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Macimorelin - AEterna Zentaris

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Drug Profile

Macimorelin - AEterna Zentaris

Alternative Names: AEZS-130; ARD-07; D-87575; EP-01572; EP-1572; Ghryvelin; JMARD-07; JMV-1843; Macimorelin acetate; Macrilen; Solorel

Latest Information Update: 01 Apr 2024

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At a glance

  • Originator AEterna Zentaris Inc
  • Developer AEterna Zentaris Inc; Consilient Health; Novo Nordisk; University of Queensland
  • Class Amides; Carboxylic acids; Diagnostic agents; Indoles; Oligopeptides; Small molecules
  • Mechanism of Action Ghrelin receptor agonists; Ghrelin receptor antagonists
  • Orphan Drug Status

    Orphan designation is assigned by a regulatory body to encourage companies to develop drugs for rare diseases.

    Yes - Somatotropin deficiency
  • New Molecular Entity Yes
  • Available For Licensing Yes - Somatotropin deficiency

Highest Development Phases

  • Marketed Somatotropin deficiency
  • Phase II Cachexia
  • Preclinical Amyotrophic lateral sclerosis

Most Recent Events

  • 27 Mar 2024 AEterna Zentaris completes enrolment in the phase III DETECT trial for Somatotropin deficiency in Georgia, Poland, Italy, Slovenia, Germany, Romania, Serbia, Slokavia, USA (PO) (NCT04786873) (EudraCT2018-001989-42)
  • 13 Jul 2023 Aeterna Zentaris plans to have scientific advice meeting with regulatory authorities to discuss next steps program development
  • 12 Apr 2023 USPTO has issued a Notice of Allowance for Aeterna’s patent application (US 17 375 709) titled, “Use of Macimorelin in Assessing Growth Hormone Deficiency in Children"
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