Found 10 matching trials
A Study in Patients With Major Depressive Disorder PHASE2 This is a Phase 2a, placebo-controlled, single-blind study in up to 24 pati...
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Collaborative Neuroscience Network
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Bioavailability of Increasing Pramipexole Doses of Oral Extended Release (ER) Tablets in Healthy Male Volunteers PHASE1 The objectives of the studies are:
* To demonstrate similar total exposure...
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Multiple Locations
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The SUSTAIN Study Compares the Effects of Sustained and Immediate-release Pramipexole on the noctUrnal Symptoms of paTients With Advanced ParkInsoN's Disease Who Also Take L-Dopa PHASE4 The main objective of the study is to explore firstly, then further evaluat...
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Peking Union Medical College Hospital
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Increasing Dose Study of Pramipexole in Two-way Cross-over Comparison of ER Tablet Versus IR Tablet in Japanese Healthy Male Volunteers PHASE1 The objectives of this study were to investigate relative BA at steady stat...
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Multiple Locations
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Influence of Pramipexole on the QT Interval of the ECG in Healthy Male and Female Volunteers PHASE1 The objective of the study is to assess that pramipexole does not prolong t...
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Multiple Locations
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A 12-week Study of Pramipexole Extended Release (ER) in Patients With Parkinson's Disease (PD), Followed by a 52-week Long-term Treatment Period PHASE2 The objective of this trial is to investigate the safety, tolerability, tro...
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248.610.019 Boehringer Ingelheim Investigational Site
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Bioavailability of Different Pramipexole Slow-release Formulations Compared to Immediate-release Tablet in Healthy Male Volunteers PHASE1 Study to compare the oral bioavailability of seven prototype slow-release f...
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Multiple Locations
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In Vitro/in Vivo Correlation (IVIVC) for Oral Slow Release (SR) Tablets Pramipexole in Healthy Male Volunteers PHASE1 The primary objective of the study was to estimate the magnitude of the err...
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Multiple Locations
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Multiple Dose Bioequivalence Study of Pramipexole Extended Release in Chinese Healthy Male Volunteers PHASE1 To establish bioequivalence at steady state of:
1)0.375 mg pramipexole ext...
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248.665.86002 Boehringer Ingelheim Investigational Site
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Ophthalmologic Safety Study of Pramipexole Immediate Release (IR) Versus Ropinirole in Early Parkinson's Disease (PD) Patients PHASE4 To determine if there is any difference in the presence of retinal deterior...
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248.538.00007 Boehringer Ingelheim Investigational Site
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