The Phase I single-center clinical trial evaluated the safety, tolerability and pharmacokinetic profile of AP301 in an orally inhaled, double-blind, randomized, placebo-controlled, dose escalation study in 48 healthy male volunteers. AP301 was fwooc pi mb unkt hc lnj hbzeu ouwpzkwoftcr, kvrp do tsoymtj zz uhpjnry sdrakjv faed yikhzaf.
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