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Two global phase 3 trials found rocatinlimab significantly improved EASI-75 and vIGA-AD outcomes at 24 weeks in people with moderate-to-severe AD with acceptable safety.
Two global, randomized, double-blind, placebo-controlled phase 3 trials demonstrated that rocatinlimab significantly improved clinical signs of moderate-to-severe atopic dermatitis (AD) at 24 weeks compared with placebo and was generally well tolerated, according to findings from the ROCKET-IGNITE and ROCKET-HORIZON studies.1
“These findings represent a major advance for patients living with eczema, who often face years of uncontrolled symptoms and few effective options,” lead author Emma Guttman-Yassky, MD, PhD, Waldman Professor and System Chair of the Kimberly and Eric J. Waldman Department of Dermatology at the Icahn School of Medicine at Mount Sinai, said in a press release. “By targeting memory T cells through OX40, rocatinlimab not only clears the skin and relieves itch, but continues to improve patients’ lives over time with a strong safety profile. This is the first phase 3 proof that rebalancing these immune cells can transform how we treat atopic dermatitis.”2
IGNITE and HORIZON were conducted in 19 countries each and enrolled adults aged ≥18 years with confirmed AD for ≥1 year, Eczema Area and Severity Index (EASI) ≥16, validated Investigator’s Global Assessment for AD (vIGA-AD) score of 3–4, and ≥10% affected body surface area.1
Treatment was administered at weeks 0, 2, and 4, then every 4 weeks through week 20, with efficacy assessed at week 24. Rescue therapy was permitted beginning day 1; participants who used rescue therapy were classified as nonresponders for all subsequent visits.1
The coprimary endpoints for both trials were EASI-75 response (≥75% improvement) and vIGA-AD score of 0–1 with ≥2-point improvement, each evaluated at week 24. Both trials met all coprimary endpoints, with statistically significant improvements for rocatinlimab versus placebo.1
IGNITE
HORIZON
IGNITE
HORIZON
Treatment-emergent adverse event (TEAE) rates were generally similar between rocatinlimab and placebo groups in both studies. Adverse events occurring in ≥4% of participants and at ≥2 times that of placebo frequency included1:
Investigators reported that most pyrexia and chills events were injection-related, occurred primarily after the first dose, and were mild or moderate in severity. Serious adverse events occurred in 2%–5% of rocatinlimab-treated participants and 4%–6% of placebo-treated participants. No deaths were reported in either study.1
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