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AllergyPhase 1NCT00298701

Tolerability of Grazax-R in Children

A Phase 1 study testing ALK Grass tablet in people with Allergy, run by ALK-Abelló A/S at 1 site in Germany.

Completed

Finished. The study has ended and is not enrolling. Results may be posted on the official record.

Official record
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Trial summary

This trial is performed to assess whether the Grazax-R treatment is safe to use in children aged 5-12 years. Read more about this study

Who is it for?
Ages 5 to 12 years
Conditions the study is for
Allergy
What is being tested?
ALK Grass tablet
Type of treatment
Pill or oral medicine
How many people
50 participants
Where
1 siteGermany
Study dates
Feb 2006to Apr 2006
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 5 to 12 years
  • All sexes
  • No healthy volunteers
  • Child

Who may be able to join

  • Grass pollen induced rhinoconjunctivitis
  • Boys and girls, 5-12 years of age
  • Positive skin prick test to grass pollen

Who cannot join

  • Previous treatment with immunotherapy

Trial locations and contacts

1 site in 1 country.

Germany1 site
  • Tangstedter Landstrasse 77

    Hamburg, 22415

Other trials in Germany

About this study

Official title: A Randomised, Double-Blind, Placebo-Controlled, Multi-Centre Phase I Trial Investigating the Safety of GRAZAX-R in Children Aged 5-12 Years With Grass Pollen Induced Rhinoconjunctivitis (With/Without Asthma)

This trial is performed to assess whether the Grazax-R treatment is safe to use in children aged 5-12 years.

Conditions
Allergy
Being tested
ALK Grass tablet
Keywords
Allergy
Medical subject headings
Hypersensitivity

What participants receive

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

  • ALK Grass tabletBiological

What is being measured

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

  1. Assessment of safety by recording of adverse events

Timeline

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

  1. First posted3 Mar 2006 (estimated)
  2. Study startFeb 2006
  3. Study completionApr 2006

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
Allocation
Randomised
Intervention model
Parallel groups
Masking
Double blind
Enrolment
50 participants
IDs, dates and publications
ClinicalTrials.gov ID
NCT00298701
Sponsor's protocol ID
GT-11
Status last verified
May 2006
First submitted
1 Mar 2006
Last updated
4 May 2006
Results posted
No

Questions about this trial

What is this clinical trial studying?

A Phase 1 study testing ALK Grass tablet in people with Allergy, run by ALK-Abelló A/S at 1 site in Germany.

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

Who may be eligible to take part?

The sponsor lists 3 inclusion and 1 exclusion criteria. 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: finished, as of the sponsor's last update on 4 May 2006. Status can change between updates, so confirm with the study contact before making plans.

Where is the study taking place?

The record lists 1 site in Germany. 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. 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 is completed, but results are not available in the source record. That does not mean the treatment did or did not work.

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?

Assessment of safety by recording of adverse events. 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 4 May 2006.

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