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A Phase 1 Combined Single and Multiple Ascending Oral Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Food Effect and Biomarker Response of ASP5502 in Healthy Adults and Participants With Primary Sjögren's Syndrome

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Trial Profile

A Phase 1 Combined Single and Multiple Ascending Oral Dose Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Food Effect and Biomarker Response of ASP5502 in Healthy Adults and Participants With Primary Sjögren's Syndrome

Status: Recruiting
Phase of Trial: Phase I

Latest Information Update: 25 Nov 2024

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At a glance

  • Drugs ASP 5502 (Primary)
  • Indications Sjogren's syndrome
  • Focus Adverse reactions; First in man
  • Sponsors Astellas Pharma Global Development

    • Most Recent Events

    • 20 Nov 2024 Time frame for primary endpoint 'Number of Participants With Adverse Events (AEs)' has been changed from upto 38 days to 58 days.
    • 29 Aug 2024 Status changed from not yet recruiting to recruiting.
    • 14 Aug 2024 New trial record

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