Treatment of Chronic Thyroid Eye Disease With MHB018A
2026年6月2日 更新者:Minghui Pharmaceutical (Hangzhou) Ltd
A Phase III, Randomized, Double-Masked, Placebo-Controlled Study to Evaluate the Efficacy of MHB018A Injection Treatment in Subjects With Chronic Moderate-to-Severe Thyroid Eye Disease
The primary objective of this study is to evaluate the efficacy of MHB018A injection compared with placebo in participants with chronic moderate-to-severe TED.
研究概览
详细说明
The primary objective of this study is to evaluate the efficacy of MHB018A injection compared with placebo in participants with chronic moderate-to-severe TED.
研究类型
介入性
注册 (估计的)
135
阶段
- 第三阶段
联系人和位置
本节提供了进行研究的人员的详细联系信息,以及有关进行该研究的地点的信息。
学习联系方式
- 姓名:CMO/ Senior Vice President of R&D
- 电话号码:86 0571-86963293
- 邮箱:jwshi@minghuipharma.com
参与标准
研究人员寻找符合特定描述的人,称为资格标准。这些标准的一些例子是一个人的一般健康状况或先前的治疗。
资格标准
适合学习的年龄
- 成人
- 年长者
接受健康志愿者
不
描述
Inclusion Criteria:
- Subjects voluntarily participating in the study and signing the informed consent form;
- Aged 18-75 years (inclusive), of any gender;
- Clinical diagnosis of chronic Thyroid Eye Disease (TED) , with symptoms in the study eye more than 12 months and less than 10 years.
- Subjects with a clinical diagnosis of moderate to severe TED at screening and baseline.
- Does not require immediate surgical ophthalmological intervention, and no corrective surgery/orbital radiotherapy is planned during the study.
- Diabetic subjects must have well-controlled stable disease.
- Sufficient bone marrow and organ function.
- Eligible subjects of childbearing potential (male and female) must agree to use reliable contraceptive methods; female subjects of childbearing potential must have a negative blood pregnancy test within 7 days before the first use of the study drug and must not be breastfeeding.
Subject is willing and able to comply with the prescribed treatment protocol and evaluations for the duration of the study.
-
Exclusion Criteria:
- Decreased best corrected visual acuity due to optic neuropathy as defined by a decrease in vision within the last 6 months of two lines of Snellen chart, new visual field defect or color defect secondary to optic nerve involvement.
- Corneal decompensation unresponsive to medical management.
- Decrease in CAS of ≥ 2 points or decrease in proptosis of ≥ 2 mm between screening and baseline.
- Free thyroxine (FT4) and free triiodothyronine (FT3) levels <50% above or below the normal reference range at screening.
- Subjects who have previously received orbital radiotherapy or ophthalmic surgery for TED.
- Subjects who received oral or intravenous corticosteroids or corticosteroid eye drops/ointments for TED within 4 weeks before the first dose; subjects who received periorbital/orbital steroid injections within 3 months before the first dose.
- Subjects who used oral or intravenous corticosteroids for reasons other than TED within 4 weeks prior to Screening, excluding local use (topical, nasal, inhalation).
- Any previous treatment with rituximab, tocilizumab, other immunosuppressive agent use within 3 months prior to Screening.
- Previous treatment targeting IGF-1R.
- Selenium and biotin must be discontinued 3 weeks prior to Screening and must not be restarted during the trial; however, taking a multivitamin that includes selenium and/or biotin is allowed.
- Use of an investigational agent for any condition within 30 days prior to Screening or anticipated use during the course of the trial.
- Identified pre-existing ophthalmic disease that, in the judgment of the Investigator, would preclude study participation or complicate interpretation of study results.
- Malignant condition in the past 5 years before signing the ICF (except successfully treated basal/squamous cell carcinoma of the skin).
- Acute cardiovascular disease history or treatment within 6 months before the first dose.
- Presence of poorly controlled hypertension with systolic blood pressure ≥ 160 mmHg or diastolic blood pressure ≥ 100 mmHg; Renal artery stenosis.
- Pregnant or lactating women.
- Drug or alcohol abuse during the screening period.
- Hearing impairment history in either ear during the screening period; or abnormal pure tone audiometry results.
- Biopsy-proven or clinically suspected inflammatory bowel disease.
- Positive results for serum virology tests (defined as pos
- Subjects who received or planned to receive live or attenuated live vaccines within 4 weeks before the first dose or during the study period.
- Subjects who underwent major surgery within 4 weeks before the first dose or are expected to undergo surgery during the study period or within 4 weeks after the study.
Known hypersensitivity to any of the components of MNB018A or prior hypersensitivity reactions to mAbs.
-
学习计划
本节提供研究计划的详细信息,包括研究的设计方式和研究的衡量标准。
研究是如何设计的?
设计细节
- 主要用途:治疗
- 分配:随机化
- 介入模型:并行分配
- 屏蔽:四人间
武器和干预
参与者组/臂 |
干预/治疗 |
|---|---|
|
实验性的:MHB018A 注射液
皮下注射MHB018A注射液,每4周一次(q4w),每次450mg。
|
MHB018A 450毫克,每4周一次(Q4W)皮下注射
|
|
安慰剂比较:MHB018A 注射安慰剂
每4周(q4w)进行一次MHB018A安慰剂的皮下注射
|
每4周(q4w)皮下注射6次MHB018A安慰剂
|
研究衡量的是什么?
主要结果指标
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
Proptosis response rate at Week 24
大体时间:Week 24
|
The percentage of subjects with a reduction in proptosis of ≥2 mm in the study eye/target eye compared to baseline, without deterioration (≥2 mm) in the fellow eye.
|
Week 24
|
次要结果测量
结果测量 |
措施说明 |
大体时间 |
|---|---|---|
|
总体响应率
大体时间:第24周
|
临床活性评分≥2分的受试者的百分比(CAS)降低和≥2mm的基线持续性降低,前提是CAS的CAS或proptosis中的CAS或propissis的相应恶化(≥2点/mm升高)。
|
第24周
|
|
伴有变化
大体时间:基线,直到第24周
|
研究眼中的基线从基线变化,如第24周通过牙科计量计测量
|
基线,直到第24周
|
|
复视回应率
大体时间:第24周
|
复视严重程度降低≥1年级的受试者百分比。
|
第24周
|
|
抗MHB018A抗体(ADA)发病率
大体时间:直到第24周,审判结束(EOT)访问
|
产生抗MHB018A抗体的受试者的百分比。
|
直到第24周,审判结束(EOT)访问
|
|
治疗期间不良事件(AEs)发生率
大体时间:截至第24周及试验结束(EOT)访视时
|
包括治疗期间出现的不良事件(TEAE)、严重不良事件(SAE)和导致提前退出研究的不良事件,以及实验室检查、12导联心电图、生命体征和体格检查。
|
截至第24周及试验结束(EOT)访视时
|
|
Pharmacokinetic Parameter Trough Concentration for MHB018A
大体时间:Week 24
|
Trough concentration (Ctrough) will be assessed using non-compartmental methods in participants randomized to the MHB018A group.
|
Week 24
|
|
Percentage of subjects with CAS of 0 or 1
大体时间:Week 24
|
The percentage of subjects with a CAS (Clinical Activity Score) of 0 or 1 in the study eye/target eye.
CAS ranges from 0 to 7, while higher scores mean a worse outcome.
|
Week 24
|
|
Change in CAS
大体时间:Week 24
|
The mean change from baseline to Week 24 in the CAS (Clinical Activity Score) in the study eye/target eye.
CAS ranges from 0 to 7, while higher scores mean worse outcome.
|
Week 24
|
|
Change in Quality of Life (GO-QOL) Scores
大体时间:Week 24
|
The mean change in scores from the Graves' Ophthalmopathy Quality of Life questionnaire compared to baseline.
The GO-QoL is a self-filled questionnaire containing 16 items.
The raw scores for items 1-8 and items 9-16 are summed separately, each yielding a total raw score ranging from 8 to 24.
Each raw score is then transformed into a 0-100 scale using the following formula: Total Score = (Raw Score - 8) ÷ 16 × 100.
Higher scores indicate better quality of life.
|
Week 24
|
合作者和调查者
在这里您可以找到参与这项研究的人员和组织。
研究记录日期
这些日期跟踪向 ClinicalTrials.gov 提交研究记录和摘要结果的进度。研究记录和报告的结果由国家医学图书馆 (NLM) 审查,以确保它们在发布到公共网站之前符合特定的质量控制标准。
研究主要日期
学习开始 (估计的)
2026年12月1日
初级完成 (估计的)
2028年7月1日
研究完成 (估计的)
2029年7月1日
研究注册日期
首次提交
2026年5月27日
首先提交符合 QC 标准的
2026年5月27日
首次发布 (实际的)
2026年6月2日
研究记录更新
最后更新发布 (实际的)
2026年6月4日
上次提交的符合 QC 标准的更新
2026年6月2日
最后验证
2026年6月1日
更多信息
此信息直接从 clinicaltrials.gov 网站检索,没有任何更改。如果您有任何更改、删除或更新研究详细信息的请求,请联系 register@clinicaltrials.gov. clinicaltrials.gov 上实施更改,我们的网站上也会自动更新.