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View Clinical Trial (Medical Research Study)
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Clinical Trial Ceftriaxone in Subjects With ALS - NCT00349622-63104 (Clinical Trial 308432)
Permalink: http://www.ClinicalConnection.com/exp/ExpandedPatientViewStudy308432.aspx
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| City: |
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St. Louis |
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State:
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MO |
| Zip Code: |
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63104 |
| Conditions: |
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Amyotrophic Lateral Sclerosis - ALS |
| Purpose: |
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The purpose of the study is to evaluate the safety and efficacy of ceftriaxone treatment in
amyotrophic lateral sclerosis (ALS).
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| Study summary: |
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It is known that nerve cells called motor neurons die in the brains and spinal cords of
people with amyotrophic lateral sclerosis (ALS). However, the cause of this cell death is
unknown. Researchers think that increased levels of a chemical called "glutamate" may be
related to the cell death. For this reason researchers want to study drugs that decrease
glutamate levels near nerves. Ceftriaxone—a semi-synthetic, third generation cephalosporin
antibiotic—may increase the level of a protein that decreases glutamate levels near nerves.
Studies of ceftriaxone in the laboratory suggest that it may protect motor neurons from
injury.
Ceftriaxone is approved by the U.S. Food and Drug Administration (FDA) for treating
bacterial infections but not for treating ALS. Also, ceftriaxone has not been given to
people over a long period of time, such as months or years. The goals of this study are to
evaluate the safety and effectiveness of ceftriaxone as a treatment for ALS, and to
determine the safety and effectiveness of long-term use of the drug in people with ALS.
A total of 600 eligible people with ALS will be enrolled in this multi-center research
study. Participants will be randomly assigned to receive treatment with ceftriaxone (2/3 of
participants) or placebo (1/3 of participants) for at least 12 months.
The study consists of three stages. The first stage, which has completed enrollment, will
look at whether ceftriaxone enters the cerebrospinal fluid (the fluid that surrounds the
spinal cord, also called CSF) in amounts that are high enough to be of possible benefit.
The second stage, which has also completed enrollment, will look at the safety and side
effects of the study drug when taken daily for at least 20 weeks. The study is currently
enrolling subjects for the third stage, which began in Spring 2009, and will determine
whether the study drug prolongs survival and slows decline in function due to ALS. |
| Criteria: |
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Inclusion Criteria:
- Participants will be people with ALS, at least 18 years of age.
- Participants must be medically able to undergo the study procedures and have a
caregiver or other individual who will be available to help with daily study
medication administration.
- Participants should live within a reasonable distance of the study site, due to
frequent study visits.
Exclusion Criteria:
- Participants cannot be taking any other experimental medications for ALS, or have a
history of sensitivity to cephalosporin antibiotics (such as Ancef, Keflex, Ceclor,
Ceftin, Lorabid, Suprax, or Fortaz). |
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| Study is available at: |
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St. Louis University
St. Louis, MO 63104
United States
Primary Contact:
Susan Eller, RN
Phone: 314-977-4867
Secondary Contact:
Sarah Titus, MPH
Email: stitus@partners.org
Phone: (617) 726-1398 |
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If you are interested in this clinical trial please use the contact information above. If you would like to get additional information about this clinical trial please visit ClinicalTrials.gov.
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| Data Source: |
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ClinicalTrials.gov |
| Date Processed: |
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March 15, 2010 |
Modifications to
this listing: |
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Only selected fields are shown, please use the link
above to view all information about this clinical trial. |
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Clinical trials are medical research studies designed to test the safety and/or
effectiveness of new drugs, devices, or treatments in humans. These studies are
conducted worldwide for a range of conditions and illnesses. Learn more about
clinical research and participating in a study at
About Clinical Trials.
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