Experimental combo targets Hard-to-Treat lymphoma
NCT ID NCT05896163
First seen Jun 25, 2026 · Last updated Jun 27, 2026 · Updated 1 time
Summary
This study tested two experimental drugs, maplirpacept and glofitamab, given after a single dose of obinutuzumab, in adults with diffuse large B-cell lymphoma (DLBCL) that had returned or not responded to prior treatments. Participants had already tried at least two standard therapies and could not or would not have a stem cell transplant. The goal was to find a safe and effective dose of the combination. However, the trial was terminated early, so full results are not available.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- maplirpacept (PF-07901801) combined with glofitamab and obinutuzumab
- What this could lead to
- If it works, this could offer a new treatment option for people with DLBCL who have run out of standard therapies and cannot have a stem cell transplant.
- What could go wrong
- This trial was terminated early, so results may be limited. It is also an early-phase study (Phase 1b/2) with a small number of participants, so safety and effectiveness are not yet proven.
This is an AI summary of the original study and may miss details. Read our disclaimer.
Study facts
What this study's own registry entry says, in plain language.
- Phase
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Phase 1/2
Runs two stages together: safety and dose first, then whether the treatment works.
- Participants
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40 people
The number who actually took part.
- Started
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Aug 2023
- Finished
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Apr 2026
- Lead sponsor
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A company
The lead sponsor is a pharmaceutical, biotech, or medical-device company.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
- Ages
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18 years and older
- Sex
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Anyone
- Healthy volunteers
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Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
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Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Key Inclusion Criteria: * Histologically confirmed diagnosis of DLBCL * Relapsed or refractory disease * Participant is not be a candidate for or is unwilling to undergo high dose chemotherapy and subsequent stem cell transplant and/or is unable to receive chimeric antigen receptor (CAR) T-cell therapy * Previous treatment with at least two prior lines of systemic therapy (for phase 2, at least 2 and no more than 4 prior lines of systemic therapy). Prior therapy must include an anti-CD20 antibody. * Adequate bone marrow, hepatic and renal function * Eastern Cooperative Oncology Group (ECOG) ≤2 Key Exclusion Criteria: * Prior treatment with anti-CD47 and/or prior glofitamab or anti-CD20 x CD3 containing regimen. Refractoriness to an obinutuzumab monotherapy containing regimen. * Prior allogeneic stem cell transplantation or autologous stem cell transplantation within 12 weeks prior to enrolment * High Grade B-Cell Lymphoma * Known active bacterial, viral, fungal, mycobacterial, parasitic, or other infection.
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Conditions
The condition(s) this trial relates to.
As listed by the trial registrant
The condition terms exactly as the trial's registrant entered them.
Contacts and locations
Locations
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Barnes-Jewish Hospital Parkview Tower
St Louis, Missouri, 63110, United States
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Gazi University I lcalth Research and Annlica1ion Cenlcr Gazi Hospilal
Ankara, 06560, Turkey (Türkiye)
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National Hospital Organization Kyushu Cancer Center
Fukuoka, 811-1395, Japan
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Rambam Health Care Campus
Haifa, Northern District, 3109601, Israel
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Sheba Medical Center
Ramat Gan, Central District, 5262100, Israel
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Shizuoka Cancer Center
Nagaizumi-cho, Shizuoka, 411-8777, Japan
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Siteman Cancer Center
St Louis, Missouri, 63108, United States
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Sourasky Medical Center
Tel Aviv, TELL ABĪB, 6423906, Israel
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University of Kansas Hospital Cambridge North Tower A
Kansas City, Kansas, 66160, United States
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Washington University School of Medicine
St Louis, Missouri, 63110, United States
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