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NCT04910568Active, not recruitingPhase 1

A Study to Evaluate Safety, Pharmacokinetics, and Activity of Cevostamab as Monotherapy and Cevostamab Plus Pomalidomide and Dexamethasone or Cevostamab Plus Daratumumab and Dexamethasone in Patients with Relapsed or Refractory Multiple Myeloma (CAMMA 1)

Source: EU CTIS (euclinicaltrials.eu) · Last updated 19 Aug 2026

Status (registry)
Active, not recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
60 (estimated)
First submitted
15 Jul 2024
Start date
8 Jul 2022
Lead sponsor
Genentech Inc.
EU CT number
2023-507019-36-00
EudraCT number
2021-000238-33

What you commit to

  • Study type: Interventional · Phase 1
  • Planned participants: 60
  • 12 sites in 6 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 (12)

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

SiteCityCountrySite status
Fakultni nemocnice Ostrava
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OstravaCzechiaActive, not recruiting
Rigshospitalet
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Copenhagen OeDenmarkActive, not recruiting
Hospital Universitari Vall d'Hebron
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BarcelonaSpainActive, not recruiting
Hospital General Universitario Gregorio Marañón
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MadridSpainActive, not recruiting
Hospital Hotel Dieu
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NantesFranceActive, not recruiting
Hopital Saint Louis
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ParisFranceActive, not recruiting
Centre Hospitalier Universitaire de Poitiers
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PoitiersFranceActive, not recruiting
Azienda Socio Sanitaria Territoriale Papa Giovanni XXIII
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BergamoItalyActive, not recruiting
Azienda Socio Sanitaria Territoriale degli Spedali Civili di Brescia
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BresciaItalyActive, not recruiting
Uniwersyteckie Centrum Kliniczne
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GdanskPolandActive, not recruiting
Pratia Hematologia Sp. Z o. o
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KatowicePolandActive, not recruiting
Uniwersytecki Szpital Kliniczny w Poznaniu
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PoznanPolandActive, not recruiting

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