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Completed

NCT Number: NCT00966563

Mangafodipir as an Adjunct to Percutaneous Coronary Intervention

The present feasibility study is designed to find out whether pre-treatment with the compound mangafodipir (PP-099) provides an additional reduction in myocardial infarct size in patients treated with primary percutaneous coronary intervention (PCI) during acute myocardial infarction (AMI).

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Key information

Age range

40 year–80 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Department of Internal Medicine, County Hospital Ryhov

Jönköping, 551 85, Sweden

About this study

Mangafodipir, manganese (Mn) dipyridoxyl diphosphate (MnDPDP) and its lipophile metabolite Mn dipyridoxyl diethylene diamide (MnPLED), are catalytic antioxidants and iron chelators. In preclinical studies these agents reduce oxidative stress induced injuries related to chemotherapy of cancer and to reperfusion/reoxygenation of ischemic/hypoxic myocardium. Accordingly, in an in vivo pig model of AMI metabolite MnPLED applied at end of ischemia and during reperfusion reduced myocardial infarct size by 55 %. Mangafodipir most likely activates salvage pathways and prevents lethal reperfusion injuries.

Other advantages are that mangafodipir is already approved as a contrast agent for MRI of liver, and that the experience for more than a decade reveals a high safety with minor and tolerable side-effects.

The present study will include 20 patients treated for their first documented AMI. They will after admission to hospital undergo primary PCI. Reopening of an occluded coronary artery will be preceded by iv. infusion of mangafodipir or placebo in two groups , each consisting of 10 patients. The primary endpoint will be release to plasma of commonly accepted biomarkers of myocardial injury (Troponin T and CK-MB) measured at admission and 6 hours after PCI. The secondary endpoints include the accumulated release of plasma biomarkers over 48 hours and direct measurement of the final myocardial infarct size at 6-10 weeks after PCI.

Who can participate

Healthy volunteers accepted: No

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Males 40-80 and females 50-80 years with first severe coronary attack
  • Chest pain up to 6 hours.
  • T segment elevation (≥ 0.2 mV in two neighbouring anterior and inferior wall leads.
  • Decided for treatment by primary PCI.
  • TIMI grade 0 flow in the occluded LAD or RCA artery
  • Written informed consent.

Exclusion criteria

  • Previous coronary artery bypass operation.
  • Previous AMI.
  • Chest pain more than 6 hours.
  • Angina within 48 hours before admission.
  • Cardiac arrest and cardiogenic shock.
  • Occlusion of the left main stem, circumflex and right coronary arteries at angiography.
  • Known hypersensitivity to mangafodipir (as contrast agent for MRI).
  • Received mangafodipir ≤ 5 weeks before admission
  • History of prior serious allergic or pseudo-allergic reaction
  • Severely reduced liver or renal function
  • Any other serious illness or medical condition
  • Fertile females
  • Phaeochromocytoma

Treatment and study plan

Mangafodipir

Drug

Administered dose: 2 µmol/kg b.w. Administration form: Ready-to-use formulation (solution). Mangafodipir or placebo (0.2 ml/kg b.w.) will be administered as an intravenous (iv.) infusion over 2-5 min prior to reopening of occluded coronary artery during PCI

Other names: Teslascan

Placebo

Drug

Primary outcomes

  1. Reduction of myocardial infarct size assessed by biomarker release to plasma

    Time frame: Before and at 2 days after PCI

Secondary outcomes

  1. Reduction of myocardial infarct size assessed by biomarker release to plasma and by magnetic resonance imaging (MRI) of the heart.

    Time frame: Accumulated biomarker release over 48 hours after PCI; MRI at 6-10 weeks after PCI.

Sponsors and collaborators

Lead sponsor

Egetis Therapeutics

Industry

Registry information

Official study title

Mangafodipir as an Adjunct to Percutaneous Coronary Intervention in Acute Myocardial Infarction (MANAMI)

Acronym: MANAMI

Important dates

Study start
2009
Primary completion
2013
Study completion
2013
First posted
Aug 27, 2009
Registry last updated
Jul 16, 2013

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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