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2023-505908-28-00CompletedPhase 1

A RANDOMIZED PHASE I, DOUBLE-BLIND, PARALLEL, COMPARATIVE ASSESSMENT OF PHARMACOKINETICS, SAFETY, PHARMACODYNAMICS, AND IMMUNOGENICITY OF LT-01 (AN OMALIZUMAB BIOSIMILAR CANDIDATE [TEST]) LYOPHYLIZED POWDER FOR SUBCUTANEOUS INJECTION VERSUS EU-APPROVED XOLAIR® LYOPHYLIZED POWDER FOR SUBCUTANEOUS INJECTION (REFERENCE) IN HEALTHY SUBJETCS: CIMA STUDY.

Source: EU CTIS (euclinicaltrials.eu) · Last updated 17 May 2025

Next steps

Status (registry)
Completed
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
68 (actual)
First submitted
27 Sept 2024
Start date
26 Feb 2025
Lead sponsor
Laboratorios Liomont S.A. de C.V.
Diseases
Asthma
EU CT number
2023-505908-28-00

What you commit to

  • Study type: Interventional · Phase 1
  • Participants enrolled: 68
  • 2 sites 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 (2)

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

SiteCityCountrySite status
Hospital de la Santa Creu i Sant PauBarcelonaSpainCompleted
Hospital del MarBarcelonaSpainCompleted

Are you the coordinator? Confirm the details

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