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2024-512390-27-00CompletedPhase 1

A first-in-human dose escalation and expansion study with the SIRPα-directed monoclonal antibody BYON4228 alone and in combination with rituximab to evaluate the safety, pharmacokinetics, pharmacodynamics and efficacy in patients with relapsed/refractory CD20 positive B-cell Non-Hodgkin’s Lymphoma (NHL)

Source: EU CTIS (euclinicaltrials.eu) · Last updated 8 Apr 2026

Next steps

Status (registry)
Completed
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
66 (actual)
First submitted
24 May 2024
Start date
9 Jun 2023
Lead sponsor
Byondis B.V.
EU CT number
2024-512390-27-00
EudraCT number
2022-002018-18

What you commit to

  • Study type: Interventional · Phase 1
  • Participants enrolled: 66
  • 10 sites in 3 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
Hospital Universitari Vall d'HebronBarcelonaSpainCompleted
Institut Catala D'oncologiaL'Hospitalet de LlobregatSpainCompleted
Hospital Universitario HM SanchinarroMadridSpainCompleted
Azienda Socio Sanitaria Territoriale degli Spedali Civili di BresciaBresciaItalyCompleted
Istituto Di Candiolo Fondazione Del Piemonte Per Loncologia IRCCSCandioloItalyCompleted
Ospedale San Raffaele S.r.l.MilanItalyCompleted
Istituto Europeo di Oncologia s.r.lMilanItalyCompleted
Azienda Unità Sanitaria Locale della RomagnaRavennaItalyCompleted
Stichting Amsterdam UMCAmsterdamNetherlandsCompleted
Radboud Universitair Medisch Centrum (Radboudumc)NijmegenNetherlandsCompleted

Are you the coordinator? Confirm the details

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