CompletedPhase 2NCT00660231
Gemcitabine and Bexarotene in Treating Patients With Progressive or Refractory Stage IB, Stage II, Stage III, or Stage IV Cutaneous T-cell Non-Hodgkin Lymphoma
Studying Aggressive primary cutaneous T-cell 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
- University College, London
- Principal Investigator
- Tim IllidgeThe Christie NHS Foundation Trust
- Intervention
- bexarotene(drug)
- Enrollment
- 36 enrolled
- Eligibility
- 18 years · All sexes
- Timeline
- 2008 – 2014
Study locations (7)
- Leeds Cancer Centre at St. James's University Hospital, Leeds, England, United Kingdom
- Saint Bartholomew's Hospital, London, England, United Kingdom
- St. Thomas' Hospital, London, England, United Kingdom
- Christie Hospital, Manchester, England, United Kingdom
- Southampton General Hospital, Southampton, England, United Kingdom
- Royal Cornwall Hospital, Truro, England, United Kingdom
- Edinburgh Cancer Centre at Western General Hospital, Edinburgh, Scotland, United Kingdom
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.
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