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A Phase 1 Ascending Single Dose Study To Evaluate The Safety, Tolerability, And Pharmacokinetics Of PF-05230901 Administered Subcutaneously To Healthy Subjects

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Trial Profile

A Phase 1 Ascending Single Dose Study To Evaluate The Safety, Tolerability, And Pharmacokinetics Of PF-05230901 Administered Subcutaneously To Healthy Subjects

Status: Discontinued
Phase of Trial: Phase I

Latest Information Update: 25 Apr 2014

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At a glance

  • Drugs PF 5230901 (Primary)
  • Indications Cachexia
  • Focus Adverse reactions
  • Sponsors Pfizer

Most Recent Events

  • 25 Apr 2014 New trial record

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