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2023-506912-41-00CompletedPhase 1

A phase 1, randomised, double-blind, placebo-controlled, single ascending dose and multiple ascending dose study to evaluate the safety, tolerability, and pharmacokinetics in healthy adult subjects after subcutaneous injection of TISA-818-Inj-5mg/mL.

Source: EU CTIS (euclinicaltrials.eu) · Last updated 27 Nov 2023

Next steps

Status (registry)
Completed
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
48 (actual)
First submitted
18 Sept 2023
Start date
9 Jan 2024
Lead sponsor
Enlitisa (Shanghai) Pharmaceutical Co. Ltd.
EU CT number
2023-506912-41-00

What you commit to

  • Study type: Interventional · Phase 1
  • Participants enrolled: 48
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of EU CTIS (euclinicaltrials.eu). It describes the study design.

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
CTC Clinical Trial Consultants ABUppsalaSwedenCompleted

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This page is information, not medical advice. Discuss any trial with your doctor.