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Zolinza® [vorinostat] capsules Reactivate Expression
Patient Product Information

Visible Improvements in CTCL
With ZOLINZA*

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Visible Improvements in CTCL With ZOLINZA
  • Cutaneous T-cell lymphomas are a heterogeneous group of cutaneous non-Hodgkin’s lymphomas,1 the 2 most common forms of which are mycosis fungoides (MF) and Sézary syndrome (SS).
Reference: 1. Willemze R, Jaffe ES, Burg G, et al. WHO-EORTC classification for cutaneous lymphomas. Blood. 2005;105:3768–3785.

Study Design

Open-label, single-agent, multicenter trial in patients (N=74) treated with ZOLINZA 400 mg once daily. Patients studied were aged 39 to 83 years (median 60 years); 48.6% female and 51.4% male; 82.4% white, 14.9% black, 1.4% Asian, and 1.4% other.

Objective response (primary end point)=either complete clinical response (CCR), defined as no evidence of disease, or partial response (PR), defined as a ≥50% decrease in SWAT skin assessment score compared with baseline. Both CCR and PR had to be maintained for at least 4 weeks.

Selected Important Safety Information

  • QTc prolongation has been observed. Monitor electrolytes and ECGs at baseline and periodically during treatment. Administer with caution in patients who have or may develop QTc prolongation. Hypokalemia or hypomagnesemia should be corrected before administering ZOLINZA.

Before prescribing ZOLINZA, please read the physician Prescribing Information. The Patient Product Information is also available.

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