As founders of PledPharma AB [1], including the main inventor of calmangafodipir [2], we have with great interest read the article entitled “Randomised open label exploratory, safety and tolerability study with calmangafodipir in patients treated with the 12-h regimen of N-acetylcysteine for paracetamol overdose—the PP100-01 for Overdose of Paracetamol (POP) trial: study protocol for a randomised controlled trial” published online by POP Trial Investigators and Dear [3] on January 8, 2019.
In the Background section of the article, POP Trial Investigators and Dear [3] state the following: “Calmangafodipir (Ca4Mn(DPDP)5) is a unique chemical species derived from mangafodipir, where 80% of the manganese in mangafodipir has been replaced with calcium. Based on the similarities between calmangafodipir and mangafodipir, it is anticipated that calmangafodipir would also exhibit SOD-dependent pharmacologic actions similar to those of mangafodipir”. We presume that they pertain the SOD-mimetic actions of these two compounds and not the SOD-dependent actions, as SOD is the admitted abbreviation of superoxide dismutases (intracellular and extracellular enzymes). Unfortunately, POP Trial Investigators and Dear have omitted an essential reference written by us and Torsten Almén (deceased January 8, 2016) [1]. This article describes the background of both calmangafodipir and mangafodipir, and their SOD-mimetic properties, so the word “anticipated” is highly misleading. The article by Brurok et al. [4] (reference 10 in POP Trial Investigators and Dear [3]) is interesting but it was published 13 years before calmangafodipir was described in a scientific journal [5]. You can find our article [1] on the sponsor’s website (https://www.pledpharma.com/pipeline/publications/), and as the title reads “Calmangafodipir [Ca4Mn(DPDP)5], mangafodipir (MnDPDP) and MnPLED with special reference to their SOD mimetic and therapeutic properties” there should be no doubt that this is the most appropriate reference to cite. The omission, whether deliberate or not, is a disservice to the reader. Furthermore, we believe that the earlier “original” work is actually the work that led to Dear’s clinical trial study.
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References
Karlsson JOG, Ignarro LJ, Lundström I, Jynge P, Almén T. Calmangafodipir [Ca4Mn(DPDP)5], mangafodipir (MnDPDP) and MnPLED with special reference to their SOD mimetic and therapeutic properties. Drug Discov Today. 2015;20:411–21.
Karlsson J, Reineke K, Kurz T, Andersson R, McLaughlin C, Jacobsson S, Näsström J. Calmangafodipir, a new chemical entity, and other metal complexes, method of preparation, compositions, and methods of treatment. US 9187509 B2. Nov 17, 2015.
POP Trial Investigators, Dear J. Randomised open label exploratory, safety and tolerability study with calmangafodipir in patients treated with the 12-h regimen of N-acetylcysteine for paracetamol overdose—the PP100-01 for Overdose of Paracetamol (POP) trial: study protocol for a randomised controlled trial published study protocol for a randomised controlled trial. Trials. 2019;20(1):27. https://doi.org/10.1186/s13063-018-3134-1.
Brurok H, Ardenkjaer-Larsen JH, Hansson G, Skarra S, Berg K, Karlsson JO, Laursen I, Jynge P. Manganese dipyridoxyl diphosphate: MRI contrast agent with antioxidative and cardioprotective properties? Biochem Biophys Res Commun. 1999;254:768–72.
Karlsson JOG, Kurz T, Flechsig NJ, Andersson RGG. Superior therapeutic index of calmangafodipir in comparison to mangafodipir as a chemotherapy adjunct. Transl Oncol. 2012;5:492–502.
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JOGK owns shares in PledPharma AB and is the main inventor of calmangafodipir (owned by PledPharma AB). IL owns shares in PledPharma AB. PJ and LJI have no competing interests.
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Karlsson, J.O.G., Jynge, P., Lundström, I. et al. Letter in response to: “Randomised open label exploratory, safety and tolerability study with calmangafodipir in patients treated with the 12-h regimen of N acetylcysteine for paracetamol overdose—the PP100-01 for Overdose of Paracetamol (POP) trial: study protocol for a randomised controlled trial”. Trials 20, 380 (2019). https://doi.org/10.1186/s13063-019-3476-3
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DOI: https://doi.org/10.1186/s13063-019-3476-3