Status:

COMPLETED

Relative Bioavailability of a Fentanyl Patch

Lead Sponsor:

Sandoz

Conditions:

Pain

Eligibility:

All Genders

18-45 years

Phase:

PHASE1

Brief Summary

Tohe purpose of this study is to demonstrate the bioequivalence of a fentanyl patch transdermal delivery system.

Eligibility Criteria

Inclusion

  • No clinically significant abnormal findings on physical exam, medical history or clinical laboratory tests on screening.

Exclusion

  • Negative test for HIV and hepatitis B and C
  • No history of drug or alcohol treatment
  • No allergies to opiates

Key Trial Info

Start Date :

September 1 2006

Trial Type :

INTERVENTIONAL

Allocation :

ACTUAL

End Date :

October 1 2006

Estimated Enrollment :

40 Patients enrolled

Trial Details

Trial ID

NCT00857753

Start Date

September 1 2006

End Date

October 1 2006

Last Update

March 29 2017

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Relative Bioavailability of a Fentanyl Patch | DecenTrialz