72 studies found for:    Progressive Supranuclear Palsy
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Rank Status Study
1 Recruiting A Study to Assess Efficacy, Safety, Tolerability, and Pharmacokinetics of ABBV-8E12 in Progressive Supranuclear Palsy
Condition: Progressive Supranuclear Palsy
Interventions: Drug: ABBV-8E12;   Drug: Placebo
2 Completed Trial of Valproic Acid in Patients With Progressive Supranuclear Palsy (Depakine)
Condition: Progressive Supranuclear Palsy
Interventions: Drug: valproic acid;   Drug: Placebo
3 Completed Safety, Tolerability, and Efficacy of Two Different Oral Doses of NP031112 Versus Placebo in the Treatment of Patients With Mild-to-Moderate Progressive Supranuclear Palsy
Condition: Progressive Supranuclear Palsy
Interventions: Drug: tideglusib;   Drug: placebo
4 Unknown  Postural Instability in Progressive Supranuclear Palsy
Conditions: Progressive Supranuclear Palsy;   Parkinson's Disease
Intervention:
5 Completed Study to Evaluate the Safety and Efficacy of Davunetide for the Treatment of Progressive Supranuclear Palsy
Condition: Progressive Supranuclear Palsy
Interventions: Drug: Davunetide;   Drug: Placebo
6 Active, not recruiting Safety, Tolerability, and Pharmacokinetics of C2N-8E12 in Subjects With Progressive Supranuclear Palsy
Condition: Progressive Supranuclear Palsy
Interventions: Drug: Single dose C2N-8E12;   Drug: Single dose placebo
7 Completed Deep TMS for the Treatment of Patients With Parkinson's Disease and Progressive Supranuclear Palsy
Conditions: Progressive Supranuclear Palsy;   Parkinson's Disease
Interventions: Device: active Deep TMS;   Device: sham Deep TMS
8 Terminated Efficacy, Tolerability and Safety of Azilect in Subjects With Progressive Supranuclear Palsy
Condition: Progressive Supranuclear Palsy
Interventions: Drug: Rasagiline;   Drug: Sugar pill
9 Unknown  Alpha-lipoic Acid/L-acetyl Carnitine for Progressive Supranuclear Palsy
Condition: Progressive Supranuclear Palsy
Intervention: Drug: alpha-lipoic acid and L-acetyl carnitine
10 Completed Rehabilitation in Patients With Progressive Supranuclear Palsy
Condition: Progressive Supranuclear Palsy
Interventions: Other: MIRT;   Other: MIRT+Lokomat
11 Recruiting A Molecular Anatomic Imaging Analysis of Tau in Progressive Supranuclear Palsy
Condition: Progressive Supranuclear Palsy
Intervention: Drug: F-18 AV 1451
12 Enrolling by invitation Extension Study of BMS-986168 in Patients With Progressive Supranuclear Palsy Who Participated in CN002003
Condition: Progressive Supranuclear Palsy
Intervention: Drug: BMS-986168
13 Completed Effects of Coenzyme Q10 in Progressive Supranuclear Palsy (PSP)
Conditions: Progressive Supranuclear Palsy;   Atypical Parkinsonism
Intervention: Drug: CoenzymeQ10
14 Completed Evaluating Cerebrospinal Fluid Biomarkers in Alzheimer's, Progressive Supranuclear Palsy Subjects, and Controls
Conditions: Alzheimer Disease;   Progressive Supranuclear Palsy
Intervention:
15 Completed Study About Safety and Efficacy of Coenzyme Q10 in Progressive Supranuclear Palsy
Condition: Progressive Supranuclear Palsy
Intervention: Drug: Coenzyme Q10
16 Active, not recruiting Multiple Ascending Dose Study of Intravenously Administered BMS-986168 in Patients With Progressive Supranuclear Palsy
Condition: Progressive Supranuclear Palsy
Interventions: Drug: BMS-986168;   Drug: Placebo
17 Completed
Has Results
A Pilot Trial of Lithium in Subjects With Progressive Supranuclear Palsy or Corticobasal Degeneration
Conditions: Progressive Supranuclear Palsy;   Corticobasal Degeneration
Intervention: Drug: Lithium
18 Recruiting Efficacy of RIVAstigmine on Motor, Cognitive and Behavioural Impairment in Progressive Supranuclear Palsy
Condition: Progressive Supranuclear Palsy (PSP)
Interventions: Drug: Rivastigmine;   Drug: Placebo
19 Recruiting Young Plasma Transfusions for Progressive Supranuclear Palsy
Condition: Progressive Supranuclear Palsy
Intervention: Other: Fresh Frozen Plasma
20 Unknown  Study of the Distractibility Syndrome in Patients With Progressive Supranuclear Palsy
Condition: Supranuclear Palsy, Progressive
Intervention: Drug: donepezil

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Study has passed its completion date and status has not been verified in more than two years.