Key Insights

Highlights

Success Rate

80% trial completion

Clinical Risk Assessment

Based on trial outcomes

Moderate Risk

Score: 52/100

Termination Rate

13.0%

3 terminated out of 23 trials

Success Rate

80.0%

-6.5% vs benchmark

Late-Stage Pipeline

39%

9 trials in Phase 3/4

Results Transparency

33%

4 of 12 completed with results

Key Signals

4 with results80% success

Data Visualizations

Phase Distribution

15Total
Not Applicable (3)
P 1 (1)
P 2 (2)
P 3 (5)
P 4 (4)

Trial Status

Completed12
Terminated3
Recruiting3
Withdrawn2
Active Not Recruiting1
Not Yet Recruiting1

Trial Success Rate

80.0%

Benchmark: 86.5%

Based on 12 completed trials

Clinical Trials (23)

Showing 20 of 20 trials
NCT06580327Not ApplicableRecruitingPrimary

Programmed Intermittent Epidural Bolus Compared With Continuous Infusion in Multiparous Women

NCT06494280Not ApplicableRecruitingPrimary

PIEB Compared With CEI on Breakthrough Pain in Nulliparous Women

NCT06790719Not Yet RecruitingPrimary

Paediatric Breakthrough Pain Assessment

NCT04011150Phase 3Recruiting

Development of Variable Volume Automated Mandatory Boluses for Patient-controlled Epidural Analgesia During Labour

NCT02278601Phase 3Active Not RecruitingPrimary

Comparison of Regimens MPIB, CIPCEA, PCEA

NCT05053308Not ApplicableWithdrawn

Proportional Dose of Sublingual Fentanyl Tablet Based on Daily Opioid Requirement

NCT05200806Phase 4Unknown

A Prospective Pilot Study of a Non-Narcotic Post-Operative Course After Colectomy

NCT02886286Phase 4Completed

Patient Controlled Intrathecal Analgesia With Bupivacaine for Chronic Low Back Pain

NCT03809455Phase 2WithdrawnPrimary

Effectiveness and Tolerance of Fentanyl Citrate in Painful Pain Induced During Diagnostic or Therapeutic Examinations in Cancer Patients

NCT03435120CompletedPrimary

Quality of Life Study Breakthrough Cancer Pain Treated in Medical Oncology Services (CAVIDIOM)

NCT02869321Phase 4Completed

Analgesic Efficacy of Transmucosal Fentanyl for Breakthrough Pain Caused by Interventional Gastrostomy

NCT02840500CompletedPrimary

Quality of Life Study in Patients With Cancer Breakthrough Pain Treated in Palliative Care Units

NCT02836379CompletedPrimary

Quality of Life Study Breakthrough Cancer Pain Treated in Radiation Oncology Services With Palliative Intent

NCT00402350Phase 1CompletedPrimary

Staccato Fentanyl Single and Multidose PK

NCT02437929CompletedPrimary

Procedural Pain in Palliative Care: Prevalence, Intensity and Treatment

NCT02050503CompletedPrimary

Intranasal Transmucosal Fentanyl Pectin for Breakthrough Cancer Pain in Radiation-induced Oropharyngeal Mucositis

NCT01901718TerminatedPrimary

An Observational, Non-Interventional Trial to Assess Patient Satisfaction and Safety of Subsys™ Spray.

NCT00236041Phase 2Completed

Efficacy/Safety Study of ACTIQ® for Opioid-Tolerant Children and Adolescents With Breakthrough Pain (BTP)

NCT01842893Phase 3CompletedPrimary

Efficacy and Safety of Fentanyl ETHYPHARM for Breakthrough Pain in Opioid-treated Patients With Cancer

NCT00236145Phase 3CompletedPrimary

Evaluate the Efficacy and Safety of ACTIQ in Patients With Cancer and Breakthrough Pain

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Research Network

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