A Study of Sativex® for Pain Relief in Patients With Advanced Malignancy.
CompletedPhase 2NCT00530764
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Brief summary (from the registry)
The purpose of this study is to determine the effective dose range and to demonstrate a non-effective dose range of Sativex in patients with advanced cancer, who experience inadequate pain relief even though they are on optimized chronic opioid therapy.
Study details
- Official title
- A Double Blind, Randomized, Placebo Controlled, Parallel Group Dose-range Exploration Study of Sativex® in Relieving Pain in Patients With Advanced Cancer, Who Experience Inadequate Analgesia During Optimized Chronic Opioid Therapy.
- Interventions
- Drug: Sativex Low Dose
- Drug: Sativex Medium Dose
- Drug: Sativex High Dose
- Sponsor
- GW Pharmaceuticals Ltd
- Collaborators
- Quintiles, Inc.
- Organization
- GWPharm
- Start date
- 2007-11
- Primary completion
- 2010-01
- Sex
- All
- Age range
- from 18 Years
- Results posted
- Yes, on ClinicalTrials.gov
- Countries
- Belgium, Canada, Chile, Czechia, Finland, France, Germany, India, Italy, Mexico, Poland, Romania, South Africa, Spain, United Kingdom, United States
- Total sites listed
- 110
Eligibility criteria
Show eligibility criteria (verbatim from the registry)
Inclusion Criteria: * The patient has advanced active cancer for which there is no known curative therapy. * The patient is able (in the investigators opinion) and willing to comply with all study requirements. * The patient has a clinical diagnosis of cancer related pain, which is not wholly alleviated with their current opioid treatment. * The patient is receiving a sustained release (SR) fixed dose of opioid therapy (excluding Methadone). N.B. The opiate therapy must be Step III according to the World Health Organization (WHO) analgesic ladder. * The patient is willing to continue to take their regular daily baseline opioid regimen (SR) at the same dose, throughout the duration of study. Exclusion Criteria: * The patient should be excluded from entering study if they have received or are due to receive during the study period; chemotherapy, hormone therapy or radiotherapy, which, in the opinion of the investigator will affect their pain. * Any history or immediate family history of schizophrenia, other psychotic illness, severe personality disorder or other significant psychiatric disorder other than depression associated with their underlying condition. * Any known or suspected history of a diagnosed dependence disorder, current heavy alcohol consumption, current use of an illicit drug or current non prescribed use of any prescription drug. * The patient has poorly controlled epilepsy or recurrent seizures (i.e. at least one year since last seizure). * The patient has experienced myocardial infarction or clinically relevant cardiac dysfunction within the last 12 months or has a cardiac disorder that, in the opinion of the investigator would put the patient at risk of a clinically relevant arrhythmia or myocardial infarction.
Canadian sites (2)
| Facility | City | Province |
|---|---|---|
| Vancouver Health Research Center | Victoria | British Columbia |
| Jewish General Hospital | Montreal | Quebec |
Source: ClinicalTrials.gov (US National Library of Medicine), snapshot October 2026. Check the registry for current recruiting status. Record: https://clinicaltrials.gov/study/NCT00530764