Frontiers in pharmacology · 2026
Safety, tolerability, pharmacokinetics, and pharmacodynamics of zapnometinib: results from a phase I clinical study.
Клиническое исследованиеСтатьяНазвание и аннотация: Перевод в очереди
Обработка статьи · этапы, ошибки и управление
Загрузка состояния…
Ошибки и ограничения
История · было → стало
Состояние обновляется каждые 5 секунд, пока блок открыт. Процент показывается только там, где известен объём работы. Пауза останавливает продолжение этапа; текущий запрос к источнику может завершиться.
Stenglein Stephan, Volk Julian, Füll Yvonne, Reh Christian, Haffner Steffen, Canisius Sebastian, Overend Tim, Planz Oliver
Аннотация
INTRODUCTION: Zapnometinib (ATR-002) is a selective MEK inhibitor designed to modulate the MAPK/ERK pathway, which plays a key role in viral infections and inflammatory diseases. Clinical characterization of its safety, tolerability, pharmacokinetics (PK), and pharmacodynamics (PD) is essential to support further development. This Phase I clinical trial was registered under EudraCT number 2021-005225-25.
METHODS: This was a Phase I, single-center, randomized, double-blind, placebo-controlled trial conducted in healthy adults. The study included three parts: a single ascending dose (SAD) phase, a multiple ascending dose (MAD) phase, and a drug-drug interaction (DDI) as well as a food-drug interaction (FDI) phase. In the SAD phase, 42 participants received single oral doses of 600, 900, 1,200, or 1,500 mg. In the MAD phase, 29 participants received daily oral doses of 900, 1,200, or 1,500 mg for 7 days. The DDI phase assessed the effect of zapnometinib on CYP2C8 and CYP2C9 activity using repaglinide and celecoxib as probe substrates.
RESULTS: Zapnometinib was well tolerated with no serious adverse events reported. Most treatment-emergent adverse events (TEAEs) were mild to moderate, including gastrointestinal symptoms (e.g., diarrhea, nausea) and headache. PK analysis showed dose-proportional increases in Cmax and AUC, with a notable food effect that increases bioavailability. PD evaluation demonstrated significant MEK inhibition, evidenced by reduced ERK phosphorylation.
DISCUSSION/CONCLUSION: This phase 1 study demonstrates that zapnometinib has a favorable safety and tolerability profile, predictable pharmacokinetics, and potent pharmacodynamic activity. The results support further clinical development of zapnometinib for therapeutic indications involving dysregulated MAPK/ERK signaling.
METHODS: This was a Phase I, single-center, randomized, double-blind, placebo-controlled trial conducted in healthy adults. The study included three parts: a single ascending dose (SAD) phase, a multiple ascending dose (MAD) phase, and a drug-drug interaction (DDI) as well as a food-drug interaction (FDI) phase. In the SAD phase, 42 participants received single oral doses of 600, 900, 1,200, or 1,500 mg. In the MAD phase, 29 participants received daily oral doses of 900, 1,200, or 1,500 mg for 7 days. The DDI phase assessed the effect of zapnometinib on CYP2C8 and CYP2C9 activity using repaglinide and celecoxib as probe substrates.
RESULTS: Zapnometinib was well tolerated with no serious adverse events reported. Most treatment-emergent adverse events (TEAEs) were mild to moderate, including gastrointestinal symptoms (e.g., diarrhea, nausea) and headache. PK analysis showed dose-proportional increases in Cmax and AUC, with a notable food effect that increases bioavailability. PD evaluation demonstrated significant MEK inhibition, evidenced by reduced ERK phosphorylation.
DISCUSSION/CONCLUSION: This phase 1 study demonstrates that zapnometinib has a favorable safety and tolerability profile, predictable pharmacokinetics, and potent pharmacodynamic activity. The results support further clinical development of zapnometinib for therapeutic indications involving dysregulated MAPK/ERK signaling.