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Safety, Tolerability And Pharmacodynamics of DM-101PX in Birch Pollen Allergy (UPSIT)

2026年10月30日 更新者:Desentum Oy

A Randomised, Double Blind, Placebo-controlled Study to Evaluate the Safety, Tolerability And Pharmacodynamics of Subcutaneous Immunotherapy With DM-101PX in Subjects With Birch Pollen Allergy

Randomized, double-blind placebo-controlled phase I trial with the primary aim to investigate safety and tolerability of DM-101-PX compared to placebo in birch pollen allergic adults. As an secondary objectives, the trial will also assess the number of participants receiving the maximum intended DM-101PX dose and to assess the effect of treatment with DM-101PX compared with placebo on blood allergy biomarkers. Expanded access to the study treatment is not available.

研究概览

地位

招聘中

详细说明

The study will be carried out in a single study site located in Germany.

研究类型

介入性

注册 (估计的)

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。

学习联系方式

研究联系人备份

学习地点

      • Hanover、德国、30625
        • 招聘中
        • Fraunhofer Institute for Toxicology and Experimental Medicine ITEM
        • 接触:

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 65年 (成人、年长者)

接受健康志愿者

不

有资格学习的性别

全部

描述

Inclusion Criteria:

  • Male or female, aged 18 to 65 years
  • Good general health
  • A documented clinical history of moderate to severe birch pollen-induced allergic rhinitis or rhinoconjunctivitis for at least 2 years with symptoms that interfere with daily activities or sleep
  • Bet v 1-specific IgE ≥0.7 kU/L (class 2) measured by ImmunoCAP® performed at the trial site at Screening or within 12 months prior to Screening
  • Positive SPT to Birch pollen whole allergen extract with a wheal diameter ≥3 mm (average of longest and orthogonal), with the negative control wheal diameter <2 mm and the positive (histamine) control wheal diameter ≥3 mm, performed at the trial site at Screening or within 12 months prior to Screening
  • Body weight ≥50 kg and body mass index within the range 18-35 kg/m2

Exclusion Criteria:

  • History or findings on physical examination of any significant disease or disorder which, in the opinion of the investigator, may put the individual at risk because of participation in the trial, influence the results of the trial or the participant's ability to participate in the trial
  • Significant rhinitis, sinusitis, and/or symptomatic respiratory allergy due to regular contact with allergens other than birch pollen that are expected to potentially interfere with the trial assessments, as assessed by the investigator
  • Persistent asthma that requires GINA Step 2 or higher treatment during the trial period, or required treatment within 4 weeks prior to Screening
  • History of uncontrolled asthma according to GINA classification in the 6 months prior to Screening or history of asthma deterioration that resulted in emergency treatment or hospitalization in the 12 months before Screening, or a life-threatening asthma attack (eg, one requiring intubation and mechanical ventilation) at any time in the past
  • Forced Expiratory Volume in one second (FEV1) <70 % of predicted, regardless of asthma status at Screening
  • History of severe drug allergy, severe angioedema, or systemic allergic reaction of Grade 3 or greater, according to the WAO classification (2024, see Section 12.5), due to any cause
  • History of acute hypersensitivity and/or anaphylaxis to protein therapeutics or components of formulation, including polyethylene glycol, or severe or significant allergies that in the opinion of the investigator could represent a substantial risk to the individual

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:治疗
  • 分配:随机化
  • 介入模型:并行分配
  • 屏蔽:三倍

武器和干预

参与者组/臂
干预/治疗
实验性的:DM-101PX for cohort 1

Weekly subcutaneous administration of ascending doses of DM-101PX for 10 weeks with dose escalation starting from 0.2 µg with slightly varying injection volumes.

Subcutaneous injection of DM-101PX

安慰剂比较:Placebo for cohort 1

Weekly subcutaneous administration of Placebo for 10 weeks

Placebo to match subcutaneous injection of DM-101PX

实验性的:Experimental: DM-101PX for cohort 2

Weekly subcutaneous administration of ascending doses of DM-101PX for 10 weeks with dose escalation starting from 0.2 µg with varying injection volumes

Subcutaneous injection of DM-101PX

安慰剂比较:Placebo for cohort 2

Weekly subcutaneous administration of Placebo for 10 weeks

Placebo to match subcutaneous injection of DM-101PX

实验性的:Experimental: DM-101PX for cohort 3

Weekly subcutaneous administration of ascending doses of DM-101PX for 10 weeks with regimens consisting of 2 initial placebo s.c. injections, followed by 8 s.c. injections with escalating doses starting from 0.2 µg and with varying injection volumes.

Subcutaneous injection of DM-101PX

安慰剂比较:Placebo for cohort 3

Weekly subcutaneous administration of Placebo for 10 weeks

Placebo to match subcutaneous injection of DM-101PX

实验性的:Experimental: DM-101PX for cohort 4

Weekly subcutaneous administration of ascending doses of DM-101PX for 10 weeks with regimens consisting of 2 initial placebo s.c. injections, followed by 8 s.c. injections with escalating doses starting from 0.2 µg and with constant varying injection volume.

Subcutaneous injection of DM-101PX

安慰剂比较:Placebo for cohort 4

Weekly subcutaneous administration of Placebo for 10 weeks

Placebo to match subcutaneous injection of DM-101PX

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
Treatment Emergent Adverse Events
大体时间:From the first dose to until 3 months from the last dose

Occurrence of treatment emergent adverse events

From the first dose to until 3 months from the last dose
Adverse Events of Special Interest
大体时间:From the first dose to until 3 months from the last dose

Occurrence of local injection site reactions and systemic allergic reactions

From the first dose to until 3 months from the last dose

次要结果测量

结果测量
措施说明
大体时间
Subjects Reaching the Maximum Intended Dose
大体时间:Through the treatment period, an average of 10 weeks

Number of subjects in each cohort who reach the maximum intended dose

Through the treatment period, an average of 10 weeks
Change in blood allergy biomarker levels
大体时间:From baseline to 3 and 12 weeks, after completion of treatment

Change in the levels of Bet v 1-specific IgE, IgG1 and IgG4

From baseline to 3 and 12 weeks, after completion of treatment

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。

赞助

调查人员

  • 首席研究员:Philipp Badorrek, MD、Fraunhofer Institute for Toxicology and Experimental Medicine ITEM

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)

2026年10月29日

初级完成 (估计的)

2027年3月1日

研究完成 (估计的)

2027年5月1日

研究注册日期

首次提交

2026年10月20日

首先提交符合 QC 标准的

2026年10月20日

首次发布 (实际的)

2026年10月27日

研究记录更新

最后更新发布 (实际的)

2026年11月3日

上次提交的符合 QC 标准的更新

2026年10月30日

最后验证

2026年10月1日

更多信息

与本研究相关的术语

其他研究编号

  • DM-101-C-005

计划个人参与者数据 (IPD)

计划共享个人参与者数据 (IPD)?

是的

IPD 计划说明

All individual participant data that underlie publicly available results will be considered for sharing

IPD 共享时间框架

Anonymized participant data will be considered for sharing once the indication has been approved by a regulatory body, if there is legal authority to share the data and there is not a reasonable likelihood of participant reidentification.

IPD 共享访问标准

Qualified researchers may request access to patient level data underlying the publication: patient level data will be anonymized and study documents will be redacted to protect the privacy of trial participants. Patient level data will be anonymized and study documents will be redacted to protect the privacy of trial participants after Desentum has received marketing authorization from major health authorities (e.g. FDA, EMA), has the legal authority to share the data, and has made the study results publicly available. Requests from qualified researchers will be reviewed by the Sponsor, and data will be shared only for scientifically sound research purposes, subject to a signed data sharing agreement and in compliance with applicable data protection legislation and participant consent.

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

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