Real-World data may reveal how well tafasitamab fights Hard-to-Treat lymphoma
NCT ID NCT07709624
First seen Jul 16, 2026 · Last updated Jul 17, 2026 · Updated 1 time
Summary
This study looks at how well the drug tafasitamab works in adults with diffuse large B-cell lymphoma (DLBCL) that has come back or not responded to previous treatment. Researchers will collect real-world data from 50 patients who are not eligible for a stem cell transplant. The main goal is to see how many patients achieve a complete or partial response to the drug.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- tafasitamab
- What this could lead to
- If successful, this study could confirm tafasitamab's effectiveness in a broader, real-world population of DLBCL patients who cannot have a stem cell transplant.
- What could go wrong
- This is an observational study, not a controlled trial, so results may be influenced by patient selection or other treatments. The small size (50 patients) limits how widely findings can be applied.
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.
- Participants
-
About 50 people
The number the study aims to enrol. It can still change while the study runs.
- Started
-
Dec 2025
- Expected to finish
-
Dec 2030
An estimate. End dates often move.
- Lead sponsor
-
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.
Who is studied
R/R DLBCL who are ineligible for ASCT
- Ages
-
18 years and older
- Sex
-
Anyone
- Healthy volunteers
-
Not accepted
This study is not open to healthy volunteers. The entry requirements below say who it is open to.
Show the full entry requirements Hide the full entry requirements
Copied word for word from the study's registry entry, so the wording is the study team's rather than ours.
Inclusion Criteria: 1. Adult patients aged ≥18 years at the time of tafasitamab initiation. 2. Patients who were initiated on tafasitamab treatment between August 1, 2024, and December 31, 2028. 3. Patients with a histologically confirmed diagnosis of DLBCL. 4. Patients ineligible for ASCT based on clinical judgment, comorbidities, or other relevant factors. 5. Patients must have relapsed or refractory disease following at least one prior systemic regimen for DLBCL, with at least one line of therapy including a CD20-targeted agent (e.g., rituximab). Exclusion Criteria: 1\. Patients who are alive but unable or unwilling to provide written informed consent. \-
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for DLBCL are added.
By submitting, you agree to our Terms of use
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
-
Tty Biopharm
Taipei, Taiwan
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can a targeted drug boost the power of stem cell transplants for tough lymphoma?
- Can a targeted pill boost Chemotherapy's punch against lymphoma?
- Off-the-Shelf immune cells take on tough lymphoma
- New cocktail aims to tame aggressive lymphoma in the very elderly
- New hope for aggressive lymphoma: triple-drug combo enters human trials
- New drug cocktail aims to tackle tough lymphoma