Literature DB >> 31492564

Gastrointestinal AEs seen in the POP trial due to SOD mimetic activity of calmangafodipir? - Authors' reply.

James W Dear1.   

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Year:  2019        PMID: 31492564      PMCID: PMC6796565          DOI: 10.1016/j.ebiom.2019.08.039

Source DB:  PubMed          Journal:  EBioMedicine        ISSN: 2352-3964            Impact factor:   8.143


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The POP Trial Investigators read with interest this letter from Dr. Karlsson [1] regarding the results of our Phase 1 trial [2]. We agree that all safety information from this trial is important for our planning of future trials. The frequency of gastrointestinal adverse events and serious adverse events in the 4 different treatment groups is already presented in Supplementary Table 2 [2]. These adverse events were nausea, vomiting or abdominal pain – all symptoms that are common after a paracetamol overdose treated with acetylcysteine. No patient in this trial developed diarrhoea.
  2 in total

1.  Principal results of a randomised open label exploratory, safety and tolerability study with calmangafodipir in patients treated with a 12 h regimen of N-acetylcysteine for paracetamol overdose (POP trial).

Authors:  Emma E Morrison; Katherine Oatey; Bernadette Gallagher; Julia Grahamslaw; Rachel O'Brien; Polly Black; Wilna Oosthuyzen; Robert J Lee; Christopher J Weir; Dennis Henriksen; James W Dear
Journal:  EBioMedicine       Date:  2019-07-13       Impact factor: 8.143

2.  Gastrointestinal AEs seen in the POP trial due to SOD mimetic activity of calmangafodipir?

Authors:  Jan Olof G Karlsson
Journal:  EBioMedicine       Date:  2019-08-26       Impact factor: 8.143

  2 in total
  1 in total

Review 1.  Chemotherapy-induced peripheral neuropathy-part 2: focus on the prevention of oxaliplatin-induced neurotoxicity.

Authors:  Kinga Sałat
Journal:  Pharmacol Rep       Date:  2020-04-28       Impact factor: 3.919

  1 in total

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