Success Metrics

Clinical Success Rate
78.6%

Based on 11 completed trials

Completion Rate
79%(11/14)
Active Trials
0(0%)
Results Posted
91%(10 trials)
Terminated
3(19%)

Phase Distribution

Ph phase_3
6
38%
Ph phase_1
6
38%
Ph phase_2
4
25%

Phase Distribution

6

Early Stage

4

Mid Stage

6

Late Stage

Phase Distribution16 total trials
Phase 1Safety & dosage
6(37.5%)
Phase 2Efficacy & side effects
4(25.0%)
Phase 3Large-scale testing
6(37.5%)

Highest Phase Reached

Phase 3

Trial Status & Enrollment

Completion Rate

68.8%

11 of 16 finished

Non-Completion Rate

31.3%

5 ended early

Currently Active

0

trials recruiting

Total Trials

16

all time

Status Distribution
Completed(11)
Terminated(5)

Detailed Status

Completed11
Terminated3
Withdrawn2

Development Timeline

Analytics

Development Status

Total Trials
16
Active
0
Success Rate
78.6%
Most Advanced
Phase 3

Trials by Phase

Phase 16 (37.5%)
Phase 24 (25.0%)
Phase 36 (37.5%)

Trials by Status

terminated319%
withdrawn213%
completed1169%

Recent Activity

Clinical Trials (16)

Showing 16 of 16 trials
NCT00529373Phase 3

A Study of MK-0822 in Postmenopausal Women With Osteoporosis to Assess Fracture Risk (MK-0822-018)

Terminated
NCT01803607Phase 3

Efficacy and Safety of Odanacatib in Postmenopausal Women Previously Treated With Oral Bisphosphonate (MK-0822-076)

Terminated
NCT01630616Phase 1

A Study of Odanacatib When Administered to Adolescents and Young Adults Treated With Glucocorticoids (MK-0822-066)

Terminated
NCT01068262Phase 1

Safety and Tolerability of Odanacatib (0822-059)

Completed
NCT01120600Phase 3

A Study to Assess Safety and Efficacy of Odanacatib (MK-0822) in Men With Osteoporosis (MK-0822-053)

Completed
NCT00885170Phase 2

A Study to Evaluate the Safety, Tolerability, and Efficacy of Odanacatib (MK-0822) in Postmenopausal Women Previously Treated With a Bisphosphonate (MK-0822-042)

Completed
NCT00729183Phase 3

Study to Evaluate Efficacy of Odanacatib (MK-0822) on Bone Mineral Density (BMD) and Bone Micro-architecture and Overall Safety in Postmenopausal Women (MK-0822-031)

Completed
NCT00620113Phase 2

Efficacy and Safety of Odanacatib (MK-0822) in Participants With Involutional Osteoporosis (MK-0822-022)

Completed
NCT00399802Phase 2

A Study to Examine the Effects of an Experimental Drug on Women With Breast Cancer and Metastatic Bone Disease (MBD)(0822-016)(COMPLETED)

Completed
NCT00112437Phase 2

A Study to Examine the Effects of an Experimental Drug on Postmenopausal Osteoporosis (MK-0822-004)

Completed
NCT00691899Phase 3

A Study to Assess the Effects of MK0822 in Prolonging Time to First Bone Metastasis in Men With Castration-Resistant Prostate Cancer (0822-030)

Withdrawn
NCT00770159Phase 1

A Study to Test Once-Weekly Doses of Odanacatib (MK0822) on Healthy Adult Females (0822-005)(COMPLETED)

Completed
NCT01552122Phase 3

Efficacy and Safety of Odanacatib in Postmenopausal Women Previously Treated With Alendronate (MK-0822-050)

Withdrawn
NCT00863525Phase 1

A Study to Assess the Effects of a Light Breakfast on the Safety, Tolerability, and Pharmacokinetics of Odanacatib (MK0822)

Completed
NCT00863590Phase 1

A Single-Dose Study of the Safety, Tolerability, and Pharmacokinetics of Odanacatib (MK0822) in Healthy Volunteers

Completed
NCT00769418Phase 1

Study of Multiple Oral Doses of Odanacatib (MK0822) in Healthy Adults (0822-002)

Completed

All 16 trials loaded

Drug Details

Intervention Type
DRUG
Total Trials
16