Medical Information Only. Always consult your healthcare provider before enrolling in any clinical trial.

COMPLETED Phase 1

A Safety Study for Cethrin (BA-210) in the Treatment of Acute Thoracic and Cervical Spinal Cord Injuries

NCT00500812 · View on ClinicalTrials.gov ↗

Study Summary

This trial is a multi-center, open-label, dose-escalation study designed to evaluate the safety, tolerability and pharmacokinetics of Cethrin in two types of spinal cord injury patients: those with a complete cervical injury or a complete thoracic injury. Dose levels from 0.3 mg - 9 mg of Cethrin will be administered.

Conditions Studied

Interventions

  • DRUG Cethrin

Study Locations (8)

Ontario

  • Sunnybrooke Health Sciences Centre — Toronto
  • Toronto Western Hospital — Toronto

Arizona

  • St. Joseph's Hospital & Medical Center — Phoenix

Ohio

  • University of Cincinnati Mayfield Clinic and Spine Institute — Cincinnati

Pennsylvania

  • Thomas Jefferson University Hospital — Philadelphia

Virginia

  • Univ.of Virginia Health System — Charlottesville

Washington

  • University of Washington Harborview Medical Center — Seattle

Quebec

  • Hopital du Sacre-Coeur de Montreal — Montreal

Trial Details

FieldValue
Enrollment Target 48 participants
Start Date 2005-02
Est. Completion 2009-02
Phase Phase 1

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Full Details on ClinicalTrials.gov ↗

What the Registry Record Tells You About NCT00500812

The ClinicalTrials.gov registry entry for NCT00500812 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 48 participants, a figure that helps gauge the scale of data the investigators plan to collect. The listed sponsor is Vertex Pharmaceuticals Incorporated, which has 82 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 Spinal Cord Injury appearing as the primary indexed condition, and to 1 intervention — of which Cethrin 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: NCT00500812 reports 8 study locations spanning 7 distinct geographic areas — top geographies include Ontario, Arizona, Ohio. 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 NCT00500812 about?

NCT00500812 is a clinical study titled "A Safety Study for Cethrin (BA-210) in the Treatment of Acute Thoracic and Cervical Spinal Cord Injuries". This trial is a multi-center, open-label, dose-escalation study designed to evaluate the safety, tolerability and pharmacokinetics of Cethrin in two types of spinal cord injury patients: those with a complete cervical injury or a complete thoracic injury. Dose levels from 0.3 mg - 9 mg of Cethrin wi...

What is the current status of trial NCT00500812?

This trial is currently completed. It is a Phase 1 study. The enrollment target is 48 participants. The study started on 2005-02. Estimated completion is 2009-02.

What conditions does trial NCT00500812 study?

This clinical trial studies the following conditions: Spinal Cord Injury. These conditions were identified from the trial registry and reflect the primary focus areas of the research.

What interventions are being tested in trial NCT00500812?

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

Who is sponsoring clinical trial NCT00500812?

This trial is sponsored by Vertex Pharmaceuticals Incorporated, which has 82 total clinical trials registered on ClinicalTrials.gov. The sponsor is responsible for the study's design, funding, and regulatory compliance.

Where is trial NCT00500812 being conducted?

This trial has 8 study locations across Arizona, Ohio, Pennsylvania, Virginia, Washington. 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