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NCT05896163CompletedPhase 1/2

C4971006: A Study to Learn About the Effects of 2 Study Medicines (Maplirpacept [PF-07901801] and Glofitamab) When Given Together in People With Relapsed or Refractory Diffuse Large B Cell Lymphoma

C4971006: A PHASE 1b/2, OPEN-LABEL STUDY OF PF-07901801 IN COMBINATION WITH GLOFITAMAB AFTER A FIXED, SINGLE DOSE OF OBINUTUZUMAB IN PARTICIPANTS WITH RELAPSED/REFRACTORY DIFFUSE LARGE B CELL LYMPHOMA NOT ELIGIBLE FOR STEM CELL TRANSPLANTATION

Source: EU CTIS (euclinicaltrials.eu) · Last updated 30 Apr 2025

Brief summary (registry, in English)

Phase 1b: to assess dose limiting toxicities (DLTs), safety and tolerability of PF-07901801 and glofitamab, after a single dose of obinutuzumab in adult participants with R/R DLBCL in order to select up to 2 doses of PF-07901801 for further evaluation in Phase 2 of the study. Phase 2: to assess the clinical anti-tumor activity of PF 07901801 in combination with glofitamab after a single dose of obinutuzumab in adult participants with R/R DLBCL.

Status (registry)
Completed
Phase (registry)
Phase 1/2
Study type
Interventional
Enrollment
34 (actual)
First submitted
24 Jan 2025
Start date
1 Jul 2025
Lead sponsor
Pfizer Inc.
NCT number
NCT05896163
EU CT number
2022-502822-41-00

What you commit to

  • Study type: Interventional · Phase 1/2
  • Participants enrolled: 34
  • 18 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, not your situation.

Who cannot take part

Copied verbatim from EU CTIS (euclinicaltrials.eu) and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Known active bacterial, viral, fungal, mycobacterial, parasitic, or other infection (excluding fungal infections of nail beds) not resolved within 72 hours prior to study enrollment.
  • Prior treatment with anti-CD47 and/or anti-SIRPα therapy and/or prior glofitamab or anti-CD20xCD3 containing regimen.

Other illness

  • Known or suspected primary or secondary CNS lymphoma or meningeal involvement; history of multifocal leukoencephalopathy; history of CNS disease.
  • Significant cardiac/cardiovascular/thromboembolic disease.

Other

  • High-grade B-Cell lymphoma NOS or High-grade B-Cell lymphoma with MYC and BCL2 rearrangements.

Who the study is looking for

  • Adults with histologically confirmed DLBCL and relapsed or refractory disease
  • Participant is not a candidate or unwilling to undergo high dose chemotherapy and subsequent autologous stem cell transplant or unable to receive approved chimeric antigen receptor T-cell therapy (CAR-T).
  • Measurable disease: at least 1 site of measurable PET-avid disease per Lugano 2014 classification.
  • Prior treatment must include at least 2 lines of systemic therapy (for Phase 2: at least 2 but no more than 4 prior lines of systemic therapy). Prior therapy must include an anti-CD20 containing regimen.
  • Adequate hematologic, hepatic and renal function.
  • Eastern Cooperative Oncology Group (ECOG) performance status ≤2.

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on EU CTIS (euclinicaltrials.eu)

Sites (18)

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

SiteCityCountrySite status
Vivantes MVZ GmbH
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BerlinGermanyCompleted
Universitaetsklinikum Halle (Saale) AöR
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Halle SaaleGermanyCompleted
Klinikum der Stadt Ludwigshafen am Rhein gGmbH
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Ludwigshafen Am RheinGermanyCompleted
Hospital Clinic de Barcelona
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BarcelonaSpainCompleted
Hospital Universitari Vall d'Hebron
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BarcelonaSpainCompleted
Hospital de la Santa Creu i Sant Pau
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BarcelonaSpainCompleted
Institut Catala D'oncologia
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L'Hospitalet de LlobregatSpainCompleted
Hospital Universitario Ramón y Cajal
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MadridSpainCompleted
Hospital Universitario Quironsalud Madrid
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Pozuelo de AlarcónSpainCompleted
Hospital Universitario Marqués de Valdecilla
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SantanderSpainCompleted
Centre Hospitalier de la Cote Basque
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BayonneFranceCompleted
Institut Bergonie
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BordeauxFranceCompleted
Centre Hospitalier Universitaire De Caen Normandie
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Caen Cedex 9FranceCompleted
Centre Hospitalier Universitaire de Lille
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LilleFranceCompleted
Institut Paoli-Calmettes
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MarseilleFranceCompleted
Centre Hospitalier Universitaire de Nantes
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NantesFranceCompleted
Hopitaux Universitaires Pitie Salpetriere
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ParisFranceCompleted
Hopital Saint Louis
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ParisFranceCompleted

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