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临床试验/NCT07228325
NCT07228325Enrolling By Invitation1 期

A Comparison of PK and PD Responses Following Single and Repeat Administration of Epinephrine Nasal FMXIN002 4.0 mg and EpiPen 0.3 mg, in Healthy Adults With Allergic Rhinitis

Nasus Pharma1 个研究点 分布在 1 个国家目标入组 50 人开始时间: 2025年11月3日最近更新:
适应症
干预措施

试验速览

阶段
1 期
状态
Enrolling By Invitation
发起方
Nasus Pharma
入组人数
50
试验地点
1
主要终点
Epinephrine level in plasma over time

研究概览

简要总结

The study will evaluate the pharmacokinetic (PK) and pharmacodynamic (PD) responses of FMXIN002, an intranasal epinephrine powder, compared with the EpiPen® intramuscular autoinjector, after single and double doses, in healthy adults with a history of allergic rhinitis.

详细描述

Fifty participants will receive single and repeat doses of both treatments under normal and nasal congestion conditions induced by nasal allergen challenge. The study will also assess the effect of repeat nasal dosing in the same versus opposite nostrils. PK parameters and hemodynamic responses will be measured, and safety and tolerability will be evaluated.

研究设计

研究类型
Interventional
分配方式
Randomized
干预模型
Sequential
主要目的
Treatment
盲法
None

入排标准

年龄范围
18 Years 至 55 Years(Adult)
性别
All
接受健康志愿者

入选标准

  • Non-smoking, male and female participants, from 18 to 55 years of age.
  • Documented positive skin allergy test at screening.
  • History of hay fever, seasonal allergies, or allergic rhinitis during the last year.
  • BMI ≥18 and < =30 kg/m
  • Females may be of childbearing or non-childbearing potential:
  • Childbearing potential:
  • o Physically capable of becoming pregnant, must be willing to use acceptable effective methods of contraception.
  • Non-childbearing potential:
  • Surgically sterile (i.e., both ovaries removed, uterus removed, or bilateral tubal ligation); and/or
  • Postmenopausal (no menstrual period for at least 12 consecutive months without any other medical cause and a FSH value consistent with being postmenopausal).
  • Able to tolerate venipuncture.
  • Be informed of the nature of the study and give written consent prior to any study procedure.
  • Willing and able to remain in the clinic for the entire duration of the confinement period.
  • Have good intravenous access on both arms and hands. -

排除标准

  • History of clinically significant neurologic, hematologic, endocrine, oncologic, pulmonary, immunologic, genitourinary, psychiatric, or cardiovascular disease or any other condition which, in the opinion of the Investigator, would jeopardize the safety of the participant or impact the validity of the study results.
  • Have clinically significant findings at screening.
  • Females who:
  • Have discontinued or changed the use of implanted, intrauterine, intravaginal, or injected hormonal contraceptives within 6 months prior to the first drug administration;
  • Have discontinued or changed the use of oral or patch hormonal contraceptives within one (1) month prior to the first drug administration;
  • Are pregnant (serum β-hCG consistent with pregnancy); or
  • Are breast-feeding.

研究组 & 干预措施

FMXIN002 Repeated doses in the same nostril

Experimental

Repeated doses of epinephrine nasal powder spray, in the same nostril, 10 minutes apart.

干预措施: FMXIN002 single dose (Drug)

FMXIN002 Repeated doses in the same nostril

Experimental

Repeated doses of epinephrine nasal powder spray, in the same nostril, 10 minutes apart.

干预措施: Epinephrine autoinjector single dose (Drug)

FMXIN002 Repeated doses in the same nostril

Experimental

Repeated doses of epinephrine nasal powder spray, in the same nostril, 10 minutes apart.

干预措施: FMXIN002 single dose + NAC (Drug)

FMXIN002 Repeated doses in the same nostril

Experimental

Repeated doses of epinephrine nasal powder spray, in the same nostril, 10 minutes apart.

干预措施: Epinephrine autoinjector double dose (Drug)

FMXIN002 Repeated doses in the same nostril

Experimental

Repeated doses of epinephrine nasal powder spray, in the same nostril, 10 minutes apart.

干预措施: FMXIN002 double dose (Drug)

FMXIN002 Repeated doses in the same nostril

Experimental

Repeated doses of epinephrine nasal powder spray, in the same nostril, 10 minutes apart.

干预措施: FMXIN002 double dose + NAC (Drug)

FMXIN002 Repeated doses in the opposite nostril

Experimental

Repeated doses of epinephrine nasal powder spray, in both nostrils, 10 minutes apart.

干预措施: FMXIN002 single dose (Drug)

FMXIN002 Repeated doses in the opposite nostril

Experimental

Repeated doses of epinephrine nasal powder spray, in both nostrils, 10 minutes apart.

干预措施: Epinephrine autoinjector single dose (Drug)

FMXIN002 Repeated doses in the opposite nostril

Experimental

Repeated doses of epinephrine nasal powder spray, in both nostrils, 10 minutes apart.

干预措施: FMXIN002 single dose + NAC (Drug)

FMXIN002 Repeated doses in the opposite nostril

Experimental

Repeated doses of epinephrine nasal powder spray, in both nostrils, 10 minutes apart.

干预措施: Epinephrine autoinjector double dose (Drug)

FMXIN002 Repeated doses in the opposite nostril

Experimental

Repeated doses of epinephrine nasal powder spray, in both nostrils, 10 minutes apart.

干预措施: FMXIN002 double dose (Drug)

FMXIN002 Repeated doses in the opposite nostril

Experimental

Repeated doses of epinephrine nasal powder spray, in both nostrils, 10 minutes apart.

干预措施: FMXIN002 double dose + NAC (Drug)

结局指标

主要结局

Epinephrine level in plasma over time

时间窗: -60 to 240 minutes post administration

Measurements in 14 timepoints

Tmax

时间窗: -60 to 240 minutes post administration

Time to maximum epinephrine level in plasma

T100pg/ml

时间窗: -60 to 240 minutes post administration

Time to reach epinephrine level of 100pg/ml in plasma

Cmax

时间窗: -60 to 240 minutes post administration

Maximum epinephrine level in plasma

AUC

时间窗: 0 to 240 minutes post administration

Total exposure to epinephrine

Blood pressure

时间窗: -60 to 120 minutes post administration

Pharmacodynamic response to epinephrine

Heart rate

时间窗: -60 to 120 minutes post administration

Pharmacodynamic response to epinephrine

Respiratory rate

时间窗: -60 to 120 minutes post administration

Pharmacodynamic response to epinephrine

次要结局

  • Safety and tolerability(Day -29 to day 50)

研究者

发起方
Nasus Pharma
申办方类型
Industry
责任方
Sponsor

研究点 (1)

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