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Trial · NCT05788289

A Study of Tafasitamab and Lenalidomide in People With Mantle Cell Lymphoma

NCT05788289, Phase 2, Terminated, Memorial Sloan Kettering Cancer Center; results first posted 2025-04-20

3 sourcestrials-2026-11-12-0.5.0

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ConductScience Library. A Study of Tafasitamab and Lenalidomide in People With Mantle Cell Lymphoma. Trials, record NCT05788289. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT05788289

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Trial

As registered on ClinicalTrials.gov, in the graph's capture of the registry.

Title
A Study of Tafasitamab and Lenalidomide in People With Mantle Cell Lymphoma
NCT number
NCT05788289
Status
Terminated
Phases
Phase 2
Enrollment
4 participants, actual
Lead sponsor
Memorial Sloan Kettering Cancer Center
Conditions
Mantle Cell Lymphoma, MCL
Interventions
Tafasitamab, Lenalidomide
First posted
2023-03-28
Last updated
2025-05-25
Results first posted
2025-04-20

Source ClinicalTrials.gov

Registered outcomes1

Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.

ListOutcomeTime frameDescription
PrimaryOverall Response Rate/ORRcompletion of 12 cycles of treatment (each cycle is 28 days) or at treatment discontinuation, whichever comes firstOverall Response Rate/ORR is defined as the percent of participants who achieve Complete Response/CR or Primary Response/PR

Outcomes1

Each outcome the trial posted results for, in ClinicalTrials.gov's words.

TypeOutcomeTime framePopulationUnitsMeasured as
PRIMARYOverall Response Rate/ORRcompletion of 12 cycles of treatment (each cycle is 28 days) or at treatment discontinuation, whichever comes firstParticipantsCOUNT_OF_PARTICIPANTS

Results by group2

Each measurement the trial posted, group by group, in the words and numbers it posted.

OutcomeGroupCategoryValueSpreadUnits
Overall Response Rate/ORRParticipants With Mantle Cell LymphomaParticipants with response1Participants
Overall Response Rate/ORRParticipants With Mantle Cell LymphomaParticipants without response3Participants

Participant flow3

How many started, completed or left each group, period by period.

PeriodMilestoneGroupParticipantsUnits counted
Overall StudySTARTEDParticipants With Mantle Cell Lymphoma4
Overall StudyCOMPLETEDParticipants With Mantle Cell Lymphoma1
Overall StudyNOT COMPLETEDParticipants With Mantle Cell Lymphoma3

Adverse events20

Each adverse event the trial posted, group by group: the participants affected out of those at risk.

TypeEventOrgan systemGroupAffectedAt riskEvents
otherAnemiaBlood and lymphatic system disordersParticipants With Mantle Cell Lymphoma14
otherFatigueGeneral disordersParticipants With Mantle Cell Lymphoma14
otherInfusion related reactionInjury, poisoning and procedural complicationsParticipants With Mantle Cell Lymphoma14
otherNauseaGastrointestinal disordersParticipants With Mantle Cell Lymphoma14
otherCreatinine increasedInvestigationsParticipants With Mantle Cell Lymphoma14
otherPlatelet count decreasedInvestigationsParticipants With Mantle Cell Lymphoma14
otherDysphagiaGastrointestinal disordersParticipants With Mantle Cell Lymphoma14
otherEdema faceGeneral disordersParticipants With Mantle Cell Lymphoma14
otherGeneralized muscle weaknessMusculoskeletal and connective tissue disordersParticipants With Mantle Cell Lymphoma14
otherRash maculo-papularSkin and subcutaneous tissue disordersParticipants With Mantle Cell Lymphoma14

Adverse event totals3

The totals the trial posted for each group.

TotalGroupAffectedAt risk
Total, all-cause mortalityParticipants With Mantle Cell Lymphoma44
Total, other adverse eventsParticipants With Mantle Cell Lymphoma44
Total, serious adverse eventsParticipants With Mantle Cell Lymphoma44

Papers0

The papers the trial lists on ClinicalTrials.gov.

None in this release.

Grants0

The grants NIH RePORTER links to the trial, newest funded first: NIH's, and some of AHRQ's, CDC's, FDA's and VA's. Each shows its title, principal investigators, organization and funder in its newest year.

None in this release.

Trial comparisons0

Comparisons of the trial's two groups, calculated by ConductScience from the counts it posted.

None in this release.

Tests0

The ConductCognition tests this trial's registered outcomes name, as ScienceGraph matched them in trial-tests-2026-11-12-0.2.1.

None in this release.

Data dates

The day each source was copied for this release.

ClinicalTrials.gov
2026-11-12
ClinicalTrials.gov
Results, from AACT
2026-03-23
AACT
NIH grant links
2026-11-13
NIH RePORTER

Sources 3

  • ClinicalTrials.gov's posted results, through CTTI's AACTFreely available. Acknowledgement requested
  • ClinicalTrials.govNo license stated
  • NIH RePORTER's clinical studies and project filesPublic domain
Each source's terms
  • ClinicalTrials.gov's posted results, through CTTI's AACTClinicalTrials.gov data via Aggregate Analysis of ClinicalTrials.gov (AACT), CTTI. CTTI makes its materials freely available and requests acknowledgement. https://aact.ctti-clinicaltrials.org/documentation/299
  • ClinicalTrials.govnone stated
  • NIH RePORTER's clinical studies and project filesPublic domain (NIH RePORTER)

ClinicalTrials.gov's data carry an international copyright outside the United States: https://clinicaltrials.gov/about-site/terms-conditions.

For software

Read this trial from software.

The record and each of its lists are JSON, twenty rows a page. No key.

GET https://conductscience.org/api/trials/v1/NCT05788289

GET https://conductscience.org/api/trials/v1/NCT05788289/registered