Targeting IRAK4 in Chronic Lymphocytic Leukemia

Trial statusNot yet recruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorIRCCS San Raffaele

About this trial

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).

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Age ≥18 years

Diagnosis of CLL

Participant is willing and able to give informed consent for participation in the study.

Disqualifiers

None

Trial population

Adult patients with CLL followed at Strategic Research Program on CLL

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

  • Peripheral blood sample collection

    Procedure/Surgery

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

Treatment groups

50 Participants
are divided into 1 treatment group
Group A: Study cohort1 intervention

Trial outcomes

Primary outcomes

1

TLR signaling

In 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).

Time frame
12 months

Secondary outcomes

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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