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Vanda Pharmaceuticals Inc

VNDA
Healthcare|Biotechnology|USA
$6.24
-0.14 (-2.19%)
DCF (FCF)
$3.02
Tangible Book
$2.76
Earnings Power
$1.56

Clinical Trials (85)

TrialConditionsPhaseStatusEnrollmentDesignDrug
NCT05648591
Safety and Tolerability of Open-Labeled Iloperidone in Adolescents
Schizophrenia, Bipolar I Disorder
P4
Recruiting100Open-labelIloperidone
NCT06961968
Randomized Withdrawal Study in Patients With Schizophrenia
Schizophrenia
P3
Recruiting400RCT, Double-blindiloperidone, placebo
NCT06138613
Motion Delos: An Open Label Safety and Efficacy of Tradipitant in Participants Affected by Motion Sickness
Motion Sickness
P3
Active705RCT, Open-labelTradipitant
NCT06701396
Evaluating the Effects of Tasimelteon Vs. Placebo in Delayed Sleep-Wake Phase Disorder (DSWPD) and the CRY1Δ11 Variant
Sleep Wake Disorders, Sleep Disorders, Circadian Rhythm
P3
Recruiting60RCT, Double-blindTasimelteon, Placebo
NCT07446439
A Study to Evaluate Tradipitant on Treating Nausea and Vomiting Induced by GLP-1R Agonist Use
Nausea and Vomiting, Obesity
P3
Recruiting280RCT, Double-blindTradipitant, Placebo
NCT04652882
Evaluating the Effects of Tasimelteon vs. Placebo in Delayed Sleep-Wake Phase Disorder (DSWPD)
Sleep Wake Disorders, Sleep Disorders, Circadian Rhythm
P3
Recruiting70RCT, Double-blindTasimelteon, Placebo
NCT06953869
Evaluating the Effects of Tasimelteon vs. Placebo in Treating Pediatric Insomnia
Insomnia Disorder
P3
Recruiting420RCT, Double-blindTasimelteon Oral Suspension, Placebo
NCT06830044
Evaluation of Efficacy and Safety of Milsaperidone as Adjunctive Therapy in Patients With Major Depressive Disorder
Major Depressive Disorder (MDD)
P3
Recruiting500RCT, Double-blindMilsaperidone, Placebo
NCT07221578
Study to Evaluate the Efficacy and Safety of VQW-765 for the On-Demand Treatment of Social Anxiety Disorder
Social Anxiety Disorder (SAD)
P3
Recruiting500RCT, Double-blindVQW-765, Placebo
NCT06836557
Open Label Safety Study of Tradipitant in Idiopathic and Diabetic Gastroparesis
Idiopathic Gastroparesis, Diabetic Gastroparesis
P3
Recruiting100Open-labelTradipitant
NCT07362017
Open Label Study to Investigate the Safety and Efficacy of Ponesimod in Moderate-to-Severe Chronic Plaque Psoriasis
Moderate-to-severe Chronic Plaque Psoriasis
P3
Recruiting300Open-labelPonesimod
NCT07065773
Safety, Tolerability and Efficacy of Trichostatin A in Patients With Mild to Severe Onychomycosis
Onychomycosis of Toenail
P2
Active50Open-labelTrichostatin A
NCT07179055
An Eight-Week Study to Evaluate the Safety and Efficacy of VSJ-110 Compared to Placebo in the Treatment of Dry Eye
Dry Eye
P2
Recruiting160RCT, Double-blindVSJ-110, Placebo
NCT07090161
Evaluation of Efficacy and Safety of Iloperidone for the Treatment of Participants With Uncontrolled Hypertension
Hypertension, Uncontrolled Hypertension
P2
Recruiting240RCT, Double-blindiloperidone, Placebo
NCT07223632
Treatment of Charcot-Marie-Tooth Disease, Axonal, Type 2S (CMT2S) in an Individual Patient
Charcot Marie Tooth Disease (CMT), Neuromuscular Diseases (NMD)
P1P2
Active1Open-labelVCA-894A
NCT03838926
Tolerability Study of Trichostatin A In Subjects With Relapsed or Refractory Hematologic Malignancies
Relapsed or Refractory Hematologic Malignancies
P1
Recruiting42Open-labelTrichostatin A
NCT01195558
Patient Registry of Blind Subjects With Sleep-related Problems
Sleep-wake Disorder in Blind Individuals
Recruiting10,000
NCT03154697
Development of Clinical Database of Individuals With Smith-Magenis Syndrome and Sleep Disturbances
Sleep Disturbances in Smith-Magenis Syndrome
Recruiting1,000
NCT02130999
Open Label Study to Assess the Absolute Bioavailability of Tasimelteon (HETLIOZ™)
Non-24-Hour-Sleep-Wake Disorder
P4
Completed14RCT, Open-labeltasimelteon 20 mg capsule, tasimelteon 2 mg I.V.
NCT02413918
Iloperidone in Mixed States of Bipolar Disorder
Bipolar Disorder
P4
Completed41Open-labeliloperidone
NCT04326426
ODYSSEY: A Study to Investigate the Efficacy of Tradipitant in Treating Severe or Critical COVID-19 Infection
Coronavirus Infection
P3
By Invite300RCT, Double-blindTradipitant, Placebo
NCT01430754
Withdrawal Study to Demonstrate the Maintenance Effect in the Treatment of Non-24-Hour Sleep-Wake Disorder
Non-24-Hour Sleep-Wake Disorder
P3
Completed20RCT, Double-blindtasimelteon, Placebo
NCT01429116
Tasimelteon for the Treatment of Non-24-hour Sleep-Wake Disorder (N24HSWD) in Blind Individuals With no Light Perception
Non-24-Hour Sleep-Wake Disorder
P3
Completed200Open-labeltasimelteon
NCT04327661
Motion Syros: A Study to Investigate the Efficacy of Tradipitant in Subjects Affected by Motion Sickness
Motion Sickness
P3
Completed366RCT, Double-blindTradipitant, Placebo
NCT03568331
Evaluating the Effects of Tradipitant vs. Placebo in Atopic Dermatitis (EPIONE)
Atopic Dermatitis
P3
Completed375RCT, Double-blindTradipitant, Placebo
NCT05366855
Study to Evaluate the Long-Term Safety and Efficacy of Imsidolimab (ANB019) in the Treatment of Subjects With GPP
Generalized Pustular Psoriasis
P3
Terminated42RCT, Double-blindDouble-blind 200 mg imsidolimab, Open-label 200 mg imsidolimab, Imsidolimab 750 mg IV/200 mg SC
NCT01428661
Melatonin Agonist Effects of Tasimelteon Versus Placebo in Patients With Major Depressive Disorder
Major Depressive Disorder
P2P3
Completed507RCT, Double-blindtasimelteon, placebo
NCT04819776
Evaluation of Efficacy and Safety of Iloperidone in the Acute Treatment of Manic or Mixed Episodes Associated With Bipolar I Disorder
Bipolar I Disorder
P3
Completed417RCT, Double-blindIloperidone, Iloperidone Placebo
NCT05361707
Evaluating the Effects of Tasimelteon in Individuals With Autism Spectrum Disorder (ASD) and Sleep Disturbances
Autism Spectrum Disorder, Sleep Disorder
P3
Unknown100Open-labelTasimelteon Oral Capsule, Tasimelteon Liquid Suspension
NCT00548340
VEC-162 Study in Adult Patients With Primary Insomnia
Primary Insomnia
P3
Completed322RCT, Double-blindVEC-162 20 mg, Placebo, VEC-162 50 mg
NCT07686081
Study to Evaluate the Efficacy and Safety of Ponesimod (VSP-128) in Patients With Moderately to Severely Active Ulcerative Colitis
Ulcerative Colitis (UC)
P3
Not Yet Recruiting150RCT, Double-blindPonesimod, Placebo
NCT04140695
Evaluating the Effects of Tradipitant vs. Placebo in Atopic Dermatitis (EPIONE2)
Atopic Dermatitis
P3
Terminated87RCT, Double-blindTradipitant, Placebo
NCT01218789
Safety Study of Tasimelteon for Treatment of Non-24-Hour-Sleep-Wake Disorder in Blind Individuals With No Light Perception
Non 24 Hour Sleep Wake Disorder
P3
Unknown140Open-labeltasimelteon
NCT00254202
Efficacy and Safety of Iloperidone Compared With Placebo and Active Control in Subjects With Acute Schizophrenia
Schizophrenia
P3
Completed593RCT, Double-blindIloperidone, Ziprasidone, Placebo
NCT05903924
Motion Serifos: A Study to Investigate the Efficacy of Tradipitant in Participants Affected by Motion Sickness
Motion Sickness
P3
Completed316RCT, Double-blindTradipitant, Placebo
NCT04028492
Evaluating the Safety and Efficacy of Tradipitant vs. Placebo in Idiopathic and Diabetic Gastroparesis
Idiopathic Gastroparesis, Diabetic Gastroparesis
P3
Completed992RCT, Double-blindTradipitant, Placebo, Open Label Tradipitant
NCT01291511
Relapse Prevention Study in Patients With Schizophrenia
Schizophrenia
P3
Completed635RCT, Double-blindIloperidone, Placebo
NCT00291187
VEC-162 Study in Healthy Adult Volunteers in a Model of Insomnia
Insomnia
P3
Completed411RCT, Double-blind20 mg VEC-162, 50 mg VEC-162, 100 mg VEC-162, Placebo
NCT03373201
Evaluating the Effects of Tasimelteon vs. Placebo on Jet Lag Type Insomnia
Jet Lag Type Insomnia
P3
Completed320RCT, Double-blindTasimelteon, Placebo
NCT02231008
Evaluating the Effects of Tasimelteon vs Placebo on Sleep Disturbances in SMS
Smith-Magenis Syndrome, Circadian
P2P3
Completed49RCT, Double-blindtasimelteon, placebo
NCT05352893
Study to Evaluate the Efficacy and Safety of Imsidolimab (ANB019) in the Treatment of Subjects With GPP
Generalized Pustular Psoriasis
P3
Completed45RCT, Double-blind750 mg Imsidolimab, 300 mg Imsidolimab
NCT01163032
Efficacy and Safety of Tasimelteon Compared With Placebo in Totally Blind Subjects With Non-24-Hour Sleep-Wake Disorder
Non-24-Hour Sleep-Wake Disorder
P3
Completed136RCT, Double-blindtasimelteon, Placebo
NCT00467441
VSF-173 Study in Healthy Adult Volunteers for Treatment of Induced Excessive Sleepiness
Excessive Somnolence
P2
Completed60RCT, Double-blindVSF-173
NCT04856917
A Study to Evaluate the Efficacy and Safety of Imsidolimab (ANB019) in the Treatment of Participants With Acne Vulgaris
Acne Vulgaris
P2
Completed123RCT, Double-blindImsidolimab, Placebo
NCT04849559
Effects of Tradipitant on Satiation, Gastric Volume, Gastric Accommodation, and Gastric Emptying in Healthy Volunteers
Healthy Volunteer
P1P2
Completed27RCT, Double-blindTradipitant, Placebo
NCT04800237
Evaluating the Effects of VQW-765 vs. Placebo in Performance Anxiety
Performance Anxiety
P2
Completed230RCT, Double-blindVQW-765, Placebo
NCT04622345
Safety and Efficacy of VSJ-110 in the Treatment of Allergic Conjunctivitis in Adults With a History of Ocular Allergies
Allergic Conjunctivitis
P2
Completed47RCT, Double-blindVSJ-110, Placebo
NCT02970968
Study to Assess the Efficacy of VLY-686 in Relieving Symptoms of Gastroparesis
Gastroparesis
P2
Completed152RCT, Double-blindVLY-686 (Tradipitant)
NCT04856930
A Study to Evaluate the Efficacy and Safety of Imsidolimab (ANB019) in the Treatment of Participants With Hidradenitis Suppurativa
Hidradenitis Suppurativa
P2
Completed149RCT, Double-blindImsidolimab, Placebo
NCT04697069
A Study to Evaluate of the Efficacy and Safety of Imsidolimab (ANB019) in the Treatment of Acneiform Rash
Acneiform Eruptions
P2
Terminated4RCT, Double-blindImsidolimab, Placebo
NCT02004041
Proof of Concept of VLY-686 in Subjects With Treatment-Resistant Pruritus Associated With Atopic Dermatitis
Treatment-resistant Pruritus Associated With Atopic Dermatitis
P2
Completed69RCT, Double-blindVLY-686, Placebo
NCT03633396
A Study to Evaluate the Efficacy and Safety of Imsidolimab (ANB019) in Adults With Palmoplantar Pustulosis
Palmoplantar Pustulosis
P2
Completed59RCT, Double-blindImsidolimab, Placebo
NCT02651714
Tradipitant in Treatment-resistant Pruritus Associated With Atopic Dermatitis
Atopic Dermatitis
P2
Completed168RCT, Double-blindTradipitant, Placebo
NCT04697056
A Study to Evaluate the Efficacy and Safety of Imsidolimab (ANB019) in the Treatment of Participants With Ichthyosis
Ichthyosis
P2
Terminated5RCT, Double-blindImsidolimab, placebo
NCT05344365
A Study to Evaluate Iloperidone for the Treatment of Parkinson's Disease Psychosis
Parkinson Disease Psychosis
P2
WithdrawnOpen-labelIloperidone
NCT03772340
Motion Sifnos: A Study to Investigate the Efficacy of Tradipitant in Subjects Affected by Motion Sickness
Motion Sickness
P2
Completed126RCT, Double-blindTradipitant, Placebo
NCT03291041
A Proof of Concept Study to Evaluate the Effects of Tasimelteon and Placebo in Travelers With Jet Lag Disorder
Jet Lag Disorder
P2
Completed25RCT, Double-blindTasimelteon, Placebo
NCT03619902
A Study to Evaluate the Efficacy and Safety of Imsidolimab (ANB019) in Adults With Generalized Pustular Psoriasis
Generalized Pustular Psoriasis
P2
Completed8Open-labelImsidolimab
NCT00490945
Safety and Efficacy of VEC-162 on Circadian Rhythm in Healthy Adult Volunteers
Circadian Rhythm Sleep Disorders
P2
Completed45RCT, Double-blindVEC-162
NCT06804603
A Study to Measure the Effects of Using Tradipitant on Nausea and Vomiting After GLP-1R Agonist Use
Obesity
P2
Completed124RCT, Double-blindTradipitant, Placebo
NCT06296966
A Study to Evaluate the Safety and Efficacy of VSJ-110 Compared to Placebo in the Treatment of Dry Eye
Dry Eye
P2
Unknown40RCT, Double-blindVSJ-110, Placebo
NCT01348100
Safety, Tolerability, and Pharmacokinetics of Iloperidone Depot in Schizophrenic Patients
Schizophrenia
P1P2
Completed81RCT, Open-labelIloperidone crystalline formulation, Iloperidone microparticle formulation, Oral iloperidone
NCT01540500
Pharmacokinetics of Tasimelteon Alone and in Combination With CYP1A2 Inhibitor, Fluvoxamine
Healthy Volunteers
P1
Completed24Open-labelTasimelteon, Fluvoxamine
NCT01271387
Pharmacokinetics of Tasimelteon in Subjects With Mild or Moderate Hepatic Impairment
Hepatic Impairment
P1
Completed29Open-labeltasimelteon
NCT06323655
Evaluation of Next-Day Residual Effects of Tasimelteon Compared With Placebo and Active Control in Healthy Subjects
Healthy Volunteers
P1
Completed48RCT, Double-blindTasimelteon, Active Control Placebo, Tasimelteon Placebo, Active Control
NCT01526746
Pharmacokinetics of Tasimelteon in Subjects With Renal Impairment and Matched Control Subjects With Relatively Normal Renal Function
Renal Impairment
P1
Completed32Open-labelTasimelteon, Tasimelteon
NCT01578057
Evaluation of the Pharmacodynamic and Pharmacokinetic Interactions of Tasimelteon and Ethanol
Pharmacodyamics and Pharmacokinetics of Tasimelteon Alone and in Combination With Ethanol
P1
Completed28RCT, Double-blindtasimelteon, Ethanol, Placebo ethanol
NCT02621385
Study to Assess the Effect of Multiple Doses of Tradipitant on CYP3A4 Using Midazolam as a Substrate in Healthy Subjects
Healthy Volunteers
P1
Completed24Open-labeltradipitant, Midazolam
NCT04712734
A Study to Evaluate Iloperidone Long-acting Injection (LAI) for the Treatment of Schizophrenia
Schizophrenia
P1
Completed42Open-labelIloperidone
NCT02776215
Study of the Pharmacokinetics and Safety of Tasimelteon in Children and Adolescents
Circadian Rhythm Sleep Disorders, Non-24 Hour Sleep-Wake Disorder
P1
Completed24Open-labeltasimelteon
NCT01919944
Study of Itch Control by VLY-686 in Healthy Volunteers After Intradermal Injections of Substance P
Pruritus
P1
Completed12RCT, Double-blindVLY-686, Placebo
NCT06494397
Pharmacokinetic Study of VHX-896 and Iloperidone Tablets Under Steady-State Conditions
Schizophrenia, Bipolar I Disorder
P1
Completed26RCT, Open-labelVHX-896 and iloperidone, Iloperidone and VHX-896
NCT04969211
Bioequivalence Study Between VHX-896 Tablets and Iloperidone Tablets in Healthy Volunteers
Healthy
P1
Completed25RCT, Open-labelVHX-896 and iloperidone, Iloperidone and VHX-896
NCT04127058
Evaluating a New Iloperidone Titration Scheme in Bipolar I Disorder or Schizophrenia
Bipolar I Disorder, Schizophrenia
P1
Completed12Open-labelIloperidone
NCT01495169
Tolerability and Pharmacokinetics of Iloperidone in Adolescent Patients
Safety and Tolerability of Iloperidone
P1
Completed33Open-labeliloperidone (oral tablet)
NCT01402076
A Study to Assess the Effect Tasimelteon on the Cytochrome P450 3A4 and 2C8 Enzymes in Healthy Subjects
Healthy Volunteers
P1
Completed24Open-labelTasimelteon, Rosiglitazone, Midazolam
NCT06803290
Food Effect Study of VHX-896 in Healthy Volunteers
Healthy
P1
Completed24RCT, Open-labelVHX-896
NCT01637636
Pharmacokinetics of Tasimelteon Alone and in Combination With a CYP3A4 Inhibitor, Ketoconazole, or a CYP3A4 Inducer, Rifampin.
Healthy
P1
Completed48Open-labeltasimelteon, tasimelteon, Rifampin, Ketoconazole
NCT01477619
Effects of Smoking, Age and Body Size on Pharmacokinetics, Safety and Tolerability on Tasimelteon in Healthy Subjects
Healthy Volunteers
P1
Completed60Open-labelTasimelteon
NCT05572281
Bioequivalence Study Between Tasimelteon Capsule Formulation and Liquid Suspension Formulation in Healthy Volunteers
Healthy
P1
Completed36RCT, Open-labelTasimelteon Oral Capsule, Tasimelteon Oral Suspension
NCT02560103
An Observational Study to Investigate the Effects of Rapid Transmeridian Travel
Jet Lag Disorder
Completed119
NCT04353401
WGS Analysis of COVID-19 Positive Patients
Coronavirus Infection, COVID-19
Completed79
NCT05922995
The Effects of Tasimelteon in Participants With REM Behavior Disorder (RBD)
REM Behavior Disorder
Early P1
Terminated20Open-labelTasimelteon
NCT04474990
Single-Patient Expanded Access Protocol for Tradipitant In A Single Patient With Gastroparesis
Gastroparesis, Diabetic Gastroparesis
AVAILABLETradipitant
NCT02180451
Observational Study to Investigate the Melatonin and Cortisol Circadian Rhythms of Individuals With Smith-Magenis Syndrome (SMS)
Smith Magenis Syndrome
Unknown8