AzTrials
AzTrials

Chronic Obstructive Pulmonary Disease (COPDPhase 1NCT02315131

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

A Phase 1 study testing TV46017 in people with Chronic Obstructive Pulmonary Disease (COPD, run by Teva Branded Pharmaceutical Products R&D, Inc. at 7 sites in 3 countries.

Terminated

Stopped early. The study ended before it was planned to and will not resume.

Official record
Search all trials

Trial summary

The primary objective of the study is to characterize the safety profile and duration of bronchodilation of a single dose of inhaled TV46017 Read more about this study

Who is it for?
Ages 20 to 75 yearsHealthy volunteers can take part
What is being tested?
TV46017
Could I receive a placebo?
Yes, some participants may receive a placebo
How many people
53 participants
Where
7 sitesin 3 countries
Study dates
Mar 2015to Aug 2015
Phase
Phase 1
Are there results?
None posted in the registry

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 20 to 75 years
  • All sexes
  • Healthy volunteers accepted
  • Adult, Older adult

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

Trial locations and contacts

7 sites in 3 countries.

7 sites in 3 countries

New Zealand3 sites
  • Teva Investigational Site 79037

    Auckland

  • Teva Investigational Site 79036

    Hamilton

  • Teva Investigational Site 79034

    Wellington

Other trials in New Zealand

United States2 sites
  • Teva Investigational Site 13034

    Raleigh, North Carolina

  • Teva Investigational Site 13033

    St Louis, Missouri

Other trials in United States

Australia2 sites
  • Teva Investigational Site 78984

    Adelaide

  • Teva Investigational Site 78985

    Nedlands

Other trials in Australia

About this study

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

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

Being tested
TV46017, Placebo
Medical subject headings
Pulmonary Disease, Chronic Obstructive

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

  • TV46017Drug

    Also called 46017

    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.

  • PlaceboDrug

    Also called Matching placebo

    Placebo Comparator

Study groups in NCT02315131
Study groupRoleWhat they receive
TV46017- Healthy VolunteersExperimentalStage 1 includes a single-dose treatment period
Receives: Drug: TV46017
Placebo - Healthy VolunteersPlacebo comparatorSome healthy subjects will be randomized to receive placebo.
Receives: Drug: Placebo
TV46017 15 μg- COPDExperimentalStage 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
Receives: Drug: TV46017
TV46017 60 μg- COPDExperimentalStage 2
Receives: Drug: TV46017
TV46017 120 μg- COPDExperimentalStage 2
Receives: Drug: TV46017
TV46017 240 μg- COPDExperimentalStage 2
Receives: Drug: TV46017

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. FEV1 AUC0-12h

    baseline adjusted forced expiratory volume in 1 second area under the curve over 12 hours

    Measured: Baseline, 12 hours

Secondary outcomes (2)
  1. FEV1

    baseline adjusted trough 12 hour

    Measured: Baseline, 12 hours

  2. Percentage of Participants with Adverse Events

    Measured: 28 Days

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted11 Dec 2014 (estimated)
  2. Study startMar 2015
  3. Primary completionAug 2015
  4. Study completionAug 2015

Why it stopped: Business decision

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 1
Primary purpose
Other
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Who is masked
Participant, Investigator
Enrolment
53 participants (actual)
IDs, dates and publications
ClinicalTrials.gov ID
NCT02315131
Sponsor's protocol ID
TV46017-COPD-10046
Status last verified
Nov 2021
First submitted
9 Dec 2014
Last updated
9 Nov 2021
Results posted
No
Data monitoring committee
No

Questions about this trial

What is this clinical trial studying?

A Phase 1 study testing TV46017 in people with Chronic Obstructive Pulmonary Disease (COPD, run by Teva Branded Pharmaceutical Products R&D, Inc. at 7 sites in 3 countries.

The full registered description is in the About this study section and the official record.

Who may be eligible to take part?

Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.

Is this clinical trial currently recruiting?

The record says: stopped early, as of the sponsor's last update on 9 Nov 2021. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 7 sites in New Zealand, United States, Australia. Whether a site is taking part right now should be confirmed with that site. See every site.

What are the possible benefits and risks?

They depend on the study and the treatment, and no study can promise a benefit. Some participants in this study may receive a placebo. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.

What does this phase mean?

Phase 1 studies test a treatment in a small group of people for the first time or in a new way, mainly to check safety and find the right dose.

Not every study follows the same path, and some studies (observational studies, device studies) have no phase.

Are results available for this study?

The study was stopped early (reason given: Business decision). Results are not available in the source record.

How can a doctor refer a patient or contact the research team?

The record lists no contact. The official record names the sponsor, who can be asked directly. AzTrials does not enrol participants or take referrals.

What does the primary outcome measure?

FEV1 AUC0-12h (time frame: Baseline, 12 hours). It is what the study was designed to measure, not a finding.

Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?

No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.

How often is this information updated?

AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 9 Nov 2021.

Free account

Log in to keep searching

You’ve used your 3 free searches. AzTrials is free: log in or create a free account to keep searching clinical trials and save the ones you want to follow.

Create a free accountLog in