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A Phase I Study to Assess The Safety and Pharmacokinetics of BB-10901 (huN901-DM1) Given as an Intravenous Infusion Weekly for Two Consecutive Weeks Every Three Weeks to Subjects With Relapsed and Relapsed Refractory CD56-Positive Multiple Myeloma.

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A Phase I Study to Assess The Safety and Pharmacokinetics of BB-10901 (huN901-DM1) Given as an Intravenous Infusion Weekly for Two Consecutive Weeks Every Three Weeks to Subjects With Relapsed and Relapsed Refractory CD56-Positive Multiple Myeloma.

Status: Completed
Phase of Trial: Phase I

Latest Information Update: 03 Nov 2021

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At a glance

  • Drugs Lorvotuzumab mertansine (Primary)
  • Indications Multiple myeloma
  • Focus Adverse reactions

    • Most Recent Events

    • 21 Mar 2011 Actual end date (Mar 2011) added as reported by ClinicalTrials.gov.
    • 21 Mar 2011 Actual end date (Mar 2011) added as reported by ClinicalTrials.gov.
    • 21 Mar 2011 Status changed from recruiting to completed as reported by ClinicalTrials.gov.

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