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NCT06453668CompletedPhase 1

A 52-week, Phase 1 Safety, Pharmacokinetic and Pharmacodynamic Study of Siplizumab in Newly Diagnosed Adult Amyotrophic Lateral Sclerosis (ALS) Patients (AURORA)

Source: EU CTIS (euclinicaltrials.eu) · Last updated 11 Jun 2026

Status (registry)
Completed
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
107 (actual)
First submitted
14 Sept 2023
Start date
6 Nov 2025
Lead sponsor
Itb-Med AB
NCT number
NCT06453668
EU CT number
2023-506174-12-00

What you commit to

  • Study type: Interventional · Phase 1
  • Participants enrolled: 107
  • 6 sites in 2 countries
  • 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, not your situation.

Sites (6)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Charite Universitaetsmedizin Berlin KöR
Coordinator of this site? Confirm its status
BerlinGermanyCompleted
Deutsches Zentrum Fuer Neurodegenerative Erkrankungen e.V.
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BonnGermanyCompleted
Universitaetsklinikum Ulm AoR
Coordinator of this site? Confirm its status
UlmGermanyCompleted
University Of Skane
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MalmoSwedenCompleted
Region Stockholm – SLSO
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StockholmSwedenCompleted
Norrlands University Hospital
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UmeåSwedenCompleted

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