Fenbendazole — Research Protocol

⚠️ RESEARCH SUMMARY — NOT A TREATMENT PROTOCOL. Discuss all findings with your healthcare provider.

Fenbendazole research for cancer is based on case reports and preclinical data. No FDA-approved oncology dosing exists for humans. Dosing regimens in published literature vary significantly. This page summarizes published research protocols. It is not a guide for self-treatment. Discuss any treatment decisions with your physician.

Research Dosing (from Published Studies)

ContextDoseRouteFrequencyNotes
Tippens case report (single patient)Dosing regimens in published literature vary — consult the cited studies for detailsOralSee cited case reportSingle case report with concurrent vitamin E, curcumin, and CBD. Uncontrolled. This is anecdotal data from one individual and cannot be generalized.
Preclinical (mouse xenograft models)1 mg/mouse (~50 mg/kg in mice)Oral gavageEvery other dayDogra et al. 2018, Sci Rep. Tumor growth inhibition reported in multiple xenograft models. Animal data; not directly applicable to humans.
Veterinary anthelmintic (approved use)Veterinary dose per labelOralPer veterinary labelFDA-approved veterinary dose. Safety profile well-established in animals. Fenbendazole is NOT approved for human use.

Pharmacokinetics

Poor oral bioavailability (~10%) in humans. Enhanced by high-fat meals (2-3x increase). Metabolized by CYP enzymes to oxfendazole (active metabolite) and fenbendazole sulfone. Half-life ~8-10 hours.

Safety Profile

Veterinary safety data is extensive. Human data is limited. Reported side effects from case reports: mild GI discomfort, transient liver enzyme elevation. Mebendazole (closely related) has more human safety data and is FDA-approved for human use.

Contraindications

Monitoring Parameters

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