringer Ingelheim Investigational Site St Louis Missouri — —
1222.52.02053 Boehringer Ingelheim Investigational Site St Louis Missouri — —
1222.52.02050 Boehringer Ingelheim Investigational Site Billings Montana — —
1222.52.02035 Boehringer Ingelheim Investigational Site Henderson Nevada — —
1222.52.02030 Boehringer Ingelheim Investigational Site Marlton New Jersey — —
1222.52.02071 Boehringer Ingelheim Investigational Site Albuquerque New Mexico — —
1222.52.02064 Boehringer Ingelheim Investigational Site Johnson City New York — —
1222.52.02087 Boehringer Ingelheim Investigational Site New Windsor New York — —
1222.52.02091 Boehringer Ingelheim Investigational Site Syracuse New York — —
1222.52.02076 Boehringer Ingelheim Investigational Site Calabash North Carolina — —
1222.52.02010 Boehringer Ingelheim Investigational Site Huntersville North Carolina — —
1222.52.02045 Boehringer Ingelheim Investigational Site Raleigh North Carolina — —
1222.52.02038 Boehringer Ingelheim Investigational Site Salisbury North Carolina — —
1222.52.02051 Boehringer Ingelheim Investigational Site Shelby North Carolina — —
1222.52.02058 Boehringer Ingelheim Investigational Site Tabor City North Carolina — —
1222.52.02013 Boehringer Ingelheim Investigational Site Winston-Salem North Carolina — —
1222.52.02062 Boehringer Ingelheim Investigational Site Cincinnati Ohio — —
1222.52.02039 Boehringer Ingelheim Investigational Site Columbus Ohio — —
1222.52.02081 Boehringer Ingelheim Investigational Site Columbus Ohio — —
1222.52.02093 Boehringer Ingelheim Investigational Site Columbus Ohio — —
1222.52.02059 Boehringer Ingelheim Investigational Site Oklahoma City Oklahoma — —
1222.52.02026 Boehringer Ingelheim Investigational Site Medford Oregon — —
1222.52.02097 Boehringer Ingelheim Investigational Site Medford Oregon — —
1222.52.02075 Boehringer Ingelheim Investigational Site Philadelphia Pennsylvania — —
1222.52.02102 Boehringer Ingelheim Investigational Site Philadelphia Pennsylvania — —
1222.52.02080 Boehringer Ingelheim Investigational Site Pittsburgh Pennsylvania — —
1222.52.02100 Boehringer Ingelheim Investigational Site Charleston South Carolina — —
1222.52.02096 Boehringer Ingelheim Investigational Site Easley South Carolina — —
1222.52.02085 Boehringer Ingelheim Investigational Site Greenville South Carolina — —
1222.52.02101 Boehringer Ingelheim Investigational Site Greenville South Carolina — —
1222.52.02065 Boehringer Ingelheim Investigational Site Hodges South Carolina — —
1222.52.02042 Boehringer Ingelheim Investigational Site Myrtle Beach South Carolina — —
1222.52.02083 Boehringer Ingelheim Investigational Site Rock Hill South Carolina — —
1222.52.02066 Boehringer Ingelheim Investigational Site Spartanburg South Carolina — —
1222.52.02095 Boehringer Ingelheim Investigational Site Spartanburg South Carolina — —
1222.52.02098 Boehringer Ingelheim Investigational Site Union South Carolina — —
1222.52.02018 Boehringer Ingelheim Investigational Site Brentwood Tennessee — —
1222.52.02086 Boehringer Ingelheim Investigational Site Arlington Texas — —
1222.52.02044 Boehringer Ingelheim Investigational Site Austin Texas — —
1222.52.02041 Boehringer Ingelheim Investigational Site El Paso Texas — —
1222.52.02027 Boehringer Ingelheim Investigational Site Fort Worth Texas — —
1222.52.02056 Boehringer Ingelheim Investigational Site Houston Texas — —
1222.52.02007 Boehringer Ingelheim Investigational Site San Antonio Texas — —
1222.52.02060 Boehringer Ingelheim Investigational Site San Antonio Texas — —
1222.52.02078 Boehringer Ingelheim Investigational Site Sugar Land Texas — —
1222.52.02082 Boehringer Ingelheim Investigational Site Waco Texas — —
1222.52.02057 Boehringer Ingelheim Investigational Site Midvale Utah — —
1222.52.02023 Boehringer Ingelheim Investigational Site Richmond Virginia — —
1222.52.02069 Boehringer Ingelheim Investigational Site Selah Washington — —
1222.52.02019 Boehringer Ingelheim Investigational Site Tacoma Washington — —
1222.52.02099 Boehringer Ingelheim Investigational Site Morgantown West Virginia — —

Site contact phone numbers, emails, and investigator names are intentionally not displayed here. Open the official ClinicalTrials.gov record for site contact information.

About this trial record page

What this page shows
Public field values for ClinicalTrials.gov record NCT01696058, including study identification, conditions, interventions, eligibility (age, sex, healthy volunteer), timeline, and U.S. site list.
What this page does not do
No medical advice, eligibility judgments, treatment recommendations, study quality scoring, or AI-generated medical summaries. No site contact phone numbers, emails, or investigator names.
Where the data comes from
Sourced from the official ClinicalTrials.gov public API. The official record is the source of truth.
Last refresh
Last update posted Nov 25, 2014 · Synced Oct 16, 2026

Related: full search, browse by condition, browse by drug or therapy, browse by sponsor, browse by U.S. city.

Open the official record

The complete public registry record, listed eligibility criteria, and available contact information for NCT01696058 live on ClinicalTrials.gov.

View official ClinicalTrials.gov record →