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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

2026年11月2日 更新者:Axxium Life, Inc.

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

地位

完全的

条件

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

介入性

注册 (实际的)

40

阶段

  • 阶段1

联系人和位置

本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。

学习地点

      • Leuven、比利时
        • Katholieke Universiteit Leuven

参与标准

研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。

资格标准

适合学习的年龄

18年 至 55年 (成人)

接受健康志愿者

是的

有资格学习的性别

全部

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

本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。

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

在这里您可以找到参与这项研究的人员和组织。

调查人员

  • 研究主任:Medical Director, MD、Vaxxinity, Inc.

研究记录日期

这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。

研究主要日期

学习开始 (实际的)

2022年7月6日

初级完成 (实际的)

2023年10月6日

研究完成 (实际的)

2023年10月6日

研究注册日期

首次提交

2022年7月20日

首先提交符合 QC 标准的

2022年7月25日

首次发布 (实际的)

2022年7月28日

研究记录更新

最后更新发布 (实际的)

2026年11月4日

上次提交的符合 QC 标准的更新

2026年11月2日

最后验证

2026年11月1日

更多信息

与本研究相关的术语

其他研究编号

  • UB-313-101

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

不

药物和器械信息、研究文件

研究美国 FDA 监管的药品

不

研究美国 FDA 监管的设备产品

不

此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.

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