Sativex

From Glioblastoma Treatments
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Property Information
Drug Name Sativex (Nabiximols)
FDA Approval Not FDA-approved in the United States; approved in several countries for spasticity due to multiple sclerosis
Used for Investigational use in glioblastoma for potential direct anti-tumor effects and symptom management
Clinical Trial Phase Phase 2 clinical trial in 2021 indicated for glioblastoma
Clinical Trial Explanation Not specified
Common Side Effects Fatigue, dizziness, nausea, mouth irritation
OS without Not specified
OS with The 2021 trial reported an increase in overall survival for glioblastoma patients treated with Sativex in combination with temozolomide compared to temozolomide alone
PFS without Not specified
PFS with Details on progression-free survival (PFS) improvement need further clarification; the trial primarily highlighted improvements in overall survival
Usefulness Rating 4
Usefulness Explanation Not specified
Toxicity Level Not specified
Toxicity Explanation Not specified

Notes: In a notable 2021 trial, Sativex, combined with temozolomide, demonstrated an increase in overall survival among glioblastoma patients, marking a promising advancement in the use of cannabinoid-based therapies for cancer treatment. These results suggest Sativex may possess anti-tumor properties in addition to its symptom management potential, warranting further research to fully understand its therapeutic benefits and mechanism of action in glioblastoma.


From Ben Williams Book: Not specified

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