drugset / Trial / NCT00145171

A Sub-Study With Patients in APO401 to Evaluate Adverse Events During Dose Introduction in Apomorphine-naïve Patients.

NCT00145171

Phase 3 Completed 56 enrolled Mylan Bertek Pharmaceuticals
Non-randomizedSingle-groupOpen-labelTreatment

Summary

APO303 is a sub-study of patients enrolled in APO401 (the long-term open label safety protocol) and was designed to evaluate adverse events, particularly blood pressure drops when standing up during first dose in patients who have not been exposed to apomorphine before.

Timeline

Start
2001-02
Primary completion
Completion
2002-08

Drugs

EvaluationDrugModalityDoseRoute
Subject Apomorphine Unknown 2 mg Subcutaneous
Subject Apomorphine Unknown 10 mg Subcutaneous

Indications