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logo MPE
  • Myeloma and AL Amyloidosis
    • About myeloma
    • About AL amyloidosis
  • What we do
      • Member and patient community programmes
        • Myeloma Awareness Month
        • MPE Masterclass
        • Scholarship programme
        • Myeloma CABs
        • MPE Myeloma and AL amyloidosis Community Taskforce
        • Advocate Development Programme
        • European Young Myeloma Patients Group
        • Reasonable Agreements between Patient Advocates and Pharmaceutical Companies (RAPP)
      • Research
        • Patient Evidence
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Solène Clavreul Head of Medical Education and Scientific Engagement at Myeloma Patients Europe MPE

SOLÈNE CLAVREUL

Solène is Head of Medical Education and Scientific Engagement. She joined the team in January 2021.

Solène holds a PhD in Neuroscience and a Master of Biology and Physiology from Sorbonne University (Paris). She studied brain development during her PhD and then worked on brain cellular diversity as a researcher at the Helmholtz Zentrum München (Germany). Early involved in education, she has been leading holiday camps for children for many years and worked in a science museum during her studies to promote science, design exhibitions and lead workshops.

Interested in science policy and particularly in the health field, she trained herself in European policy implementation, clinical data management and industrial pharma management before joining MPE.
Solène comes from France and currently lives and works in Munich, Germany. She speaks French, English and German.

Recent Posts

AELCLES report cover

AELCLÉS presents report highlighting the high socioeconomic impact of oncohaematological diseases in Spain

19 February 2026

More than 65 per cent of people living with an oncohaematological disease experience a deterioration in their employment and financial situation. This is one of the key findings of a…

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150 patients, clinicians and advocates gathered in Warsaw for a landmark hemato-oncology forum

4 February 2026

On 13–14 December in Warsaw, the Carita Foundation hosted its Hemato-Oncology Patient Forum, bringing together 150 participants including patients, clinicians, pharmaceutical representatives and volunteers.  The event marked the 15th anniversary…

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MPE response to EMA consultation on their “Reflection paper on patient experience data (PED)”

3 February 2026

Last week Myeloma Patients Europe (MPE) submitted a response to the European Medicines Agency (EMA) open consultation on their “Reflection paper on patient experience data (PED)”. PED refers to data…

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Share your treatment experience, help shape the future of myeloma care

3 February 2026

Myeloma patients may receive many different treatments throughout their care. Patients’ real-world experiences of treatments tell us how treatments work in everyday life. Myeloma Patients Europe (MPE) wants to hear…

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US Food and Drug Administration (FDA) issues draft guidance on minimal residual disease

28 January 2026

The US Food and Drug Administration (FDA) has issued draft guidance to the pharmaceutical industry on using minimal residual disease (MRD) and complete response (CR) in myeloma clinical trials as…

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Dr. Charlotte Pawlyn

ASH 2025 summary video interviews

12 December 2025

The largest haematology meeting in the world has just finished. The American Society of Hematology (ASH) Annual Congress took place in Orlando, Florida, US, where the latest research in blood…

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      • Scholarship programme
      • Myeloma CABs
      • MPE Myeloma and AL amyloidosis Community Taskforce
      • Advocate Development Programme
      • Reasonable Agreements between Patient Advocates and Pharmaceutical Companies (RAPP)
      • European Young Myeloma Patients Group
    • Research
      • Patient Evidence
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