Krystal Biotech delivered strong financial results in Q4 2025, with VYJUVEK net product revenue reaching $107.1 million and a high gross margin of 94%. The company also made significant progress in its pipeline, securing RMAT designation for KB707 and Fast Track Designation for KB111, while maintaining a robust cash position.
VYJUVEK net product revenue for Q4 2025 was $107.1 million, contributing to a full-year total of $389.1 million.
The company ended the quarter with a strong balance sheet, holding $955.9 million in cash and investments.
KB707 received Regenerative Medicine Advanced Therapy (RMAT) designation for advanced NSCLC, and KB111 received Fast Track Designation for HHD.
Over 660 reimbursement approvals for VYJUVEK were secured in the United States, with steady uptake in Germany, France, and Japan.
Krystal Biotech provided guidance for FY 2026 Non-GAAP Research and Development and Selling, General and Administrative expenses, projecting a range of $175.0 million to $195.0 million.
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