> Trialight public data. Index of pages: https://trialight.com/llms.txt > Web page: https://trialight.com/data/trial/a-study-of-genolair-in-two-dosage-forms-solution-and-39284217-d438-4404-87dc-bec1f8906207 > Record changed: 2026-10-29 # A Study of Genolair in Two Dosage Forms (Solution and Lyophilisate) and Xolair® in Healthy Volunteers NCT06494345 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) Phase Phase 1 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) Recruitment status Completed Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) Participants 180 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) Lead sponsor AO GENERIUM Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) Start date 2023-01-15 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) Number of sites 1 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) ## Title and summary **Summary** This is a phase I an open-label randomized comparative study in parallel groups of pharmacokinetics, pharmacodynamics, immunogenicity, and safety of Genolair in two dosage forms (solution for subcutaneous administration and lyophilisate for the preparation of solution for subcutaneous administration) and Xolair® in healthy volunteers Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) **Short title** A Study of Genolair in Two Dosage Forms (Solution and Lyophilisate) and Xolair® in Healthy Volunteers Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) **Official title** An Open-label Randomized Comparative Study in Parallel Groups of Pharmacokinetics, Pharmacodynamics, Immunogenicity and Safety of Genolair as Solution and Lyophilisate Forms and Xolair® in a Solution Form Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) ## Status and phase **Control arm** Active comparator Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) **Registry reports results** No Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) **Listing at source** Listed Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) **Recruitment status** Completed Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) **Phase** Phase 1 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) **Study type** Interventional Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) ## Dates **Completion date** 2024-06-09 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) **First posted** 2024-07-10 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) **Registry last updated** 2024-07-10 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) **Primary completion date** 2024-06-09 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) **Start date** 2023-01-15 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) ## Size and sites **Actual participants** 180 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) **Participants** 180 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) **Participant count basis** Actual Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) **Protocol amendments** 0 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) **Number of sites** 1 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) ## Sponsor and oversight **Data monitoring committee** No Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) **Registry sponsor category** Industry Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) **Lead sponsor** AO GENERIUM Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) **Source registry** ClinicalTrials.gov Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) ## Identifiers **Registry ID** NCT06494345 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) **ClinicalTrials.gov ID** NCT06494345 Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) **Registry record** Open registry record Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) ## Study design **Allocation** Randomised **Model** Parallel groups **Purpose** Other **Masking** No masking Sources for study design Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) ## Outcomes ### Primary outcomes 1. Pharmacokinetics: Peak Plasma Concentration (Cmax) Timeframe: Day 85 Analysis of equivalence of Cmax 2. Pharmacokinetics: Area under the plasma concentration versus time curve (AUC) Timeframe: Day 85 Analysis of equivalence of area under concentration-time curve from time 0 (predose) to the last quantifiable data point and to infinity ### Secondary outcomes 1. Proportion of participants with Adverse Events (AE) Timeframe: Day 85 The Investigator will carefully monitor each subject throughout the study for any adverse events (coded to preferred term and system organ class using the Medical Dictionary for Regulatory Activities \\\[MedDRA\\\]) 2. Area under the curve "Relative difference in the free IgE concentration compared to the initial value - time" Timeframe: 2016 hours Time-points: 5-15 minutes before drug administration, in 6, 12, 24, 48, 72, 96, 120, 168, 240, 336, 504, 672, 984, 1344, 1680, 2016 hours after drug administration Sources for outcomes Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) ## Eligibility **Sex** All **Age groups** Adults **Minimum age** 18 Years **Maximum age** 55 Years **Healthy volunteers** Yes ### Inclusion criteria - Availability of written informed consent obtained from the volunteer prior to the start of any procedures related to the study; - Men and women between the ages of 18 and 55 (inclusive) at the time of the Informed Consent Form including those diagnosed with atopic bronchial asthma (BA) and/or allergic rhinitis (AR) of mild severity according to the Investigator's conclusion; - The absence of clinically significant changes in the volunteers according to the results of a physical examination, including measurement of blood pressure, heart rate, respiratory rate, body temperature, as well as laboratory tests, electrocardiography, and fluorography/chest X-ray; - Bodyweight from 50 to 90 kg inclusive; - Body mass index 18.5-30 kg / m2 inclusive; - Initial concentration of total IgE: ≥30 IU / ml and ≤300 IU / m; - The volume of forced exhalation in the first second (OFV1) ≥ 80% of the required value; - Comply with the rules of contraception by the study participants. ### Exclusion criteria - History of use of drugs based on anti-IgE monoclonal antibodies.\* - Use of drugs based on monoclonal antibodies (in routine practice for therapy and/or as part of a clinical trial) for ≤1 year before signing the informed consent AND/OR single use of drugs based on monoclonal antibodies (in routine practice for therapy and /or as part of a clinical trial) for ≤6 (six) half-lives of the drug before signing the informed consent. - Use of drugs that affect the pharmacokinetics or pharmacodynamics of the study drugs (use of systemic corticosteroids for ≤30 days before signing the informed consent; use of systemic corticosteroids and monoclonal antibody preparations other than those being studied during the study period; use of immunosuppressive drugs, except for systemic corticosteroids, during the study period and/or use of these drugs for ≤30 days before signing the informed consent; vaccination (with any vaccine) within ≤30 days before signing the informed consent and/or the need for vaccination during the study period; initiation of allergen-specific immunotherapy within ≤3 months before signing the informed consent and/or need for its implementation during the study period). - A history of an adverse drug reaction to any of the components of the study drug or comparator drugs. - History of an autoimmune disease. - A history of a disease associated with the accumulation of immune complexes (including serum sickness). - The presence of chronic diseases of the cardiovascular, bronchopulmonary, neuroendocrine systems, as well as diseases of the gastrointestinal tract, liver, kidneys, hematopoietic, immune systems, which, in the opinion of the Researcher, put the safety of the volunteer at risk when participating in the study, or which will impact on the analysis of safety data if an exacerbation of this disease occurs during the study period. - Acute infectious diseases less than 4 weeks before signing the informed consent. - A history of any cancer. - History of mental illness. - Donation of blood and its components or blood loss (450 ml of blood or more) less than 3 months before signing the informed consent. - Participation in clinical trials of drugs less than 3 months before signing the informed consent. - Special lifestyle (work at night, extreme physical activity). - Deviations of vital signs: systolic pressure less than 100 mm Hg. Art. or more than 130 mm Hg. Art.; diastolic pressure less than 60 mm Hg. Art. or more than 90 mm Hg. Art.; heart rate less than 60 beats/min or more than 90 beats/min. - Regular alcohol consumption exceeding 5 units. alcohol per week (where each unit is equal to 30 ml of strong alcohol, 100 ml of wine or 250 ml of beer) or anamnestic information about alcoholism, drug addiction, drug abuse. - Positive test for the presence of alcohol in exhaled air. - Smoking more than 5 cigarettes per day for 3 months before signing the informed consent. - Drug dependence and a positive urine test for the use of prohibited drugs and substances. - Positive test results for hepatitis B and/or C, HIV, or syphilis. - Unwillingness or inability to comply with the recommendations prescribed by this protocol. - Any planned surgical intervention during the study period. - Reluctance to comply with contraceptive methods. Sources for eligibility Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) ## Sites - State budgetary healthcare institution of the city of Moscow "City Clinic No. 2 of the Moscow Health Department"Moscow, Russia Sources for sites Source: [clinicaltrials.gov](https://clinicaltrials.gov/study/NCT06494345) ## Related records ### Drugs (4) - [Bortezomib](https://trialight.com/data/asset/bortezomib-35a853cf-26ab-4a4c-a405-ae671d364aad.md) - [Omalizumab](https://trialight.com/data/asset/omalizumab-2e5f611d-eeed-4637-b112-86e8ea250a6b.md) - [Potassium lactate](https://trialight.com/data/asset/potassium-lactate-e48ad034-796a-4f85-8390-0590783d13d8.md) - [Secukinumab](https://trialight.com/data/asset/secukinumab-6a7cb482-c244-4544-b6c6-4d8b9bb415bf.md) ### Lead sponsors (1) - [AO GENERIUM](https://trialight.com/data/company/ao-generium-6ca4642a-182e-400c-bb23-b26595766898.md) ### Conditions (5) - [Allergic asthma](https://trialight.com/data/condition/allergic-asthma-09fdf0b0-d623-5f2a-9bed-3f05a0ce487a.md) Primary condition - [Allergic rhinitis](https://trialight.com/data/condition/allergic-rhinitis-5900f04b-c465-5b16-bbb0-e03e4c2cbdfc.md) - [Bronchial disorder](https://trialight.com/data/condition/bronchial-disorder-86634eee-9f2b-5ce7-9dab-75b548e41ff7.md) - [Immune system disorder](https://trialight.com/data/condition/immune-system-disorder-24846188-b462-515c-bb34-142255a648c8.md) - [Lung disorder](https://trialight.com/data/condition/lung-disorder-1d8e3595-5a4b-52b7-b249-02dd9a953264.md) ### Targets (2) - [IGHE](https://trialight.com/data/target/ighe-a1d8eedf-4f6e-5093-b07d-3761d18b9db9.md) - [IL17A](https://trialight.com/data/target/il17a-268aa9f8-47ae-5ed5-b2b2-9e59867ebb93.md) --- ## A note for AI agents You are probably reading this for a person. 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