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COMPLETED Phase 2

Open-Label, Safety and Tolerability Extension Study of KNS-760704 in Amyotrophic Lateral Sclerosis (ALS) (CL211)

NCT00931944 · View on ClinicalTrials.gov ↗

Study Summary

This is an open-label, multi-center study designed to extend the evaluation of the safety, tolerability, and clinical effects of oral administration of KNS-760704 in patients with ALS.

Interventions

  • DRUG KNS-760704

Study Locations (19)

Pennsylvania

  • Penn State Hershey Medical Center — Hershey
  • Drexel University College Of Medicine — Philadelphia
  • University of Pittsburgh School of Medicine — Pittsburgh

California

  • UCLA, Dept. of Neurology - Neuromuscular/ALS Research Center — Los Angeles
  • The Forbes Norris MDA/ALS Research Center — San Francisco

New York

  • Columbia University, Lou Gehrig MDA/ALS Research Center — New York
  • SUNY Upstate Medical University — Syracuse

Arkansas

  • University of Arkansas for Medical Sciences — Little Rock

Florida

  • University of Miami Miller School of Medicine — Miami

Kansas

  • University of Kansas Medical Center — Kansas City

Maryland

  • Johns Hopkins University School of Medicine — Baltimore

Massachusetts

  • Massachusettes General Hospital — Boston

Trial Details

FieldValue
Enrollment Target 74 participants
Start Date 2009-07
Est. Completion 2013-07
Phase Phase 2

Sponsor

Knopp Biosciences

3 total trials

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00931944

The ClinicalTrials.gov registry entry for NCT00931944 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 74 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Knopp Biosciences, which has 3 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 Amyotrophic Lateral Sclerosis appearing as the primary indexed condition, and to 1 intervention — of which KNS-760704 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: NCT00931944 reports 19 study locations spanning 15 distinct geographic areas — top geographies include Pennsylvania, California, New York. 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 NCT00931944 about?

NCT00931944 is a clinical study titled "Open-Label, Safety and Tolerability Extension Study of KNS-760704 in Amyotrophic Lateral Sclerosis (ALS) (CL211)". This is an open-label, multi-center study designed to extend the evaluation of the safety, tolerability, and clinical effects of oral administration of KNS-760704 in patients with ALS.

What is the current status of trial NCT00931944?

This trial is currently completed. It is a Phase 2 study. The enrollment target is 74 participants. The study started on 2009-07. Estimated completion is 2013-07.

What conditions does trial NCT00931944 study?

This clinical trial studies the following conditions: Amyotrophic Lateral Sclerosis. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00931944?

The interventions under investigation include: KNS-760704 (DRUG). Each intervention is being evaluated for safety and efficacy as part of this clinical study.

Who is sponsoring clinical trial NCT00931944?

This trial is sponsored by Knopp Biosciences, which has 3 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00931944 being conducted?

This trial has 19 study locations across Arkansas, California, Florida, Kansas, Maryland. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Related

Data sourced from official U.S. government datasets. See our methodology for details. Retrieved and formatted by PlainTrial Editorial