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A Placebo-Controlled Double-Blind Parallel-Group Dose-Titration Study to Evaluate the Efficacy and Safety of CONCERTA (Methylphenidate HCl) Extended-Release Tablets in Adults With Attention Deficit Hyperactivity Disorder at Doses of 36 mg 54 mg 72 mg 90 mg or 108 mg Per Day.
This is a randomized (patients are assigned different treatments based on chance) placebo-controlled double-blind (neither the patient nor the physician knows whether drug or placebo is being taken) parallel-group dose-titration multicenter study to ...
An Open-Label Study Evaluating the Maintenance of Clinical Effect in Adults With Schizophrenia Switched From RISPERDAL®Tablets (Risperidone) to an Equivalent Dose of a Rapidly-Dissolving Tablet Formulation of Risperdone
This trial is a non-randomized open-label single arm multicentre study aimed at evaluating the maintenance of clinical effect of the rapidly-dissolving tablet dosage form of risperidone in patients switched from their previous equivalent dose of ...
Risperidone Depot (Microspheres) Vs. Risperidone Tablets - a Non-Inferiority Efficacy Trial in Subjects With Schizophrenia
Chronic schizophrenia is a longer-term condition that is characterized by a lack of drive underactivity and slowness and social withdrawal. As with the acute form of schizophrenia delusions and hallucinations are common. Based on the severity and ...
Randomised Double-Blind Comparative Trial of PPX Tablets and Bromocriptin Tablets in Patients With Parkinson`s Disease Who Are Concomitantly Treated With L-DOPA
The trial was to investigate the efficacy and safety of Pramipexole in patients with Parkinson's disease who can be concomitantly treated with L-DOPA in a double-blindmethod using Bromocriptine tablets as comparators (phase III comparative trial). ...
A Randomized Double-Blind Placebo-Controlled Crossover Study to Compare IPX054 200 Mg and 250 Mg to Carbidopa-Levodopa Immediate-Release 200 (2x100) Mg Tablets and Carbidopa-Levodopa Controlled-Release 200 Mg Tablet in Subjects With Parkinson's Disease
The objective of this study is to compare the pharmacokinetics and pharmacodynamics of IPX054, carbidopa-levodopa immediate-release tablets, and carbidopa-levodopa controlled-release tablets in subjects with idiopathic Parkinson's disease.
Effects of Conversion From Sirolimus Oral Solution to Tablets in Renal Transplant Recipients.
Sirolimus tablets will be available more than one year after the launch of sirolimus solution. Most patients on sirolimus solution will use sirolimus tablet instead.The purpose of this study is to understand the pharmacokinetics of sirolimus tablets ...
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