A Study on the Combined Use of Tocilizumab and Flupentixol-Melitracen in the Treatment of Thyroid-Associated Ophthalmopathy

NCT ID: NCT06927375

Last Updated: 2025-04-16

Basic Information

• Recruitment Status: RECRUITING
• Clinical Phase: PHASE4
• Total Enrollment: 60 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2024-12-12
• Study Completion Date: 2026-03-12

Brief Summary

Thyroid-associated ophthalmopathy (TAO) is a serious, progressive, vision-threatening autoimmune disease that can be categorized into mild, moderate, and severe stages based on severity. The activity of TAO is commonly evaluated using the Clinical Activity Score (CAS). Tocilizumab serves as a second-line treatment option for patients with moderate to severe active TAO. Additionally, it is common for TAO patients to experience anxiety, which may exacerbate their condition and negatively impact prognosis. Therefore, we have designed this randomized controlled study to evaluate the impact of Flupentixol Melitracen (Lepan) on the treatment outcomes of participants receiving Tocilizumab (Actemra).

Detailed Description

Thyroid-associated ophthalmopathy (TAO) is a serious, progressive, vision-threatening autoimmune disease with an incidence rate of about 19-42 per 100,000. Currently, it ranks first among orbital diseases and is one of the primary causes of blindness. The extensive involvement of intraorbital tissues and the significant variability in the course of moderate to severe active TAO make its treatment outcomes uncertain, classifying it as refractory thyroid-associated ophthalmopathy. The pathogenesis of TAO has not been fully elucidated; however, activation of the thyrotropin receptor (TSHR) and insulin-like growth factor receptor-1 (IGF-1R) complex is considered a critical step in TAO, leading to abnormal immune proliferation responses within the orbit, causing hypertrophy of extraocular muscles and increased orbital fat tissue. These changes result in various clinical manifestations such as exophthalmos, diplopia, pain, and compressive optic neuropathy. Intravenous glucocorticoid therapy is recommended as the first-line treatment by guidelines, yet this treatment often leads to numerous side effects (including Cushing's facies, elevated blood pressure, glucose, and lipid levels, osteoporosis, urinary tract infections, peptic ulcers, etc.), and many patients with moderate to severe active TAO do not show significant improvement in ocular symptoms (such as impairment of eye movement, blurred vision, diplopia, etc.). Therefore, scholars at home and abroad have been committed to finding new effective treatments for refractory TAO. Biological agents represent emerging therapies for TAO, with domestic and international multicenter randomized controlled trials confirming that tocilizumab is effective in treating TAO and can be considered as a second-line treatment option for moderate to severe active TAO. Tocilizumab is a monoclonal antibody against the IL-6 receptor. Interleukin-6 (IL-6) can activate T cells and B cells and produce TSHR-stimulating immunoglobulins, and it can also directly act on preadipocytes in the orbit to promote adipose hyperplasia. Tocilizumab reduces memory B cell and immunoglobulin levels, thereby improving eye movements and clinical activity scores (CAS), and enhancing quality of life scores.

Most TAO patients exhibit proptosis, and severe cases may develop incomplete eyelid closure, resulting in exposure keratitis, corneal ulcers, and significant eye pain, photophobia, and lacrimation. Changes in appearance due to TAO and even potential blindness can cause patients to experience significant psychological stress, leading to feelings of inferiority, anxiety, depression, and other negative emotions. Additionally, patients with coexisting hyperthyroidism may exhibit irritability, insomnia, anger, and other emotional reactions. Studies have shown that serum and tear fluid IL-6 levels are elevated in TAO patients, which are hormone factors related to behavioral and emotional changes and can influence emotional regulation, including anxiety modulation, by acting on the brain. Moreover, neurogenic inflammation is considered part of the psychosomatic pathogenic mechanism of TAO. Under conditions of prolonged anxiety and psychological stress, TAO patients release norepinephrine from primary neurons, generating neurogenic inflammation, and enhance the pro-inflammatory effects of platelets and leukocytes. Anxiety and depression levels in TAO patients are higher than those in other chronic diseases, increasing the risk of unnatural deaths, including suicide, thus impacting public health. Several studies indicate that TAO significantly affects patients' quality of life, including reduced participation in daily activities and poorer emotional health, and adverse emotions like anxiety and depression might exacerbate the condition and affect prognosis.

Therefore, while treating the symptoms of thyroid-associated eye disease, attention should also be paid to the varying degrees of negative psychology experienced by these patients, necessitating enhanced psychological interventions for them. We hypothesize that in refractory TAO patients with anxiety, combined treatment with Flupentixol Melitracen might help alleviate anxiety and depressive moods, improve quality of life, facilitate treatment, and improve ocular prognosis. This clinical study aims to evaluate the efficacy of tocilizumab (Actemra) in combination with Flupentixol Melitracen (Lepan) in the treatment of refractory thyroid-associated ophthalmopathy.

Conditions

Thyroid-Associated Ophthalmopathy

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: TREATMENT
• Blinding Strategy: SINGLE

Study Groups

Tocilizumab combined with Flupentixol Melitracen

Group Type: EXPERIMENTAL

Tocilizumab(400mg) combined with Flupentixol Melitracen(0.5mg:10mg)

Intervention Type: DRUG

Tocilizumab (Actemra) is administered via intravenous infusion at a dose of 400 mg at Weeks 0, 4, and 8. Flupentixol/Melitracen is given orally at a dose of 0.5 mg/10 mg twice daily for 8 consecutive weeks starting from Week 0.

Tocilizumab

Group Type: ACTIVE_COMPARATOR

Tocilizumab(400mg)

Intervention Type: DRUG

Tocilizumab (Actemra) is administered via intravenous infusion at a dose of 400 mg at Weeks 0, 4, and 8.

Interventions

Tocilizumab(400mg) combined with Flupentixol Melitracen(0.5mg:10mg)

Tocilizumab (Actemra) is administered via intravenous infusion at a dose of 400 mg at Weeks 0, 4, and 8. Flupentixol/Melitracen is given orally at a dose of 0.5 mg/10 mg twice daily for 8 consecutive weeks starting from Week 0.

Intervention Type: DRUG

Tocilizumab(400mg)

Tocilizumab (Actemra) is administered via intravenous infusion at a dose of 400 mg at Weeks 0, 4, and 8.

Intervention Type: DRUG

Other Intervention Names

study group; control group

Eligibility Criteria

Inclusion Criteria

• Aged between 18 and 80 years (inclusive).
• Meets internationally recognized diagnostic criteria for TED with the more severely affected eye in moderate to severe active phase. Meeting any one of the following criteria qualifies as moderate to severe: an exophthalmos ≥2 mm compared with normal values for sex and race; presence of inconstant to constant diplopia; a lid retraction ≥2 mm. A Clinical Activity Score (CAS) of ≥3 or a score of 2 combined with MRI evidence indicating active disease is defined as active.
• Normal thyroid function within one month prior to enrollment: including those currently taking antithyroid drugs or not requiring medication, with FT3 and FT4 levels within normal range and TSH either normal or decreased.
• HAMA (Hamilton Anxiety Rating Scale) score of ≥14.
• Voluntary participation and provision of informed consent.

Exclusion Criteria

• Severe cardiac, hepatic, or renal insufficiency (including myocardial ischemia or myocardial infarction, arrhythmias, and heart failure; ALT, AST ≥ 3 times the upper limit of normal; eGFR < 60 ml/min/1.73 m²).
• communicable disease.
• Pregnancy or planning to become pregnant.
• Currently breastfeeding.
• Received radioactive iodine treatment or hepatitis vaccination within three months prior to enrollment.
• Received systemic immunotherapy for TAO, including oral or intravenous glucocorticoids, other immunosuppressants, or orbital radiotherapy within one month prior to enrollment.
• Planning to undergo other treatments during the course of this study.
• Severe mental disorders that affect compliance.
• Presence of other clinically significant or unstable systemic diseases.
• Patients who are unlikely to complete the entire course of treatment.

• Minimum Eligible Age: 18 Years
• Maximum Eligible Age: 80 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University

OTHER

Sponsor Role: lead

Responsible Party

lu ying li

Chief physician，head of Endocrinology department

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Yingli Lu

Role: STUDY_CHAIR

Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine, Shanghai, China

Qin Li

Role: PRINCIPAL_INVESTIGATOR

Shanghai Ninth People's Hospital, Shanghai JiaoTong University School of Medicine, Shanghai, China

Locations

Shanghai Ninth People's Hospital, Shanghai Jiaotong University School of Medicine

Shanghai, Shanghai Municipality, China

Site Status: RECRUITING

Countries

China

Central Contacts

Yingli Lu

Role: CONTACT

luyingli2008@126.com

（021）+86 13636352507

qin li

Role: CONTACT

(021) +86 13564691094

Facility Contacts

Yingli Lu

Role: primary

luyingli2008@126.com

（021）+86 13636352507

qin li

Role: backup

（021）+86 13564691094

Other Identifiers

SH9H-2024-T313-2

Identifier Type: -

Identifier Source: org_study_id