CompletedPhase 1NCT01169298
A Phase I, Multicenter, Open-label, Dose-escalation Study to Assess the Safety of Lenalidomide in Patients With Advanced Adult T-cell Leukemia-lymphoma and Peripheral T-cell Lymphomaperipheral T-cell Lymphoma
Studying Adult T-cell leukemia/lymphoma
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Celgene
- Principal Investigator
- Hiroya Asou, MD, MDCelgene KK
- Intervention
- Lenalidomide(drug)
- Enrollment
- 13 enrolled
- Eligibility
- 20 years · All sexes
- Timeline
- 2010 – 2013
Study locations (6)
- National Kyusyu Cancer Center, Fukuoka, Japan
- Imamura Bun-in Hospital, Kagoshima, Japan
- Kumamoto University Hospital, Kumamoto, Japan
- Nagasaki University Hospital, Nagasaki, Japan
- Nagoya Daini Red Cross Hospital, Nagoya, Japan
- National Cancer Center Hospital, Tokyo, Japan
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT01169298 on ClinicalTrials.govOther trials for Adult T-cell leukemia/lymphoma
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