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Past Studies
Research
Trials
Acute Stroke –
1997
Alzheimer’s Disease
- 1998
Efficacy and long
term tolerability of XXX in patients with moderately severe to severe
Alzheimer’s Disease.
Epilepsy
XXX in
combination with newer and older antiepileptic drugs and as mono-therapy.
Epilepsy -1999
Safety and
Therapeutic Effect of XXX in patients with Partial Seizures.
Acute Stroke-1999
Phase IIa.
Inpatient
HIV Neuropathy
-1999
Stroke Prevention
-1999
Phase III
Seizure Management
-2000
Phase IV
Hypercholesterolemia-2001
Vascular Dementia
-2002
Phase III
Hypercholesterolemia -2002
Migraine
Disorder-2002
Phase II
Double-Blind
Randomized Multi-center, Parallel Group Study to establish Dose
response, safety and efficacy of XXX as mono-therapy in patients with
newly diagnosed epilepsy. 2002
A 6 week, open
label, dose comparison study to evaluate the safety and efficacy of XXX versus
XXX, XXX and XXX in subjects with Hypercholesterolemia. 2001
An open label,
randomized, multi-center, Phase lllb, parallel group switching study to compare
the efficacy and safety of lipid lowering agents XXX and XXX with XXX high risk
subjects with type IIa and IIb Hypercholesterolemia. 2001
A randomized,
double-blind, placebo-controlled, parallel-group study to evaluate the efficacy
and tolerability of XXX for a single moderate or severe headache in adults
diagnosed with Migrainous disorder. 2002
A multi-center,
double-blind, randomized study to evaluate the safety and efficacy of XXX
compared with placebo in subjects with painful diabetic neuropathy. 2002
An open label
study to evaluate the safety of XXX in subjects with Painful Diabetic
Neuropathy. 2003
A multi-center,
double-blind, randomized, placebo-controlled, parallel group trial to
investigate the efficacy and safety of XXX as adjunctive therapy in subjects
with partials seizures with or without secondary generalization. 2003
An open label
extension trial to determine tolerability and efficacy of long-term oral XXX as
adjunctive therapy in patients with Partial Seizures. 2003
Safety evaluation
of XXX with opiod tolerant patients. 2003
A Phase III,
randomized, double-blind, placebo-controlled, outpatient, safety and efficacy
study of XXX in adults subjects with Chronic Insomnia. 2002
A Phase II
Double-Blind, randomized, dose ranging, placebo-controlled , multi-center,
safety and efficacy evaluation of three doses of XXX in patients with mild to
moderate dementia of the Alzheimer’s Type. 2003
A Fourteen week
placebo controlled dose response efficacy and safety study of XXX in early
Parkinson’s Disease Patients. 2003
A randomized,
double blind, placebo controlled, parallel-group, single attack study to
evaluate the onset of efficacy of a new formulation of XXX in the acute
treatment of Migraine. 2003
A dose-ranging,
placebo controlled study of XXX at the dose of XXX for 12 weeks in patients with
mild to moderate Alzheimer’s Disease. 2003
A randomized,
double-blind, placebo controlled trial to evaluate the safety and efficacy of
XXX in slowing the progression of Alzheimer’s Disease. 2003
A one year,
multi-center, randomized, double-blind, placebo-controlled evaluation of
efficacy and safety of XXX in subjects with Mild Cognitive Impairment. 2003
A 5-Week ,
randomized, Double-blind, placebo-controlled, placebo-controlled, multi-center
study of XXX in patients with Postherpetic Neuralgia who are XXX treatment
failures. 2004
A Multi-center,
open-label trial to assess subject preference of XXX, orally disintegrating
tablets, compared to conventional XXX in subjects with stable Parkinson’s
Disease. 2004
A 4-Week
randomized, Multi-center, double-blind, placebo-and-active-controlled,
parallel-group, forced-titration Phase IIb study comparing efficacy and safety
of ascending doses of XXX prolonged release up to 20mg BID to placebo in
subjects with moderate to severe chronic pain due to Osteoarthritis of the knee.
2005
A Multi-center,
randomized, double-blind, placebo controlled study assessing the safety and
efficacy of XXX in patients in patients with Postherpetic Neuralgia. 2004
A randomized,
parallel-design, multi-center study to evaluate the efficacy of XXX for the
Treatment of Chronic Low Back Pain. 2004
A randomized,
double blind, placebo-controlled, parallel group Phase 2 Study to evaluate the
Safety and Efficacy of XXXX in subjects with mild to moderate Alzheimer’s
Disease. 2004
A multi-center
double blind randomized parallel group evaluation of XXX extended release
Adjunctive therapy in subjects with Partial Seizures. 2004
A multi-center
double blind randomized parallel group evaluation of XXX extended release
adjunctive therapy in patients with primary generalized Tonic- Clonic Seizures.
2004
A multi-center
randomized double blind placebo-controlled, parallel group trial to assess the
efficacy and safety of XXX in subjects with Painful Distal Diabetic Neuropathy.
2005
A randomized
double blind parallel group, placebo controlled single –attack evaluation of the
efficacy and tolerability of XXX verses Placebo when administered during the
mild pain phase of a migraine. 2004
A multi-center,
open label follow on trial to assess the long term safety and efficacy of XXX in
subjects with Painful Distal Diabetic Neuropathy. 2004
A randomized
double blind placebo controlled study to assess the subjective response to
treatment with XXX in adult subjects with Chronic Insomnia by utilizing an
interactive voice response system for collecting diary data. 2005
Phase 3
multi-center randomized double blind placebo controlled study of the effect of
daily treatment with XXX on measures of cognitive and global function in
subjects with mild to moderate dementia of the Alzheimer’s Type. 2005
A prospective
multi-center randomized open label study with blinded raters to evaluate the
effects of immediate versus delayed switch to XXX on motor function
And quality of
life in patients with Parkinson’s disease with-end-of dose wearing off. 2005
A randomized
multi-center double blind placebo-controlled, 18-month study of the efficacy of
XXX in patients with mild to moderate dementia of the Alzheimer’s Type. 2005
A multi-center,
randomized double blind placebo controlled Five arm parallel group trial to
investigate the efficacy and safety of four different transdermal doses of XXX
in subjects with Idiopathic Restless Legs Syndrome. 2005
A pilot
randomized double blind placebo controlled study to evaluate the efficacy of XXX
and XXX in the treatment of Chronic Lumbosacral
Radiculopathy. 2005
A randomized
double blind double blind placebo-controlled study of the safety and efficacy of
XXX extended release tablets in treatment of patients with Postherpetic
Neuralgia. 2005
An open- label
exploratory study with XXX of selective measures of volumetric MRI and cognition
in patients with Moderate Dementia of the Alzheimer’s Type. 2005
Safety,
tolerability and efficacy study of oral XXX administered for ninety days in
subjects with Probable Alzheimer’s of mild to moderate Severity. 2005
A phase 2
double-blind randomized, placebo-controlled, parallel-group, multi-center
proof-of-concept study to evaluate the safety and efficacy of XXX taken in
combination with XXX for the treatment of subjects with Chronic Insomnia. 2005
A randomized,
double- blind, multi-center, placebo-controlled, cross-over study to determine
the consistency of response for XXX administered during the mild pain phase for
the acute treatment of multiple migraine attacks. 2005
A randomized,
double-blind, Placebo-controlled, Multi-center Phase 3 study to evaluate the
safety and the safety of XXX once daily and XXX twice daily for 12 weeks for the
treatment of Opiod-induced Bowel Dysfunction in Adults taking Opiod Theraphy for
persistent Non-Cancer Pain. 2005
A randomized,
double-blind, placebo-controlled, multi-center Phase 3 study to evaluate the
Long-Term Safety of XXX twice daily
for 12 months for the treatment of Opiod-Induced Bowel Dysfunction in Adults
taking Opiod Theraphy for Persistent Non-Cancer Pain. 2004
A multi-center
study evaluating the efficacy and safety of XXX as headache prophylaxis in
Migraine Patients with 15 or more headache days per 4-week
period in a 24-week, double blind, randomized, placebo-controlled,
parallel-group phase followed by a 32-week open-label extension. 2006
A double-blind,
randomized, placebo-controlled study of the efficacy, safety and tolerability of
8 week treatment of XXX in sleep disturbed community dwelling, mild to
moderately severe Alzheimer’s Disease Subjects. 2006
A randomized,
double-blind, placebo-controlled, parallel-group clinical trial to examine the
efficacy and safety of early XXX treatment versus delayed XXX treatment in
patients with new onset of Parkinson’s disease. 2006
XXX Dose-range
finding trial: A 16-week, randomized, double-blind, placebo and XXX controlled,
multi-center trial of XXX in patients with Post herpetic Neuralgia. 2006
A randomized ,
double-blind ,placebo-controlled , multi-center, phase 2 study designed to
assess the efficacy and safety of XXX immediate release in subjects with Chronic
pain from Low Back Pain or
Osteoarthritis of the Hip or Knee. 2006
A multi-center
trial evaluating the efficacy of XXX for symptomatic treatment of pain in
patients with Multiple Sclerosis. 2006
A multi-center
trial evaluating the efficacy of XXX for the symptomatic treatment of pain in
patients with Diabetic Peripheral Neuropathy. 2006
A prospective,
Multi-center clinical evaluation of XXX in combination with a XXX for the
management of chronic back pain with or without leg pain. 2006
A multi-center,
randomized, double-blind, placebo-controlled, parallel group study of the
efficacy, safety, and tolerability of XXX in XXX treated Parkinson’s disease
patients with motor fluctuations. 2006
Phase 3
multinational, randomized, double-blind, placebo controlled study of the effect
of daily treatment with XXX on measures of cognition, activities of daily living
and global function in the subjects with mild dementia of the Alzheimer’s Type.
2006
A multi-center,
randomized, double-blind, placebo-controlled, parallel- group study of oral XXX
for the treatment of Opiod Induced bowel Dysfunction in subjects with chronic
non malignant pain. 2006
Open-label,
multi-center, effectiveness and safety study of once daily XXX as mono or
adjunct therapy in patients with Idiopathic Parkinson’s Disease. 2006
Randomized
evaluation of recurrent stroke comparing XXX closure to establish current
standard of care treatment. 2006
A prospective,
5-week, open-label, randomized, multi-center, parallel-group study with a
20-week, open-label extension evaluating the tolerability and safety of
switching from XXX to an initial dose of XXX patch formulation in patients with
probable Alzheimer’s disease. 2006
An open-label
extention trial assessing the safety and tolerability of XXX in patients with
Postherpetic Neuralgia. 2006
Open label study
of the effect of daily treatment with XXX in subjects with Dementia of the
Alzheimer’s type. 2006
A randomized
double-blind, placebo and active-control, parallel-arm, phase III trial with
controlled adjustment of dose to evaluate the efficacy and safety of XXX
extended release in subjects with moderate to severe chronic pain due to
Osteoarthritis of the knee. 2007
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