Thyroid Eye Disease
Conditions
Brief summary
This is a multicenter, randomized, double-masked, placebo-controlled Phase 3 study to evaluate the efficacy, safety, immunogenicity, and population pharmacokinetic (PopPK) characteristics of KHN939 in Chinese patients with moderate-to-severe active thyroid eye disease (TED). Approximately 60 participants who meet the study eligibility criteria will be randomized in a 2:1 ratio (stratified by smoking status) to receive 8 infusions of KHN939 or placebo q3W.
Interventions
DRUGKHN939
Intravenous (IV) infusion: 20 mg/kg every 3 weeks (Q3W) for a total of 8 doses over 21 weeks
DRUGPlacebo
Intravenous (IV) infusion: placebo every 3 weeks (Q3W) for a total of 8 doses over 21 weeks
Sponsors
Beijing Kanghong Biological Medicine Co., Ltd.
Study design
Allocation
RANDOMIZED
Intervention model
PARALLEL
Primary purpose
TREATMENT
Masking
QUADRUPLE (Subject, Caregiver, Investigator, Outcomes Assessor)
Eligibility
Sex/Gender
ALL
Age
18 Years to 70 Years
Healthy volunteers
No
Inclusion criteria
1. Aged 18-70 years (inclusive) at the time of signing the informed consent form (ICF), male or female 2. Weight between 45 kg and 100 kg 3. Diagnosed with moderate-to-severe active TED: * Proptosis ≥18 mm, accompanied by at least one of the following: (a) eyelid retraction ≥2 mm; (b) moderate to severe soft tissue involvement; (c) intermittent or continuous diplopia * CAS ≥ 3 points * Duration of active TED symptoms ≤12 months prior to screening (documented by patient history or medical records) 4. Female participants of childbearing potential must have a negative serum pregnancy test during screening and agree to use an effective method of contraception from screening until 90 days after the last dose of the study drug. (Note: Women of non-childbearing potential, defined as surgically sterile or postmenopausal, are exempt.) Male participants must agree to use birth control from screening until at least 90 days after the dose of study drug. 5. Able to comply with all protocol-required procedures, examinations, and symptom reporting.
Exclusion criteria
1. Known hypersensitivity to any component of the study drug formulation, or prior hypersensitivity to any monoclonal antibodies 2. Proptosis at Day 1 (pre-dose) that has decreased by ≥2 mm relative to screening 3. CAS at Day 1 (pre-dose) that has decreased by ≥2 points relative to screening 4. Ocular conditions: * Prior or investigator-assessed diagnosis of dysthyroid optic neuropathy (DON) at screening * Corneal involvement in the study eye without improvement after appropriate treatment * Prior orbital radiotherapy or surgery for TED in the study eye (including orbital decompression, strabismus correction, eyelid correction) * Requires immediate or planned ophthalmic surgical intervention during the study period * Has any pre-existing ocular condition (e.g., high myopia, anticipated cataract surgery) that, as determined by the investigator, would preclude study participation or complicate the interpretation of study results; 5. Prior/concomitant treatments: * Cumulative corticosteroid use for TED ≥1 g methylprednisolone equivalent. \[Note: Participants receiving \<1 g and discontinued ≥30 days prior to screening are eligible\] * Corticosteroid use within 30 days of screening (except topical, intranasal, inhaled, or intra-articular) * Periorbital/periocular corticosteroid injection within 90 days of screening * Corticosteroid or non-steroidal immunosuppressant eye drops within 7 days of screening * Oral or IV non-steroidal immunosuppressants within 90 days of screening * Prior anti-CD20 antibody, IL-6 receptor antibody, teprotumumab, or teprotumumab N01 at any time * Any other investigational TED treatment (including IGF-1R or TSHR-targeting biologics) at any time * Need for selenium or vitamin supplementation for TED treatment from 21 days pre-dose through study end (multivitamins are permitted) 6. Medical history/conditions: * Medical conditions that contraindicate study drug use, including: suspected or confirmed inflammatory bowel disease (IBD), coagulopathy, Cerebrovascular accident (CVA) or transient ischemic attack (TIA) within 180 days, acute myocardial infarction (MI), unstable angina, or CABG/PCI within 180 days, severe arrhythmia, or severe systemic infection * Malignancy (treated or untreated) within 5 years prior to screening, except for the following cured or non-metastatic conditions: cutaneous squamous cell carcinoma (SCC) or basal cell carcinoma (BCC), cervical or prostate carcinoma in situ (CIS), papillary thyroid carcinoma * Uncontrolled diabetes (HbA1c ≥8.0% at screening, or initiation of a new diabetes medication, or a \>10% dose adjustment to an existing diabetes medication within 60 days prior to screening) * Poorly controlled thyroid function: defined as FT3 or FT4 deviating ≥50% from local laboratory normal range (≥1.5×ULN or ≤0.5×LLN) * Uncontrolled hypertension: defined as SBP ≥160 mmHg or DBP ≥100 mmHg; renal artery stenosis; or other evidence of clinically unstable blood pressure * 12-lead ECG with a heart rate \<50 or \>100 bpm and evidence of active cardiac disease; or any screening ECG abnormality that, in the investigator's opinion, confounds subsequent interpretation, particularly QTcF \>450 ms in males or \>470 ms in females 7. Laboratory exclusions at screening: * Alanine aminotransferase (ALT) \>3 × ULN * Aspartate aminotransferase (AST) \>3 × ULN * Serum creatinine(Cr) ≥1.5 × ULN, or glomerular filtration rate (GFR) \<30 mL/min/1.73 m² (MDRD formula) 8. Clinically significant ear disease, prior ear surgery, hearing impairment, or abnormal pure-tone audiometry (defined as a mean bone conduction threshold ≥25 dB at 0.5, 1, 2, 4 kHz, or ≥40 dB at any frequency) 9. Positive for HBsAg with HBV-DNA \>1000 IU/mL or currently receiving anti-HBV therapy; positive for HIV antibody or HCV antibody; or active syphilis 10. Participation in any drug, vaccine, or device clinical trial within 3 months prior to screening, or currently within follow-up or within 5 half-lives of another study 11. Female subjects who are pregnant or lactating 12. Any other condition deemed by the investigator as inappropriate for study participation
Design outcomes
Primary
| Measure | Time frame | Description |
|---|---|---|
| The proptosis responder rate of the study eye | Week 24 | Defined as percentage of subjects with a ≥ 2mm reduction from Baseline in proptosis in the study eye, without deterioration \[≥ 2 mm increase\] of proptosis in the non-study eye at Week 24. Proptosis assessment: amount of protrusion of the eye from the orbital rim measured by Hertel exophthalmometer. |
Secondary
| Measure | Time frame | Description |
|---|---|---|
| Proptosis responder rate in the study eye | Week 12 | See primary outcome measure description for details. |
| Overall responder rate in the study eye | week 12, week 24 | Defined as study eye CAS reduced ≥2 points from baseline AND proptosis reduced ≥2 mm from baseline,without deterioration (without deterioration: CAS increase \<2 points AND proptosis increase \<2 mm) in the fellow eye. |
| Change from baseline in proptosis measurement of the study eye | week 12, week 24 | See primary outcome measure description for details. |
| Change in Quality of Life (GO-QoL) Scores | week 12, week 24 | The GO-QoL is a 16-item self-administered questionnaire divided into 2 subsets and used to assess the perceived effects of TED by the subjects on (i) their daily physical activity as it relates to visual function, and (ii) psychosocial functioning. The range of the GO-QoL overall transformed scores is 0 to 100, where higher values correspond to better quality of life. |
| Change from baseline in Clinical Activity Score (CAS) in the study eye | week 12, week 24 | The CAS, based on the 7-item European Group on Graves' Ophthalmopathy (EUGOGO) amendment, was used to evaluate clinical activity. The CAS ranges from 0 to 7, where higher scores indicate greater disease activity (worse outcome). |
| Treatment response rate in the study eye | week 12, week 24 | Treatment response rate in the study eye (treatment response defined as meeting ≥2 of the following 4 criteria: (a) palpebral width reduction ≥2 mm; (b) ≥1 point reduction in any of the 5 CAS inflammatory items (eyelid erythema, eyelid edema, conjunctival erythema, conjunctival edema, caruncle swelling); (c) proptosis reduction ≥2 mm; (d) ocular motility improvement ≥8°; with no worsening in the contralateral eye). |
| Change from baseline in diplopia score | week 12, week 24 | Diplopia will be evaluated using the Gorman Subjective Diplopia Scale. The total score ranges from a minimum value of 0 to a maximum value of 3 (0 = no diplopia; 1 = intermittent diplopia; 2 = inconstant diplopia; 3 = constant diplopia). Higher scores mean a worse outcome (more severe diplopia condition). |
| Change from Baseline in Diplopia Questionnaire (DQ) Score | Week 12, Week 24 | The Diplopia Questionnaire (DQ) will be used to evaluate the severity and impact of diplopia. Total scores range from 0 to 100, with higher scores indicating greater symptom severity and a more significant negative impact on daily life (representing a worse outcome). |
| Percentage of subjects with a CAS value of 0 or 1 in the study eye | week 12, week 24 | — |
| Proptosis responder rate in the non-study eye | week 12, week 24 | — |
| Change from baseline in proptosis measurement in the non-study eye | week 12, week 24 | — |
Countries
China
Contacts
CONTACTZhili Niu
Outcome results
None listed