Polycythemia Vera Clinical Trials

Find Polycythemia Vera Clinical Trials Near You

A New Diagnostic Algorithm to Non-invasively Track Fibrotic Changes in Myeloproliferative Neoplasms Based on C-C Chemokine Receptor 2 Detection. From Flow Cytometry to the Development of Targeted Positron Emission Tomography Molecular Imaging. Pre-clinical Studies and First In-human Proof of Concept

Status: Recruiting
Location: See location...
Intervention Type: Diagnostic test
Study Type: Interventional
Study Phase: Not Applicable
SUMMARY

Chronic Philadelphia-negative myeloproliferative syndromes are chronic blood disorders. They include essential thrombocythemia, polycythemia vera, and myelofibrosis. Myelofibrosis may arise de novo (primary myelofibrosis) or represent the evolution of essential thrombocythemia or polycythemia vera (secondary myelofibrosis). The myelofibrotic stage-characterized, as the name implies, by the presence of bone marrow fibrosis (deposition of scar-like tissue)-is generally associated with a more severe and symptomatic disease. To date, the only way to assess fibrotic progression in these disorders is bone marrow biopsy. The aim of this project is to evaluate whether the identification, tracking, and quantification of cells expressing a specific receptor (CCR2), a selective biomarker of fibrosis, may allow early and non-invasive identification of the fibrotic stage of the disease through: * laboratory analysis on a blood sample (using flow cytometry) * use in PET-CT (positron emission tomography combined with computed tomography) of a tracer specific for the CCR2 receptor, capable of selectively binding to CCR2-expressing cells (⁶⁸Ga-DOTA-ECL1i).

Eligibility
Participation Requirements
Sex: All
Minimum Age: 18
Healthy Volunteers: f
View:

• Diagnosis of ET/PV/prePMF/overtPMF according to the WHO 2016 criteria and of SMF according to the IWG-MRT criteria (with histopathological data).

• Age \>= 18 yrs

• ECOG performance status \<=3

Locations
Other Locations
Italy
Dipartimento di Medicina e Chirurgia
RECRUITING
Parma
Contact Information
Primary
Elena Masselli, MD, PhD
elena.masselli@unipr.it
+39 0521 906655
Time Frame
Start Date: 2023-09-05
Estimated Completion Date: 2027-04-30
Participants
Target number of participants: 265
Treatments
Experimental: MPN subtypes
Patient will be tested for CCR2 expression on CD34+ cells in order to correlate imaging and flow-cytometry data.
Sponsors
Leads: Azienda Ospedaliero-Universitaria di Parma

This content was sourced from clinicaltrials.gov