Clinical trial NCT06282978 - References

Multiple Myeloma in Relapse — Study of Elranatamab for Relapsed or Refractory Myeloma in Patients Previously Exposed to Three-drug Classes

Citation(s)

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•   European Medicines Agency
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•   European Medicines Agency
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•   European Medicines Agency
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•   European Medicines Agency
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•   European Medicines Agency
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•   Food and Drug Administration
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•   Food and Drug Administration
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•   Pfizer
  PF-06863135 As Single Agent And In Combination With Immunomodulatory Agents In Relapse/Refractory Multiple Myeloma. ClinicalTrials.gov Identifier: NCT03269136. Updated July 11, 2022. Accessed September 17, 2022. https://clinicaltrials.gov/ct2/show/NCT03269136 . 2022.
•   Pfizer
  Pfizer Presents First Data from Planned Interim Analysis of Pivotal Phase 2 MagnetisMM-3 Trial of BCMA-CD3 Bispecific Antibody Elranatamab Under Investigation for Relapsed/Refractory Multiple Myeloma. Press release available at: https://www.pfizer.com/news/press-release/press-release-detail/pfizer-presents-first-data-plann ed-interim-analysis-pivotal . 2022.
•   Pfizer
  Pfizer Presents Updated Favorable Elranatamab Data from Pivotal Phase 2 MagnetisMM-3 Trial. Press release available at: https://www.pfizer.com/news/press-release/press-release-detail/pfizer-presents-updated-favora ble-elranatamab-data-pivotal . 2022.
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An Open Label, Multicenter, Phase II Study of Elranatamab as Single Agent for the Treatment of Relapsed or Refractory Myeloma in Patients Previously Exposed to Three-drug Classes (GEM-RANTAB)

Details for clinical trial NCT06282978