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Efficacy and Safety of QAX576 in Patients With Eosinophilic Esophagitis
NCT01022970 · View on ClinicalTrials.gov ↗
Study Summary
This study is designed to investigate the effects of a 12 week course of intravenous QAX576 6mg/kg every 4 weeks in reducing the number of eosinophils in the esophagus of EoE patients by 75% or greater when compared with baseline.
Conditions Studied
Interventions
- DRUG QAX576 placebo
- DRUG QAX576
Study Locations (5)
California
- Stanford Medical Center and Lucile Packard Children's Hospital — Stanford
Illinois
- Northwestern University Feinberg School of Medicine — Chicago
Minnesota
- Mayo Clinic — Minneota
Ohio
- Cincinnati Children's Hospital Medical Center — Cincinnati
Virginia
- Oral Alpan, 6210 Old Keene Mill Court, — Springfield
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 25 participants |
| Start Date | 2009-11 |
| Phase | Phase 2 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01022970
The ClinicalTrials.gov registry entry for NCT01022970 describes a study currently listed as completed. It is categorized as Phase 2, which is the standard way researchers label where a study sits along the investigational pathway from early safety work through later efficacy and post-marketing evaluation. The registered enrollment target is 25 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Novartis Pharmaceuticals, which has 792 total studies on file at ClinicalTrials.gov, and sponsors are the parties responsible for study design, oversight, and regulatory filings.
The record links to 1 condition, with Eosinophilic Esophagitis appearing as the primary indexed condition, and to 2 interventions — of which QAX576 placebo is the first listed. Interventions can include drugs, devices, procedures, behavioral programs, or observational arms, and each is tracked as a separate registry field so that downstream queries can filter accurately. When a trial lists multiple interventions, it usually reflects a multi-arm design or a comparison protocol rather than a single treatment being tested in isolation. The brief summary published in the registry is the clearest source of protocol intent and should be read before drawing conclusions from any sidebar tags.
Geographic footprint matters for practical reasons: NCT01022970 reports 5 study locations spanning 5 distinct geographic areas — top geographies include California, Illinois, Minnesota. A larger site network tends to correlate with broader recruitment capacity, but it does not imply anything about study quality, and site-level enrollment status can diverge from the overall registry status shown above. Every data point on this page comes from the public ClinicalTrials.gov dataset and is reproduced here for reference only; it is not a medical recommendation, an endorsement of the sponsor, or an invitation to enroll. Verify current status, eligibility criteria, and contact details directly at ClinicalTrials.gov, and discuss any participation decision with your own healthcare provider.
Frequently Asked Questions
What is clinical trial NCT01022970 about?
NCT01022970 is a clinical study titled "Efficacy and Safety of QAX576 in Patients With Eosinophilic Esophagitis". This study is designed to investigate the effects of a 12 week course of intravenous QAX576 6mg/kg every 4 weeks in reducing the number of eosinophils in the esophagus of EoE patients by 75% or greater when compared with baseline.
What is the current status of trial NCT01022970?
This trial is currently completed. It is a Phase 2 study. The enrollment target is 25 participants. The study started on 2009-11.
What conditions does trial NCT01022970 study?
This clinical trial studies the following conditions: Eosinophilic Esophagitis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT01022970?
The interventions under investigation include: QAX576 placebo (DRUG), QAX576 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT01022970?
This trial is sponsored by Novartis Pharmaceuticals, which has 792 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT01022970 being conducted?
This trial has 5 study locations across California, Illinois, Minnesota, Ohio, Virginia. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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