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DuoBody anti-BCMA x CD3 in relapsed or refractory multiple myeloma

THE PURPOSE OF THIS STUDY IS TO DETERMINE THE SAFE DOSE (SPECIFIC AMOUNT OF DRUG GIVEN EACH TIME) OF JNJ-64007957, HOW LONG IT STAYS IN THE BODY, HOW LONG IT REMAINS ACTIVE, AND WHETHER IT IS USEFUL IN TREATING PATIENTS WITH MULTIPLE MYELOMA, IN ORDER TO ESTABLISH WHETHER IT CAN BE USED TO HELP YOU AND IN FUTURE STUDIES OF PATIENTS WITH MULTIPLE MYELOMA.

Navarre headquarters
Madrid headquarters
Cancer Center
Diseases
Mieloma múltiple y otras gammapatías monoclonales
Status
In recruitment
headquarters
Pamplona
Early phase

Technical Summary

  • PHASE 1, FIRST-IN-HUMAN, OPEN-LABEL, DOSE-ESCALATION STUDY OF JNJ-64007957, A HUMANIZED DUOBODY BCMAXCD3 ANTIBODY, IN SUBJECTS WITH RELAPSED OR REFRACTORY MULTIPLE MYELOMA
  • Code EudraCT: 2016-002122-36
  • Protocol number: 64007957MMY1001
  • Promoter: Janssen-Cilag
  • Molecule/Drug: JNJ-64007957

* The trials only admit a limited number of patients and are subject to inclusion and exclusion criteria. The specialist who assesses your case will inform you of the conditions required to participate in the clinical trial.

More information about this clinical trial

Information offered by the Spanish Registry of Clinical Studies

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