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A Single-Center, Single-Dose, Placebo-Controlled, Randomized, Double-Blind, Ascending Dose Study to Evaluate the Safety, Tolerability and Pharmacokinetics and Pharmacodynamics of Subcutaneously Administered PL-3994 in Subjects With Controlled Hypertension

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A Single-Center, Single-Dose, Placebo-Controlled, Randomized, Double-Blind, Ascending Dose Study to Evaluate the Safety, Tolerability and Pharmacokinetics and Pharmacodynamics of Subcutaneously Administered PL-3994 in Subjects With Controlled Hypertension

Status: Completed
Phase of Trial: Phase II

Latest Information Update: 28 Dec 2021

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At a glance

  • Drugs PL 3994 (Primary)
  • Indications Essential hypertension
  • Focus Pharmacodynamics; Pharmacokinetics
  • Sponsors Palatin Technologies

    • Most Recent Events

    • 22 Feb 2011 Actual end date (July 2008) added as reported by ClinicalTrials.gov.
    • 15 Sep 2009 Results presented at the 13th Annual Scientific Meeting of the Heart Failure Society of America in Boston.
    • 23 Sep 2008 Results reported briefly in a Paladin Technologies media release.

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