Clinical Trials
20 trialsNCT06790719 2025-01-24
BEACON
University of Southampton
Not yet recruiting
NCT00263575 2024-06-18
Long-term Safety Study of Sublingual Fentanyl Tablets in Cancer Patients
Kyowa Kirin Co., Ltd.
Phase 3 Completed
NCT05053308 2023-08-07
Proportional Dose of Sublingual Fentanyl Tablet Based on Daily Opioid Requirement
Seoul National University
Phase NA Withdrawn
NCT01651910 2023-05-31
The Cancer Pain and Unmet Needs Study
University of Surrey
Terminated
NCT05037539 2022-08-31
Efficacy of Injectable Fentanyl in Sublingual Route Versus Oral Morphine Syrup for Breakthrough Pain
Department of Medical Services Ministry of Public Health of Thailand
Phase 1/2 Completed
NCT03809455 2020-04-22
FARADI
UNICANCER
Phase 2 Withdrawn
NCT03435120 2020-03-02
CAVIDIOM
Angelini Farmacéutica
Completed
NCT02869321 2019-05-13
ANTALGIP
Central Hospital, Nancy, France
Phase 4 Completed
NCT02836379 2018-03-05
CAVIDIOR
Angelini Farmacéutica
Completed
NCT02840500 2018-03-05
CAVIDIOPAL
Angelini Farmacéutica
Completed
NCT00125294 2017-09-25
Sublingual Methadone for the Management of Cancer Breakthrough Pain
AHS Cancer Control Alberta
Phase 1 Completed
NCT01326689 2017-03-08
2246-004
Kyowa Kirin Co., Ltd.
Phase 3 Completed
NCT02437929 2016-07-12
Procedural Pain in Palliative Care: Prevalence, Intensity and Treatment
Antea Foundation
Completed
NCT02050503 2015-03-17
CP073
Grupo de Investigación Clínica en Oncología Radioterapia
Completed
NCT00236041 2014-05-09
Efficacy/Safety Study of ACTIQ® for Opioid-Tolerant Children and Adolescents With Breakthrough Pain (BTP)
Teva Branded Pharmaceutical Products R&D, Inc.
Phase 2 Completed
NCT01842893 2013-05-03
ETHYFYL
Ethypharm
Phase 3 Completed
NCT00236145 2013-01-29
Evaluate the Efficacy and Safety of ACTIQ in Patients With Cancer and Breakthrough Pain
Teva Branded Pharmaceutical Products R&D, Inc.
Phase 3 Completed
NCT00842829 2012-10-01
Study of Breakthrough Cancer Pain: Assessment of Fentanyl Buccal Tablets Titration and Treatment in Opioid-Tolerant Patients
Teva Branded Pharmaceutical Products R&D, Inc.
Phase 4 Terminated
NCT00994760 2012-09-27
GENISIS
Takeda
Completed
NCT00576173 2010-04-28
An Open Label Study to Evaluate Safety, Tolerability and Clinical Utility of ULTRACET® (37.5mg Tramadol Hydrochloride/325mg Acetaminophen) for the Treatment of Breakthrough Pain in Cancer Patients
Johnson & Johnson Taiwan Ltd
Phase 4 Completed