Success Metrics

Clinical Success Rate
96.3%

Based on 26 completed trials

Completion Rate
96%(26/27)
Active Trials
5(11%)
Results Posted
19%(5 trials)
Terminated
1(2%)

Phase Distribution

Ph phase_3
9
20%
Ph phase_1
5
11%
Ph early_phase_1
1
2%
Ph not_applicable
8
18%
Ph phase_2
12
27%
Ph phase_4
6
14%

Phase Distribution

6

Early Stage

12

Mid Stage

15

Late Stage

Phase Distribution41 total trials
Early Phase 1First-in-human
1(2.4%)
Phase 1Safety & dosage
5(12.2%)
Phase 2Efficacy & side effects
12(29.3%)
Phase 3Large-scale testing
9(22.0%)
Phase 4Post-market surveillance
6(14.6%)
N/ANon-phased studies
8(19.5%)

Highest Phase Reached

Phase 4

Trial Status & Enrollment

Completion Rate

92.9%

26 of 28 finished

Non-Completion Rate

7.1%

2 ended early

Currently Active

5

trials recruiting

Total Trials

44

all time

Status Distribution
Active(7)
Completed(26)
Terminated(2)
Other(9)

Detailed Status

Completed26
unknown9
Recruiting4
Not yet recruiting1
Active, not recruiting1
Terminated1

Development Timeline

Analytics

Development Status

Total Trials
44
Active
5
Success Rate
96.3%
Most Advanced
Phase 4

Trials by Phase

Early Phase 11 (2.4%)
Phase 15 (12.2%)
Phase 212 (29.3%)
Phase 39 (22.0%)
Phase 46 (14.6%)
N/A8 (19.5%)

Trials by Status

not_yet_recruiting12%
active_not_recruiting12%
completed2659%
recruiting49%
terminated12%
unknown920%
withdrawn12%
enrolling_by_invitation12%

Recent Activity

Clinical Trials (44)

Showing 20 of 44 trialsScroll for more
NCT07568574Not Applicable

Impact of Medically Supervised Performance-Enhancing Substances (PES) on Elite Athletes

Enrolling By Invitation
NCT07492160Phase 2

Efficacy of Cabergoline in Inhibiting Lactation and Alleviating Breast Symptoms

Recruiting
NCT07043322Phase 2

Clinical Study to Evaluate Efficacy of Cabergoline to Coasting in Reducing the Incidence of Ovarian Hyperstimulation Syndrome

Recruiting
NCT07463235Phase 3

Safety and Potency of a High Cabergoline Dosage in Microprolactinomas

Recruiting
NCT06909123Phase 2

A Reduced Dose of Cabergoline for Lactation Inhibition After Second-Trimester Abortion or Pregnancy Loss

Not Yet Recruiting
NCT02288962Phase 3

Dopamine Agonist Treatment of Non-functioning Pituitary Adenomas

Active Not Recruiting
NCT01794793Phase 4

Study to Allow Access to Pasireotide for Patients Benefiting From Pasireotide Treatment in Novartis-sponsored Studies

Completed
NCT06123026Phase 4

Pharmacological Inhibition of Lactation After 16 to 20 Week Abortion

Recruiting
NCT05024422Not Applicable

Lactation Inhibition, the Efficiency of Vitamin B6 Versus Cabergoline

Completed
NCT03457389Not Applicable

Comparison of Treatment Outcome of Cabergoline According to Target Prolactin Levels in Patients With Prolactinoma

Unknown
NCT02542410Phase 2

Dopamine Receptor Agonist Therapy for Pain Relief in Women Suffering From Endometriosis: A Pilot Study

Completed
NCT01730729Early Phase 1

Cabergoline in Metastatic Breast Cancer

Completed
NCT04038749Not Applicable

Satisfaction of Patients With the Chosen Method of Inhibition of Lactation

Unknown
NCT02875587Phase 2

Cabergoline Versus Calcium Gluconate Infusion in the Prevention of Ovarian Hyperstimulation Syndrome

Completed
NCT03313661Phase 3

Co-administration of Cabergoline and Gliclazide Improve Glycemic Parameters and Lipid Profile in T2DM Patients

Unknown
NCT01535859Phase 3

Study of Cabergoline for Prevention of Ovarian Hyperstimulation Syndrome (OHSS) in In Vito Fertilization Cycles and Derivation of OHSS Biomarkers

Completed
NCT00699530

Substrate Metabolism and Insulin Sensitivity in Patients With Hyperprolactinemia Before and After Treatment

Withdrawn
NCT00652873Phase 1

Bioequivalence Study of Cabergoline Tablets and Dostinex Under Fed Conditions

Completed
NCT03271918Phase 3

Cabergoline in Nonfunctioning Pituitary Adenomas

Completed
NCT03263299Phase 4

Value of Cabergoline and Low Dose Aspirin in Poor Responders Undergoing ICSI-ET With GnRH Agonist Flare-Up-Protocol

Unknown

Drug Details

Intervention Type
DRUG
Total Trials
44