Skip to content

Targeting IRAK4 in Chronic Lymphocytic Leukemia

Targeting IRAK4 in Chronic Lymphocytic Leukemia

Status
Not yet recruiting
Phases
Unknown
Study type
Observational
Source
ClinicalTrials.gov
Registry ID
NCT07741695
Acronym
PS-CLL016
Enrollment
50
Registered
2026-08-03
Start date
2026-09-01
Completion date
2027-09-01
Last updated
2026-08-04

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Chronic Lymphocytic Leukemia (CLL)

Keywords

chronic lymphocytic leukemia, IRAK4

Brief summary

Patients with chronic lymphocytic leukemia (CLL) followed at Strategic Research Program on CLL will be enrolled and undergo sampling of additional amount of blood at the time of standard blood tests. Leukemic B cells and peripheral blood mononuclear cells (PBMC).

Detailed description

Patients with chronic lymphocytic leukemia (CLL) followed at Strategic Research Program on CLL will be enrolled and undergo sampling of additional amount of blood at the time of standard blood tests. Leukemic B cells and peripheral blood mononuclear cells (PBMC). Up to 50 ml of blood will be collected for the research project at the time of standard blood tests.

Interventions

Up to 50 ml of blood will be collected for the research project at the time of standard blood tests.

Sponsors

IRCCS San Raffaele
Lead SponsorOTHER

Study design

Observational model
COHORT
Time perspective
PROSPECTIVE

Eligibility

Sex/Gender
ALL
Age
18 Years to No maximum
Healthy volunteers
No

Inclusion criteria

* Age ≥18 years * Diagnosis of CLL * Participant is willing and able to give informed consent for participation in the study.

Exclusion criteria

\- Participant is unable or unwilling to provide informed consent for participation in the study

Design outcomes

Primary

MeasureTime frameDescription
TLR signaling12 monthsIn vitro inhibition of TLR signaling in CLL cells following exposure to IRAK4 CDAC, as assessed by modulation of downstream signaling molecules (e.g. phosphorylation status and/or degradation of key components of the TLR pathway).

Contacts

CONTACTPaolo Ghia, MD, PhD
ghia.paolo@hsr.it+390226434797
CONTACTLydia Scarfo, MD
scarfo.lydia@hsr.it+390226436119

Outcome results

None listed

Source: ClinicalTrials.gov · Data processed: Aug 5, 2026