评估 UB-313 在健康参与者中的安全性、耐受性和免疫原性的 1 期研究
一项随机、双盲、安慰剂对照、首次人体研究,以评估 UBITh® CGRP 免疫疗法 (UB-313) 在健康参与者中的安全性、耐受性和免疫原性
This first in-human (FIH) study of UB-313, an anti-calcitonin gene-related peptide based immunotherapeutic candidate, is designed to assess the safety, tolerability, and immunogenicity of 4 selected UB-313 dose regimens in healthy adults.
研究概览
详细说明
This is a single-site, randomized, double-blind, placebo-controlled, multidose regimen, FIH study of UB-313, an anti-CGRP peptide-based immunotherapy candidate. The double-blind period will include dose escalation and cohort staggering for up to 4 planned dose levels of UB-313 or placebo in 4 cohorts of healthy participants. All eligible participants will be enrolled in the study for up to 44 weeks, consisting of IM injections of UB-313 or placebo at Week 0 (Baseline, Day 1), Week 4, and Week 12. The End of Treatment (EoT) is defined as Week 16, followed by a follow-up period up to Week 44.
研究类型
注册 (实际的)
阶段
- 阶段1
联系人和位置
学习地点
-
-
-
Leuven、比利时
- Katholieke Universiteit Leuven
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-
参与标准
资格标准
适合学习的年龄
接受健康志愿者
有资格学习的性别
描述
Inclusion Criteria:
- Is a male or female aged 18 to 55 years old, inclusive, at time of informed consent.
- Has a body mass index between 18 and 30 kg/m2, inclusive at Screening, and with a minimum weight of 50 kg.
- Male participants and their partners of childbearing potential must commit to the use of highly effective contraceptives for the study duration and for at least 12 weeks after the last dose. Men must refrain from donating sperm during this same period.
- Female participants must be of nonchildbearing potential, or, for women of childbearing potential, must be willing to practice highly effective contraception throughout the duration of the study and for at least 24 weeks following the last dose.
- Other inclusion criteria apply
Exclusion Criteria:
- Has a history of clinically significant medical or psychiatric conditions, which in the opinion of the Investigator may compromise the participant's safety or the scientific value of the study, posing an unacceptable risk to the participant or interfere with the participant's ability to comply with study procedures or abide by study restrictions.
- Presents any concern by the Investigator regarding safe participation in the study or for any other reason (including contraindication to MRI) that the Investigator considers the participant inappropriate for participation in the study.
- Has a recent history (within the past year of Screening) of migraine headache.
- Has unsuitable skin characteristics for the dermal capsaicin challenge as determined by the Investigator.
- Has not demonstrated at least a 100% increase in dermal blood flow following capsaicin challenge as part of Screening procedures and measured through laser speckle contrast imaging.
- Other exclusion criteria apply
学习计划
研究是如何设计的?
设计细节
- 主要用途:预防
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:四人间
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:UB-313 Cohort 1
UB-313 100mcg administered by intramuscular (IM) injection at Week 0, Week 4 and Week 12 |
A synthetic peptide-based immunotherapy |
|
实验性的:UB-313 Cohort 2
UB-313 300mcg administered by IM injection at Week 0 and 100mcg at Week 4 and Week 12 |
A synthetic peptide-based immunotherapy |
|
实验性的:UB-313 Cohort 3
UB-313 300mcg administered by IM injection at Week 0, Week 4 and Week 12 |
A synthetic peptide-based immunotherapy |
|
实验性的:UB-313 Cohort 4
UB-313 600mcg administered by IM injection at Week 0 and 100mcg at Week 4 and Week 12 |
A synthetic peptide-based immunotherapy |
|
安慰剂比较:Placebo Comparator
Placebo (normal saline), administered by IM injection at Week 0, Week 4 and Week 12 |
Normal saline |
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Number of Participants With Treatment-Emergent Adverse Events
大体时间:44 weeks
|
The number and percentage of participants with TEAEs were tabulated. |
44 weeks
|
|
Immunogenicity Measured by Serum Anti-CGRP Antibodies.
大体时间:Weeks 0, 1, 4, 5, 8, 12, 13, 16, 20, 28, 36 and 44; Week 0, Week 16 and Week 44 are reported
|
Immunogenicity measured by blood anti-CGRP antibody titers, reported as Optical Density (OD) of 1:25 dilution. |
Weeks 0, 1, 4, 5, 8, 12, 13, 16, 20, 28, 36 and 44; Week 0, Week 16 and Week 44 are reported
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Pharmacodynamics of the Immune Response Measured by Capsaicin-induced Increase in Dermal Blood Flow
大体时间:Weeks 0, 4, 8, 12, 16, 20
|
Number of Participants with inhibition of capsaicin-induced increase in dermal blood flow |
Weeks 0, 4, 8, 12, 16, 20
|
合作者和调查者
调查人员
- 研究主任:Medical Director, MD、Vaxxinity, Inc.
研究记录日期
研究主要日期
学习开始 (实际的)
初级完成 (实际的)
研究完成 (实际的)
研究注册日期
首次提交
首先提交符合 QC 标准的
首次发布 (实际的)
研究记录更新
最后更新发布 (实际的)
上次提交的符合 QC 标准的更新
最后验证
更多信息
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