Can 3D-Printed models unlock personalized blood cancer therapies?
NCT ID NCT07759661
First seen Aug 12, 2026 · Last updated Aug 14, 2026 · Updated 2 times
Summary
This study aims to create 3D models of B-cell cancers—like chronic lymphocytic leukemia, splenic marginal-zone lymphoma, and hairy cell leukemia—using blood samples from patients. The goal is to build realistic models that mimic the tumor environment, which could help researchers test and personalize treatments. Adults with these conditions who are receiving standard care may participate by donating extra blood during routine draws.
What this could mean
Our plain-language read of the trial. This is informational only, not medical advice or a prediction.
- Active substance
- Patient-derived 3D bioprinted models
- What this could lead to
- If successful, this could lead to more personalized and effective treatments for B-cell cancers like CLL, SMZL, and HCL.
- What could go wrong
- This is an early-stage laboratory study, so the models may not perfectly mimic real patient responses, and results may not directly translate to new treatments.
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 64 people
The number the study aims to enrol. It can still change while the study runs.
- Expected to start
-
Nov 2026
An estimate. Start dates often move.
- Expected to finish
-
Nov 2029
An estimate. End dates often move.
- Lead sponsor
-
Other sponsor
The registry's catch-all category, for sponsors it does not file as a company, a government agency, or a research network.
Who can take part
This study's own entry requirements. Only the study team can say for certain whether you qualify.
Who is studied
Adult patients with CLL, SMZL, HCL followed at participating clinical sites
- 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: * Age ≥18 years * Diagnosis of CLL, SMZL or HCL * Participant is willing and able to autonomously give informed consent for participation in the study. Exclusion Criteria: \- Participant is unable or unwilling to provide informed consent for participation in the study
Get updates
Get notified about this study
Sign up to get updates when this study changes or when new studies for Chronic lymphocytic leukemia (CLL) are added.
Genom att skicka in godkänner du våra Användarvillkor
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.
How to take part
Only the study team decides who joins. These are the ways to reach them.
-
The places running it
1 site. The list below names each one and where it is.
-
The official record
ClinicalTrials.gov lists the study team's own contact details, including names and phone numbers. We don't republish those.
-
A doctor treating you
A doctor who knows your case can contact a study site on your behalf, and can tell you whether this study is worth pursuing at all.
Contacts and locations
Locations
-
IRCCS Ospedale San Raffaele
Milan, MI, 20132, Italy
More trials for these conditions
Other studies related to the condition(s) this trial covers.
- Can a bispecific antibody wipe out residual leukemia cells in High-Risk CLL?
- Can a Two-Drug combo keep CLL at bay for years? a 10-Year watch begins
- Could a protein blocker quiet Leukemia's alarm system?
- Supercharged immune cells take aim at cancer and viruses in one shot
- Leukemia drug study probes thinking and memory side effects
- Smart blood pressure cuffs could protect cancer patients from heart risks