JPRN-jRCT2080220654UnknownPhase 1
Phase I, open label, dose ascending study of BCX1777 (oral) in patients with recurrent or refractory T/NK-cell malignancies
Mundipharma K.K.0 sites24 target enrollmentStarted: January 8, 2009Last updated:
Conditions
Trial Snapshot
- Phase
- Phase 1
- Sponsor
- Enrollment
- 24
Study Overview
Brief Summary
No summary available.
Study Design
- Study Type
- Interventional
Eligibility Criteria
- Ages
- >= 20age old to ot applicable (—)
- Sex
- All
Inclusion Criteria
- •Inclusion Criteria (excerpted)
- •- Histologically documented with histopathological diagnosis from biopsy, T/NK-cell malignancies (WHO classification). Precursor T-cell lymphoblastic leukemia/lymphoma (T-ALL/T-LBL) should be excluded in this study
- •- A patient with recurrent, relapse or refractory T/NK-cekk malignancies who has received at lease one chemotherapeutic regimen
Exclusion Criteria
- •Exclusion criteria (excerpted)
- •- Pregnant, breast-feeding female, female with a possibility of becoming pregnant (fertile female; in the case of female before menopause or within a year from menopause, the patient sho is positive in the pregnancy test conducted within 14 days before the start of administration), or male and fertile female unwilling to practice appropriate contraception during the 2 mounths after the final administration.
- •- Active serious infection not controlled by oral or intravenous antibiotics.
Investigators
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