Tiomolibdic acid (trade name Decuprate) is a chelating agent under investigation for the treatment of cancer and of Wilson's disease,[1] a rare and potentially fatal disease in which the body cannot regulate copper. It is developed by Wilson Therapeutics and used in form of the salt bis-choline tetrathiomolybdate.
Wilson's disease is an autosomal recessivegenetic disorder that is manifested by serious hepatic, neurologic or psychiatric symptoms. The disease is fatal if left untreated. It is estimated that 1 individual in every 30,000 to 100,000 worldwide has Wilson's disease.[2]
Bis-choline tetrathiomolybdate has been evaluated in clinical trials in patients with various forms of cancer[3][4][5] and has received orphan designation in the US and EU as a potential therapy against Wilson's disease.[6][7]
Pharmacology
Mechanism of action
Tiomolibdic acid selectively forms highly stable complexes with copper and proteins. These complexes are then believed to be primarily excreted via the bile, restoring the normal excretion route of copper that is impaired in patients with Wilson's disease.[8][9][10]
The binding and excretion mechanism is stable; whereas many de-coppering agents form unstable complexes that are excreted via urine.[11]
Clinical trials
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As of November 2014, a Phase 2, multi-centre, open-label study was recruiting newly diagnosed Wilson's disease patients 18 and older to evaluate the efficacy and safety of bis-choline tetrathiomolybdate administration over a 24-week period.[12][13]
The data suggest that bis-choline tetrathiomolybdate can rapidly lower and control toxic free copper levels and improve clinical symptoms in Wilson's disease patients. The data also suggest that it is generally well tolerated, with the potential for a reduced risk of neurological worsening after initiation of therapy compared to existing therapies.[22][23][24]
Dosing
Previous clinical studies with bis-choline tetrathiomolybdate in oncology patients have shown that it can lower and maintain copper levels using a once or twice daily oral dosing.[4][5] This may be helpful since untreated Wilson's disease may lead to death within several years of the onset of symptoms,[27] and medication use should continue throughout the patient's lifespan. Patient compliance is crucial for clinical improvement, and it is a particular challenge for Wilson's disease patients taking de-coppering treatments.[28]
Society and culture
Names
Tiomolibdic acid is the recommended International nonproprietary name (INN).[29]
References
^"Tiomolibdic acid". National Center for Advancing Translational Sciences. Retrieved 30 December 2021. This article incorporates text from this source, which is in the public domain.
^ abBerenson JR, Boccia RV, Bashey A, Levine AM, Koc ON, Callahan JA, et al. (2006). "Phase I Study of the [Cu, Zn] Superoxide Dismutase (SOD1) Inhibitor ATN-224 (Bis-Choline Tetrathiomolybdate) in Patients with Advanced Hematologic Malignancies Presentation at the Amer Soc Hematol 2006 Annual Meeting". Blood. 108. Abstract 2593.
^McQuaid A, Mason J (February 1991). "A comparison of the effects of penicillamine, trientine, and trithiomolybdate on [35S]-labeled metallothionein in vitro; implications for Wilson's disease therapy". Journal of Inorganic Biochemistry. 41 (2): 87–92. doi:10.1016/0162-0134(91)80002-y. PMID2033396.
^Ogra Y, Ohmichi M, Suzuki KT (October 1995). "Systemic dispositions of molybdenum and copper after tetrathiomolybdate injection in LEC rats". Journal of Trace Elements in Medicine and Biology. 9 (3): 165–9. Bibcode:1995JTEMB...9..165O. doi:10.1016/S0946-672X(11)80042-8. PMID8605606.
^Říha M, Karlíčková J, Filipský T, Macáková K, Hrdina R, Mladěnka P (June 2013). "Novel method for rapid copper chelation assessment confirmed low affinity of D-penicillamine for copper in comparison with trientine and 8-hydroxyquinolines". Journal of Inorganic Biochemistry. 123: 80–7. doi:10.1016/j.jinorgbio.2013.02.011. PMID23563391.
^Clinical trial number NCT02273596 for "Efficacy and Safety Study of WTX101 in Adult Wilson Disease Patients" at ClinicalTrials.gov
^Brewer GJ, Dick RD, Grover DK, LeClaire V, Tseng M, Wicha M, et al. (January 2000). "Treatment of metastatic cancer with tetrathiomolybdate, an anticopper, antiangiogenic agent: Phase I study". Clinical Cancer Research. 6 (1): 1–10. PMID10656425.
^Henry NL, Dunn R, Merjaver S, Pan Q, Pienta KJ, Brewer G, et al. (2006). "Phase II trial of copper depletion with tetrathiomolybdate as an antiangiogenesis strategy in patients with hormone-refractory prostate cancer". Oncology. 71 (3–4): 168–75. doi:10.1159/000106066. PMID17641535. S2CID25861052.
^Redman BG, Esper P, Pan Q, Dunn RL, Hussain HK, Chenevert T, et al. (May 2003). "Phase II trial of tetrathiomolybdate in patients with advanced kidney cancer". Clinical Cancer Research. 9 (5): 1666–72. PMID12738719.
^ abBrewer GJ, Askari F, Dick RB, Sitterly J, Fink JK, Carlson M, et al. (August 2009). "Treatment of Wilson's disease with tetrathiomolybdate: V. Control of free copper by tetrathiomolybdate and a comparison with trientine". Translational Research. 154 (2): 70–7. doi:10.1016/j.trsl.2009.05.002. PMID19595438.
^Członkowska A, Tarnacka B, Litwin T, Gajda J, Rodo M (June 2005). "Wilson's disease-cause of mortality in 164 patients during 1992-2003 observation period". Journal of Neurology. 252 (6): 698–703. doi:10.1007/s00415-005-0720-4. PMID15742108. S2CID34212689.
^World Health Organization (2010). "International nonproprietary names for pharmaceutical substances (INN): recommended INN: list 63". WHO Drug Information. 24 (1). hdl:10665/74530.
External links
"Tiomolibdic acid". Drug Information Portal. U.S. National Library of Medicine.