Trial · NCT04974216
Study of Tafasitamab and Lenalinomide Associated to Rituximab in Frontline Diffuse Large B-Cell Lymphoma Patients of 80 y/o or Older
NCT04974216, Phase 2, Active not recruiting, The Lymphoma Academic Research Organisation
3 sourcestrials-2026-11-12-0.5.0
Cite this record
ConductScience Library. Study of Tafasitamab and Lenalinomide Associated to Rituximab in Frontline Diffuse Large B-Cell Lymphoma Patients of 80 y/o or Older. Trials, record NCT04974216. Release trials-2026-11-12-0.5.0, 12 Nov 2026. https://conductscience.org/library/trials/NCT04974216
On this page
Trial
As registered on ClinicalTrials.gov, in the graph's capture of the registry.
- Title
- Study of Tafasitamab and Lenalinomide Associated to Rituximab in Frontline Diffuse Large B-Cell Lymphoma Patients of 80 y/o or Older
- NCT number
- NCT04974216
- Status
- Active not recruiting
- Phases
- Phase 2
- Enrollment
- 71 participants, actual
- Lead sponsor
- The Lymphoma Academic Research Organisation
- Conditions
- DLBCL
- Interventions
- Tafasitamab, Lenalidomide, Rituximab
- First posted
- 2021-07-23
- Last updated
- 2026-06-04
Source ClinicalTrials.gov
Registered outcomes18
Each outcome the trial registered, primary first, in ClinicalTrials.gov's words.
| List | Outcome | Time frame | Description |
|---|---|---|---|
| Primary | Overall Response Rate (ORR) by local assessment | 3 months (3 cycles of 28 days) | LOCAL ASSESSMENT : Complete Metabolic Response + Partial Metabolic Response based according to Lugano Response Criteria |
| Secondary | Number of Serious Adverse Events (SAE) of patients treated with lenalidomide and tafasitamab | 13 months | |
| Secondary | Number of SAE of patients who switched to RminiCHOP | 7 months | |
| Secondary | Progression free survival (PFS) | 2 years | |
| Secondary | Overall survival (OS) | 2 years | |
| Secondary | Overall Response Rate (ORR) by central assessment | 3 months (3 cycles of 28 days) | CENTRAL ASSESSMENT : Complete Metabolic Response + Partial Metabolic Response based according to Lugano Response Criteria |
| Secondary | Complete Metabolic Response (CMR) by local assessment | 3 months (3 cycles of 28 days) | LOCAL ASSESSMENT |
| Secondary | Complete Metabolic Response (CMR) by central assessment | 3 months (3 cycles of 28 days) | CENTRAL ASSESSMENT |
| Secondary | Complete Metabolic Response (CMR) by local assessment | 6 months (6 cycles of 28 days) | LOCAL ASSESSMENT |
| Secondary | Complete Metabolic Response (CMR) by central assessment | 6 months (6 cycles of 28 days) | CENTRAL ASSESSMENT |
1 to 10 of 18Source ClinicalTrials.gov
See all 18 registered outcomesOutcomes0
Each outcome the trial posted results for, in ClinicalTrials.gov's words.
None in this release.
Results by group0
Each measurement the trial posted, group by group, in the words and numbers it posted.
None in this release.
Participant flow0
How many started, completed or left each group, period by period.
None in this release.
Adverse events0
Each adverse event the trial posted, group by group: the participants affected out of those at risk.
None in this release.
Adverse event totals0
The totals the trial posted for each group.
None in this release.
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.
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/NCT04974216
GET https://conductscience.org/api/trials/v1/NCT04974216/registered