VALCHLOR® (mechlorethamine) gel is an alkylating drug indicated for the topical treatment of Stage IA and IB mycosis fungoides–type cutaneous T-cell lymphoma (MF-CTCL) in patients who have received prior skin-directed therapy
Proven treatment with an FDA-approved formulation1
VALCHLOR gel* is a clear, quick-drying formulation of mechlorethamine2
Applied at the patient's discretion
Can be used with emollients2
2 hours before/after application
Clear, non-greasy gel2
Once dry, unlikely to stain clothing/sheets
5-10 minutes after application
- Mechlorethamine (nitrogen mustard) is an effective topical treatment for cutaneous lymphoma with nearly 70 years of data2,3
*Each tube of VALCHLOR gel contains gel 0.016% w/w of mechlorethamine (equivalent to 0.02% mechlorethamine HCl).2
VALCHLOR gel is the only FDA-approved topical formulation of mechlorethamine
manufactured with consistent quality for your patients.2
- Lymphoma Research Foundation. Getting the facts: cutaneous T-cell lymphoma. Lymphoma Research Foundation website. https://lymphoma.org/wp-content/uploads/2017/06/LRF_FACTSHEET_Cutaneous_TCell_Lymphoma_CTCL.pdf. Updated August 2017. Accessed November 19, 2018.
- VALCHLOR [package insert]. Iselin, NJ: Helsinn Therapeutics US, Inc.; January 2020.
- Lessin SR, Duvic M, Guitart J, et al. Topical chemotherapy in cutaneous T-cell lymphoma: positive results of a randomized, controlled, multicenter trial testing the efficacy and safety of a novel mechlorethamine, 0.02%, gel in mycosis fungoides. Arch Dermatol. 2012;E1-E8.