- ICH GCP
- Amerikanska kliniska prövningsregistret
- Klinisk prövning NCT07720648
A Phase III Study of KHN939 in Chinese Patients With Moderate-to-Severe Inactive Thyroid Eye Disease (Halo-2)
22 juli 2026 uppdaterad av: Beijing Kanghong Biological Medicine Co., Ltd.
A Multicenter, Randomized, Double-masked, Placebo-Controlled Phase III Clinical Study to Evaluate the Efficacy and Safety of KHN939 in the Treatment of Moderate-to-Severe Inactive Thyroid Eye Disease (TED) in China.
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 inactive thyroid eye disease (TED).
Approximately 117 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.
Studieöversikt
Status
Har inte rekryterat ännu
Betingelser
Intervention / Behandling
Studietyp
Interventionell
Inskrivning (Beräknad)
117
Fas
- Fas 3
Kontakter och platser
Det här avsnittet innehåller kontaktuppgifter för dem som genomför studien och information om var denna studie genomförs.
Studiekontakt
- Namn: Zhili Niu
- Telefonnummer: +86-028-87516260
- E-post: niuzhili@cnkh.com
Studieorter
-
-
Shanghai Municipality
-
Shanghai, Shanghai Municipality, Kina, 200135
- Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University
-
Kontakt:
- Study Team
- Telefonnummer: +86-028-87509966/87508866
- E-post: khn939_trial@cnkh.com
-
-
Deltagandekriterier
Forskare letar efter personer som passar en viss beskrivning, så kallade behörighetskriterier. Några exempel på dessa kriterier är en persons allmänna hälsotillstånd eller tidigare behandlingar.
Urvalskriterier
Åldrar som är berättigade till studier
- Vuxen
- Äldre vuxen
Tar emot friska volontärer
Nej
Beskrivning
Inclusion Criteria:
- Aged 18-70 years (inclusive) at the time of signing the informed consent form (ICF), male or female
- Weight between 45 kg and 100 kg (inclusive)
Diagnosed with moderate-to-severe inactive 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 ≤ 2 points in each eye
- CAS ≤ 2 in each eye for 6 months prior to screening (based on medical records); or meets all of the following criteria for ≥ 6 months prior to screening (based on patient self-report or medical records): no progression of proptosis, no new-onset or progressive TED-related diplopia, no new-onset inflammatory TED symptoms
- The time since initial TED diagnosis is ≥ 2 years and < 10 years prior to screening (documented by patient history or medical records)
- 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.
- Able to comply with all protocol-required procedures, examinations, and symptom reporting
Exclusion Criteria:
- Known hypersensitivity to any component of the study drug formulation, or prior hypersensitivity to any monoclonal antibodies
- Proptosis at Day 1 (pre-dose) that has decreased by ≥2 mm relative to screening
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
Prior/concomitant treatments:
- Use of oral or intravenous glucocorticoids within 30 days prior to screening
- Periorbital/periocular corticosteroid injection within 90 days of screening
- Oral or IV non-steroidal immunosuppressants within 90 days of screening
- Corticosteroid or non-steroidal immunosuppressant eye drops within 7 days of screening
- Received teprotumumab or teprotumumab N01 at any time prior to screening
- Received anti-CD20 antibody therapy within 12 months prior to screening
- Received anti-interleukin-6 receptor (anti-IL-6R) antibody therapy within 6 months prior to screening
- Received any other investigational therapy for TED at any time prior to screening (including, but not limited to, biologics targeting IGF-1R, FcRn, or TSHR)
- Received any other monoclonal antibody therapy within 90 days prior to screening
- Need for selenium or vitamin supplementation for TED treatment from 21 days pre-dose through study end (multivitamins are permitted)
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
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)
- 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)
- 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
- 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
- Female subjects who are pregnant or lactating
- Any other condition deemed by the investigator as inappropriate for study participation
Studieplan
Det här avsnittet ger detaljer om studieplanen, inklusive hur studien är utformad och vad studien mäter.
Hur är studien utformad?
Designdetaljer
- Primärt syfte: Behandling
- Tilldelning: Randomiserad
- Interventionsmodell: Parallellt uppdrag
- Maskning: Fyrdubbla
Vapen och interventioner
Deltagargrupp / Arm |
Intervention / Behandling |
|---|---|
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Experimentell: KHN939 20 mg/kg
8 infusions of KHN939 q3W for a total of 21 weeks
|
Intravenous (IV) infusion: 20 mg/kg every 3 weeks (Q3W) for a total of 8 doses over 21 weeks
|
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Placebo-jämförare: Placebo
8 infusions of placebo q3W for a total of 21 weeks
|
Intravenous (IV) infusion: placebo every 3 weeks (Q3W) for a total of 8 doses over 21 weeks
|
Vad mäter studien?
Primära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
|
The proptosis responder rate of the study eye
Tidsram: 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.
|
Week 24
|
Sekundära resultatmått
Resultatmått |
Åtgärdsbeskrivning |
Tidsram |
|---|---|---|
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Proptosis responder rate in the study eye
Tidsram: Week 12
|
See primary outcome measure description for details.
|
Week 12
|
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Change from baseline in proptosis measurement of the study eye
Tidsram: week 12, week 24
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See primary outcome measure description for details.
|
week 12, week 24
|
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Change in Quality of Life (GO-QoL) Scores
Tidsram: 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.
|
week 12, week 24
|
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Change from baseline in Clinical Activity Score (CAS) in the study eye
Tidsram: 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).
|
week 12, week 24
|
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Change from baseline in diplopia score
Tidsram: 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).
|
week 12, week 24
|
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Percentage of subjects with a CAS value of 0 or 1 in the study eye
Tidsram: week 12, week 24
|
week 12, week 24
|
|
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Proptosis responder rate in the non-study eye
Tidsram: week 12, week 24
|
week 12, week 24
|
|
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Change from baseline in proptosis measurement in the non-study eye
Tidsram: week 12, week 24
|
week 12, week 24
|
|
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Change from baseline in ocular motility of the study eye
Tidsram: week 12, week 24
|
week 12, week 24
|
|
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The number, incidence, severity, and relevance to study drugs or treatments of all ocular and other systemic AEs, TEAEs, AESIs, and SAEs
Tidsram: From the Screening period through study completion, with each participant completing all study visits over approximately 28 weeks, comprising a Screening Period (up to 4 weeks), a Treatment Period (21 weeks), and a Safety Follow-up Period (3 weeks).
|
From the Screening period through study completion, with each participant completing all study visits over approximately 28 weeks, comprising a Screening Period (up to 4 weeks), a Treatment Period (21 weeks), and a Safety Follow-up Period (3 weeks).
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|
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Incidence of anti-drug antibodies (ADA) and neutralizing antibodies (NAbs)
Tidsram: Up to Week 24
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Up to Week 24
|
|
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Serum Drug Concentration
Tidsram: Pre-dose and end-of-infusion at Doses 1, 2, 3, and 5, with additional samples at Week 1 and Week 24 (or early termination), up to Week 24
|
Serum drug concentrations will be collected at the following scheduled time points:
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Pre-dose and end-of-infusion at Doses 1, 2, 3, and 5, with additional samples at Week 1 and Week 24 (or early termination), up to Week 24
|
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Change from Baseline in Diplopia Questionnaire (DQ) Score
Tidsram: 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).
|
Week 12, Week 24
|
Samarbetspartners och utredare
Det är här du hittar personer och organisationer som är involverade i denna studie.
Studieavstämningsdatum
Dessa datum spårar framstegen för inlämningar av studieposter och sammanfattande resultat till ClinicalTrials.gov. Studieposter och rapporterade resultat granskas av National Library of Medicine (NLM) för att säkerställa att de uppfyller specifika kvalitetskontrollstandarder innan de publiceras på den offentliga webbplatsen.
Studera stora datum
Studiestart (Beräknad)
1 augusti 2026
Primärt slutförande (Beräknad)
1 maj 2027
Avslutad studie (Beräknad)
1 juni 2027
Studieregistreringsdatum
Först inskickad
10 juli 2026
Först inskickad som uppfyllde QC-kriterierna
17 juli 2026
Första postat (Faktisk)
22 juli 2026
Uppdateringar av studier
Senaste uppdatering publicerad (Faktisk)
23 juli 2026
Senaste inskickade uppdateringen som uppfyllde QC-kriterierna
22 juli 2026
Senast verifierad
1 juni 2026
Mer information
Termer relaterade till denna studie
Ytterligare relevanta MeSH-villkor
- Sjukdomar i det endokrina systemet
- Genetiska sjukdomar, medfödda
- Autoimmuna sjukdomar
- Immunsystemets sjukdomar
- Ögonsjukdomar
- Ögonsjukdomar, ärftliga
- Graves sjukdom
- Exoftalmos
- Orbitala sjukdomar
- Struma
- Hypertyreos
- Sköldkörtelsjukdomar
- Medfödda, ärftliga och neonatala sjukdomar och abnormiteter
- Graves Oftalmopati
Andra studie-ID-nummer
- KHN939-60102
Läkemedels- och apparatinformation, studiedokument
Studerar en amerikansk FDA-reglerad läkemedelsprodukt
Nej
Studerar en amerikansk FDA-reglerad produktprodukt
Nej
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