Phase
Condition
Lymphoproliferative Disorders
Bone Neoplasm
Multiple Myeloma
Treatment
Elranatamab (PF-06863135)
Clinical Study ID
Ages > 18 All Genders
Study Summary
Eligibility Criteria
Inclusion
Inclusion Criteria:
- Male or female, 18 years or older (at the time consent is obtained).
- Patient who, in the investigator's opinion, is able to comply with the protocolrequirements.
- Prior diagnosis of MM as defined according to IMWG criteria.
- Patient has given voluntary written informed consent before performance of anystudy-related procedure not part of normal medical care, with the understanding thatconsent may be withdrawn by the patient at any time without prejudice to their futuremedical care.
- Relapse multiple myeloma patients that have received at least 1 or 2 prior lines oftherapy including at least to one proteasome inhibitor (bortezomib, carfilzomib orixazomib), one immunomodulatory drug (lenalidomide is mandatory and patients can bealso have been exposed to pomalidomide) and at least one anti-CD38 monoclonal antibody (daratumumab or isatuximab).
- Patients must be refractory to the last line of therapy, defined as progression whilereceiving treatment or in the first 60 days after the last dose of treatment.
- Patient must have a measurable secretory disease defined as either serum monoclonalprotein of ≥ 0,5 g/dl or urine monoclonal (light chain) protein ≥ 200 mg/24 h. Forpatients in whom disease is only measurable by serum FLC, the involved FLC should be ≥ 10mg/dL (100 mg/L), with an abnormal serum FLC ratio.
Exclusion
Exclusion Criteria:
- Subject has a diagnosis of primary amyloidosis, monoclonal gammopathy of undeterminedsignificance (MGUS), smoldering multiple myeloma (SMM), POEMS syndrome (defined by thepresence of peripheral neuropathy, organomegaly, endocrinopathy, monoclonalplasma-cells proliferative disorder, and skin changes) or plasma cell leukemia.
- Prior anti-BCMA treatment.
- Subject has peripheral neuropathy or neuropathic pain grade 2 or higher, as defined bythe National Cancer Institute Terminology Criteria for Adverse Events (NCI CTCAE)Version 5.
- History of Guillain-Barré syndrome (GBS) or GBS variants, or history of any Grade ≥3peripheral motor polyneuropathy.
- Stem cell transplant within 12 weeks prior to enrolment.
Study Design
Study Description
Connect with a study center
Hospital Clínico Universitario de Santiago ~ CHUS
Santiago De Compostela, A Coruña 15706
SpainSite Not Available
Institut Catala d'Oncologia (ICO) Badalona - Hospital Universitari Germans Trias i Pujol
Badalona, Barcelona 08916
SpainSite Not Available
Institut Catala d'Oncologia (ICO) Hospital Duran i Reynals
L'Hospitalet De Llobregat, Barcelona 08908
SpainSite Not Available
Hospital Universitario Marqués de Valdecilla
Santander, Cantabria 39008
SpainSite Not Available
Hospital Universitario de Jerez de la Frontera
Jerez De La Frontera, Cádiz 11407
SpainSite Not Available
Hospital Son Llàtzer
Palma De Mallorca, Illes Balears 07198
SpainSite Not Available
CHU de Gran Canaria Doctor Negrín
Las Palmas De Gran Canaria, Las Palmas 35010
SpainSite Not Available
Hospital HM Sanchinarro
Sanchinarro, Madrid 28050
SpainSite Not Available
Hospital Clínico Universitario Virgen de la Arrixaca
El Palmar, Murcia 30120
SpainSite Not Available
Clinica Universidad Navarra (CUN)
Pamplona, Navarra 31008
SpainSite Not Available
H. Clínic i Provincial de Barcelona
Barcelona, 08036
SpainSite Not Available
Hospital de Cabueñes
Gijón, 33394
SpainActive - Recruiting
Instituto de Investigación Sanitaria Hospital 12 de Octubre
Madrid, 28041
SpainSite Not Available
Hospital Clínico Universitario Salamanca
Salamanca, 37007
SpainActive - Recruiting
C.H. de Toledo (Virgen de la Salud)
Toledo, 45005
SpainSite Not Available
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