bavisant: Clinical Trials

9 trials of bavisant, newest first

ClinicalTrials Daily  ·  Areas  ·  Conditions  ·  Drugs  ·  Sponsors  ·  

7 completed, 2 withdrawn. 5 Phase 1, 4 Phase 2.

By phase and status

PhaseTrialsStatus
Phase 15Completed 4, Withdrawn 1
Phase 24Completed 3, Withdrawn 1

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Trials newest first · largest first

Tick up to 5 trials to compare them side by side (eligibility, arms, endpoints, adverse events) in a Literature Matrix.

TrialPhaseStatusSponsorEnrollmentStartUpdated
BEN-2001 in Parkinson Disease Patients With Excessive Daytime Sleepiness
BEN-2001, Placebo - Excessive Daytime Sleepiness, Parkinson Disease
Phase 2CompletedBenevolentAI Bio2442017-11-102025-03-10
Effect of JNJ 31001074 on Urge to Drink in Alcohol-Dependent Adults
JNJ-31001074, Placebo - Alcoholism
Phase 2WithdrawnJanssen Research & Development, LLC2011-08-012012-04-30
A Drug Interaction Study of JNJ-31001074 and Ketoconazole in Healthy Volunteers
JNJ-31001074; ketoconazole - Healthy, Pharmacokinetics
Phase 1CompletedJohnson & Johnson Pharmaceutical Research & Development, L.L.C.142009-11-012010-04-30
A Study to Characterize the Pharmacokinetics and Effect of Food on JNJ-31001074 in Healthy Volunteers
JNJ-31001074 - Healthy, Pharmacokinetics
Phase 1CompletedJohnson & Johnson Pharmaceutical Research & Development, L.L.C.202009-06-012010-04-26
A Study to Evaluate Pharmacokinetics, Safety and Tolerability After a Single Dose Administration of JNJ-31001074 in Pediatric Patients (12-17 Years) With Attention Deficit Hyperactivity Disorder (ADHD)
JNJ-31001074 - Attention Deficit Hyperactivity Disorder, Attention Deficit Disorders With Hyperactivity
Phase 1CompletedJohnson & Johnson Pharmaceutical Research & Development, L.L.C.182009-05-012010-04-16
A Study to Evaluate Pharmacokinetics, Safety and Tolerability After a Single Dose Administration of of JNJ-31001074 in Children (6-11 Years) With Attention Deficit Hyperactivity Disorder (ADHD)
JNJ-31001074 - Attention Deficit Hyperactivity Disorder, Attention Deficit Disorders With Hyperactivity
Phase 1CompletedJohnson & Johnson Pharmaceutical Research & Development, L.L.C.182009-05-012010-04-16
A Study to Evaluate 3 Different Doses of JNJ-31001074 in the Treatment of Adults With Attention-Deficit/Hyperactivity Disorder (ADHD)
Atomoxetine 80 mg/d, Placebo, OROS methylphenidate HCl 54 mg/d - Attention Deficit Hyperactivity Disorder
Phase 2CompletedJohnson & Johnson Pharmaceutical Research & Development, L.L.C.4302009-05-012013-03-04
A Safety and Effectiveness Study of JNJ-31001074 in Adults With Attention-Deficit/Hyperactivity Disorder.
Placebo, JNJ-31001074 - Attention Deficit Hyperactivity Disorder
Phase 2CompletedJohnson & Johnson Pharmaceutical Research & Development, L.L.C.322007-12-012014-05-13
A Study to Evaluate the Pharmacokinetic Drug Interaction Between Multiple Doses of JNJ-31001074 and a Single Dose of an Oral Contraceptive Containing Ethinyl Estradiol and Levonorgestrel in Women
JNJ-31001074 - Pharmacokinetics, Drug Interactions
Phase 1WithdrawnJohnson & Johnson Pharmaceutical Research & Development, L.L.C.2016-09-20

Conditions studied

Attention Deficit Disorder with Hyperactivity (4)  ·  Alcohol-Related Disorders (1)  ·  Alcoholism (1)  ·  Disorders of Excessive Somnolence (1)  ·  Mental Disorders (1)  ·  Parkinson Disease (1)  ·  Substance-Related Disorders (1)

Sponsors

Johnson & Johnson Pharmaceutical Research & Development, L.L.C. (7)  ·  BenevolentAI Bio (1)  ·  Janssen Research & Development, LLC (1)

Countries

United States (4)

Top investigators

William G Ondo, M.D (1)

Results publications

PMID 22519922