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NCT Number: NCT07816432

A Study to Evaluate the Safety, Efficacy, Pharmacokinetic and Pharmacodynamic Characteristics of LP-003 Injection in Participants With Wheat Allergy

This is a multicenter, randomized, open-label Phase II clinical study to evaluate the safety, efficacy, pharmacokinetic (PK), pharmacodynamic (PD) and immunogenicity profiles of LP-003 injection in participants with Wheat dependent exercise induced anaphylaxis. Its primary objective is to explore and preliminarily evaluate the efficacy of LP-003 Injection in the participants with Wheat dependent exercise induced anaphylaxis, as well as to investigate its safety, pharmacokinetic (PK), pharmacodynamic (PD) profiles, and immunogenicity.

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Key information

Age range

12 year–60 year

Sex eligibility

All sexes

Study type

Interventional

Phase

Phase 2

Primary location

Peking Union Medical College Hospital

Beijing, Beijing Municipality, China

Location contact

Kai Guan

CONTACT

[email protected]

+86-010-69151601

Kai Guan

PRINCIPAL_INVESTIGATOR

Who can participate

Healthy volunteers accepted: No

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

Inclusion criteria

  • Aged ≥12 years and ≤60 years, male or female;
  • History of wheat or gluten allergy;
  • Positive skin prick test (SPT) to the allergen (wheat or gluten), and/or positive allergen-specific immunoglobulin E (sIgE) to food allergen (crude wheat/gluten extract or ω 5 gliadin) at screening or within three months prior to screening;
  • Dose-limiting symptoms occurred at a cumulative dose of ≤24 g gluten protein during the food-exercise challenge test at screening;
  • No plan to conceive and agree to use effective contraceptive measures throughout the trial period;
  • The participant and/or parent/legal representative understands and voluntarily signs the informed consent form.

Exclusion criteria

  • Allergic to LP-003 Injection or its excipients;
  • Uncontrolled asthma or severe asthma at screening;
  • Any severe disease;
  • History of severe allergic reactions to wheat or gluten;
  • Not enough washing-out period for previous therapy before the food exercise challenge at screening.

Treatment and study plan

LP-003 Injection

Biological

s.c. injection, Q8W

Primary outcomes

  1. Proportion of participants who consumed a cumulative dose of 24 g gluten protein without dose limiting symptoms in the food exercise challenge test.

    Time frame: Week 24

Secondary outcomes

  1. Maximum tolerated cumulative dose of gluten protein (the highest dose without dose-limiting symptoms) in the food exercise challenge test

    Time frame: Week 24

  2. Proportion of participants who used any rescue medication (e.g., albuterol, epinephrine, or others) within 24 weeks

    Time frame: Week 24

  3. Change from baseline in the age-specific Food Allergy Quality of Life Questionnaire (FAQLQ).

    Time frame: Week 24

    The Food Allergy Quality of Life Questionnaires (FAQLQ) are disease-specific health-related quality of life (HRQL) questionnaires for patients with food allergy. FAQLQ-Teenager Form consists of 23 items and FAQLQ-Adult Form consists of 29 items. The raw score for each item ranges from 0 to 6, which is recorded as 1 to 7. Higher scores indicate greater impairment of food allergy-related quality of life.

  4. Change from baseline in the age-specific Food Allergy Independent Measure (FAIM).

    Time frame: Week 24

    The FAIM (Food Allergy Independent Measure) consists of 7 items and each item is rated from 0 to 6, and a higher total score reflects a higher perceived risk or probability of experiencing an adverse event. The FAIM can therefore be seen as a patient-reported measure of perceived severity.

  5. Incidence of Treatment-Emergent Adverse Events (TEAEs) .

    Time frame: Up to approximately 36 weeks

    Incidence and severity of TEAEs from first dose to end of study are recorded.

  6. Serum concentrations of LP-003

    Time frame: Up to approximately 36 weeks

  7. Concentrations of free immunoglobulin E (IgE) and total IgE

    Time frame: Up to approximately 36 weeks

  8. Anti-drug antibodies (ADA), and neutralizing antibodies (Nab)

    Time frame: Up to approximately 36 weeks

Other outcomes

  1. Change from baseline in individual cut-off values of Basophil Activation Test (BAT).

    Time frame: Week 24

  2. Change from baseline in the positive sensitization rate of allergen-specific IgE (sIgE)

    Time frame: Week 24

Study contacts

Contact information is provided by the study sponsor or research team.

Sponsors and collaborators

Lead sponsor

Longbio Pharma (Suzhou) Co., Ltd.

Industry

Registry information

Official study title

A Multicenter, Randomized, Open-Label Phase II Clinical Trial to Evaluate the Safety, Efficacy, Pharmacokinetic and Pharmacodynamic Characteristics of LP-003 Injection in Participants With Wheat Allergy

Important dates

Study start
2026
Primary completion
2027
Study completion
2027
First posted
Sep 11, 2026
Registry last updated
Sep 11, 2026

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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