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Recruiting NCT05259553

NCT05259553 Biomarkers in Multiple Myeloma

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Clinical Trial Summary
NCT ID NCT05259553
Status Recruiting
Phase
Sponsor Centre Hospitalier Universitaire de Saint Etienne
Condition Hematological Patients
Study Type INTERVENTIONAL
Enrollment 70 participants
Start Date 2022-05-20
Primary Completion 2025-10-30

Eligibility & Interventions

Sex All sexes
Min Age 18 Years
Max Age N/A
Study Type INTERVENTIONAL
Interventions
Blood samples

Eligibility Fast-Check

Enter your details for a quick preliminary check. This does not replace medical advice.

What to Expect as a Participant

You will actively receive the study intervention — which may be a drug, biologic, device, or procedure.

This trial targets 70 participants in total. It began in 2022-05-20 with a primary completion date of 2025-10-30.

⚠ This information is for research awareness only. Always consult your physician before joining any clinical trial. Participation is voluntary and you may withdraw at any time.

Brief Summary

The association between multiple myeloma (MM) and venous thromboembolism (VTE) is well known. Indeed, the incidence of VTE is increased in patients with newly diagnosed MM and in patients treated by immunomodulatory drugs in combination with glucocorticoids. Moreover, the clinical outcome of MM is supposed to be correlated to the risk of thrombosis. At the biological level, a number of hemostasis abnormalities participate in increasing VTE incidence. Yet, data on predictive biomarkers linked to VTE are limited.

Eligibility Criteria

Inclusion Criteria: * Patient affiliated to a social security regimen or beneficiary of the same * Signed written informed consent form * Confirmed diagnosis of de novo multiple myeloma, non-previously treated and requiring treatment. Exclusion Criteria: * Pregnant women * Patient under guardianship or deprived of his liberty or any condition that may affect the patient's ability to understand and sign the informed consent * Refusing participation * Patient whose follow-up or life expectancy is less than 6 months.

Contact & Investigator

Central Contact

Emilie Chalayer, MD

✉ emilie.chalayer@chu-st-etienne.fr

📞 04 77 91 70 00

Principal Investigator

Emilie Chalayer, MD

PRINCIPAL INVESTIGATOR

CHU de Saint-Etienne

Frequently Asked Questions

Who can join the NCT05259553 clinical trial?

This trial is open to participants of all sexes, aged 18 Years or older, studying Hematological Patients. Full inclusion and exclusion criteria are listed in the Eligibility Criteria section. Always confirm your eligibility with the research team before applying.

Is NCT05259553 currently recruiting?

Yes, NCT05259553 is actively recruiting participants. Contact the research team at emilie.chalayer@chu-st-etienne.fr for enrollment information.

Where is the NCT05259553 trial being conducted?

This trial is being conducted at Lyon, France, Saint-Etienne, France.

Who is sponsoring the NCT05259553 clinical trial?

NCT05259553 is sponsored by Centre Hospitalier Universitaire de Saint Etienne. The principal investigator is Emilie Chalayer, MD at CHU de Saint-Etienne. The trial plans to enroll 70 participants.

ClinicalMetric — Independent clinical trial intelligence platform. Not affiliated with NIH, ClinicalTrials.gov, the U.S. FDA, or any pharmaceutical company, hospital, or clinical research organization. Trial data is sourced from ClinicalTrials.gov for informational purposes only and does not constitute medical advice. Do not make any treatment, enrollment, or health decisions based solely on information found here — always consult a qualified healthcare professional. Full Disclaimer  ·  Last Reviewed: April 2026  ·  Data Methodology