Trials / Completed
CompletedNCT00874978
The Efficacy and Safety of Lenalidomide Monotherapy in Red Blood Cell Transfusion Dependent Subjects With Myelodysplastic Syndrome (MDS) Associated With Del (5q) Abnormality
The Efficacy and Safety of Lenalidomide (Revlimid®) Monotherapy in Red Blood Cell Transfusion Dependent Subjects With Myelodysplastic Syndrome Associated With Del (5q) Cytogenetic Abnormality
- Status
- Completed
- Phase
- Phase 2
- Study type
- Interventional
- Enrollment
- 36 (estimated)
- Sponsor
- King's College Hospital NHS Trust · Academic / Other
- Sex
- All
- Age
- 18 Years
- Healthy volunteers
- Not accepted
Summary
The purpose of this study is to evaluate the efficacy of lenalidomide treatments to achieve haematopoietic improvement in subjects with low- or intermediate-1 risk International Prognostic Scoring System1 (IPSS) myelodysplastic syndrome (MDS) associated with a del (5q31-33) cytogenetic abnormality.
Conditions
Interventions
| Type | Name | Description |
|---|---|---|
| DRUG | lenalidomide | Oral lenalidomide 10mg (two 5mg capsules) daily on days 1-21 every 28 days for up to 6 cycles. |
Timeline
- Start date
- 2005-01-01
- Primary completion
- 2016-05-01
- Completion
- 2016-05-01
- First posted
- 2009-04-03
- Last updated
- 2019-02-27
Locations
1 site across 1 country: United Kingdom
Source: ClinicalTrials.gov record NCT00874978. Inclusion in this directory is not an endorsement.