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Clinical Trials/JPRN-jRCT2080220654
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

Sponsor
Mundipharma K.K.

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