Post-authorisation Study of Biological Relapse in Patients With Multiple Myeloma

NCT02394210 · Status: TERMINATED · Type: OBSERVATIONAL · Enrollment: 415

Last updated 2021-09-14

No results posted yet for this study

Summary

Post-authorisation prospective follow-up study to assess the clinical impact on time to progression (TTP) from the start of anti- multiple myeloma treatment at the onset of asymptomatic relapse/biological progression versus start of treatment at the time of symptomatic relapse.

Conditions

Sponsors & Collaborators

  • Celgene

    lead INDUSTRY

Principal Investigators

  • Mireya Navarro, MD · Celgene

Eligibility

Min Age
18 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2013-05-14
Primary Completion
2021-05-18
Completion
2021-05-18

Countries

  • Spain

Study Locations

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Entities

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT02394210 on ClinicalTrials.gov