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A Study of IBI3031 in Participants With Thyroid Eye Disease

13 de julho de 2026 atualizado por: Innovent Biologics (Suzhou) Co. Ltd.

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

This is a multicenter, randomized, double-masked, placebo-controlled, single/multiple-dose-escalation trial conducted in Chinese participants with Thyroid Eye Disease (TED), aiming to evaluate the safety and tolerability of IBI3031 administered via subcutaneous or intravenous injection.

Visão geral do estudo

Status

Recrutamento

Descrição detalhada

IBI3031 is an IGF-1R(Insulin-like growth factor 1 receptor)/TSHR(Thyroid-stimulating hormone receptor) bispecific antibody with potential synergistic therapeutic efficacy in TED and modulatory effects on thyroid function. As the first-in-human trial of IBI3031, this study evaluates the safety, tolerability, PK(Pharmacokinetics)/PD(Pharmacodynamics) profiles, immunogenicity, and efficacy of IBI3031 in TED participants. The trial is conducted in two stages: Stage 1- a single-ascending-dose (SAD) study involving single SC or IV administration of IBI3031; Stage 2- a multiple-ascending-dose (MAD) study involving three SC administrations of IBI3031. Approximately 66 TED participants are planned for enrollment: 36 in Stage 1 (allocated at a 3:1 ratio) and 30 in Stage 2 (allocated at a 4:1 ratio).

Tipo de estudo

Intervencional

Inscrição (Estimado)

66

Estágio

  • Fase 1

Contactos e Locais

Esta seção fornece os detalhes de contato para aqueles que conduzem o estudo e informações sobre onde este estudo está sendo realizado.

Contato de estudo

Estude backup de contato

  • Nome: funan liu
  • Número de telefone: 024-83281137
  • E-mail: lfn540@126.com

Locais de estudo

    • Liaoning
      • Shenyang, Liaoning, China, 110001
        • Recrutamento
        • The First Hospital of China Medical University
        • Contato:

Critérios de participação

Os pesquisadores procuram pessoas que se encaixem em uma determinada descrição, chamada de critérios de elegibilidade. Alguns exemplos desses critérios são a condição geral de saúde de uma pessoa ou tratamentos anteriores.

Critérios de elegibilidade

Idades elegíveis para estudo

  • Adulto
  • Adulto mais velho

Aceita Voluntários Saudáveis

Não

Descrição

Key Inclusion Criteria:

  1. Written informed consent.
  2. Aged between 18 and 75 years at screening.
  3. Weight between 45 kg and 100 kg.
  4. 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;
  5. Exophthalmos ≥ 18 mm in the study eye at baseline. (Only applicable to Stage 2)
  6. Participants must be clinically and biochemically euthyroid, or have mild hypothyroidism or mild-to-moderate hyperthyroidism at screening.
  7. Positive for Thyrotrophin Receptor Antibody (TRAb) at screening.
  8. 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.
  9. 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):

  1. 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;
  2. Participants previously diagnosed with dysthyroid optic neuropathy (DON), or with DON as determined by the investigator at screening;
  3. Patients with corneal ulcers that are not relieved after treatment at the investigator's discretion;
  4. 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);
  5. 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).
  6. 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);
  7. Scheduled radioactive iodine therapy or thyroidectomy at any time before screening or during the study;
  8. 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;
  9. Cumulative dose of glucocorticoids used to treat TED ≥ 1 g of methylprednisolone equivalents within 90 days prior to screening;
  10. Oral or intravenous glucocorticoids within 30 days prior to screening;
  11. Peribulbar/periorbital injection of glucocorticoids within 90 days prior to screening;
  12. Oral or intravenous administration of any other non-steroidal immunosuppressants within 90 days prior to screening;
  13. Use of glucocorticoid eye drops/ointments or use of non-steroidal immunosuppressant eye drops within 14 days prior to screening;
  14. 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;
  15. 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;
  16. Use of any other monoclonal antibody within 90 days prior to screening;
  17. Have received live vaccines within 180 days prior to screening, or plan to receive live vaccines during the study;
  18. Female participants in pregnancy or lactation.

Plano de estudo

Esta seção fornece detalhes do plano de estudo, incluindo como o estudo é projetado e o que o estudo está medindo.

Como o estudo é projetado?

Detalhes do projeto

  • Finalidade Principal: Tratamento
  • Alocação: Randomizado
  • Modelo Intervencional: Atribuição Paralela
  • Mascaramento: Triplo

Armas e Intervenções

Grupo de Participantes / Braço
Intervenção / Tratamento
Comparador de Placebo: SAD Dose 4 - Placebo Control Group
Subjects receive matching placebo to the treatment group.
subcutaneous injection or intravenous infusion.
Experimental: 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.
subcutaneous injection or intravenous infusion.
Experimental: SAD Dose 4 - IBI3031A101 Treatment Group
Subjects receive single-dose IBI3031A101 at different dose levels to evaluate safety, tolerability and pharmacokinetics.
subcutaneous injection or intravenous infusion.
Comparador de Placebo: MAD Dose 1 - Placebo Control Group
Multiple ascending dose (MAD) phase. Subjects receive matching placebo to the treatment group.
subcutaneous injection or intravenous infusion.
Experimental: 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.
subcutaneous injection or intravenous infusion.
Comparador de Placebo: MAD Dose 3 - Placebo Control Group
Multiple ascending dose (MAD) phase. Subjects receive matching placebo to the treatment group.
subcutaneous injection or intravenous infusion.
Experimental: SAD Dose 5 - IBI3031A101 Treatment Group
Subjects receive single-dose IBI3031A101 at different dose levels to evaluate safety, tolerability and pharmacokinetics.
subcutaneous injection or intravenous infusion.
Comparador de Placebo: MAD Dose 2 - Placebo Control Group
Multiple ascending dose (MAD) phase. Subjects receive matching placebo to the treatment group.
subcutaneous injection or intravenous infusion.
Comparador de Placebo: SAD - Dose 1 - Placebo Control Group
Subjects receive matching placebo to the treatment group.
subcutaneous injection or intravenous infusion.
Experimental: 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)
subcutaneous injection or intravenous infusion.
Experimental: SAD Dose 2 - IBI3031A101 Treatment Group
Subjects receive single-dose IBI3031A101 at different dose levels to evaluate safety, tolerability and pharmacokinetics.
subcutaneous injection or intravenous infusion.
Comparador de Placebo: SAD Dose 5 - Placebo Control Group
Subjects receive matching placebo to the treatment group.
subcutaneous injection or intravenous infusion.
Comparador de Placebo: SAD Dose 3 - Placebo Control Group
Subjects receive matching placebo to the treatment group.
subcutaneous injection or intravenous infusion.
Experimental: 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.
Comparador de Placebo: SAD - Dose 2 - Placebo Control Group
Subjects receive matching placebo to the treatment group.
subcutaneous injection or intravenous infusion.
Experimental: SAD Dose 1 - IBI3031A101 Treatment Group
Subjects receive single-dose IBI3031A101 at different dose levels to evaluate safety, tolerability and pharmacokinetics.
subcutaneous injection or intravenous infusion.

O que o estudo está medindo?

Medidas de resultados primários

Medida de resultado
Descrição da medida
Prazo
Number, incidence rate, severity, and association with the study drug of Adverse Events (AEs)
Prazo: up to Day 85 for SAD;up to Day 337 for MAD
The number, incidence rate, severity, and association with the study drug of all AEs occurring throughout the trial will be summarized.
up to Day 85 for SAD;up to Day 337 for MAD
Number, incidence rate, severity, and association with the study drug of Treatment-Emergent Adverse Events (TEAEs)
Prazo: up to Day 85 for SAD;up to Day 337 for MAD
The number, incidence rate, severity, and association with the study drug of all TEAEs after study drug administration will be summarized.
up to Day 85 for SAD;up to Day 337 for MAD
Number, incidence rate, severity, and association with the study drug of Serious Adverse Events (SAEs)
Prazo: up to Day 85 for SAD;up to Day 337 for MAD
The number, incidence rate, severity, and association with the study drug of all SAEs will be summarized.
up to Day 85 for SAD;up to Day 337 for MAD
Change in systolic and diastolic blood pressure after dosing in each dose group(Unit of Measure: mmHg)
Prazo: up to Day 85 for SAD;up to Day 337 for MAD
Systolic and diastolic blood pressure will be measured and recorded at each specified time point
up to Day 85 for SAD;up to Day 337 for MAD
Number of participants with clinically significant abnormal findings in complete physical examination(Unit of Measure: participants)
Prazo: up to Day 85 for SAD;up to Day 337 for MAD
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
up to Day 85 for SAD;up to Day 337 for MAD
Changes in hematology laboratory parameters before and after dosing in each dose group
Prazo: up to Day 85 for SAD;up to Day 337 for MAD
Changes in hematology parameters including white blood cell count, red blood cell count, hemoglobin, and platelet count will be recorded.
up to Day 85 for SAD;up to Day 337 for MAD
Changes in blood chemistry laboratory parameters before and after dosing in each dose group
Prazo: up to Day 85 for SAD;up to Day 337 for MAD
Changes in blood chemistry parameters including liver and renal function, electrolytes, and blood glucose will be recorded.
up to Day 85 for SAD;up to Day 337 for MAD
Changes in urinalysis laboratory parameters before and after dosing in each dose group
Prazo: up to Day 85 for SAD;up to Day 337 for MAD
Changes in urinalysis parameters including urine protein, urine occult blood, and urine leukocytes will be recorded.
up to Day 85 for SAD;up to Day 337 for MAD
Changes in thyroid function laboratory parameters before and after dosing in each dose group
Prazo: up to Day 85 for SAD;up to Day 337 for MAD
Changes in thyroid function parameters including thyroid-stimulating hormone, free triiodothyronine, and free thyroxine will be recorded.
up to Day 85 for SAD;up to Day 337 for MAD
Number of subjects with abnormal ECG changes before and after administration in each dose group
Prazo: up to Day 85 for SAD;up to Day 337 for MAD
up to Day 85 for SAD;up to Day 337 for MAD
Changes in pure-tone audiometry results before and after dosing in each dose group
Prazo: up to Day 85 for SAD;up to Day 337 for MAD
Changes in hearing thresholds at each frequency (500 Hz, 1000 Hz, 2000 Hz, 4000 Hz) will be recorded.
up to Day 85 for SAD;up to Day 337 for MAD
Change in heart rate after dosing in each dose group (Unit of Measure: beats per minute)
Prazo: up to Day 85 for SAD;up to Day 337 for MAD
Heart rate will be measured and recorded at each specified time point.
up to Day 85 for SAD;up to Day 337 for MAD
Change in body temperature after dosing in each dose group(Unit of Measure: °C)
Prazo: up to Day 85 for SAD;up to Day 337 for MAD
Body temperature will be measured and recorded at each specified time point.
up to Day 85 for SAD;up to Day 337 for MAD
Change in respiratory rate after dosing in each dose group( Unit of Measure: breaths per minute)
Prazo: up to Day 85 for SAD;up to Day 337 for MAD
Respiratory rate will be measured and recorded at each specified time point.
up to Day 85 for SAD;up to Day 337 for MAD

Medidas de resultados secundários

Medida de resultado
Descrição da medida
Prazo
Area Under the Curve (AUC) of the serum concentration-time profile
Prazo: up to Day 85 for SAD;up to Day 337 for MAD
up to Day 85 for SAD;up to Day 337 for MAD
Maximum Concentration (Cmax) of the drug in serum
Prazo: up to Day 85 for SAD;up to Day 337 for MAD
up to Day 85 for SAD;up to Day 337 for MAD
Clearance (CL)
Prazo: up to Day 85 for SAD;up to Day 337 for MAD
up to Day 85 for SAD;up to Day 337 for MAD
Volume of Distribution (Vd)
Prazo: up to Day 85 for SAD;up to Day 337 for MAD
up to Day 85 for SAD;up to Day 337 for MAD
Elimination Half-life (t1/2)
Prazo: up to Day 85 for SAD;up to Day 337 for MAD
up to Day 85 for SAD;up to Day 337 for MAD
Production of anti-drug antibodies (ADAs) and/or neutralizing antibodies (NAbs) in serum
Prazo: up to Day 85 for SAD;up to Day 337 for MAD
up to Day 85 for SAD;up to Day 337 for MAD
Proportion of participants with proptosis response
Prazo: 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
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
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
Proportion of participants with overall response
Prazo: 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
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)
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
Number of subjects with changes in proptosis from baseline after dosing
Prazo: 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
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
Proportion of participants with CAS = 0 or 1
Prazo: 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
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
CAS change from baseline
Prazo: 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
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
Proportion of participants with diplopia response
Prazo: 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
Defined as a ≥1-point reduction in diplopia
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
Total score of the Graves' Ophthalmopathy Quality of Life
Prazo: 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
The effect of thyroid eye disease on social activities and appearance during the past 1 week.
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

Colaboradores e Investigadores

É aqui que você encontrará pessoas e organizações envolvidas com este estudo.

Datas de registro do estudo

Essas datas acompanham o progresso do registro do estudo e os envios de resumo dos resultados para ClinicalTrials.gov. Os registros do estudo e os resultados relatados são revisados ​​pela National Library of Medicine (NLM) para garantir que atendam aos padrões específicos de controle de qualidade antes de serem publicados no site público.

Datas Principais do Estudo

Início do estudo (Real)

30 de junho de 2026

Conclusão Primária (Estimado)

15 de junho de 2027

Conclusão do estudo (Estimado)

28 de dezembro de 2027

Datas de inscrição no estudo

Enviado pela primeira vez

19 de maio de 2026

Enviado pela primeira vez que atendeu aos critérios de CQ

27 de maio de 2026

Primeira postagem (Real)

3 de junho de 2026

Atualizações de registro de estudo

Última Atualização Postada (Real)

14 de julho de 2026

Última atualização enviada que atendeu aos critérios de controle de qualidade

13 de julho de 2026

Última verificação

1 de julho de 2026

Mais Informações

Termos relacionados a este estudo

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Estuda um medicamento regulamentado pela FDA dos EUA

Não

Estuda um produto de dispositivo regulamentado pela FDA dos EUA

Não

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