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2023-505796-76-00CompletedPhase 1

Phase 1b safety study of xevinapant, weekly cisplatin, and radiotherapy in participants with unresected LA SCCHN

Source: EU CTIS (euclinicaltrials.eu) · Last updated 6 Jun 2024

Next steps

Status (registry)
Completed
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
12 (actual)
First submitted
10 Aug 2023
Start date
18 Jan 2024
Lead sponsor
Merck Healthcare KGaA
EU CT number
2023-505796-76-00

What you commit to

  • Study type: Interventional · Phase 1
  • Participants enrolled: 12
  • 10 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 design.

Sites (10)

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

SiteCityCountrySite status
Antwerp University HospitalEdegemBelgiumCompleted
Universitair Ziekenhuis GentGentBelgiumCompleted
Algemeen Ziekenhuis GroeningeKortrijkBelgiumCompleted
Hopital De LibramontLibramont-ChevignyBelgiumCompleted
VitazSint-NiklaasBelgiumCompleted
Institut Català d'OncologiaGironaSpainCompleted
Hospital Universitario Lucus AugustiLugoSpainCompleted
Hospital Universitario Fundación Jiménez DíazMadridSpainCompleted
Clinica Universidad de NavarraMadridSpainCompleted
University Hospital Virgen Del Rocio S.L.SevillaSpainCompleted

Are you the coordinator? Confirm the details

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