ClinicalTrials.gg
CompletedNCT00400660Updated Sep 29, 2017

A First Time In Human Study To Assess The Compound GSK615915

A Phase 1 interventional study of GSK615915A and Placebo in Bronchospasm, sponsored by GlaxoSmithKline. Completed at 1 site in United Kingdom. Open to participants aged 18 Years to 60 Years, including healthy volunteers. Per ClinicalTrials.gov, last updated 2017-09-29.

Sponsored by GlaxoSmithKline · Phase 1, Interventional, and Treatment

From the registry’s dates

  • Registered 11 months after the study started (first participant enrolled Nov 2005, registered Nov 2006).
Phase
Phase 1
Study type
Interventional
Enrollment
46
Allocation
Randomized
Ages
18 Years to 60 Years
Sex
All
01

Study summary

GSK615915A is being developed as a novel surfactant for use in the formulation of GSK's future generation of Metered Dose Inhalers (MDIs). A surfactant in a MDI would provide a more stable drug suspension, this in turn will produce a consistent dose of drug being delivered with each puff.

02

Conditions studied

  • Bronchospasm

Browse trials for

Keywords

  • GSK615915 asthma surfactant MDI
03

In context

Bronchial Spasm

44 studies on the registry are indexed under Bronchial Spasm; 4 are open to participants now.

This study's enrollment of 46 is below the median of 70 across 29 interventional studies indexed under Bronchial Spasm.

Browse Bronchial Spasm studies →

Lead sponsor

GlaxoSmithKline is the lead sponsor of 3,650 studies on the registry; 118 are open to participants now.

Of its 264 completed or terminated interventional studies of FDA-regulated products, 241 (91%) have results posted.

Counted across the registry records on this site, refreshed daily.

04

Who can participate

Ages eligible
18 Years to 60 Years
Sexes eligible
All
Accepts healthy volunteers
Yes

Go through the criteria one by one — yes, no or not sure — and take the list to your doctor or the study team. Kept in this browser only.

Inclusion criteria

  • Women of non-child bearing potential.
  • Body weight = 50 kg (110 lbs) for men and = 45 kg for women and (BMI) within the range 19.0-30.0 kg/m²
  • The subject is a current non-smoker who has not used any tobacco products in the last 12 months with a pack history of = 10 pack years.
  • The subject has demonstrated the ability to correctly use a metered dose inhaler device.
  • If asthmatic:

The subject must be clinically stable The subject has a baseline = 80% of predicted.

Exclusion criteria

Exclusion Criteria:

  • As a result of the medical interview, physical examination or screening investigations, the Physician Responsible considers the volunteer unfit for the study.
  • The subject has a history of allergy to , MDI propellants, or a history of drug or other allergy that, in the opinion of the physician responsible makes the volunteer unfit to participate.
  • The subject has recently participated in another clinical trial.
  • The subject has used prescription or non-prescription drugs, including vitamins, herbal and dietary supplements (including St John’s Wort) within 7 or 14 days.
  • The subject has an average weekly alcohol intake of greater than 21 units if male or 14 units if female, or an average daily intake of greater than 3 units regularly, where 1 unit is equivalent to a half-pint (220mL) of beer or 1 (25ml) measure of spirits or 1 glass (125ml) of wine.
  • Any history of breathing problems (e.g. history of asthmatic symptoms).
  • The subject is infected with the , , or virus.
  • The subject is has a positive drugs of abuse test.
  • The subject has had a respiratory tract infection within 4 weeks of the start of the study.
  • The subject has a past or present disease, which as judged by the Doctor, may affect the outcome of this study.
  • The subject has a history of life-threatening asthma.
  • The subject has taken inhaled, nasal or dermal within 4 weeks or oral steroids within 8 weeks of the start of the study.
  • The subject has taken long acting inhaled beta 2 agonists within 96 hours before the screening visit.
  • The subject has taken short acting inhaled beta 2 agonists within 8 hours before the screening visit.
  • The subject is unable to abstain from other drugs that may interfere with the conduct of the study or its interpretation.
  • The subject has ongoing rhinitis that requires treatment.
Terms in these criteria, in plain language(7)

Underlined terms in the criteria open these too. Explained by clinicaltrials.gg, not part of the registry record. The study team decides who can take part.

BMI (body mass index)

Weight in kilograms divided by height in metres squared. Example: 70 kg and 1.75 m gives 70 ÷ (1.75 × 1.75) ≈ 22.9.

What counts as overweight or obesity differs between countries (some use lower cut-offs), so go by the range the study states.

FEV1

From a breathing test (spirometry): how much air you can blow out in the first second. Often given as a percentage of what is expected for your age, height and sex.

Excipients

The other ingredients in a medicine besides the active drug, such as fillers, colours or preservatives.

Hepatitis B tests

Hepatitis B is a virus that infects the liver. These are separate tests: HBsAg positive usually means a current infection (a recent vaccination can briefly cause it too); total anti-HBc (HBcAb) positive means an infection now or in the past; HBV DNA measures how much virus is in the blood.

Some studies accept a past infection if HBV DNA is undetectable, sometimes with antiviral medicine during the study. Check what this study allows.

Hepatitis C tests

Hepatitis C is a virus that infects the liver. An HCV antibody test can stay positive after an infection has cleared (and is occasionally positive without one); an HCV RNA test shows whether the virus is there now.

After treatment, hepatitis C counts as cured when HCV RNA is still undetectable 12 weeks or more after the treatment ended. Studies often accept people cured this way.

HIV

The human immunodeficiency virus, which weakens the immune system.

Many studies now accept people whose HIV is controlled on treatment, judged by the viral load and the CD4 count. Check the limits this study sets.

Corticosteroids (steroids)

Anti-inflammatory medicines such as prednisone, prednisolone and dexamethasone — not the anabolic steroids used for muscle.

Studies differ in what they allow: check which steroid medicines, routes (tablets, injections, creams, inhalers, eye drops) and doses this study accepts.

05

Study design

Phase
Phase 1
Primary purpose
Treatment
Allocation
Randomized
Intervention model
Crossover assignment
Enrollment
46 participants (actual)

Study arms

  • Experimental
    Subjects receiving treatment sequence 1: Part 1

    Eligible subjects will receive placebo followed by GSK615915A with a starting dose of 250 micrograms.

    Drug: GSK615915A · Drug: Placebo

  • Experimental
    Subjects receiving treatment sequence 2: Part 1

    Eligible subjects will receive GSK615915A with a starting dose of 250 micrograms followed by placebo.

    Drug: GSK615915A · Drug: Placebo

  • Experimental
    Subjects receiving treatment sequence 1: Part 2

    Eligible subjects will receive placebo followed by GSK615915A with a starting dose of 250 micrograms.

    Drug: GSK615915A · Drug: Placebo

  • Experimental
    Subjects receiving treatment sequence 2: Part 2

    Eligible subjects will receive GSK615915A with a starting dose of 250 micrograms followed by placebo.

    Drug: GSK615915A · Drug: Placebo

  • Experimental
    Subjects receiving GSK615915A: Part 3

    Eligible subjects will receive GSK615915A with a starting dose of 250 micrograms.

    Drug: GSK615915A

  • Experimental
    Subjects receiving placebo: Part 3

    Eligible subjects will receive placebo.

    Drug: Placebo

Interventions

  • DrugGSK615915A

    GSK615915A inhaler will be given with a dose of 250 micrograms per metered actuation and 120 actuations per inhaler.

  • DrugPlacebo

    Subjects will also receive placebo inhaler.

06

What researchers measure

Primary outcomes

  1. Side effects Lung function Blood tests Heart rate and blood pressure Heart monitored (ECG)

    Time frame: Up to 18 weeks

Secondary outcomes

  1. Levels of GSK615915A and any breakdown products in the blood and urine.

    Time frame: Up to 18 weeks

07

Study locations

1 site
  • GSK Investigational Site
    Edinburgh, West Lothian EH14 4AP, United Kingdom
08

Timeline

Tracking since Sep 25, 2026
ElapsedEstimatedEstimated, not yet reached

Ran from Nov 2005 to primary completion in Jul 2006, 7 months.

How these figures are worked out, and which studies are left out of them.

Registered
Nov 15, 2006
First posted
Nov 17, 2006
StartActual
Nov 23, 2005
Primary completionActual
Jul 3, 2006
CompletionActual
Jul 3, 2006
Last update
Sep 29, 2017
What these dates mean
Start.
When the first participant enrolled; while estimated, when the study expects to open to recruitment.
Primary completion.
When the last participant was examined or treated to collect data for the study's main question, its primary outcome. A study that stopped early gives the date its data collection stopped.
Completion.
When the last participant's last visit took place, for every outcome, secondary ones and side effects included: the end of the study. Often later than primary completion, sometimes the same day.
Actual and Est.
Actual means the registry says the date has happened. Est. (estimated) is a date the sponsor plans or expects. It can still move, and the sponsor is expected to change it to actual once it has passed.
No changes since tracking began. The registry record was last updated on Sep 29, 2017, before this site started recording changes on Sep 25, 2026. Its history is on ClinicalTrials.gov ↗
09

Registry details

Key details

Study ID
NCT00400660
Lead sponsor
GlaxoSmithKline
Responsible party
Sponsor
First posted
Nov 17, 2006
Start date
Nov 23, 2005
Primary completion
Jul 3, 2006
Completion
Jul 3, 2006
Last update
Sep 29, 2017

Study contacts

GSK Clinical Trials
study director · GlaxoSmithKline
View the source record on ClinicalTrials.gov ↗

Not currently enrolling

This study is completed, as verified in Sep 2017. You cannot join it, but the record below documents what was studied.

Follow this study

Get an email when the registry record changes — status, dates, results — or when someone posts here.

Sign in to follow

Discussion

Questions and observations about this study, from anyone following it. Not medical advice, and not a channel to the study team — their contact details are on the registry record.

Sign in to join the discussion. Reading takes no account; posting does. You choose a display name, and a pseudonym is the default.

Nothing here yet. If you are running this trial, taking part in it, or weighing whether to, this is the place to say so.

Start the discussion