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Completed

NCT Number: NCT05449535

Study of JYB1904 (an Anti-immunoglobulin E Antibody) in Healthy Chinese Subjects

This phase Ia study is meant to evaluate the tolerability, safety, pharmacokinetics, preliminary pharmacodynamics, and immunogenicity of single-dose JYB1904, an anti-immunoglobulin E (IgE) antibody, in healthy Chinese subjects.

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Key information

Conditions

Age range

18 year–50 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 1

Primary location

Shulan (Hangzhou) Hospital

Hangzhou, Zhejiang, 310000, China

About this study

This first-in-human study with a dose-escalation design is meant to evaluate the tolerability, safety, pharmacokinetics, preliminary pharmacodynamics, and immunogenicity of single-dose JYB1904 in healthy Chinese subjects.

The sequential dose levels (sample size) of JYB1904 are set at five different dose, with additional two JYB1904 placebo subjects in each group. The active comparator is omalizumab (Xolair).

Dosage and administration: single-dose; subcutaneous injection in the deltoid region of the upper arm.

Who can participate

Healthy volunteers accepted: Yes

Only the study team can determine whether someone qualifies for participation.

Inclusion criteria

  • Able to understand the study and provide written informed consent voluntarily, and comply with the requirements;
  • Healthy Chinese subjects aged 18-50 years, male or female;
  • Normal or abnormal but without clinical significance reports of physical examinations, vital signs, clinical laboratory tests and others.

Exclusion criteria

  • Surgery history within 6 months prior to screening or any surgery schedule during the study;
  • Last visit in previous drug clinical trial within 3 months prior to screening;
  • Acute diseases occur or receive any medication during the screening period;
  • Other conditions unsuitable for the study confirmed by the investigator.

Treatment and study plan

JYB1904

Drug

Dosage form: injection, solution; Usage and dosage matching:dose 1, dose 2, dose 3, dose 4, dose 5; single-dose; subcutaneous injection in the deltoid region of the upper arm.

Omalizumab

Drug

Dosage form: injection, powder, lyophilized, for solution; Usage and dosage matching:dose 1; single-dose; subcutaneous injection in the deltoid region of the upper arm.

Other names: Xolair

JYB1904 Placebo

Drug

Dosage form: injection, solution; Usage and dosage matching:dose 1, dose 2, dose 3, dose 4, dose 5; single-dose; subcutaneous injection in the deltoid region of the upper arm.

Primary outcomes

  1. Adverse events (AEs)

    Time frame: Baseline through 168 days post-dose

    Incidence and features of AEs assessed by CTCAE v5.0

Secondary outcomes

  1. Serum concentrations of JYB1904 and Omalizumab

    Time frame: Baseline through 168 days post-dose

    Serum JYB1904 and Omalizumab assessed by pre-specified methods, and related pharmacokinetic parameters analysis

  2. Serum concentrations of total/free IgE

    Time frame: Baseline through 168 days post-dose

    Serum total/free IgE assessed by a pre-specified method, and related pharmacodynamic parameters analysis

  3. Serum concentrations of anti-drug antibody (ADA) and neutralizing antibody (Nab)

    Time frame: Baseline through 168 days post-dose

    Serum ADA and Nab assessed by pre-specified methods, and related immunogenic features analysis

Sponsors and collaborators

Lead sponsor

Jemincare

Industry

Registry information

Official study title

Phase Ia Study to Evaluate the Tolerability, Safety, Pharmacokinetics, Preliminary Pharmacodynamics, and Immunogenicity of Single-dose JYB1904 in Healthy Chinese Subjects

Important dates

Study start
2022
Primary completion
2023
Study completion
2023
First posted
Jul 8, 2022
Registry last updated
Jun 27, 2023

OpenTrials presents study information sourced from ClinicalTrials.gov. The official registry record should be consulted for the latest information.

View the official ClinicalTrials.gov record (opens in a new tab)

This listing is for discovery and informational purposes only. It is not medical advice, does not guarantee that a study is recruiting, and does not determine eligibility. Contact the study team and a qualified healthcare professional when considering participation.

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