Multiple MyelomaPhase 3NCT06152575
MagnetisMM-32: A Study to Learn About the Study Medicine Called Elranatamab in People With Multiple Myeloma (MM) That Has Come Back After Taking Other Treatments (Including Prior Treatment With an Anti-CD38 Antibody and Lenalidomide)
A Phase 3 study testing Elranatamab, Elotuzumab and Pomalidomide in people with Multiple Myeloma, run by Pfizer at 270 sites in 27 countries.
Trial summary
The purpose of this study is to learn about the study medicine called elranatamab.This study aims to compare elranatamab to other medicines for the treatment of MM (a type of cancer). This study is seeking participants who: Are 18 years of age or older and have MM. Have received treatments before for MM. Read more about this study
- Who is it for?
- Ages 18 years and older
- Conditions the study is for
- Multiple Myeloma
- What is being tested?
- Elranatamab, Elotuzumab and Pomalidomide
- Type of treatment
- Pill or oral medicine, Injection or infusion
- Could I receive a placebo?
- No, everyone receives an active treatment
- How many people
- 492 participants
- Where
- 270 sitesin 27 countries
- Study dates
- 8 Feb 2024to 30 Dec 2027
- Phase
- Phase 3
- Are there results?
- Not yet: the study is under way
Key requirements
Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.
- Ages 18 years and older
- All sexes
- No healthy volunteers
- Adult, Older adult
Who may be able to join
- Prior diagnosis of multiple myeloma as defined by International Myeloma Working Group (IMWG) criteria and previously received 1 to 4 prior lines of therapy including prior anti-cluster of differentiation 38 (CD38) antibody and prior lenalidomide.
- Documented evidence of progressive disease or failure to achieve a response to last line of therapy per IMWG criteria.
- Measurable disease defined as at least 1 of the following: (a) Serum M-protein ≥0.5 g/dL; (b) Urinary M-protein excretion ≥200 mg/24 hours; (c) Serum involved immunoglobulin FLC ≥10 mg/dL AND abnormal serum immunoglobulin kappa to lambda FLC ratio (<0.26 or >1.65).
- Have clinical laboratory values within the specified range.
- ECOG (Eastern Cooperative Oncology Group) performance status ≤2.
- Not pregnant or breastfeeding and willing to use contraception.
Who cannot join
- Smoldering multiple myeloma.
- Plasma cell leukemia.
- Amyloidosis.
- Polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy and skin abnormalities (POEMS) syndrome.
- Known central nervous system (CNS) involvement or clinical signs of myelomatous meningeal involvement.
- Stem cell transplant within 12 weeks prior to enrolment, or active graft versus host disease.
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- Any active, uncontrolled bacterial, fungal, or viral infection.
- Any other active malignancy within 3 years prior to enrolment (exceptions include, adequately treated basal cell or squamous cell skin cancer, carcinoma in situ)
- Previous treatment with a B cell maturation antigen (BCMA)-directed therapy or CD3-redirecting therapy.
- Unable to receive investigator's choice therapy.
- Live attenuated vaccine within 4 weeks of the first dose of study intervention.
- Administration with an investigational product (e.g. drug or vaccine) within 30 days preceding the first dose of study intervention used in this study.
Trial locations and contacts
270 sites in 27 countries. Contact the study team or a site near you to ask about taking part.
270 sites in 27 countries
United States100 sites, 93 recruiting
- Recruiting
American Oncology Partners, P.A. Dba MidAmerica Cancer Care
Belton, Missouri, 64012
- Recruiting
Beverly Hills Cancer Center
Beverly Hills, California, 90211
- Recruiting
Beth Israel Deaconess Medical Center
Boston, Massachusetts, 02215
- Recruiting
BIDMC Research Pharmacy
Boston, Massachusetts, 02215
- Recruiting
Endeavor Health - Swedish Hospital
Chicago, Illinois, 60625
- Recruiting
Oncology Hematology Care Clinical Trials, LLC
Cincinnati, Ohio, 45211
- Recruiting
TriHealth Cancer Institute-Good Samaritan Hospital
Cincinnati, Ohio, 45220
- Recruiting
Oncology Hematology Care Clinical Trials, LLC
Cincinnati, Ohio, 45236
- Recruiting
The Jewish Hospital
Cincinnati, Ohio, 45236
- Recruiting
Oncology Hematology Care Clinical Trials, LLC
Cincinnati, Ohio, 45242
- Recruiting
TriHealth Cancer Institute- Thomas Comprehensive Care Center
Cincinnati, Ohio, 45242
- Recruiting
Oncology Hematology Care Clinical Trials, LLC
Cincinnati, Ohio, 45245
- Recruiting
Cleveland Clinic
Cleveland, Ohio, 44195
- Recruiting
Clovis Community Medical Center
Clovis, California, 93611
- Recruiting
Community Cancer Institute
Clovis, California, 93611
- Recruiting
Sylvester Comprehensive Cancer Center - The Lennar Foundation Medical Center
Coral Gables, Florida, 33146
- Recruiting
Baylor University Medical Center, Investigational Drug Services, Department of Pharmacy
Dallas, Texas, 75246
- Recruiting
Baylor University Medical Center
Dallas, Texas, 75246
- Recruiting
University of Miami Hospital and Clinics - Deerfield Beach
Deerfield Beach, Florida, 33442
- Recruiting
Sylvester Comprehensive Cancer Center- Doral
Doral, Florida, 33166
- Recruiting
Clinical Research Advisors (Encino Satellite Location)
Encino, California, 91316
- Recruiting
Endeavor Health - Evanston Hospital
Evanston, Illinois, 60201
- Recruiting
Sanford Fargo Medical Center
Fargo, North Dakota, 58102
- Recruiting
UCHealth Poudre Valley Hospital
Fort Collins, Colorado, 80524
- Recruiting
UCHealth Harmony
Fort Collins, Colorado, 80528
- Recruiting
University of California San Francisco
Fresno, California, 93701
- Recruiting
Community Regional Medical Center
Fresno, California, 93721
- Recruiting
Endeavor Health - Glenbrook Hospital Ambulatory Care Center
Glenview, Illinois, 60026
- Active, not recruiting
Western Regional Medical Center, Inc. dba. City of Hope Phoenix
Goodyear, Arizona, 85338
- Recruiting
UCHealth Greeley Hospital
Greeley, Colorado, 80634
- Active, not recruiting
St Francis Cancer Center
Greenville, South Carolina, 29607
- Active, not recruiting
WMCHealth Advanced Physician Services
Hawthorne, New York, 10532
- Recruiting
Endeavor Health - Highland Park Hospital Health Center 1
Highland Park, Illinois, 60035
- Recruiting
Sylvester Comprehensive Cancer Center - Hollywood
Hollywood, Florida, 33021
- Recruiting
Houston Methodist Cancer Center Infusion
Houston, Texas, 77030
- Recruiting
Houston Methodist Hospital - Department of Pharmacy
Houston, Texas, 77030
- Recruiting
Houston Methodist Hospital Cancer Center
Houston, Texas, 77030
- Recruiting
Houston Methodist Clear Lake Hospital (St. John)
Houston, Texas, 77058
- Recruiting
Houston Methodist Willowbrook Hospital
Houston, Texas, 77070
- Recruiting
Houston Methodist West Hospital
Houston, Texas, 77094
- Recruiting
MIVA Medical
Independence, Missouri, 64057
- Recruiting
Community Health Network, Inc.
Indianapolis, Indiana, 46227
- Recruiting
Community Health Network, Inc.
Indianapolis, Indiana, 46250
- Recruiting
Community Health Network, Inc.
Indianapolis, Indiana, 46256
- Active, not recruiting
Hoag Health Center Irvine
Irvine, California, 92618
- Active, not recruiting
Hoag Hospital Irvine
Irvine, California, 92618
- Recruiting
American Oncology Partners, P.A. Dba MidAmerica Cancer Care
Kansas City, Kansas, 66112
- Recruiting
Kansas City VA Medical Center
Kansas City, Missouri, 64128
- Recruiting
American Oncology Partners, P.A. Dba MidAmerica Cancer Care
Kansas City, Missouri, 64132
- Recruiting
Northwell Health/ RJ Zuckerberg Cancer Center
Lake Success, New York, 11042
- Recruiting
Ascentist Doctors' Hospital
Leawood, Kansas, 66211
- Recruiting
Bryan Medical Center
Lincoln, Nebraska, 68506
- Recruiting
NHO Revive Research Institute, LLC
Lincoln, Nebraska, 68506
- Recruiting
UCHealth Longs Peak Hospital
Longmont, Colorado, 80504
- Recruiting
UCHealth Longs Peak Medical Center
Longmont, Colorado, 80504
- Recruiting
Clinical Research Advisors (Korea Town Satellite Location)
Los Angeles, California, 90020
- Recruiting
Clinical Research Advisors (West Hollywood Satellite Location)
Los Angeles, California, 90048
- Recruiting
Valkyrie Clinical Trials
Los Angeles, California, 90067
- Recruiting
UCHealth - Medical Center of the Rockies
Loveland, Colorado, 80538
- Recruiting
Joe Arrington Cancer Research and Treatment Center
Lubbock, Texas, 79410
- Recruiting
University of Wisconsin Carbone Cancer Center - Eastpark Medical Center
Madison, Wisconsin, 53718
- Recruiting
University of Wisconsin Carbone Cancer Center-University Hospital
Madison, Wisconsin, 53792
- Recruiting
North Shore University Hospital
Manhasset, New York, 11030
- Recruiting
American Oncology Partners, P.A. Dba MidAmerica Cancer Care
Merriam, Kansas, 66204
- Recruiting
Sylvester Comprehensive Cancer Center
Miami, Florida, 33136
- Recruiting
University of Miami Hospital and Clinics - Griffin Cancer Research Building
Miami, Florida, 33136
- Recruiting
University of Miami Hospital and Clinics
Miami, Florida, 33136
- Recruiting
Baptist Hospital of Miami
Miami, Florida, 33176
- Recruiting
Miami Cancer Institute at Baptist Health, Inc.
Miami, Florida, 33176
- Recruiting
Sylvester Comprehensive Cancer Center- Kendall
Miami, Florida, 33176
- Recruiting
Infirmary Cancer Care
Mobile, Alabama, 36607
- Recruiting
WVU Cancer Institute
Morgantown, West Virginia, 26506
- Recruiting
Atlantic Health System Morristown Medical Center
Morristown, New Jersey, 07960
- Recruiting
Ascension St. Thomas Hospital
Nashville, Tennessee, 37203
- Recruiting
Tennessee Oncology, PLLC - Investigational Drug Services
Nashville, Tennessee, 37203
- Recruiting
Tennessee Oncology, PLLC - Nashville Elliston Place Plaza Center for Blood Cancers
Nashville, Tennessee, 37203
- Recruiting
Tennessee Oncology, PLLC - Nashville Elliston Place Plaza DDU
Nashville, Tennessee, 37203
- Recruiting
Tennessee Oncology, PLLC - Nashville Elliston Place Plaza Medical Oncology & Hematology
Nashville, Tennessee, 37203
- Recruiting
Long Island Jewish Medical Center
New Hyde Park, New York, 11040
- Active, not recruiting
Hoag Memorial Hospital Presbyterian
Newport Beach, California, 92663
- Recruiting
Mission Community Hospital (Satellite Site)
Panorama City, California, 91402
- Recruiting
AHN West Penn Hospital
Pittsburgh, Pennsylvania, 15224
- Recruiting
BRCR Global
Plantation, Florida, 33322
- Recruiting
BRCR Medical Center Inc
Plantation, Florida, 33322
- Recruiting
Brcr Medical Center, Inc.
Plantation, Florida, 33322
- Recruiting
HCA Florida Westside Hospital
Plantation, Florida, 33324
- Recruiting
Rodhe Island Hospital
Providence, Rhode Island, 02903
- Recruiting
The Miriam Hospital
Providence, Rhode Island, 02906
- Recruiting
University of California Davis (UC Davis) Comprehensive Cancer Center
Sacramento, California, 95817
- Recruiting
University of California
Sacramento, California, 95817
- Recruiting
Simmons Cancer Institute at SIU
Springfield, Illinois, 62702
- Recruiting
Springfield Clinic Main Campus
Springfield, Illinois, 62703
- Recruiting
HSHS St. John's Hospital
Springfield, Illinois, 62769
- Recruiting
Springfield Memorial Hospital
Springfield, Illinois, 62781
- Recruiting
Houston Methodist Sugar Land Hospital
Sugar Land, Texas, 77479
- Recruiting
BRCR Medical Center Inc.
Tamarac, Florida, 33321
- Recruiting
Baylor Scott & White Medical Center - Temple
Temple, Texas, 76508
- Recruiting
Houston Methodist The Woodlands Hospital
The Woodlands, Texas, 77385
- Active, not recruiting
Westchester Medical Center
Valhalla, New York, 10595
- Recruiting
Midwestern Regional Medical Center, Inc. dba City of Hope Chicago
Zion, Illinois, 60099
Brazil19 sites, 19 recruiting
- Recruiting
Hospital Amaral Carvalho
Jaú, São Paulo, 17210-080
- Recruiting
Instituto Oncomed de Educação e Pesquisa
Niterói, Rio de Janeiro, 24220-070
- Recruiting
Oncomed Clínica Oncológica
Niterói, Rio de Janeiro, 24220-300
- Recruiting
Hospital Moinhos de Vento
Porto Alegre, Rio Grande do Sul, 90035-001
- Recruiting
Centro Gaucho Integrado De Oncologia, Hematologia, Ensino E Pesquisa
Porto Alegre, Rio Grande do Sul, 90110-270
- Recruiting
Centro de Pesquisa Clínica - Área Administrativa
Porto Alegre, Rio Grande do Sul, 90850-170
- Recruiting
Hospital Mae de Deus
Porto Alegre, Rio Grande do Sul, 90880-480
- Recruiting
Hospital das Clínicas da Faculdade de Medicina de Ribeirão Preto da Universidade de São Paulo (USP)
Ribeirão Preto, São Paulo, 14051-140
- Recruiting
Instituto de Educação, Pesquisa e Gestão em Saúde
Rio de Janeiro, 20775-001
- Recruiting
Americas Centro de Oncologia Integrado
Rio de Janeiro, 22775001
- Recruiting
Instituto de Educação, Pesquisa e Gestão em Saúde
Rio de Janeiro, 22793-080
- Recruiting
Instituto D'Or de Pesquisa e Ensino (IDOR) - Filial Salvador
Salvador, Estado de Bahia, 41253-190
- Recruiting
Instituto D'Or de Pesquisa e Ensino (IDOR)
São Paulo, São Paulo, 04543-000
- Recruiting
ESHO Empresa de Serviços Hospitalares S.A/ Hospital Samaritano de Higienópolis
São Paulo, 01232-010
- Recruiting
Instituto D'Or de Pesquisa e Ensino (IDOR)
São Paulo, 01401-002
- Recruiting
HU UNIFESP / SPDM - Hospital São Paulo
São Paulo, 04024-002
- Recruiting
Universidade Federal de Sao Paulo
São Paulo, 04024-002
- Recruiting
Clínica Médica São Germano S/S Ltda
São Paulo, 04537-080
- Recruiting
Clínica Médica São Germano LTDA
SP, São Paulo, 04537-080
United Kingdom18 sites, 18 recruiting
- Recruiting
Betsi Cadwaladr University Health Board
Bangor, Gwynedd, LL57 2PW
- Recruiting
Queen Elizabeth Hospital Birmingham
Birmingham, England, B15 2TH
- Recruiting
Glan Clwyd Hospital
Bodelwyddan, Denbighshire [SIR Ddinbych Gb-ddb], LL18 5UJ
- Recruiting
Royal Bournemouth Hospital
Bournemouth, Dorset, BH7 7DW
- Recruiting
Kent and Canterbury Hospital
Canterbury, CT1 3NG
- Recruiting
Eastbourne District General Hospital
Eastbourne, EAST Sussex, BN21 2UD
- Recruiting
Barts Health NHS Trust
London, Greater London, E1 1BB
- Recruiting
St Bartholomew's Hospital
London, London, CITY of, EC1A 7BE
- Recruiting
Guy's & St Thomas' NHS Foundation Trust
London, London, CITY of, SE1 9RT
- Recruiting
King's College Hospital
London, London, CITY of, SE5 9RL
- Recruiting
Royal Marsden Hospital (Sutton)
London, Sutton, SM2 5PT
- Recruiting
Maidstone Hospital
Maidstone, KENT, ME16 9QQ
- Recruiting
Milton Keynes Hospital
Milton Keynes, Buckinghamshire, MK6 5LD
- Recruiting
Churchill Hospital
Oxford, Oxfordshire, OX3 7LE
- Recruiting
Poole Hospital
Poole, Dorset, BH15 2JB
- Recruiting
Royal Stoke University Hospital
Stoke-on-Trent, Staffordshire, ST4 6QG
- Recruiting
New Cross Hospital
Wolverhampton, WV10 0QP
- Recruiting
Worthing Hospital
Worthing, EAST Sussex, BN11 2DH
France15 sites, 13 recruiting
- Recruiting
Centre Hospitalier de la Côte Basque
Bayonne, 64109
- Recruiting
Centre Hospitalier Universitaire de Poitiers
City/Town/Village, Vienne, 86021
- Recruiting
Henri Mondor Hospital
Créteil, Val-de-marne, 94010
- Recruiting
CHD Vendee
La Roche-sur-Yon, 85925
- Recruiting
Centre Hospitalier du Mans
Le Mans, 72037
- Recruiting
Centre Hospitalier Universitaire de Nantes - L' Hopital l'hôtel-Dieu
Nantes, Pays de la Loire Region, 44000
- Recruiting
Hôpital Universitaire Necker Enfants Malades
Paris, 75015
- Recruiting
Hopitaux Universitaires Paris Centre-Hopital Cochin
Paris, 75679
- Recruiting
CHU Bordeaux Haut-Leveque
Pessac, Aquitaine, 33600
- Recruiting
Hôpital NOVO
Pontoise, Val-d'oise, 95300
- Recruiting
Centre Hospitalier de Cornouaille
Quimper, 29107
- Recruiting
Institut Universitaire du Cancer Toulouse - Oncopole - CHU de TOULOUSE
Toulouse, Haute-garonne, 31100
- Recruiting
Centre Hospitalier Régional Universitaire de Tours - Hôpital Bretonneau
Tours, 37044
- Active, not recruiting
Centre Hospitalier Bretagne Atlantique
Vannes, 56000
- Active, not recruiting
Centre Hospitalier Bretagne Atlantique
Vannes, 56017
Japan14 sites, 14 recruiting
- Recruiting
Nippon Medical School Hospital
Bunkyo-ku, Tokyo, 113-8603
- Recruiting
Kagoshima University Hospital
Kagoshima, 890-8520
- Recruiting
Kobe City Medical Center General Hospital
Kobe, Hyōgo, 650-0047
- Recruiting
Yamanashi Prefectural Central Hospital
Kofu, Yamanashi, 400-8506
- Recruiting
Japanese Foundation for Cancer Research
Koto, Tokyo, 135-8550
- Recruiting
The Cancer Institute Hospital of JFCR
Koto, Tokyo, 135-8550
- Recruiting
University Hospital,Kyoto Prefectural University of Medicine
Kyoto, 602-8566
- Recruiting
Gunma University Hospital
Maebashi, Gunma, 371-8511
- Recruiting
Ehime Prefectural Central Hospital
Matsuyama, Ehime, 790-0024
- Recruiting
National Hospital Organization Okayama Medical Center
Okayama, 701-1192
- Recruiting
National Hospital Organization Shibukawa Medical Center
Shibukawa, Gunma, 377-0280
- Recruiting
Iwate Medical University Hospital
Shiwa-gun Yahaba-cho, Iwate, 028-3695
- Recruiting
Toyohashi Municipal Hospital
Toyohashi, Aichi-ken, 441-8570
- Recruiting
Yamagata University Hospital
Yamagata, 990-9585
Italy12 sites, 4 recruiting
- Recruiting
Azienda Ospedaliero Universitaria delle Marche
Ancona, The Marches, 60126
- Active, not recruiting
IRCCS Azienda Ospedaliero-Universitaria di Bologna, Policlinico di Sant'Orsola
Bologna, 40138
- Active, not recruiting
Azienda Ospedaliera Universitaria Careggi
Florence, Tuscany, 50134
- Active, not recruiting
Azienda Socio Sanitaria Ovest milanese
Legnano, Milano, 20025
- Active, not recruiting
IRCCS - Istituto Romagnolo per lo Studio dei Tumori (IRST) "Dino Amadori"
Meldola (FC), 47014
- Recruiting
P.O. San Carlo Borromeo- ASST SANTI PAOLO E CARLO
Milan, Lombardy, 20153
- Active, not recruiting
Istituto Europeo di Oncologia IRCCS
Milan, 20141
- Recruiting
ASST Santi Paolo e Carlo Ospedale San Paolo
Milan, 20142
- Active, not recruiting
A.O.U. Policlinico Paolo Giaccone
Palermo, Sicily, 90127
- Recruiting
Ospedale Civile dello Spirito Santo
Pescara, 65124
- Active, not recruiting
Azienda Ospedaliero Universitaria Pisana
Pisa, Tuscany, 56126
- Active, not recruiting
Azienda Ospedaliero-Universitaria Città della Salute e della Scienza di Torino
Turin, Piedmont, 10126
Spain12 sites
- Active, not recruiting
Institut Català d'Oncologia (ICO) - Badalona
Badalona, Barcelona [barcelona], 08916
- Active, not recruiting
OSI Ezkerraldea-Enkarterri-Cruces - Hospital Universitario Cruces
Barakaldo, Basque Country, 48903
- Active, not recruiting
Hospital Clínic de Barcelona
Barcelona, Catalunya [cataluña], 08036
- Active, not recruiting
Institut Català d'Oncologia (ICO) - Girona
Girona, Girona [gerona], 17007
- Active, not recruiting
Hospital General Universitario Gregorio Marañon
Madrid, 28007
- Active, not recruiting
Hospital Universitario HM Sanchinarro
Madrid, 28050
- Active, not recruiting
H.R.U Málaga - Hospital General
Málaga, 29010
- Active, not recruiting
Hospital General Universitario Morales Meseguer
Murcia, Galicia [galicia], 30008
- Active, not recruiting
Hospital Universitario de Salamanca - Complejo Asistencial Universitario de Salamanca
Salamanca, 37007
- Active, not recruiting
Hospital Universitari Mutua Terrassa
Terrassa, Barcelona [barcelona], 08221
- Active, not recruiting
ASCIRES ECG Médica S.L
Valencia, Valenciana, Comunitat, 46004
- Active, not recruiting
Hospital Universitari i Politecnic La Fe
Valencia, 46026
Germany9 sites, 9 recruiting
- Recruiting
Vivantes Klinikum Am Urban
Berlin, 10249
- Recruiting
Vivantes Klinikum Am Urban
Berlin, 10967
- Recruiting
Universitätsklinikum Bonn
Bonn, North Rhine-Westphalia, 53127
- Recruiting
Medizinische Universität Lausitz - Carl Thiem
Cottbus, 03048
- Recruiting
Universitaetsklinikum Freiburg
Freiburg im Breisgau, Baden-Wurttemberg, 79106
- Recruiting
St. Barbara-Klinik Hamm-Heessen
Hamm, 59073
- Recruiting
Klinikum Nürnberg Nord
Nuremberg, Bavaria, 90419
- Recruiting
Robert Bosch Krankenhaus GmbH
Stuttgart, Baden-Wurttemberg, 70376
- Recruiting
Universitaetsklinikum Ulm
Ulm, Baden-Wurttemberg, 89081
Australia7 sites, 7 recruiting
- Recruiting
Sunshine Coast University Hospital
Birtinya, Queensland, 4575
- Recruiting
Blacktown Hospital
Blacktown, New South Wales, 2148
- Recruiting
Royal Brisbane and Women's Hospital
Brisbane, Queensland, 4029
- Recruiting
Concord Repatriation General Hospital
Concord, New South Wales, 2139
- Recruiting
St Vincent's Hospital (Melbourne)
Fitzroy, Victoria, 3065
- Recruiting
Barwon Health
Geelong, Victoria, 3220
- Recruiting
Sir Charles Gairdner Hospital, Haematology Clinical Trials
Nedlands, Western Australia, 6009
Croatia7 sites, 7 recruiting
- Recruiting
Klinicki bolnicki centar Osijek
Osijek, 31000
- Recruiting
Klinicki bolnicki centar Rijeka
Rijeka, 51000
- Recruiting
Klinicki bolnicki centar Split
Split, 21 000
- Recruiting
Sestre milosrdnice University Hospital Center
Zagreb, 10 000
- Recruiting
University Hospital Center Zagreb
Zagreb, 10 000
- Recruiting
Klinicka bolnica Dubrava
Zagreb, 10000
- Recruiting
Klinicka bolnica Merkur
Zagreb, 10000
Chile6 sites, 6 recruiting
- Recruiting
FALP
Providencia, Santiago Metropolitan, 7500836
- Recruiting
FALP
Providencia, Santiago Metropolitan, 7500966
- Recruiting
FALP
Santiago, Santiago Metropolitan, 7500921
- Recruiting
Clínica Inmunocel
Santiago, Santiago Metropolitan, 7580206
- Recruiting
Clínica Universidad de Los Andes
Santiago, Santiago Metropolitan, 7620157
- Recruiting
Clínica Alemana de Santiago
Santiago, Santiago Metropolitan, 7650568
Belgium5 sites, 5 recruiting
- Recruiting
UZ Brussel
Brussels, Bruxelles-capitale, Région de, 1090
- Recruiting
Grand Hôpital de Charleroi
Gilly, Hainaut, 6060
- Recruiting
Centre Hospitalier Epicura
Hornu, Hainaut, 7301
- Recruiting
CHR Verviers - La Tourelle
Verviers, Liège, 4800
- Recruiting
Université Catholique de Louvain-Namur - Centre Hospitalier Universitaire Dinant-Godinne - Site Godi
Yvoir, Namur, 5530
Greece5 sites
- Active, not recruiting
University General Hospital of Alexandroupoli
Alexandroupoli, Anatolikí Makedonía KAI Thráki, 681 00
- Active, not recruiting
Alexandra General Hospital of Athens
Athens, Attikí, 115 28
- Active, not recruiting
University Hospital of Ioannina
Ioannina, Ípeiros, 455 00
- Active, not recruiting
"Theagenio" Cancer Hospital of Thessaloniki
Thessaloniki, Kentrikí Makedonía, 54639
- Active, not recruiting
G. Papanikolaou General Hospital
Thessaloniki, Thessaloníki, 570 10
Israel5 sites, 5 recruiting
- Recruiting
Soroka Medical Center
Beersheba, Southern District, 8410101
- Recruiting
Hadassah Medical Center
Jerusalem, Jerusalem, 9112001
- Recruiting
Rabin Medical Center
Petah Tikva, Central District, 4910021
- Recruiting
Sheba Medical Center
Ramat Gan, Central District, 5265601
- Recruiting
Sourasky Medical Center
Tel Aviv, TELL ABĪB, 6423906
Argentina4 sites, 4 recruiting
- Recruiting
Instituto Alexander Fleming
Ciudad Autónoma de Buenos Aires, Buenos Aires, C1426ANZ
- Recruiting
Hospital Italiano de Buenos Aires
Ciudad de Buenos Aires, Buenos Aires F.D., C1199ABB
- Recruiting
Hospital Italiano de La Plata
La Plata, 1900
- Recruiting
Hospital Universitario Austral
Pilar, Buenos Aires, 1629
Norway4 sites, 4 recruiting
- Recruiting
Akershus Universitetssykehus
Lørenskog, Akershus, 1478
- Recruiting
Oslo Universitetssykehus Ullevål
Oslo, 0450
- Recruiting
Sykehuset i Vestfold
Tønsberg, Vestfold, 3103
- Recruiting
St. Olavs Hospital
Trondheim, Sør-trøndelag, 7030
Slovakia4 sites
- Active, not recruiting
Fakultna nemocnica s poliklinikou F.D.Roosevelta Banska Bystrica
Banská Bystrica, Banská Bystrica Region, 97517
- Active, not recruiting
Narodny onkologicky ustav
Bratislava, 833 10
- Active, not recruiting
Univerzitna nemocnica Bratislava, Nemocnica sv. Cyrila a Metoda
Bratislava, 851 07
- Active, not recruiting
Univerzitna Nemocnica L. Pasteura Kosice
Košice, Košice Region, 040 11
Canada3 sites, 3 recruiting
- Recruiting
The Moncton Hospital
Moncton, New Brunswick, E1C 6Z8
- Recruiting
Jewish General Hospital
Montreal, Quebec, H3T 1E2
- Recruiting
l'Hôpital du Sacré-Cœur-de-Montréal
Montreal, Quebec, H4J 1C5
Denmark3 sites, 3 recruiting
- Recruiting
Aalborg Universitetshospital, Syd
Aalborg, North Denmark, 9000
- Recruiting
Aarhus Universitetshospital, Skejby
Aarhus, Central Jutland, 8200
- Recruiting
Rigshospitalet
Copenhagen Ø, DK 2100
Finland3 sites
- Active, not recruiting
Helsinki University Hospital - Comprehensive Cancer Center (HYKS - Syöpäkeskus)
Helsinki, Uusimaa, 00029
- Active, not recruiting
Oulun yliopistollinen sairaala
Oulu, 90220
- Active, not recruiting
Turku University Hospital
Turku, Southwest Finland, 20520
Netherlands3 sites
- Active, not recruiting
Albert Schweitzer Ziekenhuis, locatie Dordwijk
Dordrecht, South Holland, 3318 AT
- Active, not recruiting
Maastricht UMC+
Maastricht, Limburg, 6229 HX
- Active, not recruiting
Erasmus Medisch Centrum
Rotterdam, South Holland, 3015 GD
South Korea3 sites, 3 recruiting
- Recruiting
Seoul National University Hospital
Seoul, Seoul-teukbyeolsi [seoul], 03080
- Recruiting
Severance Hospital, Yonsei University Health System
Seoul, Seoul-teukbyeolsi [seoul], 03722
- Recruiting
Samsung Medical Center
Seoul, Seoul-teukbyeolsi [seoul], 06351
Czechia2 sites, 2 recruiting
- Recruiting
Fakultní nemocnice Brno Bohunice
Brno, Brno-město, 625 00
- Recruiting
Fakultni nemocnice Kralovske Vinohrady
Prague, Praha 10, 100 34
Portugal2 sites
- Active, not recruiting
2Ca Braga
Braga, 4710-243
- Active, not recruiting
Instituto Português de Oncologia de Lisboa Francisco Gentil
Lisbon, Lisbon District, 1099-023
Sweden2 sites
- Active, not recruiting
Falu Lasarett
Falun, 791 31
- Active, not recruiting
Universitetssjukhuset Örebro
Örebro, Örebro LÄN [se-18], 701 85
Taiwan2 sites, 2 recruiting
- Recruiting
China Medical University Hospital
Taichung, 404332
- Recruiting
Taichung Veterans General Hospital
Taichung, 407
Slovenia1 site, 1 recruiting
- Recruiting
University Medical Centre Ljubljana
Ljubljana, 1000
About this study
Official title: A PHASE 3, OPEN-LABEL STUDY OF ELRANATAMAB MONOTHERAPY VERSUS ELOTUZUMAB, POMALIDOMIDE, DEXAMETHASONE (EPd) OR POMALIDOMIDE, BORTEZOMIB, DEXAMETHASONE (PVd) OR CARFILZOMIB, DEXAMETHASONE (Kd) IN PARTICIPANTS WITH RELAPSED/REFRACTORY MULTIPLE MYELOMA WHO RECEIVED PRIOR ANTI-CD38 DIRECTED THERAPY
The purpose of this study is to learn about the study medicine called elranatamab.This study aims to compare elranatamab to other medicines for the treatment of MM (a type of cancer).
This study is seeking participants who:
Read more
- Are 18 years of age or older and have MM.
- Have received treatments before for MM.
- Have MM that has returned or not responded to their most recent treatment.
Half of the participants will receive elranatamab. The other half of participants will receive a combination therapy selected by the study doctor. The selected combination therapy will include 2 to 3 different medicines commonly used to treat MM.
Elranatamab will be given as a shot under the skin at the study clinic about once a week. This may change to a smaller number of shots later in the study.
The medicines in the combination therapy will be taken by mouth (at home or at the study clinic) AND will be given either as:
- a shot under the skin at the study clinic
- through a needle in the vein at the study clinic The number of times these medicines will be taken depends on what combination therapy the study doctor selects.
Participants may continue to receive elranatamab or a combination therapy until their MM is no longer responding. The study team will see how each participant is doing with the study treatment during regular visits at the study clinic. The study team will continue to follow-up with participants after study treatment with telephone contacts (or visits).
The study will compare the experiences of people receiving elranatamab to those people receiving a combination therapy. This will help learn about the safety and how effective elranatamab is.
- Conditions
- Multiple Myeloma
- Being tested
- Elranatamab, Elotuzumab, Pomalidomide, Dexamethasone, Bortezomib
- Keywords
- Elranatamab, B-Cell Maturation Antigen, BCMA, Bispecific antibody, BCMA-CD3 bispecific antibody, Myeloma, Multiple myeloma, Relapsed multiple myeloma, Refractory multiple myeloma, MagnetisMM, MagnetisMM-32, Pomalidomide, Elotuzumab, Bortezomib, Carfilzomib, PF-06863135
- Medical subject headings
- Multiple Myeloma, Neoplasms, Plasma Cell
What participants receive
What participants receive. In a randomised study each person is assigned to one group by chance.
ElranatamabDrug
Elranatamab will be administered subcutaneously
ElotuzumabDrug
Elotuzumab will be administered intravenously
PomalidomideDrug
Pomalidomide will be administered orally
DexamethasoneDrug
Dexamethasone will be administered orally
BortezomibDrug
Bortezomib will be administered subcutaneously or intravenously
CarfilzomibDrug
Carfilzomib will be administered intravenously
| Study group | Role | What they receive |
|---|---|---|
| Elranatamab | Experimental | Participants will receive elranatamab monotherapy Receives: Drug: Elranatamab |
| Investigator's Choice | Active comparator | Participants will receive either Elotuzumab, Pomalidomide and Dexamethasone (EPd), or Pomalidomide, Bortezomib and Dexamethasone (PVd), or Carfilzomib and Dexamethasone (Kd) Receives: Drug: Elotuzumab; Drug: Pomalidomide; Drug: Dexamethasone; Drug: Bortezomib; Drug: Carfilzomib |
What is being measured
The primary outcome is the main question the study is designed to answer.
Progression free survival per International Myeloma Working Group criteria
From date of randomization to date of progressive disease, discontinuation from study, death, or censoring, whichever occurs first
Measured: Up to approximately 5 years
Secondary outcomes (17)
Overall survival
From date of randomization to date of discontinuation from study, death, or censoring, whichever occurs first
Measured: Up to approximately 5 years
Progression free survival on next-line treatment per International Myeloma Working Group criteria
From date of randomization to date of second objective disease progression, discontinuation from the study, death, or censoring, whichever occurs first
Measured: Up to approximately 5 years
Objective response rate per International Myeloma Working Group criteria
From date of randomization to date of progressive disease, discontinuation from study, death, or start of new anticancer therapy
Measured: Up to approximately 5 years
Duration of response per International Myeloma Working Group criteria
From date of confirmed objective response to date of progressive disease, discontinuation from study, death, or censoring, whichever occurs first
Measured: Up to approximately 5 years
Very good partial response or better response rate per International Myeloma Working Group criteria
From date of randomization to date of progressive disease, discontinuation from study, death, or start of new anticancer therapy, whichever occurs first
Measured: Up to approximately 5 years
Complete response rate per International Myeloma Working Group criteria
From date of randomization to date of progressive disease, discontinuation from study, death, or start of new anticancer therapy, whichever occurs first
Measured: Up to approximately 5 years
Duration of complete response per International Myeloma Working Group criteria
From date of confirmed complete response to date of progressive disease, discontinuation from study, death, or censoring, whichever occurs first
Measured: Up to approximately 5 years
Time to response per International Myeloma Working Group criteria
From date of randomization to date of confirmed objective response
Measured: Up to approximately 5 years
Minimal residual disease negativity rate per International Myeloma Working Group criteria
From date of randomization to date of progressive disease, discontinuation from study, death, or start of new anticancer therapy, whichever occurs first
Measured: Up to approximately 5 years
Sustained minimal residual disease negativity rate per International Myeloma Working Group criteria
From date of randomization to date of progressive disease, discontinuation from study, death, or start of new anticancer therapy, whichever occurs first
Measured: Up to approximately 5 years
Duration of minimal residual disease negativity rate per International Myeloma Working Group criteria
From date of minimal residual disease negativity to date of relapse, death, or censoring, whichever occurs first
Measured: Up to approximately 5 years
Frequency of treatment-emergent adverse events
Measured: From date of first dose of study intervention up to 90 days after last study intervention administration
Frequency of abnormal laboratory results
Measured: From date of first dose of study intervention up to 90 days after last study intervention administration
Free elranatamab serum trough concentration [Ctrough]
Measured: From date of first dose of elranatamab up to approximately 14 days after last dose of elranatamab
Elranatamab immunogenicity by anti-drug antibodies against elranatamab
Measured: From date of first dose of elranatamab up to approximately 14 days after last dose of elranatamab
Health-related quality of life by European Organization for Research and Treatment of Cancer Quality of Life Questionnaire - Core 30
Change from baseline scores
Measured: From date of informed consent up to approximately 35 days after last administration of study intervention
Health-related quality of life by European Organization for Research and Treatment of Cancer Quality of Life Questionnaire - Myeloma 20
Change from baseline scores
Measured: From date of informed consent up to approximately 35 days after last administration of study intervention
Timeline
From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.
- First posted30 Nov 2023
- Study start8 Feb 2024
- Primary completion30 Aug 2026 (estimated)
- Study completion30 Dec 2027 (estimated)
Resources
- Official record on ClinicalTrials.govThe registry entry this page is built from, with its full change history.
- Other trials for Multiple MyelomaStudies of the same condition, open and under way.
- More trials run by PfizerThe sponsor's other registered studies.
- What the trial phases meanHow a treatment moves from first tests in people to approval.
More details
For doctors and researchers: how the study is designed, who runs it, and its registry IDs.
Study design
- Study type
- Interventional
- Phase
- Phase 3
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Enrolment
- 492 participants (estimated)
Sponsor and investigators
- Lead sponsor
- Pfizer
- Sponsor type
- Industry (pharma, biotech, devices)
- Responsible party
- Sponsor
- Investigators
- Pfizer CT.gov Call Center, Study director, Pfizer
IDs, dates and publications
- ClinicalTrials.gov ID
- NCT06152575
- Sponsor's protocol ID
- C1071032
- Other IDs
- MAGNETISMM-32, 2023-507871-23-00, 2023
- Status last verified
- Aug 2026
- First submitted
- 17 Nov 2023
- Last updated
- 24 Aug 2026
- Results posted
- No
- Data monitoring committee
- Yes
- FDA-regulated drug
- Yes
- FDA-regulated device
- No
- Individual data sharing
- Yes: Pfizer will provide access to individual de-identified participant data and related study documents (e.g. protocol, Statistical Analysis Plan (SAP), Clinical Study Report (CSR)) upon request from qualified researchers, and subject to certain criteria, conditions, and exceptions. Further details on Pfizer's data sharing criteria and process for requesting access can be found at: https://www.pfizer.com/science/clinical\_trials/trial\_data\_and\_results/data\_requests.
- Expanded access
- Available
Study at a glance
From the registry record, last updated by the sponsor on 24 Aug 2026. Recruitment status is as the sponsor reported it: confirm with the study team.
- Official title
- A PHASE 3, OPEN-LABEL STUDY OF ELRANATAMAB MONOTHERAPY VERSUS ELOTUZUMAB, POMALIDOMIDE, DEXAMETHASONE (EPd) OR POMALIDOMIDE, BORTEZOMIB, DEXAMETHASONE (PVd) OR CARFILZOMIB, DEXAMETHASONE (Kd) IN PARTICIPANTS WITH RELAPSED/REFRACTORY MULTIPLE MYELOMA WHO RECEIVED PRIOR ANTI-CD38 DIRECTED THERAPY
- ClinicalTrials.gov ID
- NCT06152575
- Acronym / sponsor ID
- C1071032
- Conditions
- Multiple Myeloma
- Keywords
- Elranatamab, B-Cell Maturation Antigen, BCMA, Bispecific antibody, BCMA-CD3 bispecific antibody, Myeloma, Multiple myeloma, Relapsed multiple myeloma
- Phase
- Phase 3
- Study type
- Interventional
- Recruitment status
- Recruiting
- Enrolment
- 492 participants (estimated)
- Lead sponsor
- PfizerIndustry (pharma, biotech, devices)
- Study start
- 8 Feb 2024 (actual)
- Primary completion
- 30 Aug 2026 (estimated)
- Study completion
- 30 Dec 2027 (estimated)
- First posted
- 30 Nov 2023 (actual)
- Results
- Not posted in the source record
Clinical summary
The research question as the sponsor registered it. This describes what the study plans to test, not what it found.
The purpose of this study is to learn about the study medicine called elranatamab.This study aims to compare elranatamab to other medicines for the treatment of MM (a type of cancer).
This study is seeking participants who:
- Are 18 years of age or older and have MM.
- Have received treatments before for MM.
- Have MM that has returned or not responded to their most recent treatment.
Half of the participants will receive elranatamab. The other half of participants will receive a combination therapy selected by the study doctor. The selected combination therapy will include 2 to 3 different medicines commonly used to treat MM.
Elranatamab will be given as a shot under the skin at the study clinic about once a week. This may change to a smaller number of shots later in the study.
The medicines in the combination therapy will be taken by mouth (at home or at the study clinic) AND will be given either as:
- a shot under the skin at the study clinic
- through a needle in the vein at the study clinic The number of times these medicines will be taken depends on what combination therapy the study doctor selects.
Participants may continue to receive elranatamab or a combination therapy until their MM is no longer responding. The study team will see how each participant is doing with the study treatment during regular visits at the study clinic. The study team will continue to follow-up with participants after study treatment with telephone contacts (or visits).
The study will compare the experiences of people receiving elranatamab to those people receiving a combination therapy. This will help learn about the safety and how effective elranatamab is.
Study design
- Primary purpose
- Treatment
- Allocation
- Randomised
- Intervention model
- Parallel groups
- Masking
- None (open label)
- Number of arms
- 2
| Arm | Type | Receives |
|---|---|---|
| Elranatamab | Experimental | Drug: ElranatamabParticipants will receive elranatamab monotherapy |
| Investigator's Choice | Active comparator | Drug: Elotuzumab, Drug: Pomalidomide, Drug: Dexamethasone, Drug: Bortezomib, Drug: CarfilzomibParticipants will receive either Elotuzumab, Pomalidomide and Dexamethasone (EPd), or Pomalidomide, Bortezomib and Dexamethasone (PVd), or Carfilzomib and Dexamethasone (Kd) |
Who may qualify
- Ages
- 18 years and older
- Sex
- All
- Healthy volunteers
- Not accepted
- Age groups
- Adult, Older adult
Key inclusion criteria (6 listed)
- Prior diagnosis of multiple myeloma as defined by International Myeloma Working Group (IMWG) criteria and previously received 1 to 4 prior lines of therapy including prior anti-cluster of differentiation 38 (CD38) antibody and prior lenalidomide.
- Documented evidence of progressive disease or failure to achieve a response to last line of therapy per IMWG criteria.
- Measurable disease defined as at least 1 of the following: (a) Serum M-protein ≥0.5 g/dL; (b) Urinary M-protein excretion ≥200 mg/24 hours; (c) Serum involved immunoglobulin FLC ≥10 mg/dL AND abnormal serum immunoglobulin kappa to lambda FLC ratio (<0.26 or >1.65).
- Have clinical laboratory values within the specified range.
- ECOG (Eastern Cooperative Oncology Group) performance status ≤2.
Key exclusion criteria (12 listed)
- Smoldering multiple myeloma.
- Plasma cell leukemia.
- Amyloidosis.
- Polyneuropathy, organomegaly, endocrinopathy, monoclonal gammopathy and skin abnormalities (POEMS) syndrome.
- Known central nervous system (CNS) involvement or clinical signs of myelomatous meningeal involvement.
Eligibility is decided by the study team after screening; this overview does not establish that a patient qualifies. Full inclusion and exclusion criteria.
Interventions
| Intervention | Type | Arms |
|---|---|---|
| ElranatamabElranatamab will be administered subcutaneously | Drug | Elranatamab |
| ElotuzumabElotuzumab will be administered intravenously | Drug | Investigator's Choice |
| PomalidomidePomalidomide will be administered orally | Drug | Investigator's Choice |
| DexamethasoneDexamethasone will be administered orally | Drug | Investigator's Choice |
| BortezomibBortezomib will be administered subcutaneously or intravenously | Drug | Investigator's Choice |
| CarfilzomibCarfilzomib will be administered intravenously | Drug | Investigator's Choice |
Primary outcome
Progression free survival per International Myeloma Working Group criteria
Time frame: Up to approximately 5 years
From date of randomization to date of progressive disease, discontinuation from study, death, or censoring, whichever occurs first
17 secondary outcomes
Overall survival
Time frame: Up to approximately 5 years
Progression free survival on next-line treatment per International Myeloma Working Group criteria
Time frame: Up to approximately 5 years
Objective response rate per International Myeloma Working Group criteria
Time frame: Up to approximately 5 years
Duration of response per International Myeloma Working Group criteria
Time frame: Up to approximately 5 years
Very good partial response or better response rate per International Myeloma Working Group criteria
Time frame: Up to approximately 5 years
Complete response rate per International Myeloma Working Group criteria
Time frame: Up to approximately 5 years
Duration of complete response per International Myeloma Working Group criteria
Time frame: Up to approximately 5 years
Time to response per International Myeloma Working Group criteria
Time frame: Up to approximately 5 years
Minimal residual disease negativity rate per International Myeloma Working Group criteria
Time frame: Up to approximately 5 years
Sustained minimal residual disease negativity rate per International Myeloma Working Group criteria
Time frame: Up to approximately 5 years
Duration of minimal residual disease negativity rate per International Myeloma Working Group criteria
Time frame: Up to approximately 5 years
Frequency of treatment-emergent adverse events
Time frame: From date of first dose of study intervention up to 90 days after last study intervention administration
Frequency of abnormal laboratory results
Time frame: From date of first dose of study intervention up to 90 days after last study intervention administration
Free elranatamab serum trough concentration [Ctrough]
Time frame: From date of first dose of elranatamab up to approximately 14 days after last dose of elranatamab
Elranatamab immunogenicity by anti-drug antibodies against elranatamab
Time frame: From date of first dose of elranatamab up to approximately 14 days after last dose of elranatamab
Health-related quality of life by European Organization for Research and Treatment of Cancer Quality of Life Questionnaire - Core 30
Time frame: From date of informed consent up to approximately 35 days after last administration of study intervention
Health-related quality of life by European Organization for Research and Treatment of Cancer Quality of Life Questionnaire - Myeloma 20
Time frame: From date of informed consent up to approximately 35 days after last administration of study intervention
Results and safety
This study is still under way. Results are not available in the source record yet.
Research links
- Official record on ClinicalTrials.govLast updated by the sponsor 24 Aug 2026.
- To obtain contact information for a study center near you, click here.Link provided by the sponsor.
- MagnetisMM-32Link provided by the sponsor.
- Individual participant dataSharing planned: Yes. Pfizer will provide access to individual de-identified participant data and related study documents (e.g. protocol, Statistical Analysis Plan (SAP), Clinical Study Report (CSR)) upon request from qualified researchers, and subject to certain criteria, conditions, and exceptions. Further details on Pfizer's data sharing criteria and process for requesting access can be found at: https://www.pfizer.com/science/clinical_trials/trial_data_and_results/data_requests.
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Referral and contact
AzTrials does not enrol participants or take referrals. Contact the study team or a site listed below; they decide who can take part.
Pfizer CT.gov Call Center study director
Pfizer
270 sites in 27 countries: see every site and its status.
Questions about this trial
What is this clinical trial studying?
A Phase 3 study testing Elranatamab, Elotuzumab and Pomalidomide in people with Multiple Myeloma, run by Pfizer at 270 sites in 27 countries.
The full registered description is in the About this study section and the official record.
Who may be eligible to take part?
The sponsor lists 6 inclusion and 12 exclusion criteria. Eligibility is decided by the study team after screening, so read the full criteria and contact a listed site.
Is this clinical trial currently recruiting?
The record says: looking for participants now, as of the sponsor's last update on 24 Aug 2026. Status can change between updates, so confirm with the study contact before making plans.
Where is the study taking place?
The record lists 270 sites in United States, Brazil, United Kingdom, France, Japan and 22 more countries. Whether a site is taking part right now should be confirmed with that site. See every site.
What are the possible benefits and risks?
They depend on the study and the treatment, and no study can promise a benefit. The study team explains the known risks during informed consent, before anyone joins; the record itself does not list them.
What does this phase mean?
Phase 3 studies compare the treatment with the current standard treatment or a placebo in a large group, to confirm how well it works and watch for side effects.
Not every study follows the same path, and some studies (observational studies, device studies) have no phase.
Are results available for this study?
This study is still under way. Results are not available in the source record yet.
How can a doctor refer a patient or contact the research team?
Contact Pfizer CT.gov Call Center (1-800-718-1021, ClinicalTrials.gov_Inquiries@pfizer.com), or a site near the patient. AzTrials does not enrol participants or take referrals.
What does the primary outcome measure?
Progression free survival per International Myeloma Working Group criteria (time frame: Up to approximately 5 years). It is what the study was designed to measure, not a finding.
Where can I read the original study information?
Does a listing mean the treatment is approved or proven to work?
No. A listing means the study is registered. It does not show that the treatment is safe, works, or is approved by a regulator.
How often is this information updated?
AzTrials copies changed records from ClinicalTrials.gov every night and reloads the whole registry every week. The sponsor last updated this record on 24 Aug 2026.