Ibogaine in the treatment of chronic hepatitis C. Howard S. Lotsof. President Dora Weiner Foundation Staten Island, NY http://www.doraweiner.org. Invitational Ibogaine forum Warsaw 2007 Wednesday 16 May Hotel Sofitel Victoria. Tabernanthe iboga source of ibogaine.
Howard S. Lotsof.
Dora Weiner Foundation
Staten Island, NY
Invitational Ibogaine forum
Wednesday 16 May
Hotel Sofitel Victoria
Found in West African rain forests
Courtesy Jason Callan
President and Founder
1973: Non A, Non B hepatitis is described
1989: HCV RNA virus identified
1990: Anti HCV effects of ibogaine reported
2005: Patent application for ibogaine to treat chronic HCV filed
Most common viral infection in the
New infections per year 1990 - 242,000
New infections per year 2001 - 25,000
New infections per year 2004 - 25,000
Greater than 75% of IVDUs test positive
The discovery of ibogaine’s use in treating both chemical dependence and HCV was by ibogaine activist advocates who were themselves treated or self-treated with ibogaine.
Scientific research followed patent development in the treatment of chemical dependence and it is hoped the same will be true for ibogaine related HCV research.
Rapid method for interrupting the narcotic addiction syndrome, US 4,499,096 (1985)
Rapid method for interrupting the cocaine and amphetamine abuse syndrome US 4,587,243 (1986)
Rapid method for attenuating the alcohol dependency syndrome, US 4,957,523 (1989)
Rapid method for interrupting or attenuating the nicotine/tobacco dependency syndrome, US 5,026,697 (1991)
Rapid method for interrupting or attenuating poly-drug dependency syndromes, US 5, 124,994 (1992)
A thirty-three year old male diagnosed with HCV and using 1/4 gram of heroin a day was administered 25 mg/kg ibogaine HCl. Following administration of ibogaine heroin use ceased along with swelling of the liver and pain in the area of the liver.
A sixty year old male testing positive for HCV RNA genotype I, administered the following dose regimens of ibogaine HCl. Subject weighed 79 kg. Doses administered were as total doses and not mg/kg. Day 1: 10 mg, Day 2: 20 mg, Day 3: 20 mg, Day 4: 30 mg, Day 5: 50 mg, Day 6: 75 mg, Day 8: 100 mg.Day 10: 150 mg, Day 14: 300 mg. HCV RNA UL/ml was reduced from 780,000 to 644,000, Pretreatment Alkaline Phosphatase was 99, AST was 103 and ALT 195. Post treatment Alkaline Phosphatase was 88, AST 89 and ALT 127. An additional 250 mg ibogaine HCl reduced HCV RNA UL/ml to 154,000. Further testing showed continued reduction to HCV RNA UL/ml 78,200
A forty-two year old female testing positive for HCV RNA type 3. RNA IU/ml was 12,600,000. Subject was administered a total of 27 mg/kg ibogaine HCl in the following regimen:
6 x 2 mg/kg
1 x 12 mg/kg
1 x 3 mg/kg
HCV RNA IU/ml was reduced to 50,100. Prior to ibogaine treatment patient’s urine was dark and stool light. Post treatment color of urine and stool returned to normal.
Repetitive low dosing with ibogaine provided continuous depression of viral load.
Genotype 3 appears highly responsive in keeping with results of interferon riboviron therapy.
Continued reduction in viral load after stopping of ibogaine therapy observed.
Less toxic than current HCV therapies.
Interest of pharmaceutical companies with experience in development of HCV drugs.
Preclinical confirmation of efficacy if possible.
Phase I/II clinical studies to confirm findings and establish preferred dose regimen.