Cabergoline: Clinical Trials

8 trials of Cabergoline, newest first

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6 completed, 1 active not recruiting, 1 not yet recruiting. 8 Phase 1, 2 Phase 2.

By phase and status

PhaseTrialsStatus
Phase 18Completed 6, Active not recruiting 1, Not yet recruiting 1
Phase 22Completed 2

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Trials (filtered) newest first · largest first

All 8 trials

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

TrialPhaseStatusSponsorEnrollmentStartUpdated
A Study to Assess the Safety, Tolerability and Pharmacokinetics of Viaca (Sildenafil + Cabergoline) Compared With Sildenafil and Cabergoline
Viaca, Sildenafil 50 mg, Cabergoline 0.5 MG - Erectile Dysfunctions, Healthy Volunteer
Phase 1Not yet recruitingYanping Kong302026-08-012026-07-28
A Study on Bioequivalence of Cabergoline Tablets in Human Body
Cabergoline tablets test formulation, Cabergoline tablets reference formulation - Hyperprolactinemia
Phase 1Active not recruitingChangchun GeneScience Pharmaceutical Co., Ltd.722025-06-302025-11-17
Clinical Guidance for Proper Treatment of Unexplained Resistant Hyperprolactinemia.
cabergoline 1.5-2 mg/week).orally daily for 1 month plus health education, cabergoline 1.5-2 mg/week).orally daily for 1 month without health education - Health Education
Phase 1CompletedWoman's Health University Hospital, Egypt1202020-02-012023-05-25
A Pilot Study of Cabergoline for the Treatment of Cocaine Dependence
Placebo, Cabergoline - Cocaine Dependence, Cocaine Abuse
Phase 1CompletedBaylor College of Medicine112011-07-012012-07-27
Compare the Efficacy of Human Albumin With Cabergoline to Prevent Ovarian Hyper Stimulation in Assisted Reproductive Technology (ART) Program
Cabergoline, Control - Ovarian Hyperstimulation Syndrome
Phase 1 / Phase 2CompletedRoyan Institute102009-06-012015-05-06
Effect of Cabergoline on Weight and Glucose Tolerance
Cabergoline, placebo - Body Weight, Impaired Glucose Tolerance in Obese
Phase 1 / Phase 2CompletedColumbia University402002-04-012015-10-14
Bioequivalence Study of Cabergoline Tablets and Dostinex Under Fasting Conditions
Cabergoline, Dostinex - To Determine Bioequivalence Under Fasting Conditions
Phase 1CompletedPar Pharmaceutical, Inc.402001-08-012008-04-04
Bioequivalence Study of Cabergoline Tablets and Dostinex Under Fed Conditions
Cabergoline, Dostinex - To Determine Bioequivalence Under Fed Conditions
Phase 1CompletedPar Pharmaceutical, Inc.242001-07-012017-09-26

Conditions studied

Hyperprolactinemia (2)  ·  Body Weight (1)  ·  Cocaine-Related Disorders (1)  ·  Erectile Dysfunction (1)  ·  Fasting (1)  ·  Health Education (1)  ·  Lecithin Cholesterol Acyltransferase Deficiency (1)  ·  Ovarian Hyperstimulation Syndrome (1)  ·  Substance-Related Disorders (1)

Sponsors

Par Pharmaceutical, Inc. (2)  ·  Baylor College of Medicine (1)  ·  Changchun GeneScience Pharmaceutical Co., Ltd. (1)  ·  Columbia University (1)  ·  Royan Institute (1)  ·  Woman's Health University Hospital, Egypt (1)  ·  Yanping Kong (1)

Countries

Canada (2)  ·  United States (2)  ·  Australia (1)  ·  China (1)  ·  Egypt (1)  ·  Iran (1)

Top investigators

Eric Masson, Pharm.D. (2)  ·  Ashraf Moini, MD (1)  ·  Atef M Darwish, Prof (1)  ·  Emma Trowbridge, MD (1)  ·  Eniseh Tehraninejad, MD (1)  ·  Judith Korner, MD, PHD (1)  ·  Marzieh Shiva, MD (1)

Results publications

PMID 22231013