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A Double-blind, Randomized, Placebo-controlled, Sponsor-open, Single Ascending Dose (SAD) and Multiple Ascending Dose (MAD) Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of TD-5202 in Healthy Subjects

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Trial Profile

A Double-blind, Randomized, Placebo-controlled, Sponsor-open, Single Ascending Dose (SAD) and Multiple Ascending Dose (MAD) Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of TD-5202 in Healthy Subjects

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 02 Dec 2020

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At a glance

  • Drugs TD 5202 (Primary)
  • Indications Inflammatory bowel diseases
  • Focus Adverse reactions; First in man; Pharmacokinetics
  • Sponsors Theravance Biopharma

    • Most Recent Events

    • 13 Oct 2020 Results presented at the 28th United European Gastroenterology Week
    • 13 Dec 2019 Status changed from recruiting to completed.
    • 05 Nov 2019 According to Theravance Biopharma media release, results are expected in 1H 2020

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