Clinical Trials - VNDA

NCT IDTitleStatusPhasesStart DateCompletion DatePrimary Completion Date
NCT07179055An Eight-Week Study to Evaluate the Safety and Efficacy of VSJ-110 Compared to Placebo in the Treatment of Dry EyeRECRUITINGPHASE22025-102026-092026-09
NCT07090161Evaluation of Efficacy and Safety of Iloperidone for the Treatment of Participants With Uncontrolled HypertensionNOT_YET_RECRUITINGPHASE22025-07-282026-112026-10
NCT06961968Randomized Withdrawal Study in Patients With SchizophreniaRECRUITINGPHASE32025-05-142027-112027-11
NCT07065773Safety, Tolerability and Efficacy of Trichostatin A in Patients With Mild to Severe OnychomycosisRECRUITINGPHASE22025-05-052026-052026-03
NCT06953869Evaluating the Effects of Tasimelteon vs. Placebo in Treating Pediatric InsomniaRECRUITINGPHASE32025-04-212028-012027-11
NCT06830044Evaluation of Efficacy and Safety of Milsaperidone as Adjunctive Therapy in Patients With Major Depressive DisorderRECRUITINGPHASE32025-03-032028-032028-03
NCT06804603A Study to Measure the Effects of Using Tradipitant on Nausea and Vomiting After GLP-1R Agonist UseRECRUITINGPHASE22025-02-252025-09-012025-09-01
NCT06701396Evaluating the Effects of Tasimelteon Vs. Placebo in Delayed Sleep-Wake Phase Disorder (DSWPD) and the CRY1Δ11 VariantRECRUITINGPHASE32024-10-082025-06-302025-06-30
NCT06494397Pharmacokinetic Study of VHX-896 and Iloperidone Tablets Under Steady-State ConditionsCOMPLETEDPHASE12024-07-112024-10-242024-10-24
NCT06296966A Study to Evaluate the Safety and Efficacy of VSJ-110 Compared to Placebo in the Treatment of Dry EyeRECRUITINGPHASE22024-02-292024-072024-07
NCT06836557Open Label Safety Study of Tradipitant in Idiopathic and Diabetic GastroparesisRECRUITINGPHASE32024-01-092025-122025-12
NCT05903924Motion Serifos: A Study to Investigate the Efficacy of Tradipitant in Participants Affected by Motion SicknessCOMPLETEDPHASE32023-09-092024-04-242024-04-06
NCT05648591Safety and Tolerability of Open-Labeled Iloperidone in AdolescentsRECRUITINGPHASE42023-05-242026-11-302026-03-31
NCT06138613Motion Delos: An Open Label Safety and Efficacy of Tradipitant in Participants Affected by Motion SicknessRECRUITINGPHASE32023-02-272025-04-302025-04-30
NCT06803290Food Effect Study of VHX-896 in Healthy VolunteersCOMPLETEDPHASE12022-06-212022-12-272022-12-27
NCT05344365A Study to Evaluate Iloperidone for the Treatment of Parkinson's Disease PsychosisWITHDRAWNPHASE22022-062023-112023-11
NCT05572281Bioequivalence Study Between Tasimelteon Capsule Formulation and Liquid Suspension Formulation in Healthy VolunteersCOMPLETEDPHASE12022-05-182022-06-152022-06-15
NCT05366855Long-Term Safety and Efficacy of Imsidolimab (ANB019) in Subjects With Generalized Pustular PsoriasisTERMINATEDPHASE32022-04-212024-07-172024-02-08
NCT05352893Study to Evaluate the Efficacy and Safety of Imsidolimab (ANB019) in the Treatment of Subjects With GPPCOMPLETEDPHASE32022-04-142023-08-172023-08-17
NCT04327661Motion Syros: A Study to Investigate the Efficacy of Tradipitant in Subjects Affected by Motion SicknessCOMPLETEDPHASE32021-11-152023-04-122023-04-01
NCT05361707Evaluating the Effects of Tasimelteon in Individuals With Autism Spectrum Disorder (ASD) and Sleep DisturbancesRECRUITINGPHASE32021-07-282025-072025-07
NCT04856930A Study to Evaluate the Efficacy and Safety of Imsidolimab (ANB019) in the Treatment of Participants With Hidradenitis SuppurativaCOMPLETEDPHASE22021-07-072022-12-142022-07-15
NCT04969211Bioequivalence Study Between VHX-896 Tablets and Iloperidone Tablets in Healthy VolunteersCOMPLETEDPHASE12021-06-302021-10-132021-10-13
NCT04856917A Study to Evaluate the Efficacy and Safety of Imsidolimab (ANB019) in the Treatment of Participants With Acne VulgarisCOMPLETEDPHASE22021-05-152022-03-292022-02-01
NCT04697069A Study to Evaluate of the Efficacy and Safety of Imsidolimab (ANB019) in the Treatment of Acneiform RashTERMINATEDPHASE22021-05-042021-12-132021-12-13
NCT04819776Evaluation of Efficacy and Safety of Iloperidone in the Acute Treatment of Manic or Mixed Episodes Associated With Bipolar I DisorderCOMPLETEDPHASE32021-03-222023-08-162022-09-07
NCT04800237Evaluating the Effects of VQW-765 vs. Placebo in Performance AnxietyCOMPLETEDPHASE22021-02-232022-08-022022-08-02
NCT04849559Effects of Tradipitant on Satiation, Gastric Volume, Gastric Accommodation, and Gastric Emptying in Healthy VolunteersCOMPLETEDPHASE1, PHASE22021-02-012021-09-242021-09-24
NCT04697056A Study to Evaluate the Efficacy and Safety of Imsidolimab (ANB019) in the Treatment of Participants With IchthyosisTERMINATEDPHASE22021-01-252021-11-192021-11-19
NCT04712734A Study to Evaluate Iloperidone Long-acting Injection (LAI) for the Treatment of SchizophreniaCOMPLETEDPHASE12021-01-132022-08-302022-08-30
NCT04652882Evaluating the Effects of Tasimelteon Vs. Placebo in Delayed Sleep-Wake Phase Disorder (DSWPD)RECRUITINGPHASE32020-12-092025-122025-12
NCT04622345Safety and Efficacy of VSJ-110 in the Treatment of Allergic Conjunctivitis in Adults With a History of Ocular AllergiesCOMPLETEDPHASE22020-11-212021-06-282021-05-22
NCT04326426ODYSSEY: A Study to Investigate the Efficacy of Tradipitant in Treating Severe or Critical COVID-19 InfectionENROLLING_BY_INVITATIONPHASE32020-04-132020-08-312020-08-01
NCT04140695Evaluating the Effects of Tradipitant vs. Placebo in Atopic Dermatitis (EPIONE2)TERMINATEDPHASE32019-10-212020-10-142020-10-14
NCT04127058Evaluating a New Iloperidone Titration Scheme in Bipolar I Disorder or SchizophreniaCOMPLETEDPHASE12019-10-072019-11-272019-11-27
NCT04028492Evaluating the Safety and Efficacy of Tradipitant vs. Placebo in Idiopathic and Diabetic GastroparesisCOMPLETEDPHASE32019-08-202025-02-212025-02-21
NCT03633396A Study to Evaluate the Efficacy and Safety of Imsidolimab (ANB019) in Adults With Palmoplantar PustulosisCOMPLETEDPHASE22019-05-202021-04-232021-04-23
NCT03619902A Study to Evaluate the Efficacy and Safety of Imsidolimab (ANB019) in Adults With Generalized Pustular PsoriasisCOMPLETEDPHASE22019-01-302021-01-202021-01-20
NCT03772340Motion Sifnos: A Study to Investigate the Efficacy of Tradipitant in Subjects Affected by Motion SicknessCOMPLETEDPHASE22018-12-202019-06-272019-06-06
NCT03838926Tolerability Study of Trichostatin A In Subjects With Relapsed or Refractory Hematologic MalignanciesRECRUITINGPHASE12018-09-272025-122025-12
NCT06323655Evaluation of Next-Day Residual Effects of Tasimelteon Compared With Placebo and Active Control in Healthy SubjectsCOMPLETEDPHASE12018-07-192018-08-282018-08-28
NCT03568331Evaluating the Effects of Tradipitant vs. Placebo in Atopic Dermatitis (EPIONE)COMPLETEDPHASE32018-07-092019-12-272019-12-27
NCT03373201Evaluating the Effects of Tasimelteon vs. Placebo on Jet Lag Type InsomniaCOMPLETEDPHASE32017-10-162018-03-052018-03-05
NCT02970968Study to Assess the Efficacy of VLY-686 in Relieving Symptoms of GastroparesisCOMPLETEDPHASE22016-112018-122018-11
NCT02776215Study of the Pharmacokinetics and Safety of Tasimelteon in Children and AdolescentsCOMPLETEDPHASE12016-10-042017-12-202017-12-20
NCT03291041A Proof of Concept Study to Evaluate the Effects of Tasimelteon and Placebo in Travelers With Jet Lag DisorderCOMPLETEDPHASE22016-072017-112017-11
NCT02651714Tradipitant in Treatment-resistant Pruritus Associated With Atopic DermatitisCOMPLETEDPHASE22016-01-192017-08-042017-08-04
NCT02621385Study to Assess the Effect of Multiple Doses of Tradipitant on CYP3A4 Using Midazolam as a Substrate in Healthy SubjectsCOMPLETEDPHASE12015-112016-02
NCT02231008Evaluating the Effects of Tasimelteon vs Placebo on Sleep Disturbances in SMSCOMPLETEDPHASE2, PHASE32015-092022-012018-11-19
NCT02130999Open Label Study to Assess the Absolute Bioavailability of Tasimelteon (HETLIOZâ„¢)COMPLETEDPHASE42014-052014-052014-05
NCT02004041Proof of Concept of VLY-686 in Subjects With Treatment-Resistant Pruritus Associated With Atopic DermatitisCOMPLETEDPHASE22013-12-102015-02-192015-02-19
NCT01919944Study of Itch Control by VLY-686 in Healthy Volunteers After Intradermal Injections of Substance PCOMPLETEDPHASE12013-082013-112013-11
NCT01637636Pharmacokinetics of Tasimelteon Alone and in Combination With a CYP3A4 Inhibitor, Ketoconazole, or a CYP3A4 Inducer, Rifampin.COMPLETEDPHASE12012-062012-082012-08
NCT01578057Evaluation of the Pharmacodynamic and Pharmacokinetic Interactions of Tasimelteon and EthanolCOMPLETEDPHASE12012-042012-062012-06
NCT01540500Pharmacokinetics of Tasimelteon Alone and in Combination With CYP1A2 Inhibitor, FluvoxamineCOMPLETEDPHASE12012-022012-032012-03
NCT01526746Pharmacokinetics of Tasimelteon in Subjects With Renal Impairment and Matched Control Subjects With Relatively Normal Renal FunctionCOMPLETEDPHASE12012-022012-062012-06
NCT01477619Effects of Smoking, Age and Body Size on Pharmacokinetics, Safety and Tolerability on Tasimelteon in Healthy SubjectsCOMPLETEDPHASE12011-112012-012012-01
NCT01495169Tolerability and Pharmacokinetics of Iloperidone in Adolescent PatientsCOMPLETEDPHASE12011-102015-022015-02
NCT01429116Tasimelteon for the Treatment of Non-24-hour Sleep-Wake Disorder (N24HSWD) in Blind Individuals With no Light PerceptionCOMPLETEDPHASE32011-102015-012015-01
NCT01428661Melatonin Agonist Effects of Tasimelteon Versus Placebo in Patients With Major Depressive DisorderCOMPLETEDPHASE2, PHASE32011-092013-052013-01
NCT01430754Withdrawal Study to Demonstrate the Maintenance Effect in the Treatment of Non-24-Hour Sleep-Wake DisorderCOMPLETEDPHASE32011-092012-122012-12
NCT01402076A Study to Assess the Effect Tasimelteon on the Cytochrome P450 3A4 and 2C8 Enzymes in Healthy SubjectsCOMPLETEDPHASE12011-082011-082011-08
NCT01291511Relapse Prevention Study in Patients With SchizophreniaCOMPLETEDPHASE32011-022015-032014-03
NCT01271387Pharmacokinetics of Tasimelteon in Subjects With Mild or Moderate Hepatic ImpairmentCOMPLETEDPHASE12011-012011-082011-08
NCT01218789Safety Study of Tasimelteon for Treatment of Non-24-Hour-Sleep-Wake Disorder in Blind Individuals With No Light PerceptionACTIVE_NOT_RECRUITINGPHASE32010-10-282024-12-052024-12-05
NCT01163032Efficacy and Safety of Tasimelteon Compared With Placebo in Totally Blind Subjects With Non-24-Hour Sleep-Wake DisorderCOMPLETEDPHASE32010-082012-112012-11
NCT00548340VEC-162 Study in Adult Patients With Primary InsomniaCOMPLETEDPHASE32007-112008-062008-02
NCT00291187VEC-162 Study in Healthy Adult Volunteers in a Model of InsomniaCOMPLETEDPHASE32006-022006-082006-08
NCT00254202Efficacy and Safety of Iloperidone Compared With Placebo and Active Control in Subjects With Acute SchizophreniaCOMPLETEDPHASE32005-11-182007-03-212006-09-26
NCT00490945Safety and Efficacy of VEC-162 on Circadian Rhythm in Healthy Adult VolunteersCOMPLETEDPHASE22004-072005-032005-03
NCT00467441VSF-173 Study in Healthy Adult Volunteers for Treatment of Induced Excessive SleepinessCOMPLETEDPHASE2