Disulfiram
DrugDisulfiram 400 mg daily
NCT Number: NCT02678975
Disulfiram (Antabuse®) is a well-tolerated, cheap, generic drug that has been in use since the 1950s to treat alcoholism. There is now an increasing amount of independent preclinical data to support disulfiram as an anticancer agent. The potency of disulfiram as an anticancer agent seems strengthened by copper.
The investigators aim is to investigate disulfiram and copper-supplement as add-on treatment in glioblastoma patients with recurrence receiving alkylating chemotherapy.
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Notify Me18 year and older
All sexes
Interventional
Phase 2 / Phase 3
Cancer Clinic, St.Olavs University Hospital, Trondheim, Norway
Disulfiram (Antabuse®) is a well-tolerated, cheap, generic drug that has been in use since the 1950s to treat alcoholism. There is now an increasing amount of independent preclinical data to support disulfiram as an anticancer agent. The potency of disulfiram as an anticancer agent seems strengthened by copper. There is now anecdotal clinical evidence of disulfiram as an anticancer agent. So far no clinical studies have been published in glioma patients, but two small, uncontrolled studies are planned according to clinicaltrials.gov. with search 1st November 2015.
The investigators aim to investigate disulfiram and copper-supplement as add-on treatment in glioblastoma patients with recurrence receiving alkylating chemotherapy. The study will be performed as a multicenter RCT including patients in Norway and Sweden. This will serve as a proof-of concept study.
The primary end-point is survival at 6 months
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
a. However increased levels are seen together with ongoing acute phase reaction as determined by elevated C-reactive protein (ceruloplasmin is elevated as part of the same process) it is possible to retest after normalization of C-reactive protein.
Exclusion criteria
Disulfiram 400 mg daily
nutritional supplement with copper, 2 mg daily
Alkylating antineoplastic agent
Other names: lomustine (CCNU), PCV or temozolomide
Time frame: Proportion of alive participants at 6 months
Time frame: Proportion without progression at 6 and 12 months
Using RANO criteria applied by local investigators
Time frame: Proportion of alive participants at 12 and 24 months
Time frame: Median overall survival assessed at 6 months and 24 months after last included participant
Using Kaplan Meier plots and log-rank test
Time frame: Assessed at baseline and month 3, 6, 9, 12, 15, 18, 21, 24
EuroQol 5D (generic)
Time frame: Baseline and first follow-up scan being scheduled at 3 months post-inclusion
Tumor volumes are assessed using semi-automatic segmentation
Time frame: Assessed month 1, 2, 3, 4, 5, 6, 7, 8, 9, 10, 11, 12, 15, 18, 21, 24, but analyzed as cumulative burden at 6 and 24 months
Cumulative burden at 6 and 24 months
Sahlgrenska University Hospital
Other
DIRECT (DIsulfiram REsponse as add-on to ChemoTherapy in Recurrent) Glioblastoma: A Randomized Controlled Trial
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View the official ClinicalTrials.gov record (opens in a new tab)This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.
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