search
Back to results

Study in Healthy Volunteers and COPD Patients to Evaluate the Efficacy and Safety of Inhaled TV46017

Primary Purpose

Chronic Obstructive Pulmonary Disease (COPD

Status
Terminated
Phase
Phase 1
Locations
International
Study Type
Interventional
Intervention
TV46017
Placebo
Sponsored by
Teva Branded Pharmaceutical Products R&D, Inc.
About
Eligibility
Locations
Arms
Outcomes
Full info

About this trial

This is an interventional other trial for Chronic Obstructive Pulmonary Disease (COPD

Eligibility Criteria

20 Years - 75 Years (Adult, Older Adult)All SexesAccepts Healthy Volunteers

Stage 1 Inclusion Criteria (healthy volunteers):

  • The subject is a male or female 20 to 75 years of age, inclusive, weighing 50 to 80 kg with a body mass index (BMI) of less than 30 kg/m2. Note: Every effort should be made to enroll approximately equal numbers of men and women in each group.
  • The subject is in good health as determined by medical and psychiatric history, physical examination, electrocardiogram (ECG), serum chemistry, hematology, urinalysis, and serology.
  • Other criteria apply, please contact the investigator for more information

Stage 2 Inclusion Criteria (COPD patients):

  • Current or former cigarette smokers with a history of cigarette smoking of ≥10 pack years at the SV (number of cigarette packs smoked per day multiplied by the number of years smoked; eg, 2 packs/day for 3 years equals a 6 pack year history).
  • Diagnosis of COPD as defined by the Global Initiative for Chronic Obstructive Lung Disease guidelines.
  • Male or female; 40 to 75 years of age, inclusive.
  • Patient is free of any other medical conditions or concomitant treatment that could interfere with study conduct, influence the interpretation of study observations/results, or put the patient at increased risk during the study.
  • Other criteria apply, please contact the investigator for more information

Stage 1 Exclusion Criteria (healthy volunteers):

  • History or current evidence of a clinically significant or uncontrolled disease.
  • Any disorder that may interfere with the absorption, distribution, metabolism or excretion of study drugs.
  • History of severe allergy to milk protein.
  • Active smokers or former smokers who quit within 3 months of the first dose of study drug. Former smokers with greater than five-pack years (ie, the equivalent of one pack per day for five years) are also excluded.
  • Other criteria apply, please contact the investigator for more information

Stage 2 Exclusion Criteria (COPD patients):

  • Recent history of hospitalization due to an exacerbation of airway disease within 3 months.
  • Need for increased treatments of COPD within 6 weeks prior to the SV.
  • Occurrence of a COPD exacerbation, which is not resolved by 4 weeks or more prior to the SV/informed consent. (Note: An exacerbation of COPD is defined as any worsening of the patient's baseline COPD symptoms requiring any treatment other than rescue albuterol or the patient's regular maintenance therapy. This includes requiring the use of systemic corticosteroids, antibiotics, and/or emergency room visit or hospitalization.)
  • History of and/or current diagnosis of asthma.
  • Known α1 antitrypsin deficiency, active lung infections (such as tuberculosis or pneumonia), and lung cancer are absolute exclusionary conditions. A patient who, in the opinion of the investigator, has any other significant respiratory condition in addition to COPD should be excluded. Examples may include clinically significant noncystic bronchiectasis, pulmonary hypertension, sarcoidosis, or interstitial lung disease. Allergic rhinitis is not exclusionary.
  • Other criteria apply, please contact the investigator for more information

Sites / Locations

  • Teva Investigational Site 13033
  • Teva Investigational Site 13034
  • Teva Investigational Site 78984
  • Teva Investigational Site 78985
  • Teva Investigational Site 79037
  • Teva Investigational Site 79036
  • Teva Investigational Site 79034

Arms of the Study

Arm 1

Arm 2

Arm 3

Arm 4

Arm 5

Arm 6

Arm Type

Experimental

Placebo Comparator

Experimental

Experimental

Experimental

Experimental

Arm Label

TV46017- Healthy Volunteers

Placebo - Healthy Volunteers

TV46017 15 μg- COPD

TV46017 60 μg- COPD

TV46017 120 μg- COPD

TV46017 240 μg- COPD

Arm Description

Stage 1 includes a single-dose treatment period

Some healthy subjects will be randomized to receive placebo.

Stage 2 includes two 24 hour treatment periods with approximately 7 days of washout in between each treatment period; and open label ipratropium bromide pressurized metered-dose inhaler hydrofluoroalkane (HFA) will be administered

Stage 2

Stage 2

Stage 2

Outcomes

Primary Outcome Measures

FEV1 AUC0-12h
baseline adjusted forced expiratory volume in 1 second area under the curve over 12 hours

Secondary Outcome Measures

FEV1
baseline adjusted trough 12 hour
Percentage of Participants with Adverse Events

Full Information

First Posted
December 9, 2014
Last Updated
November 5, 2021
Sponsor
Teva Branded Pharmaceutical Products R&D, Inc.
search

1. Study Identification

Unique Protocol Identification Number
NCT02315131
Brief Title
Study in Healthy Volunteers and COPD Patients to Evaluate the Efficacy and Safety of Inhaled TV46017
Official Title
A 2-Stage, Single-Dose Study in Healthy Volunteers and COPD Patients With an Open Label Ipratropium Bromide Reference to Evaluate the Efficacy, Pharmacokinetics, and Safety Profile of Inhaled TV46017
Study Type
Interventional

2. Study Status

Record Verification Date
November 2021
Overall Recruitment Status
Terminated
Why Stopped
Business decision
Study Start Date
March 2015 (undefined)
Primary Completion Date
August 2015 (Actual)
Study Completion Date
August 2015 (Actual)

3. Sponsor/Collaborators

Responsible Party, by Official Title
Sponsor
Name of the Sponsor
Teva Branded Pharmaceutical Products R&D, Inc.

4. Oversight

Data Monitoring Committee
No

5. Study Description

Brief Summary
The primary objective of the study is to characterize the safety profile and duration of bronchodilation of a single dose of inhaled TV46017

6. Conditions and Keywords

Primary Disease or Condition Being Studied in the Trial, or the Focus of the Study
Chronic Obstructive Pulmonary Disease (COPD

7. Study Design

Primary Purpose
Other
Study Phase
Phase 1
Interventional Study Model
Parallel Assignment
Masking
ParticipantInvestigator
Allocation
Randomized
Enrollment
53 (Actual)

8. Arms, Groups, and Interventions

Arm Title
TV46017- Healthy Volunteers
Arm Type
Experimental
Arm Description
Stage 1 includes a single-dose treatment period
Arm Title
Placebo - Healthy Volunteers
Arm Type
Placebo Comparator
Arm Description
Some healthy subjects will be randomized to receive placebo.
Arm Title
TV46017 15 μg- COPD
Arm Type
Experimental
Arm Description
Stage 2 includes two 24 hour treatment periods with approximately 7 days of washout in between each treatment period; and open label ipratropium bromide pressurized metered-dose inhaler hydrofluoroalkane (HFA) will be administered
Arm Title
TV46017 60 μg- COPD
Arm Type
Experimental
Arm Description
Stage 2
Arm Title
TV46017 120 μg- COPD
Arm Type
Experimental
Arm Description
Stage 2
Arm Title
TV46017 240 μg- COPD
Arm Type
Experimental
Arm Description
Stage 2
Intervention Type
Drug
Intervention Name(s)
TV46017
Other Intervention Name(s)
46017
Intervention Description
TV46017 15, 60, 120, and 240 μg; 4 ascending doses of inhaled TV46017 with an ipratropium bromide reference to evaluate the single administration of 4 ascending doses of inhaled TV46017 in COPD patients.
Intervention Type
Drug
Intervention Name(s)
Placebo
Other Intervention Name(s)
Matching placebo
Intervention Description
Placebo Comparator
Primary Outcome Measure Information:
Title
FEV1 AUC0-12h
Description
baseline adjusted forced expiratory volume in 1 second area under the curve over 12 hours
Time Frame
Baseline, 12 hours
Secondary Outcome Measure Information:
Title
FEV1
Description
baseline adjusted trough 12 hour
Time Frame
Baseline, 12 hours
Title
Percentage of Participants with Adverse Events
Time Frame
28 Days

10. Eligibility

Sex
All
Minimum Age & Unit of Time
20 Years
Maximum Age & Unit of Time
75 Years
Accepts Healthy Volunteers
Accepts Healthy Volunteers
Eligibility Criteria
Stage 1 Inclusion Criteria (healthy volunteers): The subject is a male or female 20 to 75 years of age, inclusive, weighing 50 to 80 kg with a body mass index (BMI) of less than 30 kg/m2. Note: Every effort should be made to enroll approximately equal numbers of men and women in each group. The subject is in good health as determined by medical and psychiatric history, physical examination, electrocardiogram (ECG), serum chemistry, hematology, urinalysis, and serology. Other criteria apply, please contact the investigator for more information Stage 2 Inclusion Criteria (COPD patients): Current or former cigarette smokers with a history of cigarette smoking of ≥10 pack years at the SV (number of cigarette packs smoked per day multiplied by the number of years smoked; eg, 2 packs/day for 3 years equals a 6 pack year history). Diagnosis of COPD as defined by the Global Initiative for Chronic Obstructive Lung Disease guidelines. Male or female; 40 to 75 years of age, inclusive. Patient is free of any other medical conditions or concomitant treatment that could interfere with study conduct, influence the interpretation of study observations/results, or put the patient at increased risk during the study. Other criteria apply, please contact the investigator for more information Stage 1 Exclusion Criteria (healthy volunteers): History or current evidence of a clinically significant or uncontrolled disease. Any disorder that may interfere with the absorption, distribution, metabolism or excretion of study drugs. History of severe allergy to milk protein. Active smokers or former smokers who quit within 3 months of the first dose of study drug. Former smokers with greater than five-pack years (ie, the equivalent of one pack per day for five years) are also excluded. Other criteria apply, please contact the investigator for more information Stage 2 Exclusion Criteria (COPD patients): Recent history of hospitalization due to an exacerbation of airway disease within 3 months. Need for increased treatments of COPD within 6 weeks prior to the SV. Occurrence of a COPD exacerbation, which is not resolved by 4 weeks or more prior to the SV/informed consent. (Note: An exacerbation of COPD is defined as any worsening of the patient's baseline COPD symptoms requiring any treatment other than rescue albuterol or the patient's regular maintenance therapy. This includes requiring the use of systemic corticosteroids, antibiotics, and/or emergency room visit or hospitalization.) History of and/or current diagnosis of asthma. Known α1 antitrypsin deficiency, active lung infections (such as tuberculosis or pneumonia), and lung cancer are absolute exclusionary conditions. A patient who, in the opinion of the investigator, has any other significant respiratory condition in addition to COPD should be excluded. Examples may include clinically significant noncystic bronchiectasis, pulmonary hypertension, sarcoidosis, or interstitial lung disease. Allergic rhinitis is not exclusionary. Other criteria apply, please contact the investigator for more information
Overall Study Officials:
First Name & Middle Initial & Last Name & Degree
Teva Medical Expert, MD
Organizational Affiliation
Teva Branded Pharmaceutical Products R&D, Inc.
Official's Role
Study Director
Facility Information:
Facility Name
Teva Investigational Site 13033
City
Saint Louis
State/Province
Missouri
Country
United States
Facility Name
Teva Investigational Site 13034
City
Raleigh
State/Province
North Carolina
Country
United States
Facility Name
Teva Investigational Site 78984
City
Adelaide
Country
Australia
Facility Name
Teva Investigational Site 78985
City
Nedlands
Country
Australia
Facility Name
Teva Investigational Site 79037
City
Auckland
Country
New Zealand
Facility Name
Teva Investigational Site 79036
City
Hamilton
Country
New Zealand
Facility Name
Teva Investigational Site 79034
City
Wellington
Country
New Zealand

12. IPD Sharing Statement

Learn more about this trial

Study in Healthy Volunteers and COPD Patients to Evaluate the Efficacy and Safety of Inhaled TV46017

We'll reach out to this number within 24 hrs