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  • Myeloma and AL Amyloidosis
    • About myeloma
    • About AL amyloidosis
  • What we do
      • Member and patient community programmes
        • Myeloma Awareness Month 2025
        • 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)
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Category: MPE

MPE Publishes 2021: Year in Review
MPEFebruary 9, 2022
Myeloma Patients Europe appoints joint CEOs
MPEMarch 27, 2023
CAR T interviews 768x432 1
Horizon2020 CARAMBA CAR-T interview series
MPEJune 15, 2023
2023: Year in Review
MPEDecember 4, 2023
Join MPE’s webinar on Access Barriers to Clinical Trials in CEE Countries
Access, MPEOctober 20, 2022
Anxiety, depression and quality of life tied to caregivers’ coping mechanisms
MPENovember 21, 2022
MPE appointed to new HTA Stakeholder Network
MPEMay 10, 2023
MPE attending International Myeloma Society (IMS) Annual Meeting in Athens
MPESeptember 25, 2023
EMA CHMP gives positive recommendation to elranatamab for the treatment of relapsed or refractory myeloma
Access, MPE, MyelomaOctober 13, 2023
ESMO 2023 | Patient Advocacy Track highlights challenges in access, caregiver support and digitalisation
Conferences, MPEOctober 27, 2023
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  • Myeloma and AL Amyloidosis
    • About myeloma
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    • Member and patient community programmes
      • Myeloma Awareness Month 2025
      • MPE Masterclass
      • 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
      • Horizon Europe
      • IMI
    • Access and Policy
      • Myeloma Access Atlas
      • CEE workgroup on Access
      • Myeloma and AL amyloidosis Clinical Trial Navigator
      • EU HTA regulation
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