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An Extension Study of KRN23 in Adults With X-Linked Hypophosphatemia
NCT01571596 · View on ClinicalTrials.gov ↗
Study Summary
The primary purpose of this study is to assess the safety and efficacy of repeated subcutaneous (SC) injections of KRN23 in adult subjects with X-Linked Hypophosphatemia (XLH).
Conditions Studied
Interventions
- DRUG KRN23
Study Locations (6)
California
- University of California San Francisco — San Francisco
Connecticut
- Yale University School of Medicine — New Haven
Indiana
- Clinical Research Center, Indiana University School of Medicine — Indianapolis
North Carolina
- Duke Clinical Research Unit — Durham
Texas
- University of Texas Health Science Center at Houston — Houston
Quebec
- Shriners Hospital for Children - Canada — Montreal
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 23 participants |
| Start Date | 2012-02 |
| Est. Completion | 2014-06 |
| Phase | Phase 1 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01571596
The ClinicalTrials.gov registry entry for NCT01571596 describes a study currently listed as completed. It is categorized as Phase 1, 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 23 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Kyowa Kirin Co., which has 8 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 X-linked Hypophosphatemia appearing as the primary indexed condition, and to 1 intervention — of which KRN23 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: NCT01571596 reports 6 study locations spanning 6 distinct geographic areas — top geographies include California, Connecticut, Indiana. 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 NCT01571596 about?
NCT01571596 is a clinical study titled "An Extension Study of KRN23 in Adults With X-Linked Hypophosphatemia". The primary purpose of this study is to assess the safety and efficacy of repeated subcutaneous (SC) injections of KRN23 in adult subjects with X-Linked Hypophosphatemia (XLH).
What is the current status of trial NCT01571596?
This trial is currently completed. It is a Phase 1 study. The enrollment target is 23 participants. The study started on 2012-02. Estimated completion is 2014-06.
What conditions does trial NCT01571596 study?
This clinical trial studies the following conditions: X-linked Hypophosphatemia. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT01571596?
The interventions under investigation include: KRN23 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT01571596?
This trial is sponsored by Kyowa Kirin Co., which has 8 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT01571596 being conducted?
This trial has 6 study locations across California, Connecticut, Indiana, North Carolina, Texas. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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