
Vanda Pharmaceuticals Inc
VNDAHealthcare|Biotechnology|USA
$6.24
-0.14 (-2.19%)
DCF (FCF)
$3.02
Tangible Book
$2.76
Earnings Power
$1.56
Clinical Trials (85)
| Trial | Conditions | Phase | Status | Enrollment | Design | Drug |
|---|---|---|---|---|---|---|
| NCT05648591 Safety and Tolerability of Open-Labeled Iloperidone in Adolescents | Schizophrenia, Bipolar I Disorder | P4 | Recruiting | 100 | Open-label | Iloperidone |
| NCT06961968 Randomized Withdrawal Study in Patients With Schizophrenia | Schizophrenia | P3 | Recruiting | 400 | RCT, Double-blind | iloperidone, placebo |
| NCT06138613 Motion Delos: An Open Label Safety and Efficacy of Tradipitant in Participants Affected by Motion Sickness | Motion Sickness | P3 | Active | 705 | RCT, Open-label | Tradipitant |
| 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 | Recruiting | 60 | RCT, Double-blind | Tasimelteon, Placebo |
| NCT07446439 A Study to Evaluate Tradipitant on Treating Nausea and Vomiting Induced by GLP-1R Agonist Use | Nausea and Vomiting, Obesity | P3 | Recruiting | 280 | RCT, Double-blind | Tradipitant, Placebo |
| NCT04652882 Evaluating the Effects of Tasimelteon vs. Placebo in Delayed Sleep-Wake Phase Disorder (DSWPD) | Sleep Wake Disorders, Sleep Disorders, Circadian Rhythm | P3 | Recruiting | 70 | RCT, Double-blind | Tasimelteon, Placebo |
| NCT06953869 Evaluating the Effects of Tasimelteon vs. Placebo in Treating Pediatric Insomnia | Insomnia Disorder | P3 | Recruiting | 420 | RCT, Double-blind | Tasimelteon 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 | Recruiting | 500 | RCT, Double-blind | Milsaperidone, 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 | Recruiting | 500 | RCT, Double-blind | VQW-765, Placebo |
| NCT06836557 Open Label Safety Study of Tradipitant in Idiopathic and Diabetic Gastroparesis | Idiopathic Gastroparesis, Diabetic Gastroparesis | P3 | Recruiting | 100 | Open-label | Tradipitant |
| 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 | Recruiting | 300 | Open-label | Ponesimod |
| NCT07065773 Safety, Tolerability and Efficacy of Trichostatin A in Patients With Mild to Severe Onychomycosis | Onychomycosis of Toenail | P2 | Active | 50 | Open-label | Trichostatin 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 | Recruiting | 160 | RCT, Double-blind | VSJ-110, Placebo |
| NCT07090161 Evaluation of Efficacy and Safety of Iloperidone for the Treatment of Participants With Uncontrolled Hypertension | Hypertension, Uncontrolled Hypertension | P2 | Recruiting | 240 | RCT, Double-blind | iloperidone, 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 | Active | 1 | Open-label | VCA-894A |
| NCT03838926 Tolerability Study of Trichostatin A In Subjects With Relapsed or Refractory Hematologic Malignancies | Relapsed or Refractory Hematologic Malignancies | P1 | Recruiting | 42 | Open-label | Trichostatin A |
| NCT01195558 Patient Registry of Blind Subjects With Sleep-related Problems | Sleep-wake Disorder in Blind Individuals | Recruiting | 10,000 | — | — | |
| NCT03154697 Development of Clinical Database of Individuals With Smith-Magenis Syndrome and Sleep Disturbances | Sleep Disturbances in Smith-Magenis Syndrome | Recruiting | 1,000 | — | — | |
| NCT02130999 Open Label Study to Assess the Absolute Bioavailability of Tasimelteon (HETLIOZ™) | Non-24-Hour-Sleep-Wake Disorder | P4 | Completed | 14 | RCT, Open-label | tasimelteon 20 mg capsule, tasimelteon 2 mg I.V. |
| NCT02413918 Iloperidone in Mixed States of Bipolar Disorder | Bipolar Disorder | P4 | Completed | 41 | Open-label | iloperidone |
| NCT04326426 ODYSSEY: A Study to Investigate the Efficacy of Tradipitant in Treating Severe or Critical COVID-19 Infection | Coronavirus Infection | P3 | By Invite | 300 | RCT, Double-blind | Tradipitant, 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 | Completed | 20 | RCT, Double-blind | tasimelteon, 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 | Completed | 200 | Open-label | tasimelteon |
| NCT04327661 Motion Syros: A Study to Investigate the Efficacy of Tradipitant in Subjects Affected by Motion Sickness | Motion Sickness | P3 | Completed | 366 | RCT, Double-blind | Tradipitant, Placebo |
| NCT03568331 Evaluating the Effects of Tradipitant vs. Placebo in Atopic Dermatitis (EPIONE) | Atopic Dermatitis | P3 | Completed | 375 | RCT, Double-blind | Tradipitant, 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 | Terminated | 42 | RCT, Double-blind | Double-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 | Completed | 507 | RCT, Double-blind | tasimelteon, 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 | Completed | 417 | RCT, Double-blind | Iloperidone, Iloperidone Placebo |
| NCT05361707 Evaluating the Effects of Tasimelteon in Individuals With Autism Spectrum Disorder (ASD) and Sleep Disturbances | Autism Spectrum Disorder, Sleep Disorder | P3 | Unknown | 100 | Open-label | Tasimelteon Oral Capsule, Tasimelteon Liquid Suspension |
| NCT00548340 VEC-162 Study in Adult Patients With Primary Insomnia | Primary Insomnia | P3 | Completed | 322 | RCT, Double-blind | VEC-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 Recruiting | 150 | RCT, Double-blind | Ponesimod, Placebo |
| NCT04140695 Evaluating the Effects of Tradipitant vs. Placebo in Atopic Dermatitis (EPIONE2) | Atopic Dermatitis | P3 | Terminated | 87 | RCT, Double-blind | Tradipitant, 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 | Unknown | 140 | Open-label | tasimelteon |
| NCT00254202 Efficacy and Safety of Iloperidone Compared With Placebo and Active Control in Subjects With Acute Schizophrenia | Schizophrenia | P3 | Completed | 593 | RCT, Double-blind | Iloperidone, Ziprasidone, Placebo |
| NCT05903924 Motion Serifos: A Study to Investigate the Efficacy of Tradipitant in Participants Affected by Motion Sickness | Motion Sickness | P3 | Completed | 316 | RCT, Double-blind | Tradipitant, Placebo |
| NCT04028492 Evaluating the Safety and Efficacy of Tradipitant vs. Placebo in Idiopathic and Diabetic Gastroparesis | Idiopathic Gastroparesis, Diabetic Gastroparesis | P3 | Completed | 992 | RCT, Double-blind | Tradipitant, Placebo, Open Label Tradipitant |
| NCT01291511 Relapse Prevention Study in Patients With Schizophrenia | Schizophrenia | P3 | Completed | 635 | RCT, Double-blind | Iloperidone, Placebo |
| NCT00291187 VEC-162 Study in Healthy Adult Volunteers in a Model of Insomnia | Insomnia | P3 | Completed | 411 | RCT, Double-blind | 20 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 | Completed | 320 | RCT, Double-blind | Tasimelteon, Placebo |
| NCT02231008 Evaluating the Effects of Tasimelteon vs Placebo on Sleep Disturbances in SMS | Smith-Magenis Syndrome, Circadian | P2P3 | Completed | 49 | RCT, Double-blind | tasimelteon, placebo |
| NCT05352893 Study to Evaluate the Efficacy and Safety of Imsidolimab (ANB019) in the Treatment of Subjects With GPP | Generalized Pustular Psoriasis | P3 | Completed | 45 | RCT, Double-blind | 750 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 | Completed | 136 | RCT, Double-blind | tasimelteon, Placebo |
| NCT00467441 VSF-173 Study in Healthy Adult Volunteers for Treatment of Induced Excessive Sleepiness | Excessive Somnolence | P2 | Completed | 60 | RCT, Double-blind | VSF-173 |
| NCT04856917 A Study to Evaluate the Efficacy and Safety of Imsidolimab (ANB019) in the Treatment of Participants With Acne Vulgaris | Acne Vulgaris | P2 | Completed | 123 | RCT, Double-blind | Imsidolimab, Placebo |
| NCT04849559 Effects of Tradipitant on Satiation, Gastric Volume, Gastric Accommodation, and Gastric Emptying in Healthy Volunteers | Healthy Volunteer | P1P2 | Completed | 27 | RCT, Double-blind | Tradipitant, Placebo |
| NCT04800237 Evaluating the Effects of VQW-765 vs. Placebo in Performance Anxiety | Performance Anxiety | P2 | Completed | 230 | RCT, Double-blind | VQW-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 | Completed | 47 | RCT, Double-blind | VSJ-110, Placebo |
| NCT02970968 Study to Assess the Efficacy of VLY-686 in Relieving Symptoms of Gastroparesis | Gastroparesis | P2 | Completed | 152 | RCT, Double-blind | VLY-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 | Completed | 149 | RCT, Double-blind | Imsidolimab, Placebo |
| NCT04697069 A Study to Evaluate of the Efficacy and Safety of Imsidolimab (ANB019) in the Treatment of Acneiform Rash | Acneiform Eruptions | P2 | Terminated | 4 | RCT, Double-blind | Imsidolimab, 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 | Completed | 69 | RCT, Double-blind | VLY-686, Placebo |
| NCT03633396 A Study to Evaluate the Efficacy and Safety of Imsidolimab (ANB019) in Adults With Palmoplantar Pustulosis | Palmoplantar Pustulosis | P2 | Completed | 59 | RCT, Double-blind | Imsidolimab, Placebo |
| NCT02651714 Tradipitant in Treatment-resistant Pruritus Associated With Atopic Dermatitis | Atopic Dermatitis | P2 | Completed | 168 | RCT, Double-blind | Tradipitant, Placebo |
| NCT04697056 A Study to Evaluate the Efficacy and Safety of Imsidolimab (ANB019) in the Treatment of Participants With Ichthyosis | Ichthyosis | P2 | Terminated | 5 | RCT, Double-blind | Imsidolimab, placebo |
| NCT05344365 A Study to Evaluate Iloperidone for the Treatment of Parkinson's Disease Psychosis | Parkinson Disease Psychosis | P2 | Withdrawn | — | Open-label | Iloperidone |
| NCT03772340 Motion Sifnos: A Study to Investigate the Efficacy of Tradipitant in Subjects Affected by Motion Sickness | Motion Sickness | P2 | Completed | 126 | RCT, Double-blind | Tradipitant, 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 | Completed | 25 | RCT, Double-blind | Tasimelteon, Placebo |
| NCT03619902 A Study to Evaluate the Efficacy and Safety of Imsidolimab (ANB019) in Adults With Generalized Pustular Psoriasis | Generalized Pustular Psoriasis | P2 | Completed | 8 | Open-label | Imsidolimab |
| NCT00490945 Safety and Efficacy of VEC-162 on Circadian Rhythm in Healthy Adult Volunteers | Circadian Rhythm Sleep Disorders | P2 | Completed | 45 | RCT, Double-blind | VEC-162 |
| NCT06804603 A Study to Measure the Effects of Using Tradipitant on Nausea and Vomiting After GLP-1R Agonist Use | Obesity | P2 | Completed | 124 | RCT, Double-blind | Tradipitant, 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 | Unknown | 40 | RCT, Double-blind | VSJ-110, Placebo |
| NCT01348100 Safety, Tolerability, and Pharmacokinetics of Iloperidone Depot in Schizophrenic Patients | Schizophrenia | P1P2 | Completed | 81 | RCT, Open-label | Iloperidone crystalline formulation, Iloperidone microparticle formulation, Oral iloperidone |
| NCT01540500 Pharmacokinetics of Tasimelteon Alone and in Combination With CYP1A2 Inhibitor, Fluvoxamine | Healthy Volunteers | P1 | Completed | 24 | Open-label | Tasimelteon, Fluvoxamine |
| NCT01271387 Pharmacokinetics of Tasimelteon in Subjects With Mild or Moderate Hepatic Impairment | Hepatic Impairment | P1 | Completed | 29 | Open-label | tasimelteon |
| NCT06323655 Evaluation of Next-Day Residual Effects of Tasimelteon Compared With Placebo and Active Control in Healthy Subjects | Healthy Volunteers | P1 | Completed | 48 | RCT, Double-blind | Tasimelteon, 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 | Completed | 32 | Open-label | Tasimelteon, 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 | Completed | 28 | RCT, Double-blind | tasimelteon, 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 | Completed | 24 | Open-label | tradipitant, Midazolam |
| NCT04712734 A Study to Evaluate Iloperidone Long-acting Injection (LAI) for the Treatment of Schizophrenia | Schizophrenia | P1 | Completed | 42 | Open-label | Iloperidone |
| NCT02776215 Study of the Pharmacokinetics and Safety of Tasimelteon in Children and Adolescents | Circadian Rhythm Sleep Disorders, Non-24 Hour Sleep-Wake Disorder | P1 | Completed | 24 | Open-label | tasimelteon |
| NCT01919944 Study of Itch Control by VLY-686 in Healthy Volunteers After Intradermal Injections of Substance P | Pruritus | P1 | Completed | 12 | RCT, Double-blind | VLY-686, Placebo |
| NCT06494397 Pharmacokinetic Study of VHX-896 and Iloperidone Tablets Under Steady-State Conditions | Schizophrenia, Bipolar I Disorder | P1 | Completed | 26 | RCT, Open-label | VHX-896 and iloperidone, Iloperidone and VHX-896 |
| NCT04969211 Bioequivalence Study Between VHX-896 Tablets and Iloperidone Tablets in Healthy Volunteers | Healthy | P1 | Completed | 25 | RCT, Open-label | VHX-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 | Completed | 12 | Open-label | Iloperidone |
| NCT01495169 Tolerability and Pharmacokinetics of Iloperidone in Adolescent Patients | Safety and Tolerability of Iloperidone | P1 | Completed | 33 | Open-label | iloperidone (oral tablet) |
| NCT01402076 A Study to Assess the Effect Tasimelteon on the Cytochrome P450 3A4 and 2C8 Enzymes in Healthy Subjects | Healthy Volunteers | P1 | Completed | 24 | Open-label | Tasimelteon, Rosiglitazone, Midazolam |
| NCT06803290 Food Effect Study of VHX-896 in Healthy Volunteers | Healthy | P1 | Completed | 24 | RCT, Open-label | VHX-896 |
| NCT01637636 Pharmacokinetics of Tasimelteon Alone and in Combination With a CYP3A4 Inhibitor, Ketoconazole, or a CYP3A4 Inducer, Rifampin. | Healthy | P1 | Completed | 48 | Open-label | tasimelteon, tasimelteon, Rifampin, Ketoconazole |
| NCT01477619 Effects of Smoking, Age and Body Size on Pharmacokinetics, Safety and Tolerability on Tasimelteon in Healthy Subjects | Healthy Volunteers | P1 | Completed | 60 | Open-label | Tasimelteon |
| NCT05572281 Bioequivalence Study Between Tasimelteon Capsule Formulation and Liquid Suspension Formulation in Healthy Volunteers | Healthy | P1 | Completed | 36 | RCT, Open-label | Tasimelteon Oral Capsule, Tasimelteon Oral Suspension |
| NCT02560103 An Observational Study to Investigate the Effects of Rapid Transmeridian Travel | Jet Lag Disorder | Completed | 119 | — | — | |
| NCT04353401 WGS Analysis of COVID-19 Positive Patients | Coronavirus Infection, COVID-19 | Completed | 79 | — | — | |
| NCT05922995 The Effects of Tasimelteon in Participants With REM Behavior Disorder (RBD) | REM Behavior Disorder | Early P1 | Terminated | 20 | Open-label | Tasimelteon |
| NCT04474990 Single-Patient Expanded Access Protocol for Tradipitant In A Single Patient With Gastroparesis | Gastroparesis, Diabetic Gastroparesis | AVAILABLE | — | — | Tradipitant | |
| NCT02180451 Observational Study to Investigate the Melatonin and Cortisol Circadian Rhythms of Individuals With Smith-Magenis Syndrome (SMS) | Smith Magenis Syndrome | Unknown | 8 | — | — |