Clinical Trials Directory

Trials / Sponsors / Acorda Therapeutics

Acorda Therapeutics

Industry · 38 registered clinical trials.

StatusTrialPhaseStarted
CompletedPharmacokinetic Study of CVT-301 (Levodopa Inhalation Powder)
Parkinson's Disease
Phase 12019-03-05
CompletedA Study of the Pulmonary Safety and Pharmacokinetics of Zolmitriptan Inhalation Powder
Migraine
Phase 12016-09-01
CompletedA Study of the Safety and Tolerability of a Single Dose Administration of CVT-301 (Levodopa Inhalation Powder)
Parkinson's Disease
Phase 12016-06-01
CompletedA Study to Compare Two Dose Strengths of CVT-301 (Levodopa Inhalation Powder) With an Oral Dose of Sinemet® (C
Parkinson Disease
Phase 12016-06-01
CompletedA Pharmacokinetic Study to Assess Dose Proportionality, Safety and Tolerability of Diazepam Nasal Spray in Hea
Healthy
Phase 12016-01-01
CompletedA Study of the Safety and Pharmacokinetics of Levodopa Following Administration of CVT 301 (Levodopa Inhalatio
Asthma
Phase 12015-12-01
CompletedA Study of the Safety and Levodopa Pharmacokinetics Following Single Dose Administration of CVT 301 (Levodopa
Smoking
Phase 12015-12-01
CompletedSafety and Pharmacokinetics (PK) Study of Single Ascending Doses of CVT-427 (Zolmitriptan Inhalation Powder) I
Migraine
Phase 12015-11-01
TerminatedBioavailability, Safety and Tolerability of Diazepam Nasal Spray Versus Diazepam Rectal Gel (Diastat®)
Refractory Epilepsy
Phase 22015-06-01
CompletedAn Intravenous Infusion Study of rHIgM22 in Patients With Multiple Sclerosis Immediately Following a Relapse
Multiple Sclerosis, Acute Relapsing
Phase 12015-04-01
TerminatedStudy to Evaluate the Long-Term Safety, Tolerability and Efficacy of Dalfampridine.
Post-ischemic Stroke
Phase 32015-04-01
CompletedTwelve Month Safety and Efficacy Study of CVT-301 In Parkinson's Disease Patients With OFF Episodes
Idiopathic Parkinson's Disease
Phase 32015-03-01
CompletedRandomized Safety Study of CVT-301 Compared to an Observational Control Group
Idiopathic Parkinson's Disease
Phase 32015-03-01
TerminatedAn Open-Label, Safety and Tolerability Study of Chronic Intermittent Use of Diazepam Nasal Spray.
Epilepsy
Phase 22014-12-01
CompletedA Study to Evaluate the Efficacy and Safety of Two Dose Strengths of Dalfampridine Extended Release Tablets.
Post-Ischemic Stroke
Phase 32014-12-01
CompletedEfficacy and Safety Study of CVT-301 In Parkinson's Disease Patients With OFF Episodes
Idiopathic Parkinson's Disease
Phase 32014-11-01
CompletedA Double-Blind Pharmacokinetic Interaction Study Evaluating the Effect of a Single IV Infusion of GGF2 or Plac
Heart Failure
Phase 12013-09-01
TerminatedAC105 in Patients With Acute Traumatic Spinal Cord Injury
Acute Spinal Cord Injury
Phase 22013-07-01
CompletedEfficacy and Safety Study of Inhaled CVT 301 in Parkinson's Disease Patients for Treatment of OFF Episodes
Idiopathic Parkinson's Disease
Phase 22013-04-01
CompletedA Study to Define the ECG Effects of Tizanidine Compared to Placebo and the Positive Control, Moxifloxacin, in
Spasticity
Phase 22013-04-01
CompletedAn Intravenous Infusion Study of rHIgM22 in Patients With Multiple Sclerosis
Multiple Sclerosis
Phase 12013-03-01
CompletedSafety, Pharmacokinetics and Efficacy Study of CVT-301 Inpatients With Parkinson's Disease and "Off" Episodes
Idiopathic Parkinson's Disease
Phase 22012-05-01
CompletedA Phase 2b Study of Dalfampridine 10mg Extended Release Tablet in Subjects With Chronic Deficits After Ischemi
Ischemic Stroke
Phase 22012-05-01
CompletedAn Open Label, Proof of Concept Study to Evaluate the Effects of Dalfampridine Withdrawal on Gait and Balance
Multiple Sclerosis
2012-01-01
CompletedSafety and Tolerability of Dalfampridine in Subjects With Cerebral Palsy
Cerebral Palsy (CP)
Phase 12011-12-01
CompletedA Pharmacokinetic Study of a Single-Dose of Diazepam Nasal Spray in Adult Epileptic Patients Experiencing a Se
Epilepsy
Phase 22011-09-01
TerminatedPhase 1b Study of Tizanidine in Pediatric Patients With Cerebral Palsy
Spasticity Due to Cerebral Palsy
Phase 12011-05-01
CompletedStudy of Fampridine-ER Tablets in Patients With Multiple Sclerosis
Multiple Sclerosis
Phase 32011-03-01
CompletedPharmacokinetics (PK) of Dalfampridine-ER 7.5 mg BID in Healthy Volunteers and Subjects With Mild or Moderate
Renal Insufficiency
Phase 12011-01-01
CompletedSingle Ascending Doses of GGF2 in Patients With Left Ventricular Dysfunction and Symptomatic Heart Failure
Heart Failure
Phase 12010-12-01
CompletedOpen-Label Extension Study to Evaluate the Safety, Tolerability and Activity of Oral Fampridine-SR in Patients
Multiple Sclerosis
Phase 32007-08-01
CompletedStudy of Fampridine-SR Tablets in Multiple Sclerosis Patients
Multiple Sclerosis
Phase 32007-05-01
CompletedOpen-Label Extension Study to Evaluate the Safety, Tolerability and Activity of Oral Fampridine-SR Tablets in
Multiple Sclerosis
Phase 32006-06-01
CompletedStudy of Oral Fampridine-SR in Multiple Sclerosis
Multiple Sclerosis
Phase 32005-05-01
CompletedOpen-Label Extension Study to Evaluate the Safety, Tolerability and Activity of Oral Fampridine-SR in Patients
Multiple Sclerosis
Phase 32003-11-01
CompletedSafety and Efficacy Study of Oral Fampridine-SR in Patients With Multiple Sclerosis
Multiple Sclerosis
Phase 22003-02-01
CompletedSafety and Efficacy of Oral Fampridine-SR for the Treatment of Spasticity Resulting From Spinal Cord Injury
Spinal Cord Injury, Muscle Spasticity
Phase 32002-07-01
CompletedSafety and Efficacy of Oral Fampridine-Sustained Release (SR) for the Treatment of Spasticity Resulting From S
Spinal Cord Injury, Muscle Spasticity
Phase 32002-06-01