- ICH GCP
- Реестр клинических исследований США
- Клиническое испытание NCT07622368
A Study of IBI3031 in Participants With Thyroid Eye Disease
A Phase I Clinical Study to Evaluate the Safety, Tolerability, and Pharmacokinetics of Single and Multiple Ascending Doses of IBI3031 in Participants With Thyroid Eye Disease
Обзор исследования
Статус
Условия
Вмешательство/лечение
Подробное описание
Тип исследования
Регистрация (Оцененный)
Фаза
- Фаза 1
Контакты и местонахождение
Контакты исследования
- Имя: Zhongyan shan
- Номер телефона: 024-83282152
- Электронная почта: Shanzhongyan@medmal.com.cn
Учебное резервное копирование контактов
- Имя: funan liu
- Номер телефона: 024-83281137
- Электронная почта: lfn540@126.com
Места учебы
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Liaoning
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Shenyang, Liaoning, Китай, 110001
- Рекрутинг
- The First Hospital of China Medical University
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Контакт:
- Zhongyan Dan
- Номер телефона: 02483282152
- Электронная почта: shanzhongyan@hotmail.com
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Критерии участия
Критерии приемлемости
Возраст, подходящий для обучения
- Взрослый
- Пожилой взрослый
Принимает здоровых добровольцев
Описание
Key Inclusion Criteria:
- Written informed consent.
- Aged between 18 and 75 years at screening.
- Weight between 45 kg and 100 kg.
Moderate-to-severe active TED:
- CAS ≥ 3 in the study eye at screening and baseline;
- Usually associated with at least two of the following: lid retraction ≥ 2 mm, moderate or severe soft tissue involvement, exophthalmos ≥ 3 mm above normal, and/or inconstant or constant diplopia;
- ≤ 12 months since the onset of active TED symptoms according to subjects' chief complaint or medical record at screening;
- Exophthalmos ≥ 18 mm in the study eye at baseline. (Only applicable to Stage 2)
- Participants must be clinically and biochemically euthyroid, or have mild hypothyroidism or mild-to-moderate hyperthyroidism at screening.
- Positive for Thyrotrophin Receptor Antibody (TRAb) at screening.
- No prior treatment with antithyroid medications and/or thyroid hormone replacement therapy, or having taken antithyroid medications and/or thyroid hormone replacement therapy on a stable dose for at least 6 weeks prior to the first dose, or having not been treated with antithyroid medications and/or thyroid hormone replacement therapy due to intolerable side effects for at least 6 weeks prior to the first dose.
- Infertile female participants or fertile female participants with negative blood pregnancy test results during the screening period and agree to take contraceptive measures from screening to 120 days after the last dose; male participants should agree to use contraceptive measures from screening to 120 days after the last dose.
Key Exclusion Criteria:
Participants to be excluded (Participants meeting any of the following criteria will be regarded as ineligible):
- The CAS of the study eye at baseline is reduced by ≥ 2 points compared with that at screening, or the proptosis of the study eye at baseline is reduced by ≥ 2 mm compared with that at screening;
- Participants previously diagnosed with dysthyroid optic neuropathy (DON), or with DON as determined by the investigator at screening;
- Patients with corneal ulcers that are not relieved after treatment at the investigator's discretion;
- Presence of other non-TED ophthalmic diseases that may affect the interpretation of study results or the safety of participants as determined by the investigator (e.g., proptosis not primarily caused by TED);
- At screening, clinical or laboratory evidence of significant hypothyroidism (presence of clinical symptoms of hypothyroidism, or FT3 or FT4 (Free Thyroxine)<0.5×lower limit of normal [LLN], or TSH>1.5×upper limit of normal [ULN]); or severe hyperthyroidism during the screening period (FT3 and FT4(Free Thyroxine)>2×ULN, or presence of thyroid storm).
Other medical history and abnormal test results during the screening period that are judged by the investigator to be clinically significant, may cause the participant to fail to comply with the study protocol or complete the trial, or endanger safety, including but not limited to:
- History of hepatic insufficiency (Child-Pugh Class B or C) or liver cirrhosis; aspartate aminotransferase (AST) or alanine aminotransferase (ALT) > 2 × ULN at screening;
- Glomerular filtration rate (GFR) < 60 ml/min/1.73 m2;
- Poorly controlled diabetes mellitus or hypertension;
- Confirmed or clinically suspected inflammatory bowel disease, gastrointestinal bleeding, or peptic ulcer disease.
- History of of chronic or recurrent infections; opportunistic infection within 180 days prior to screening;
- Positive for human immunodeficiency virus antibody (HIV Ab), hepatitis C virus antibody (HCV Ab), non-specific syphilis antibody (e.g., RPR(Rapid Plasma Reagin), TRUST), hepatitis B virus surface antigen (HBsAg) or e-antigen (HBeAg), or interferon-gamma release assay (IGRA).
- History of tinnitus or other hearing impairment in either ear during the screening period; or abnormal pure tone audiometry results (defined as an average bone conduction hearing threshold of ≥ 25 dB(decibe) at 0.5, 1, 2, and 4 kHz(kilohertz), or a bone conduction hearing threshold of ≥ 40 dB at any frequency);
- Scheduled radioactive iodine therapy or thyroidectomy at any time before screening or during the study;
- Scheduled orbital radiotherapy at any time before screening or during the study, or surgical treatment for TED, including orbital decompression, strabismus surgery, and eyelid surgery;
- Cumulative dose of glucocorticoids used to treat TED ≥ 1 g of methylprednisolone equivalents within 90 days prior to screening;
- Oral or intravenous glucocorticoids within 30 days prior to screening;
- Peribulbar/periorbital injection of glucocorticoids within 90 days prior to screening;
- Oral or intravenous administration of any other non-steroidal immunosuppressants within 90 days prior to screening;
- Use of glucocorticoid eye drops/ointments or use of non-steroidal immunosuppressant eye drops within 14 days prior to screening;
- Received antibody therapy targeting IGF-1R, TSHR, CD20(cluster of differentiation antigen 20), IL-6, or IL-6 receptor (IL-6R) at any time before screening;
- Received any other TED therapeutic drugs under development (including but not limited to biologics targeting IGF-1R, FcRn(neonatal Fc recepto), IL-6, or IL-6R) at any time before screening;
- Use of any other monoclonal antibody within 90 days prior to screening;
- Have received live vaccines within 180 days prior to screening, or plan to receive live vaccines during the study;
- Female participants in pregnancy or lactation.
Учебный план
Как устроено исследование?
Детали дизайна
- Основная цель: Уход
- Распределение: Рандомизированный
- Интервенционная модель: Параллельное назначение
- Маскировка: Тройной
Оружие и интервенции
Группа участников / Армия |
Вмешательство/лечение |
|---|---|
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Плацебо Компаратор: SAD Dose 4 - Placebo Control Group
Subjects receive matching placebo to the treatment group.
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subcutaneous injection or intravenous infusion.
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Экспериментальный: MAD Dose 2- IBI3031A101 Treatment Group
Multiple ascending dose (MAD) phase.
Subjects receive repeated doses of IBI3031A101 to evaluate safety, tolerability and steady-state pharmacokinetics.
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subcutaneous injection or intravenous infusion.
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Экспериментальный: SAD Dose 4 - IBI3031A101 Treatment Group
Subjects receive single-dose IBI3031A101 at different dose levels to evaluate safety, tolerability and pharmacokinetics.
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subcutaneous injection or intravenous infusion.
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Плацебо Компаратор: MAD Dose 1 - Placebo Control Group
Multiple ascending dose (MAD) phase.
Subjects receive matching placebo to the treatment group.
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subcutaneous injection or intravenous infusion.
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Экспериментальный: MAD Dose 1- IBI3031A101 Treatment Group
Multiple ascending dose (MAD) phase.
Subjects receive repeated doses of IBI3031A101 to evaluate safety, tolerability and steady-state pharmacokinetics.
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subcutaneous injection or intravenous infusion.
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Плацебо Компаратор: MAD Dose 3 - Placebo Control Group
Multiple ascending dose (MAD) phase.
Subjects receive matching placebo to the treatment group.
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subcutaneous injection or intravenous infusion.
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Экспериментальный: SAD Dose 5 - IBI3031A101 Treatment Group
Subjects receive single-dose IBI3031A101 at different dose levels to evaluate safety, tolerability and pharmacokinetics.
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subcutaneous injection or intravenous infusion.
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Плацебо Компаратор: MAD Dose 2 - Placebo Control Group
Multiple ascending dose (MAD) phase.
Subjects receive matching placebo to the treatment group.
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subcutaneous injection or intravenous infusion.
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Плацебо Компаратор: SAD - Dose 1 - Placebo Control Group
Subjects receive matching placebo to the treatment group.
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subcutaneous injection or intravenous infusion.
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Экспериментальный: SAD Dose 3 - IBI3031A101 Treatment Group
Subjects receive single-dose IBI3031A101 at different dose levels to evaluate safety, tolerability and pharmacokinetics.(at the same dose level as Arm 2 but via [different route/method)
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subcutaneous injection or intravenous infusion.
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Экспериментальный: SAD Dose 2 - IBI3031A101 Treatment Group
Subjects receive single-dose IBI3031A101 at different dose levels to evaluate safety, tolerability and pharmacokinetics.
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subcutaneous injection or intravenous infusion.
|
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Плацебо Компаратор: SAD Dose 5 - Placebo Control Group
Subjects receive matching placebo to the treatment group.
|
subcutaneous injection or intravenous infusion.
|
|
Плацебо Компаратор: SAD Dose 3 - Placebo Control Group
Subjects receive matching placebo to the treatment group.
|
subcutaneous injection or intravenous infusion.
|
|
Экспериментальный: MAD Dose 3- IBI3031A101 Treatment Group
Multiple ascending dose (MAD) phase.
Subjects receive repeated doses of IBI3031A101 to evaluate safety, tolerability and steady-state pharmacokinetics.
|
subcutaneous injection or intravenous infusion.
|
|
Плацебо Компаратор: SAD - Dose 2 - Placebo Control Group
Subjects receive matching placebo to the treatment group.
|
subcutaneous injection or intravenous infusion.
|
|
Экспериментальный: SAD Dose 1 - IBI3031A101 Treatment Group
Subjects receive single-dose IBI3031A101 at different dose levels to evaluate safety, tolerability and pharmacokinetics.
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subcutaneous injection or intravenous infusion.
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Что измеряет исследование?
Первичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
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Number, incidence rate, severity, and association with the study drug of Adverse Events (AEs)
Временное ограничение: up to Day 85 for SAD;up to Day 337 for MAD
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The number, incidence rate, severity, and association with the study drug of all AEs occurring throughout the trial will be summarized.
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up to Day 85 for SAD;up to Day 337 for MAD
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Number, incidence rate, severity, and association with the study drug of Treatment-Emergent Adverse Events (TEAEs)
Временное ограничение: up to Day 85 for SAD;up to Day 337 for MAD
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The number, incidence rate, severity, and association with the study drug of all TEAEs after study drug administration will be summarized.
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up to Day 85 for SAD;up to Day 337 for MAD
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Number, incidence rate, severity, and association with the study drug of Serious Adverse Events (SAEs)
Временное ограничение: up to Day 85 for SAD;up to Day 337 for MAD
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The number, incidence rate, severity, and association with the study drug of all SAEs will be summarized.
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up to Day 85 for SAD;up to Day 337 for MAD
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Change in systolic and diastolic blood pressure after dosing in each dose group(Unit of Measure: mmHg)
Временное ограничение: up to Day 85 for SAD;up to Day 337 for MAD
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Systolic and diastolic blood pressure will be measured and recorded at each specified time point
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up to Day 85 for SAD;up to Day 337 for MAD
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Number of participants with clinically significant abnormal findings in complete physical examination(Unit of Measure: participants)
Временное ограничение: up to Day 85 for SAD;up to Day 337 for MAD
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A complete physical examination will be performed at each specified time point, including assessment of general appearance, respiratory system, cardiovascular system, abdomen, skin, head and neck (including ears, nose, and throat), lymph nodes, thyroid gland, musculoskeletal system (including spine and extremities), and neurological system.
Any finding that is new or worsened from baseline and deemed clinically significant by the investigator will be
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up to Day 85 for SAD;up to Day 337 for MAD
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Changes in hematology laboratory parameters before and after dosing in each dose group
Временное ограничение: up to Day 85 for SAD;up to Day 337 for MAD
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Changes in hematology parameters including white blood cell count, red blood cell count, hemoglobin, and platelet count will be recorded.
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up to Day 85 for SAD;up to Day 337 for MAD
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Changes in blood chemistry laboratory parameters before and after dosing in each dose group
Временное ограничение: up to Day 85 for SAD;up to Day 337 for MAD
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Changes in blood chemistry parameters including liver and renal function, electrolytes, and blood glucose will be recorded.
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up to Day 85 for SAD;up to Day 337 for MAD
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Changes in urinalysis laboratory parameters before and after dosing in each dose group
Временное ограничение: up to Day 85 for SAD;up to Day 337 for MAD
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Changes in urinalysis parameters including urine protein, urine occult blood, and urine leukocytes will be recorded.
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up to Day 85 for SAD;up to Day 337 for MAD
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Changes in thyroid function laboratory parameters before and after dosing in each dose group
Временное ограничение: up to Day 85 for SAD;up to Day 337 for MAD
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Changes in thyroid function parameters including thyroid-stimulating hormone, free triiodothyronine, and free thyroxine will be recorded.
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up to Day 85 for SAD;up to Day 337 for MAD
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Number of subjects with abnormal ECG changes before and after administration in each dose group
Временное ограничение: up to Day 85 for SAD;up to Day 337 for MAD
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up to Day 85 for SAD;up to Day 337 for MAD
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Changes in pure-tone audiometry results before and after dosing in each dose group
Временное ограничение: up to Day 85 for SAD;up to Day 337 for MAD
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Changes in hearing thresholds at each frequency (500 Hz, 1000 Hz, 2000 Hz, 4000 Hz) will be recorded.
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up to Day 85 for SAD;up to Day 337 for MAD
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Change in heart rate after dosing in each dose group (Unit of Measure: beats per minute)
Временное ограничение: up to Day 85 for SAD;up to Day 337 for MAD
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Heart rate will be measured and recorded at each specified time point.
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up to Day 85 for SAD;up to Day 337 for MAD
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Change in body temperature after dosing in each dose group(Unit of Measure: °C)
Временное ограничение: up to Day 85 for SAD;up to Day 337 for MAD
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Body temperature will be measured and recorded at each specified time point.
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up to Day 85 for SAD;up to Day 337 for MAD
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Change in respiratory rate after dosing in each dose group( Unit of Measure: breaths per minute)
Временное ограничение: up to Day 85 for SAD;up to Day 337 for MAD
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Respiratory rate will be measured and recorded at each specified time point.
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up to Day 85 for SAD;up to Day 337 for MAD
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Вторичные показатели результатов
Мера результата |
Мера Описание |
Временное ограничение |
|---|---|---|
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Area Under the Curve (AUC) of the serum concentration-time profile
Временное ограничение: up to Day 85 for SAD;up to Day 337 for MAD
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up to Day 85 for SAD;up to Day 337 for MAD
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Maximum Concentration (Cmax) of the drug in serum
Временное ограничение: up to Day 85 for SAD;up to Day 337 for MAD
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up to Day 85 for SAD;up to Day 337 for MAD
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Clearance (CL)
Временное ограничение: up to Day 85 for SAD;up to Day 337 for MAD
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up to Day 85 for SAD;up to Day 337 for MAD
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Volume of Distribution (Vd)
Временное ограничение: up to Day 85 for SAD;up to Day 337 for MAD
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up to Day 85 for SAD;up to Day 337 for MAD
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Elimination Half-life (t1/2)
Временное ограничение: up to Day 85 for SAD;up to Day 337 for MAD
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up to Day 85 for SAD;up to Day 337 for MAD
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Production of anti-drug antibodies (ADAs) and/or neutralizing antibodies (NAbs) in serum
Временное ограничение: up to Day 85 for SAD;up to Day 337 for MAD
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up to Day 85 for SAD;up to Day 337 for MAD
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Proportion of participants with proptosis response
Временное ограничение: Day 8, Day 29, Day 57, and Day 85 for single ascending dose (SAD) stage; Week 5, Week 9, Week 13, Week 17, Week 21, Week 29, Week 37, and Week 49 for multiple ascending dose (MAD) stage
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Defined as a ≥2 mm reduction in proptosis in the study eye from baseline, without a ≥2 mm increase in proptosis in the fellow eye
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Day 8, Day 29, Day 57, and Day 85 for single ascending dose (SAD) stage; Week 5, Week 9, Week 13, Week 17, Week 21, Week 29, Week 37, and Week 49 for multiple ascending dose (MAD) stage
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Proportion of participants with overall response
Временное ограничение: Day 8, Day 29, Day 57, and Day 85 for single ascending dose (SAD) stage; Week 5, Week 9, Week 13, Week 17, Week 21, Week 29, Week 37, and Week 49 for multiple ascending dose (MAD) stage
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Defined as a ≥2-point reduction in the Clinical Activity Score (CAS) from baseline in the study eye, a ≥2 mm reduction in proptosis in the study eye from baseline, and no worsening in the fellow eye (worsening defined as a ≥2-point increase in CAS or a ≥2 mm increase in proptosis)
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Day 8, Day 29, Day 57, and Day 85 for single ascending dose (SAD) stage; Week 5, Week 9, Week 13, Week 17, Week 21, Week 29, Week 37, and Week 49 for multiple ascending dose (MAD) stage
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Number of subjects with changes in proptosis from baseline after dosing
Временное ограничение: Day 8, Day 29, Day 57, and Day 85 for single ascending dose (SAD) stage; Week 5, Week 9, Week 13, Week 17, Week 21, Week 29, Week 37, and Week 49 for multiple ascending dose (MAD) stage
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Day 8, Day 29, Day 57, and Day 85 for single ascending dose (SAD) stage; Week 5, Week 9, Week 13, Week 17, Week 21, Week 29, Week 37, and Week 49 for multiple ascending dose (MAD) stage
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Proportion of participants with CAS = 0 or 1
Временное ограничение: Day 8, Day 29, Day 57, and Day 85 for single ascending dose (SAD) stage; Week 5, Week 9, Week 13, Week 17, Week 21, Week 29, Week 37, and Week 49 for multiple ascending dose (MAD) stage
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Day 8, Day 29, Day 57, and Day 85 for single ascending dose (SAD) stage; Week 5, Week 9, Week 13, Week 17, Week 21, Week 29, Week 37, and Week 49 for multiple ascending dose (MAD) stage
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CAS change from baseline
Временное ограничение: Day 8, Day 29, Day 57, and Day 85 for single ascending dose (SAD) stage; Week 5, Week 9, Week 13, Week 17, Week 21, Week 29, Week 37, and Week 49 for multiple ascending dose (MAD) stage
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Day 8, Day 29, Day 57, and Day 85 for single ascending dose (SAD) stage; Week 5, Week 9, Week 13, Week 17, Week 21, Week 29, Week 37, and Week 49 for multiple ascending dose (MAD) stage
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Proportion of participants with diplopia response
Временное ограничение: Day 8, Day 29, Day 57, and Day 85 for single ascending dose (SAD) stage; Week 5, Week 9, Week 13, Week 17, Week 21, Week 29, Week 37, and Week 49 for multiple ascending dose (MAD) stage
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Defined as a ≥1-point reduction in diplopia
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Day 8, Day 29, Day 57, and Day 85 for single ascending dose (SAD) stage; Week 5, Week 9, Week 13, Week 17, Week 21, Week 29, Week 37, and Week 49 for multiple ascending dose (MAD) stage
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Total score of the Graves' Ophthalmopathy Quality of Life
Временное ограничение: Day 8, Day 29, Day 57, and Day 85 for single ascending dose (SAD) stage; Week 5, Week 9, Week 13, Week 17, Week 21, Week 29, Week 37, and Week 49 for multiple ascending dose (MAD) stage
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The effect of thyroid eye disease on social activities and appearance during the past 1 week.
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Day 8, Day 29, Day 57, and Day 85 for single ascending dose (SAD) stage; Week 5, Week 9, Week 13, Week 17, Week 21, Week 29, Week 37, and Week 49 for multiple ascending dose (MAD) stage
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Соавторы и исследователи
Даты записи исследования
Изучение основных дат
Начало исследования (Действительный)
Первичное завершение (Оцененный)
Завершение исследования (Оцененный)
Даты регистрации исследования
Первый отправленный
Впервые представлено, что соответствует критериям контроля качества
Первый опубликованный (Действительный)
Обновления учебных записей
Последнее опубликованное обновление (Действительный)
Последнее отправленное обновление, отвечающее критериям контроля качества
Последняя проверка
Дополнительная информация
Термины, связанные с этим исследованием
Дополнительные соответствующие термины MeSH
- Заболевания эндокринной системы
- Генетические заболевания, врожденные
- Аутоиммунные заболевания
- Заболевания иммунной системы
- Глазные болезни
- Заболевания глаз, наследственные
- Болезнь Грейвса
- Экзофтальм
- Орбитальные заболевания
- Зоб
- Гипертиреоз
- Заболевания щитовидной железы
- Врожденные, наследственные и неонатальные заболевания и аномалии
- Офтальмопатия Грейвса
Другие идентификационные номера исследования
- CIBI3031A101
Информация о лекарствах и устройствах, исследовательские документы
Изучает лекарственный продукт, регулируемый FDA США.
Изучает продукт устройства, регулируемый Управлением по санитарному надзору за качеством пищевых продуктов и медикаментов США.
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