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Phase IIa, Open Label, Dose Ascending Study to Determine the Maximum Tolerated Dose, Safety and Tolerability, Pharmacokinetics and Pharmacodynamics of a Single Dose of Lanreotide PRF in Subjects With Acromegaly Previously Treated and Controlled With Either Octreotide LAR or Lanreotide Autogel

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Trial Profile

Phase IIa, Open Label, Dose Ascending Study to Determine the Maximum Tolerated Dose, Safety and Tolerability, Pharmacokinetics and Pharmacodynamics of a Single Dose of Lanreotide PRF in Subjects With Acromegaly Previously Treated and Controlled With Either Octreotide LAR or Lanreotide Autogel

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 17 Sep 2021

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At a glance

  • Drugs Lanreotide (Primary)
  • Indications Acromegaly
  • Focus Adverse reactions; First in man; Pharmacokinetics
  • Sponsors Ipsen

    • Most Recent Events

    • 16 May 2019 This trial has been completed in United Kingdom, according to European Clinical Trials Database.
    • 22 Dec 2017 Status changed from active, no longer recruiting to completed.
    • 12 Dec 2017 The trial has been completed in Lithuania as per European Clinical Trials Database record; EudraCT2014-002389-62

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