NCT02921802

A Study of Special Use Results Surveillance of Revlimid 5mg Capsules

Revlimid 5 mg Capsules Special Use-results Surveillance (All-case Surveillance)

• Status: Completed
• Phase: —
• Study type: Observational
• Enrollment: 4,626 (actual)
• Sponsor: Celgene · Industry
• Sex: All
• Age: 18 Years
• Healthy volunteers: Not accepted

Summary

To understand the safety and efficacy of Revlimid® 5 mg Capsules (hereinafter referred to as Revlimid) in all patients who are treated with it under the actual condition of use pursuant to the conditions of approval. 1. Planned registration period This period started on the date of initial marketing of Revlimid and will end at the time when the planned number of patients to be enrolled is reached. 2. Planned surveillance period This period started on the date of initial marketing of Revlimid and will end on the day when the approval condition related to all-case surveillance is terminated.

Conditions

• Multiple Myeloma
• Myelodysplastic Syndromes

Timeline

• Start date: 2010-07-20
• Primary completion: 2013-03-29
• Completion: 2013-03-29
• First posted: 2016-10-03
• Last updated: 2022-06-14

Locations

1 site across 1 country: Japan