A Safety Study of Sativex Compared With Placebo (Both With Dose-intense Temozolomide) in Recurrent Glioblastoma Patients
|The safety and scientific validity of this study is the responsibility of the study sponsor and investigators. Listing a study does not mean it has been evaluated by the U.S. Federal Government. Read our disclaimer for details.|
|ClinicalTrials.gov Identifier: NCT01812616|
Recruitment Status : Completed
First Posted : March 18, 2013
Last Update Posted : December 20, 2022
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|Condition or disease||Intervention/treatment||Phase|
|Cancer||Drug: Sativex Drug: Placebo||Phase 1 Phase 2|
|Study Type :||Interventional (Clinical Trial)|
|Actual Enrollment :||21 participants|
|Intervention Model:||Parallel Assignment|
|Masking:||Quadruple (Participant, Care Provider, Investigator, Outcomes Assessor)|
|Official Title:||A Two Part Study to Assess the Tolerability, Safety and Pharmacodynamics of Sativex in Combination With Dose-intense Temozolomide in Patients With Recurrent Glioblastoma|
|Study Start Date :||September 2014|
|Actual Primary Completion Date :||June 2016|
|Actual Study Completion Date :||June 2016|
Experimental: Sativex and Dose-Intense Temozolomide
Patients will received Sativex and Dose-Intense Temozolomide in a double-blind manner
Administered orally as a spray to the cheek according to a standard dose titration regimen, until patients reach a maximum tolerated dose (maximum 12 sprays per day). Each spray delivers 100 μl (Δ9tetrahydrocannabinol (THC), 27 mg/ml: Cannabidiol (CBD), 25 mg/ml).
Placebo Comparator: Placebo and Dose-Intense Temozolomide
Patients will received placebo and Dose-Intense Temozolomide and in double-blind manner
Administered orally as a spray to the cheek according to a standard dose titration regimen, until patients reach a maximum tolerated dose (maximum 12 sprays per day). Each spray delivers 100 μl ethanol:propylene glycol (50:50) excipients, with peppermint oil (0.05%) flavouring and Food, Drugs & Cosmetics (FD&C)certified color additives; FD&C Yellow No.5 (E102 tartrazine) (0.0260%), FD&C Yellow No.6 (E110 sunset yellow) (0.0038%), FD&C Red No. 40 (E129 Allura red AC) (0.00330%) and FD&C Blue No.1 (E133 Brilliant blue FCF) (0.00058%).
Other Name: Placebo comparator
- Incidence of Adverse Events as a Measure of Patient Safety. [ Time Frame: Study Day 1 - Day 358 ]Adverse events will be coded according to the current medical dictionary for regular activities graded using the Common Terminology Criteria for Adverse Events criteria. The number of patients who experienced an adverse event whilst on treatment will be presented.
- The number of patients with Progression Free Survival at six months (PFS6) [ Time Frame: Study Day 1 - Day 190 ]PFS6 will be assessment at Visit 11 (Day 190). Progression of disease will be determined from Response Assessment in Neuro-Oncology tumour assessment (based on Magnetic Resonance Imaging scans). The number of patients with PFS6 will be presented for the individual treatment groups.
- Overall Survival [ Time Frame: Study Day 1 - Day 358 ]Overall survival will be assessed at the end of the treatment visit (Day 358 or at early termination). The number of surviving patients in each group from the randomisation phase (Part B) will be presented.
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|Ages Eligible for Study:||18 Years and older (Adult, Older Adult)|
|Sexes Eligible for Study:||All|
|Accepts Healthy Volunteers:||No|
- Patient is willing and able to give informed consent for participation in the study.
- Patient is aged 18 years or above.
- Histopathologically confirmed diagnosis of grade four Glioblastoma Multiforme as per World Health Organisation classification.
- Evidence of patients first tumour progression (as determined by Revised Assessment in Neuro-Oncology) following radiation and first line chemotherapy with Temozolomide.
- If taking steroids, then the dose must be stable or decreasing.
- Karnofsky performance scale of 60% or greater.
- Patient is able (in the investigators opinion) and willing to comply with all study requirements.
- Patient is willing for his or her name to be notified to the responsible authorities for participation in this study, as applicable in individual countries.
- Patient is willing to allow his or her primary care practitioner and consultant, if appropriate, to be notified of participation in the study.
- Patients with Glioblastoma Multiforme secondary to low-grade glioma or anaplastic glioma (anaplastic astrocytoma or anaplastic oligodendroglioma).
- Patients currently receiving treatment for recurrent Glioblastoma Multiforme.
- Less than a four week interval since prior chemotherapy.
- Less than a 12 week interval since prior radiotherapy unless there is either: a) histopathology confirmation of recurrent tumour, or b) new enhancement on Magnetic Resonance Imaging outside of the radiotherapy treatment field.
- Presence of extra-cranial metastatic disease.
- Any surgery, including intracranial biopsy (not including minor diagnostic procedures such as lymph node biopsy) within two weeks of baseline disease assessments; or not fully recovered from any side effects of previous procedures.
- Any history of a different malignancy unless the patient has remained disease-free for at least three years and are at low risk for recurrence of that malignancy (cervical cancer in situ, and basal cell or squamous cell carcinoma of the skin are exempt from this criterion if treatment has occurred).
- Have previously received first line chemotherapy other than Temozolomide.
- Presents with Leptomeningeal dissemination.
- Have previously received stereotactic radiotherapy, convection enhanced delivery or brachytherapy (as gliosis/scarring from these modalities may limit delivery).
- The patient is currently using or has used cannabis or cannabinoid based medications within 30 days of study entry and is unwilling to abstain for the duration of the study.
- Any known or suspected history of a substance abuse/dependence disorder, current heavy alcohol consumption (>60g of pure alcohol per day for men, >40 g of pure alcohol per day for women), current use of an illicit drug or current non prescribed use of any prescription drug.
- 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.
- Has experienced myocardial infarction or clinically significant 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 clinically significant arrhythmia or myocardial infarction.
- Has grade 3 or above toxicity by Common Terminology Criteria for Adverse Events criteria.
- Female patients of child bearing potential and male patients whose partner is of child bearing potential, unless willing to ensure that they or their partner use effective contraception, for example, oral contraception, double barrier, intra-uterine device, during the study and for three months thereafter (however a male condom should not be used in conjunction with a female condom).
- Female patients who are pregnant, lactating or planning pregnancy during the course of the study and for three months thereafter.
- Patient who have received an Investigational Medicinal Product within the four weeks prior to the screening visit.
- Any other significant disease or disorder which, in the opinion of the investigator, may either put the patient at risk because of participation in the study, or may influence the result of the study, or the patient's ability to participate in the study.
- Travel outside the country of residence planned during the study.
- Patients previously enrolled into this study and received either Investigational Medicinal Product or Dose-Intense Temozolomide.
- Any known or suspected hypersensitivity to cannabinoids or any of the excipients of the Investigational Medicinal Product.
- Any known allergy to or other intolerability to Temozolomide.
- Following a physical examination, the patient has any abnormalities that, in the opinion of the investigator would prevent the patient from safe participation in the study.
- Unwilling to abstain from donation of blood during the study.
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01812616
|Klinik für Onkologie, Hämatologie und Stammzelltransplantation, Universitätsklinikum Aachen RWTH|
|Aachen, Germany, 52074|
|Neurologie des Klinikums Altenburger Land|
|Altenburg, Germany, 04600|
|Zentrum für Neuroonkologie der Universität Duesseldorf|
|Duesseldorf, Germany, 40225|
|Strahlenklinik der Universität Erlangen|
|Erlangen, Germany, 91054|
|The Clatterbridge Cancer Centre NHS Foundation Trust|
|Bebington, Wirral, United Kingdom, CH63 4JY|
|St James's Institute of Oncology, St James's University Hospital|
|Leeds, Yorkshire, United Kingdom, LS9 7TF|
|Bristol Haematology & Oncology Centre|
|Bristol, United Kingdom, BS2 8ED|
|Queen's Centre for Haematology & Oncology, Castle Hill Hospital|
|Cottingham, United Kingdom, HU16 5JQ|
|West of Scotland Beatson Cancer Centre|
|Glasgow, United Kingdom, G12 0YN|
|Guy's & St Thomas' NHS Foundation Trust, of St Thomas' Hospital|
|London, United Kingdom, SE1 7EH|
|The Christie NHS Foundation Trust|
|Manchester, United Kingdom, M20 4BX|
|Responsible Party:||Jazz Pharmaceuticals|
|Other Study ID Numbers:||
GWCA1208 Part B
|First Posted:||March 18, 2013 Key Record Dates|
|Last Update Posted:||December 20, 2022|
|Last Verified:||December 2022|
Neoplasms, Germ Cell and Embryonal
Neoplasms by Histologic Type
Neoplasms, Glandular and Epithelial
Neoplasms, Nerve Tissue
Sensory System Agents
Peripheral Nervous System Agents
Physiological Effects of Drugs