AI Article Synopsis

  • PA9159, a new glucocorticoid nasal spray, was tested in healthy Chinese volunteers to assess its safety, tolerability, and effects on cortisol secretion during a first-in-human clinical study.
  • The study involved 60 participants and utilized a double-blinded, randomized, placebo-controlled design with both single and multiple ascending dose cohorts, with doses ranging from 10-80 µg.
  • Results indicated that PA9159 was safe and well-tolerated, with mild nasal side effects and minimal impact on morning serum cortisol levels, while pharmacokinetic measurements showed effective absorption and half-lives of around 8-21 hours across different dosing groups.

Article Abstract

Objective: PA9159 (previously named VSG159) is a structurally novel and highly potent glucocorticoid that plays a role in the late development of autoimmune and inflammatory diseases. The current first-in-human ascending-dose study of the PA9159 nasal spray was conducted in healthy Chinese volunteers to evaluate its pharmacokinetics, safety, and tolerability. In addition, the effects of PA9159 on serum cortisol secretion were investigated.

Methods: This was a double-blinded, randomized, placebo-controlled clinical study that included four single-dose groups in the single ascending dose cohort (SAD) and two multiple-dose groups in the multiple ascending dose cohort (MAD), with dose ranges of 10-80 μg and 20-40 μg, respectively. PA9159 was administered bilaterally via nasal spray once only or once daily for seven days. Pharmacokinetic, safety, and tolerability profiles were evaluated.

Results: A total of 60 participants completed the study. PA9159 doses of up to 80 μg in the SAD and up to 40 μg in the MAD were shown to be safe and tolerable. The most common treatment-related AEs were mild and transient local nasal AEs. Morning serum cortisol levels approximately remained unchanged in both the single-dose and multiple-dose groups. PA9159 was quantified in 41.8 % (368/880) of the samples in all treatment groups, including 25.2 % (105/416) of the SAD and 56.7 % (263/464) of the MAD. The majority (>80.0 %) of PA9159 plasma concentrations ranged from 0.5 to 2 pg/mL in determined samples. The mean AUC of PA9159 in the SAD was 0.91, 1.39±0.68, 11.40±9.91, and 46.30±25.80 h*pg/mL in the 10 to 80 ug single group. The mean terminal half-life time (t) was 8.43 h and 8.97±2.28 h in 40 ug and 80 ug single group, respectively. The mean AUC of PA9159 in the MAD was 31.70±7.04, 44.20±20.60 h*pg /mL, and the t was 16.00±4.18 h, 21.20±10.20 h in the 20 ug and 40 ug multiple groups, respectively. The median T was approximately 6 h in both the SAD and MAD cohorts.

Conclusions: The PA9159 nasal spray was generally safe and well tolerated, and the effects of PA9159 on serum cortisol levels were limited. The plasma concentration and systemic exposure to PA9159 were very low. These findings support the necessity for further clinical studies on PA9159 nasal spray in patients suffering from allergic rhinitis.

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Source
http://dx.doi.org/10.1016/j.ejps.2024.106764DOI Listing

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