Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.
Efficacy and Safety Study of KIACTA in Preventing Renal Function Decline in AA Amyloidosis
NCT01215747 · View on ClinicalTrials.gov ↗
Study Summary
The primary purpose of this study is to assess the efficacy and safety of treatment with Kiacta in adult patients with AA Amyloidosis.
Conditions Studied
Interventions
- DRUG Placebo
- DRUG KIACTA (eprodisate disodium)
Study Locations (20)
Other
- UZ Leuven — Leuven
- Al Hussain University Hospital — Cairo
- Tartu University Hospital — Tartu
- Helsingin yliopistollinen keskussairaala / Meilahti — Helsinki
- Hôpital Henri Mondor — Créteil
- Hôpital Claude Huriez — Lille
- Tbilisi Heart and Vascular Clinic Ltd — Tbilisi
- Universität Heidelberg — Heidelberg
- Regency Hospital — Kanpur
- Muljibhai Patel Urological Hospital — Nadiād
- Sir Ganga Ram Hospital — New Delhi
- Bnei Zion Medical Center — Haifa
- The Chaim Sheba Medical Center — Ramat Gan
- IRCCS Policlinico San Matteo — Pavia
- Pauls Stradins Clinical University Hospital — Riga
- Hospital of Lithuanian University of Health Sciences Kaunas Clinics — Kaunas
- Vilnius University Hospital Santariskiu Klinikos — Vilnius
California
- Raffi Minasian MD a Medical Corporation — Glendale
Massachusetts
- Boston Medical Center — Boston
Ohio
- Ohio State University Medical Center — Columbus
Trial Details
| Field | Value |
|---|---|
| Enrollment Target | 261 participants |
| Start Date | 2010-11 |
| Est. Completion | 2016-03 |
| Phase | Phase 3 |
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Full Details on ClinicalTrials.gov ↗What the Registry Record Tells You About NCT01215747
The ClinicalTrials.gov registry entry for NCT01215747 describes a study currently listed as completed. It is categorized as Phase 3, 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 261 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is C.T. Development America, which has 1 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 Amyloidosis appearing as the primary indexed condition, and to 2 interventions — of which 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: NCT01215747 reports 20 study locations spanning 4 distinct geographic areas — top geographies include Other, California, Massachusetts. 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 NCT01215747 about?
NCT01215747 is a clinical study titled "Efficacy and Safety Study of KIACTA in Preventing Renal Function Decline in AA Amyloidosis". The primary purpose of this study is to assess the efficacy and safety of treatment with Kiacta in adult patients with AA Amyloidosis.
What is the current status of trial NCT01215747?
This trial is currently completed. It is a Phase 3 study. The enrollment target is 261 participants. The study started on 2010-11. Estimated completion is 2016-03.
What conditions does trial NCT01215747 study?
This clinical trial studies the following conditions: Amyloidosis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.
What interventions are being tested in trial NCT01215747?
The interventions under investigation include: Placebo (DRUG), KIACTA (eprodisate disodium) (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.
Who is sponsoring clinical trial NCT01215747?
This trial is sponsored by C.T. Development America, which has 1 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.
Where is trial NCT01215747 being conducted?
This trial has 20 study locations across California, Massachusetts, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.
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