Safety and Efficacy of QAX576 in Adults With Moderate Persistent Allergic Asthma

NCT ID: NCT00598104

Last Updated: 2016-03-04

Study Results

Results pending

The study team has not published outcome measurements, participant flow, or safety data for this trial yet. Check back later for updates.

Basic Information

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Recruitment Status

WITHDRAWN

Clinical Phase

PHASE1/PHASE2

Study Classification

INTERVENTIONAL

Study Start Date

2008-01-31

Brief Summary

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This study will evaluate the safety and efficacy of QAX576 against asthma attacks in adults with moderate persistent allergic asthma

Detailed Description

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Conditions

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Asthma

Study Design

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Allocation Method

RANDOMIZED

Intervention Model

PARALLEL

Primary Study Purpose

TREATMENT

Blinding Strategy

DOUBLE

Participants Investigators

Study Groups

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1

Group Type EXPERIMENTAL

QAX576

Intervention Type DRUG

2

Group Type PLACEBO_COMPARATOR

Placebo

Intervention Type DRUG

Interventions

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QAX576

Intervention Type DRUG

Placebo

Intervention Type DRUG

Eligibility Criteria

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Inclusion Criteria

* History of asthma attacks
* Taking inhaled corticosteroids
* Non-smoking

Exclusion Criteria

* Women of child-bearing potential
* History of respiratory disease other than asthma
* History of severe allergy to food or drugs
* Previous use of monoclonal antibodies
* Very low or high body weight
Minimum Eligible Age

18 Years

Maximum Eligible Age

55 Years

Eligible Sex

ALL

Accepts Healthy Volunteers

No

Sponsors

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Novartis

INDUSTRY

Sponsor Role lead

Responsible Party

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Responsibility Role SPONSOR

Principal Investigators

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NOVARTIS

Role: PRINCIPAL_INVESTIGATOR

Novartis investigative site

Other Identifiers

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CQAX576A2103

Identifier Type: -

Identifier Source: org_study_id

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