Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

NCT00414141 · ClinicalTrials.gov registry record · Phase 3

Efficacy and Safety/Tolerability of Grass MATA MPL

A Phase 3 study, sponsored by Allergy Therapeutics.

Completed
Registry status
Phase 3
Development phase
1,028
Enrollment target

NCT00414141 is a Phase 3 study that has completed, run by Allergy Therapeutics. The registered enrollment target is 1,028 participants.

View on ClinicalTrials.gov ↗

View your shortlist →

The verdict

NCT00414141, a Phase 3 study, has completed, sponsored by Allergy Therapeutics.

COMPLETED
Registry status
Phase 3
Development phase
1,028 participants
Enrollment target

Study Summary

Grass MATA MPL has been developed by Allergy Therapeutics (UK) Ltd. to provide pre-seasonal specific immunotherapy for patients with proven type I hypersensitivity to cross reacting grass pollens causing rhinitis and/or conjunctivitis with or without mild to moderate asthma bronchiale. The purpose of this study is to compare the efficacy of Grass MATA MPL versus placebo in grass-allergic subjects following 4 subcutaneous injections of study medication administered before the start of the 2007 grass pollen season.

Interventions

  • BIOLOGICAL Placebo
  • BIOLOGICAL Grass MATA MPL

Trial Details

FieldValue
Enrollment Target 1,028 participants
Start Date 2006-11
Est. Completion 2007-11
Phase Phase 3

Sponsor

Allergy Therapeutics

12 total trials

What the Registry Record Tells You About NCT00414141

The ClinicalTrials.gov registry entry for NCT00414141 describes a study currently listed as completed, categorized as Phase 3. The registered enrollment target is 1,028 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Allergy Therapeutics, which has 12 total studies on file at ClinicalTrials.gov.

The record links to 0 conditions, and to 2 interventions - of which Placebo is the first listed.

NCT00414141 reports 0 study locations.

Frequently Asked Questions

What is clinical trial NCT00414141 about?

NCT00414141 is a clinical study titled "Efficacy and Safety/Tolerability of Grass MATA MPL". Grass MATA MPL has been developed by Allergy Therapeutics (UK) Ltd. to provide pre-seasonal specific immunotherapy for patients with proven type I hypersensitivity to cross reacting grass pollens causing rhinitis and/or conjunctivitis with or without mild to moderate asthma bronchiale. The purpose o...

What is the current status of trial NCT00414141?

This trial is currently completed. It is a Phase 3 study. The enrollment target is 1,028 participants. The study started on 2006-11. Estimated completion is 2007-11.

What interventions are being tested in trial NCT00414141?

The interventions under investigation include: Placebo (BIOLOGICAL), Grass MATA MPL (BIOLOGICAL).

Who is sponsoring clinical trial NCT00414141?

This trial is sponsored by Allergy Therapeutics, which has 12 total clinical trials registered on ClinicalTrials.gov.

Data sourced from official public datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial

Every figure on PlainTrial is rendered directly from the ClinicalTrials.gov registry, no number is typed in by an editor. This page mirrors this trial's own ClinicalTrials.gov registry record, live from the dataset. See our editorial standards & corrections policy, the methodology behind these numbers, or report a data error.