A Study for Participants With Relapsed Cutaneous T-Cell Lymphoma
Trial ID or NCT#
Status
Purpose
The purpose of the study is to determine the efficacy and safety of enzastaurin in participants with Cutaneous T-Cell Lymphoma (CTCL) who failed prior therapies.
Official Title
A Phase 2, Open-Label, Multicenter Study of Single-Agent Enzastaurin in Patients With Relapsed Cutaneous T-Cell Lymphoma
Eligibility Criteria
- * Histologically confirmed mycosis fungoides or Sezary Syndrome.* Stage IB to IVB disease at screening.* Recurrent or refractory disease after at least 1 prior systemic therapy.* Have adequate organ function defined as:
- * Hepatic: total bilirubin ≤1.5 times the upper limit of normal (ULN); alanine transaminase/aspartate transaminase (ALT/AST) ≤2.5 times the ULN. * Renal: serum creatinine ≤1.5 times the ULN. * Adequate bone marrow reserve: platelets ≥75 \* 10\^9/Liters (L); absolute neutrophil count (ANC) ≥1.0 \* 10\^9/L.* At least 30 days must have passed since other treatment for CTCL.
- * Receiving concurrent treatment for CTCL.* Unable to swallow tablets.* Receiving high potency oral or topical steroids. Low potency oral steroid may be permitted in participants who have been on a stable dose for at least 4 weeks prior to screening. Oral or topical antihistamine is allowed.* Unable to discontinue use of carbamazepine, phenobarbital, or phenytoin.* Have a serious concomitant systemic disorder or Human Immunodeficiency Virus (HIV).* Have a serious cardiac condition such as myocardial infarction within past 6 months, angina, or heart disease as defined by the New York Heart Association (NYHA) Class III or IV.* Have electrocardiogram (ECG) abnormalities.* Are pregnant or breastfeeding.
Investigator(s)
Contact us to find out if this trial is right for you.
Contact
Natalie Viakhireva
6507238949
View on ClinicalTrials.gov