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Thyroid-Associated OphthalmopathyPhase 4NCT06927375

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

A Phase 4 study testing Tocilizumab(400mg) combined with Flupentixol Melitracen(0.5mg:10mg) and Tocilizumab(400mg) in people with Thyroid-Associated Ophthalmopathy, run by Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University at 1 site in China.

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Sites and contacts
Official record

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Trial 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). Read more about this study

Who is it for?
Ages 18 to 80 years
Conditions the study is for
Thyroid-Associated Ophthalmopathy
What is being tested?
Tocilizumab(400mg) combined with Flupentixol Melitracen(0.5mg:10mg) and Tocilizumab(400mg)
Could I receive a placebo?
No, everyone receives an active treatment
How many people
60 participants
Where
1 siteChina
Study dates
12 Dec 2024to 12 Mar 2026
Phase
Phase 4

Key requirements

Who can take part, as listed by the sponsor. Only the study team can confirm whether you are eligible, so take this list to your doctor.

  • Ages 18 to 80 years
  • All sexes
  • No healthy volunteers
  • Adult, Older adult

Who may be able to join

  • 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.

Who cannot join

  • 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.
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  • 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.

Trial locations and contacts

1 site in 1 country. Contact the study team or a site near you to ask about taking part.

China1 site, 1 recruiting
  • Shanghai Ninth People's Hospital, Shanghai Jiaotong University School of Medicine

    Shanghai, Shanghai Municipality, 200011

    Yingli Lu, (021)+86 13636352507, luyingli2008@126.com

    qin li, (021)+86 13564691094

    Recruiting

Other trials in China

About this study

Official title: Clinical Study on the Combined Use of Tocilizumab and Flupentixol-Melitracen in the Treatment of Thyroid-Associated Ophthalmopathy: A Prospective Exploratory Study

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).

Read the 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.

Being tested
Tocilizumab(400mg) combined with Flupentixol Melitracen(0.5mg:10mg), Tocilizumab(400mg)
Keywords
Thyroid Eye Disease, Graves Orbitopathy, Thyroid Associated Ophthalmopathy, TAO, TED
Medical subject headings
Graves Ophthalmopathy

What participants receive

What participants receive. In a randomised study each person is assigned to one group by chance.

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

    Also called study group

    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(400mg)Drug

    Also called control group

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

Study groups in NCT06927375
Study groupRoleWhat they receive
Tocilizumab combined with Flupentixol MelitracenExperimentalNot described
Receives: Drug: Tocilizumab(400mg) combined with Flupentixol Melitracen(0.5mg:10mg)
TocilizumabActive comparatorNot described
Receives: Drug: Tocilizumab(400mg)

What is being measured

The primary outcome is the main question the study is designed to answer.

  1. comprehensive score

    The comprehensive score has a maximum of 30 points. It is calculated as follows:the half score of TED-QoL (Thyroid Eye Disease Quality of Life questionnaire) (15 points), plus the higher value of CAS (Clinical Activity Score) between the two eyes (7 points). Additionally, one point is added for each symptom present in the participant: tearing, photophobia, dry eye, blurred vision. Also included are diplopia score (3 points) and restricted eye movement score (1 point). The study investigates changes in the comprehensive score before and after treatment in two groups.

    Measured: week12

Secondary outcomes (8)
  1. Go-qol

    The change from baseline in the Graves' Ophthalmopathy Quality of Life (GO-QoL) Questionnaire visual function score and psychosocial function score, and the total score.

    Measured: week 12

  2. TED-QoL

    The change from baseline in the TED-QoL.

    Measured: week 12

  3. CAS Decrease by ≥2 Points

    The proportion of participants whose higher CAS value decreased by ≥2 points compared to baseline.

    Measured: week 12

  4. CAS Change Value

    The change in CAS value compared to baseline for participants.

    Measured: week 12

  5. Diplopia Improvement

    The proportion of participants whose diplopia score decreased by ≥1 point.

    Measured: week 12

  6. Proptosis Change

    The change in proptosis (eye protrusion) compared to baseline for participants

    Measured: week 12

  7. overall response

    The proportion of participants who experience reduction of proptosis ≥2 mm and reduction of CAS ≥2 points

    Measured: week 12

  8. The comprehensive score of TED-QoL and CAS

    The comprehensive score has a maximum of 14 points. It is calculated as follows:the 7/30 score of TED-QoL (Thyroid Eye Disease Quality of Life questionnaire) (7 points), plus the higher value of CAS (Clinical Activity Score) between the two eyes (7 points).The study investigates changes in the comprehensive score before and after treatment in two groups.

    Measured: week12

Timeline

From the start of the study to its completion; the mark is today. Estimated dates are the sponsor’s plan.

  1. First posted15 Apr 2025
  2. Study start12 Dec 2024
  3. Primary completion12 Nov 2025 (estimated)
  4. Study completion12 Mar 2026 (estimated)

Resources

More details

For doctors and researchers: how the study is designed, who runs it, and its registry IDs.

Study design
Study type
Interventional
Phase
Phase 4
Primary purpose
Treatment
Allocation
Randomised
Intervention model
Parallel groups
Masking
Single blind
Who is masked
Investigator
Enrolment
60 participants (estimated)
IDs, dates and publications
ClinicalTrials.gov ID
NCT06927375
Sponsor's protocol ID
SH9H-2024-T313-2
Status last verified
Apr 2025
First submitted
7 Apr 2025
Last updated
16 Apr 2025
Results posted
No
Data monitoring committee
No
FDA-regulated drug
No
FDA-regulated device
No
Individual data sharing
No

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