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A Study of IBI3031 in Participants With Thyroid Eye Disease

2026年7月13日 更新者: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.

調査の概要

状態

募集

詳細な説明

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).

研究の種類

介入

入学 (推定)

66

段階

  • フェーズ 1

連絡先と場所

このセクションには、調査を実施する担当者の連絡先の詳細と、この調査が実施されている場所に関する情報が記載されています。

研究連絡先

研究連絡先のバックアップ

  • 名前:funan liu
  • 電話番号:024-83281137
  • メール:lfn540@126.com

研究場所

    • Liaoning
      • Shenyang、Liaoning、中国、110001
        • 募集
        • The First Hospital of China Medical University
        • コンタクト:

参加基準

研究者は、適格基準と呼ばれる特定の説明に適合する人を探します。これらの基準のいくつかの例は、人の一般的な健康状態または以前の治療です。

適格基準

就学可能な年齢

  • 大人
  • 高齢者

健康ボランティアの受け入れ

いいえ

説明

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.

研究計画

このセクションでは、研究がどのように設計され、研究が何を測定しているかなど、研究計画の詳細を提供します。

研究はどのように設計されていますか?

デザインの詳細

  • 主な目的:処理
  • 割り当て:ランダム化
  • 介入モデル:並列代入
  • マスキング:トリプル

武器と介入

参加者グループ / アーム
介入・治療
プラセボコンパレーター:SAD Dose 4 - Placebo Control Group
Subjects receive matching placebo to the treatment group.
subcutaneous injection or intravenous infusion.
実験的: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.
実験的: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.
プラセボコンパレーター:MAD Dose 1 - Placebo Control Group
Multiple ascending dose (MAD) phase. Subjects receive matching placebo to the treatment group.
subcutaneous injection or intravenous infusion.
実験的: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.
プラセボコンパレーター:MAD Dose 3 - Placebo Control Group
Multiple ascending dose (MAD) phase. Subjects receive matching placebo to the treatment group.
subcutaneous injection or intravenous infusion.
実験的: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.
プラセボコンパレーター:MAD Dose 2 - Placebo Control Group
Multiple ascending dose (MAD) phase. Subjects receive matching placebo to the treatment group.
subcutaneous injection or intravenous infusion.
プラセボコンパレーター:SAD - Dose 1 - Placebo Control Group
Subjects receive matching placebo to the treatment group.
subcutaneous injection or intravenous infusion.
実験的: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.
実験的: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.
プラセボコンパレーター:SAD Dose 5 - Placebo Control Group
Subjects receive matching placebo to the treatment group.
subcutaneous injection or intravenous infusion.
プラセボコンパレーター:SAD Dose 3 - Placebo Control Group
Subjects receive matching placebo to the treatment group.
subcutaneous injection or intravenous infusion.
実験的: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.
プラセボコンパレーター:SAD - Dose 2 - Placebo Control Group
Subjects receive matching placebo to the treatment group.
subcutaneous injection or intravenous infusion.
実験的: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.

この研究は何を測定していますか?

主要な結果の測定

結果測定
メジャーの説明
時間枠
Number, incidence rate, severity, and association with the study drug of Adverse Events (AEs)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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

二次結果の測定

結果測定
メジャーの説明
時間枠
Area Under the Curve (AUC) of the serum concentration-time profile
時間枠: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
時間枠: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)
時間枠: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)
時間枠: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)
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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
時間枠: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

協力者と研究者

ここでは、この調査に関係する人々や組織を見つけることができます。

研究記録日

これらの日付は、ClinicalTrials.gov への研究記録と要約結果の提出の進捗状況を追跡します。研究記録と報告された結果は、国立医学図書館 (NLM) によって審査され、公開 Web サイトに掲載される前に、特定の品質管理基準を満たしていることが確認されます。

主要日程の研究

研究開始 (実際)

2026年6月30日

一次修了 (推定)

2027年6月15日

研究の完了 (推定)

2027年12月28日

試験登録日

最初に提出

2026年5月19日

QC基準を満たした最初の提出物

2026年5月27日

最初の投稿 (実際)

2026年6月3日

学習記録の更新

投稿された最後の更新 (実際)

2026年7月14日

QC基準を満たした最後の更新が送信されました

2026年7月13日

最終確認日

2026年7月1日

詳しくは

本研究に関する用語

医薬品およびデバイス情報、研究文書

米国FDA規制医薬品の研究

いいえ

米国FDA規制機器製品の研究

いいえ

この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。

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