TY - JOUR
T1 - Development of an oral regimen of unithiol for the treatment of snakebite envenoming
T2 - a phase 1 open-label dose-escalation safety trial and pharmacokinetic analysis in healthy Kenyan adults
AU - Abouyannis, Michael
AU - Nyambura, Yvonne K.
AU - Ngome, Samson
AU - Riako, Debra
AU - Musyoki, Jennifer
AU - Muiruri, Charles
AU - Orindi, Benedict
AU - Else, Laura
AU - Amara, Alieu
AU - Dickinson, Laura
AU - Clare, Rachel H.
AU - Albulescu, Laura Oana
AU - Westhorpe, Adam P.
AU - Kool, Jeroen
AU - Adetifa, Ifedayo
AU - Ndungu, Francis M.
AU - FitzGerald, Richard
AU - Khoo, Saye
AU - Lalloo, David G.
AU - Casewell, Nicholas R.
AU - Hamaluba, Mainga
N1 - Publisher Copyright:
© 2025 The Authors
PY - 2025/3/14
Y1 - 2025/3/14
N2 - Background: Viperidae snakes are responsible for many of the 94,000 deaths caused by snakebite envenoming each year. The most pathological venom component of this globally diverse family of snakes are the zinc-dependent snake venom metalloproteinase (SVMP) enzymes, which can be inhibited by the metal chelator, unithiol. A short-course oral regimen, readily available and rapidly deployed ahead of hospital admission is needed. Methods: This open-label, phase 1 clinical trial assessed the safety of single ascending oral, multiple ascending oral, and single ascending intravenous doses of unithiol in 64 healthy adult volunteers from Kilifi County, Kenya. The multiple dose stage was informed by an interim safety and pharmacokinetic analysis, and predefined target plasma concentrations. Plasma concentrations of unithiol were measured using high-performance liquid chromatography-mass spectrometry, and safety was described by full adverse event reporting. Findings: 175 individuals were screened, and 64 (median age 30 years, IQR 25–38 years) received the study drug. There were no dose limiting toxicities or serious adverse events. There were 61 solicited adverse events, 17 related unsolicited adverse events, and 53 laboratory adverse events, all of mild or moderate severity. The maximum oral dose of 1500 mg was well tolerated and associated with the following pharmacokinetic parameters: Cmax 14.7 μg/mL, Tmax 2.9 h, T1/2 18.4 h, and AUC0-∞ 204.5 μg.h/mL. Interpretation: The phase 2 recommended dose (1500 mg loading dose, followed by 900 mg doses at 6-h and 24-h) has no safety concerns, and has promising pharmacokinetic properties for clinical use. Unithiol is affordable, stable at room temperature, and has the potential to be given orally in remote rural clinics. Its further development for snakebite indication is warranted. Funding: Wellcome Trust, Bloomsbury Set, and Cures Within Reach.
AB - Background: Viperidae snakes are responsible for many of the 94,000 deaths caused by snakebite envenoming each year. The most pathological venom component of this globally diverse family of snakes are the zinc-dependent snake venom metalloproteinase (SVMP) enzymes, which can be inhibited by the metal chelator, unithiol. A short-course oral regimen, readily available and rapidly deployed ahead of hospital admission is needed. Methods: This open-label, phase 1 clinical trial assessed the safety of single ascending oral, multiple ascending oral, and single ascending intravenous doses of unithiol in 64 healthy adult volunteers from Kilifi County, Kenya. The multiple dose stage was informed by an interim safety and pharmacokinetic analysis, and predefined target plasma concentrations. Plasma concentrations of unithiol were measured using high-performance liquid chromatography-mass spectrometry, and safety was described by full adverse event reporting. Findings: 175 individuals were screened, and 64 (median age 30 years, IQR 25–38 years) received the study drug. There were no dose limiting toxicities or serious adverse events. There were 61 solicited adverse events, 17 related unsolicited adverse events, and 53 laboratory adverse events, all of mild or moderate severity. The maximum oral dose of 1500 mg was well tolerated and associated with the following pharmacokinetic parameters: Cmax 14.7 μg/mL, Tmax 2.9 h, T1/2 18.4 h, and AUC0-∞ 204.5 μg.h/mL. Interpretation: The phase 2 recommended dose (1500 mg loading dose, followed by 900 mg doses at 6-h and 24-h) has no safety concerns, and has promising pharmacokinetic properties for clinical use. Unithiol is affordable, stable at room temperature, and has the potential to be given orally in remote rural clinics. Its further development for snakebite indication is warranted. Funding: Wellcome Trust, Bloomsbury Set, and Cures Within Reach.
KW - Envenoming
KW - Phase 1 clinical trial
KW - Snakebite
KW - Unithiol
KW - Snake Bites/drug therapy
KW - Administration, Oral
KW - Humans
KW - Middle Aged
KW - Male
KW - Kenya
KW - Healthy Volunteers
KW - Animals
KW - Antivenins/administration & dosage
KW - Adult
KW - Female
UR - https://www.scopus.com/pages/publications/85218871520
UR - https://www.scopus.com/inward/citedby.url?scp=85218871520&partnerID=8YFLogxK
U2 - 10.1016/j.ebiom.2025.105600
DO - 10.1016/j.ebiom.2025.105600
M3 - Article (journal)
C2 - 40020260
AN - SCOPUS:85218871520
SN - 2352-3964
VL - 113
JO - eBioMedicine
JF - eBioMedicine
M1 - 105600
ER -