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Phase 1 Clinical Trial to Evaluate Safety, Tolerability, Pharmacokinetics and Pharmacodynamics of DWP212525 in Healthy Volunteers

StatusRecruiting
PhasePhase 1
Started
View on ClinicalTrials.gov ↗

Record History

  1. Notable Primary completion date: Jun 30, 2026 to Dec 30, 2026 Primary endpoints: 6 to 4 · Enrollment target: 76 to 84 · Completion date: Jun 30, 2026 to Mar 30, 2027 · 5 morev3 Show 8 more changesShow less
    • Primary endpoints: 6 to 4
    • Enrollment target: 76 to 84
    • Completion date: Jun 30, 2026 to Mar 30, 2027
    • Interventions: DWP212525 100mg (Drug), DWP212525 10mg (Drug), DWP212525 200mg (Drug), DWP212525 30mg (Drug), DWP212525 400mg (Drug), DWP212525 50mg… to DWP212525 XXmg (Drug), DWP212525 placebo (Drug)
    • Study arms: 10 to 11
    • Eligibility criteria shortened, about 2 words
    • Study description shortened, about 1 word
    • Study title expanded, about 3 words

    See this version in full on ClinicalTrials.gov ↗

  2. Minor Site contact updated Study title expanded, about 6 wordsv2 Show 1 more changeShow less
    • Study title expanded, about 6 words

    See this version in full on ClinicalTrials.gov ↗

  3. Minor Study First Submitted
  • Stopped: an ongoing trial was terminated, suspended or withdrawn.
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
  • Minor: routine progress and housekeeping, such as sites added or enrollment closed.
The safety and tolerability of single and multiple administration of DWP212525
Trial Details
NCT Number NCT06736587
Lead Sponsor Daewoong Pharmaceutical Co. LTD.
Conditions Autoimmune Diseases
Enrollment 84 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov