Success Metrics

Clinical Success Rate
100.0%

Based on 11 completed trials

Completion Rate
100%(11/11)
Active Trials
0(0%)
Results Posted
18%(2 trials)

Phase Distribution

Ph phase_2
2
18%
Ph early_phase_1
1
9%
Ph phase_1
8
73%

Phase Distribution

9

Early Stage

2

Mid Stage

0

Late Stage

Phase Distribution11 total trials
Early Phase 1First-in-human
1(9.1%)
Phase 1Safety & dosage
8(72.7%)
Phase 2Efficacy & side effects
2(18.2%)

Highest Phase Reached

Phase 2

Trial Status & Enrollment

Completion Rate

100.0%

11 of 11 finished

Non-Completion Rate

0.0%

0 ended early

Currently Active

0

trials recruiting

Total Trials

11

all time

Status Distribution
Completed(11)

Detailed Status

Completed11

Development Timeline

Analytics

Development Status

Total Trials
11
Active
0
Success Rate
100.0%
Most Advanced
Phase 2

Trials by Phase

Early Phase 11 (9.1%)
Phase 18 (72.7%)
Phase 22 (18.2%)

Trials by Status

completed11100%

Recent Activity

Clinical Trials (11)

Showing 11 of 11 trials
NCT05935280Early Phase 1

Mechanism of Human Cold Pain Perception - Involvement of TRPA1, TRPM8, Nav1.7 and Nav1.8

Completed
NCT01769274Phase 2

Evaluation Of The Efficacy And Safety Of Single Doses Of PF-05089771 In Patients With Primary (Inherited) Erythromelalgia

Completed
NCT01529346Phase 2

Efficacy Of PF-05089771 In Treating Postoperative Dental Pain

Completed
NCT01854996Phase 1

Relative Bioavailability With PF-05089771 Capsule Versus Oral Dispersion

Completed
NCT01772264Phase 1

Safety And Tolerability Study Of BID Titration Scheme With PF-05089771

Completed
NCT01529671Phase 1

A Safety And Tolerability Study Of PF-05089771 In Healthy Subjects And In Subjects With Otseoarthritis Of The Knee

Completed
NCT01690351Phase 1

A Study Comparing PF-05089771 TS Capsule To PF-05089771 TS Oral Dispersion In The Fasted State

Completed
NCT01563497Phase 1

A Study Comparing PF-05089771 TS Tablet to PF-05089771 TS Oral Dispersion In The Fasted State And To PF-05089771 TS Tablet In The Fasted And Fed State

Completed
NCT01259882Phase 1

A Single Dose Escalation Study In Healthy Volunteers To Determine The Pharmacokinetics, Safety And Tolerability Of PF-05089771 In Healthy Volunteers

Completed
NCT01365637Phase 1

The Safety and Tolerability of PF-05089771 Will be Investigated in Healthy Subjects Over a 14 Day Dosing Period.

Completed
NCT01165736Phase 1

To Calculate the Pharmacokinetics (Concentration of Compound in and Rate of Excretion From the Blood) Following a Very Low Dose of Compound Which Will Not Have Any Pharmacological Activity

Completed

All 11 trials loaded

Drug Details

Intervention Type
DRUG
Total Trials
11