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2023-503404-89-00RecruitingPhase 1

A study to evaluate the Safety, Pharmacokinetics, and Activity of Subcutaneous Cevostamab (BFCR4350A) in Patients with Relapsed or Refractory Multiple Myeloma (CAMMA 3)

Source: EU CTIS (euclinicaltrials.eu) · Last updated 24 Aug 2026

Next steps

Status (registry)
Recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
45 (estimated)
First submitted
8 Jul 2024
Start date
8 Dec 2021
Lead sponsor
Genentech Inc.
EU CT number
2023-503404-89-00
EudraCT number
2021-002307-36

What you commit to

  • Study type: Interventional · Phase 1
  • Planned participants: 45
  • 6 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 (6)

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

SiteCityCountrySite status
Universitair Ziekenhuis GentGentBelgiumRecruiting
UZ BrusselJetteBelgiumRecruiting
Evangelismos S AAthensGreeceRecruiting
Alexandra HospitalAthensGreeceRecruiting
Azienda Ospedaliero-Universitaria Di Bologna IRCCS Istituto Di Ricerca E Di Cura A Carattere ScientificoBolognaItalyRecruiting
Humanitas Mirasole S.p.A.RozzanoItalyRecruiting

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