- ICH GCP
- 미국 임상 시험 레지스트리
- 임상시험 NCT07720648
A Phase III Study of KHN939 in Chinese Patients With Moderate-to-Severe Inactive Thyroid Eye Disease (Halo-2)
2026년 7월 22일 업데이트: 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.
연구 개요
연구 유형
중재적
등록 (추정된)
117
단계
- 3단계
연락처 및 위치
이 섹션에서는 연구를 수행하는 사람들의 연락처 정보와 이 연구가 수행되는 장소에 대한 정보를 제공합니다.
연구 연락처
- 이름: Zhili Niu
- 전화번호: +86-028-87516260
- 이메일: niuzhili@cnkh.com
연구 장소
-
-
Shanghai Municipality
-
Shanghai, Shanghai Municipality, 중국, 200135
- Shanghai Ninth People's Hospital Affiliated to Shanghai Jiao Tong University
-
연락하다:
- Study Team
- 전화번호: +86-028-87509966/87508866
- 이메일: khn939_trial@cnkh.com
-
-
참여기준
연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.
자격 기준
공부할 수 있는 나이
- 성인
- 고령자
건강한 자원 봉사자를 받아들입니다
아니
설명
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
공부 계획
이 섹션에서는 연구 설계 방법과 연구가 측정하는 내용을 포함하여 연구 계획에 대한 세부 정보를 제공합니다.
연구는 어떻게 설계됩니까?
디자인 세부사항
- 주 목적: 치료
- 할당: 무작위
- 중재 모델: 병렬 할당
- 마스킹: 네 배로
무기와 개입
참가자 그룹 / 팔 |
개입 / 치료 |
|---|---|
|
실험적: 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
|
|
위약 비교기: 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
|
연구는 무엇을 측정합니까?
주요 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
The proptosis responder rate of the study eye
기간: 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
|
2차 결과 측정
결과 측정 |
측정값 설명 |
기간 |
|---|---|---|
|
Proptosis responder rate in the study eye
기간: Week 12
|
See primary outcome measure description for details.
|
Week 12
|
|
Change from baseline in proptosis measurement of the study eye
기간: week 12, week 24
|
See primary outcome measure description for details.
|
week 12, week 24
|
|
Change in Quality of Life (GO-QoL) Scores
기간: 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
|
|
Change from baseline in Clinical Activity Score (CAS) in the study eye
기간: 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
|
|
Change from baseline in diplopia score
기간: 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
|
|
Percentage of subjects with a CAS value of 0 or 1 in the study eye
기간: week 12, week 24
|
week 12, week 24
|
|
|
Proptosis responder rate in the non-study eye
기간: week 12, week 24
|
week 12, week 24
|
|
|
Change from baseline in proptosis measurement in the non-study eye
기간: week 12, week 24
|
week 12, week 24
|
|
|
Change from baseline in ocular motility of the study eye
기간: week 12, week 24
|
week 12, week 24
|
|
|
The number, incidence, severity, and relevance to study drugs or treatments of all ocular and other systemic AEs, TEAEs, AESIs, and SAEs
기간: 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).
|
|
|
Incidence of anti-drug antibodies (ADA) and neutralizing antibodies (NAbs)
기간: Up to Week 24
|
Up to Week 24
|
|
|
Serum Drug Concentration
기간: 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:
|
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
|
|
Change from Baseline in Diplopia Questionnaire (DQ) Score
기간: 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
|
공동 작업자 및 조사자
여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.
연구 기록 날짜
이 날짜는 ClinicalTrials.gov에 대한 연구 기록 및 요약 결과 제출의 진행 상황을 추적합니다. 연구 기록 및 보고된 결과는 공개 웹사이트에 게시되기 전에 특정 품질 관리 기준을 충족하는지 확인하기 위해 국립 의학 도서관(NLM)에서 검토합니다.
연구 주요 날짜
연구 시작 (추정된)
2026년 8월 1일
기본 완료 (추정된)
2027년 5월 1일
연구 완료 (추정된)
2027년 6월 1일
연구 등록 날짜
최초 제출
2026년 7월 10일
QC 기준을 충족하는 최초 제출
2026년 7월 17일
처음 게시됨 (실제)
2026년 7월 22일
연구 기록 업데이트
마지막 업데이트 게시됨 (실제)
2026년 7월 23일
QC 기준을 충족하는 마지막 업데이트 제출
2026년 7월 22일
마지막으로 확인됨
2026년 6월 1일
추가 정보
이 정보는 변경 없이 clinicaltrials.gov 웹사이트에서 직접 가져온 것입니다. 귀하의 연구 세부 정보를 변경, 제거 또는 업데이트하도록 요청하는 경우 register@clinicaltrials.gov. 문의하십시오. 변경 사항이 clinicaltrials.gov에 구현되는 즉시 저희 웹사이트에도 자동으로 업데이트됩니다. .