Validation of a Platelet Proteomic Assay for Diagnosing and Monitoring Prostate Cancer

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexMale
Age40+
SponsorDuke University

About this trial

This is a single center study evaluating whether a new blood test based on platelet proteins rather than plasma proteins can improve detection of prostate cancer and evaluate the degree of serious disease. Currently, doctors rely on multiple tests such as PSA, MRI scans and biopsies to do the same evaluation. Researchers are trying to see if HeLP™ can be a safe and accurate alternative.

The study is inviting men who are being seen for suspicion of prostate cancer (based on symptoms or previous lab results). If they agree to be in the study, the research team will take a sample of their blood at the time they are getting a repeat PSA test or having Imaging. The research test does not affect the care they are already receiving and takes 3 extra tubes of blood (\~3 tbsp).

The research team is aiming to include 300 participants total. They believe 278 people are needed to confidently compare results between people with and without prostate cancer.

They will do an interim analysis halfway through the study, once samples from 150 subjects have been collected.

The research is considered low risk-no more uncomfortable or dangerous than a blood draw. There is a risk of loss of privacy, but researchers are taking strong steps to protect privileged information. That includes proper data handling, secure, storage, and making sure the study team is trained in research ethics.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients ≥ 40 years of age

All patients with suspicion of PCa

Disqualifiers

Men who have previously undergone treatment for prostate cancer.

Men with prior diagnosis of prostate cancer.

Men with severe, irreversible coagulopathy.

Men on anticoagulant therapies or those who have taken antiplatelet agents such as aspirin, NSAIDs (ibuprofen, entrophen, naproxen, diclofenac etc), clopidrogel, prasugrel, ticagrelor, or dipyridamole in the 7 days preceding blood collection.

Trial population

All subjects meeting eligibility criteria will be offered participation in this research study. The study is not relevant to women. The terminally ill subjects, students, children or volunteers-will not be included.

Trial design

Design model

Case-only

Time perspective

Prospective

Treatments tested in this trial

  • HeLP TM

    Device

    lab test for prostate cancer

Treatment groups

300 Participants
are divided into 2 treatment groups
Group A: Control Group1 intervention
Group B: Case Group1 intervention

Trial outcomes

Primary outcomes

1

Levels of HeLP™ proteins in the platelets of patients suspected to have PCa

Researchers will define the levels of HeLP™ proteins in the platelets of patients suspected to have PCa based on assessment within Duke Health compared to standard of care like PSA, mpMRI PI-RADS and other biomarkers (if available).

Time frame
Baseline
2

Diagnostic accuracy as reported by area under the curve (AUC)

Overall diagnostic accuracy of clinical variables including PSA, PI-RADS scoring, Hessian Map and other biomarkers (if available) will be determined and compared using receiving operating curve/area under curve analysis.

Time frame
Baseline

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Duke University

Lead sponsor

Hessian Labs Inc

Collaborator