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Trial of Xyrem® (Sodium Oxybate) for the Treatment of Narcolepsy - Article


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Ofloxacin Ear Solution

Floxin Otic



Clinical Trial: Trial of Xyrem® (Sodium Oxybate) for the Treatment of Narcolepsy

This study is currently recruiting patients.
Verified by Orphan Medical August 2005

Sponsored by: Orphan Medical
Information provided by: Orphan Medical
ClinicalTrials.gov Identifier: NCT00132873

Purpose

Long-term, open-label, extension of the OMC-SXB-7 trial. Participants from the OMC-SXB-7 open-label trial may be entered without any requirement as to length of participation in that trial.

Approximately 70 patients are expected to participate at up to 6 investigative centers located in Canada. The trial will continue for up to 24 months or until marketing approval, whichever occurs sooner.

Condition Intervention Phase
Narcolepsy
 Drug: Xyrem (sodium oxybate) oral solution
Phase III

MedlinePlus related topics:  Sleep Disorders

Study Type: Interventional
Study Design: Educational/Counseling/Training, Non-Randomized, Open Label, Uncontrolled, Single Group Assignment, Safety Study

Official Title: Long-Term, Open-Label, Multi-Center Extension Trial of Xyrem® (Sodium Oxybate) Oral Solution for the Treatment of Narcolepsy

Further Study Details: 
Primary Outcomes: Adverse experiences; Vital signs
Expected Total Enrollment:  70

Study start: October 2004;  Expected completion: December 2005
Last follow-up: December 2005;  Data entry closure: December 2005

This trial will be conducted as a long-term, open-label, extension of the OMC-SXB-7 trial. Participants from the OMC-SXB-7 open-label trial may be entered without any requirement as to length of participation in that trial.

Approximately 70 patients are expected to participate at up to 6 investigative centers located in Canada. The trial will continue for up to 24 months or until marketing approval, whichever occurs sooner.

Eligibility

Ages Eligible for Study:  12 Years and above,  Genders Eligible for Study:  Both
Criteria

Inclusion Criteria:

  • Remained on satisfactory treatment with Xyrem® therapy in the OMC-SXB-7 trial
  • Signed and dated an informed consent

Exclusion Criteria:

-

Location and Contact Information

Please refer to this study by ClinicalTrials.gov identifier  NCT00132873


Canada, Ontario
      Brain and Sleep Diagnostic Centre, Toronto,  Ontario,  M8X 2W2,  Canada; Recruiting
Mortimer Mamelak  416-231-5770 

More Information

Study ID Numbers:  OMC-SXB-27
Last Updated:  August 19, 2005
Record first received:  August 18, 2005
ClinicalTrials.gov Identifier:  NCT00132873
Health Authority: United States: Food and Drug Administration
ClinicalTrials.gov processed this record on 2005-08-23

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Page Updated: June 1, 2005
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