A Clinical Study of SYS6023 Combination Therapy for Advanced Breast Cancer
A Phase II Clinical Study Evaluating the Efficacy and Safety of SYS6023 Combination Therapy for Unresectable Locally Advanced or Metastatic Breast Cancer
調査の概要
詳細な説明
This is an open-label, multicenter Phase II clinical study conducted in subjects with advanced breast cancer.
The study aims to evaluate the safety/tolerability, pharmacokinetics, and preliminary efficacy of SYS6023 in combination with other agents in subjects with advanced breast cancer.
Eligible subjects will receive SYS6023 in combination with HB1901 or KN026, with each treatment cycle lasting 3 weeks, until disease progression, intolerable toxicity, initiation of new anti-tumor therapy, withdrawal of informed consent, loss to follow-up, or death, whichever occurs first.
研究の種類
入学 (推定)
段階
- フェーズ2
連絡先と場所
研究連絡先
- 名前:Clinical Trials Information Group Officer
- 電話番号:86-0311-69085587
- メール:ctr-contact@cspc.cn
研究連絡先のバックアップ
- 名前:Qingyuan Zhang, M.D.
- 電話番号:86-13313612989
- メール:sy86298276@163.com
研究場所
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Heilonjiang
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Harbin、Heilonjiang、中国、150000
- 募集
- Affiliated Tumor Hospital of Harbin
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コンタクト:
- Qingyuan Zhang, M.D.
- 電話番号:+86-13313612989
- メール:sy86298276@163.com
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-
参加基準
適格基準
就学可能な年齢
- 大人
- 高齢者
健康ボランティアの受け入れ
説明
Inclusion Criteria:
- 1. Age ≥ 18 years old;
- 2. Histologically or cytologically confirmed unresectable locally advanced or metastatic breast cancer:
- 3. Sufficient tumor specimens must be provided for biomarker testing (human epidermal growth factor receptor 3-HER3), preferably obtained during or after the most recent treatment period; During safety run-in period, subjects who cannot provide sufficient tissue samples may be screened after sponsor's evaluation and approval;
- 4. Documented disease progression or intolerability with the most recent systemic anti-tumor treatment;
- 5. According to RECIST 1.1, at least one evaluable lesion (safety run-in period) or measurable lesion (cohort expansion phase);
- 6. ECOG PS score 0-1;
- 7. Expected survival ≥ 3 months;
- 8. Adequate organ function with laboratory tests meeting criteria (no blood transfusion or hematopoietic growth factor therapy within 14 days before testing): ANC ≥ 1.5 × 10^9/L PLT ≥ 100 × 10^9/L Hb ≥ 90 g/L TBIL ≤ 1.5 × ULN ALT, AST ≤ 2.5 × ULN; for participants with liver metastasis, ALT and AST ≤ 5 × ULN Creatinine clearance rate (Ccr) > 35 mL/min (calculated according to Cockcroft-Gault formula) Activated partial thromboplastin time (APTT) ≤ 1.5 × ULN; International normalized ratio (INR) ≤ 1.5 × ULN Left ventricular ejection fraction (LVEF) ≥ 55% (only applicable to Cohort 2)
- 9. Eligible individuals with reproductive potential must agree to use reliable contraceptive methods (hormonal contraceptives, barrier methods, or abstinence) with their partners during the trial and for at least 7 months after the last dose; Women of childbearing potential must have a negative blood pregnancy test within 7 days before enrollment;
- 10. Fully understand this clinical trial and voluntarily sign the written informed consent form.
Exclusion Criteria:
- 1. Prior treatment with HER3-targeted ADC therapy;
- 2. Applicable to Cohort 1: a. Prior treatment with any topoisomerase I inhibitor-loaded ADC therapy; b. Current presence or impending visceral crisis that has caused or may cause impending organ damage and/or other life-threatening complications;
- 3. Applicable to Cohort 2: a. Prior exposure to anthracyclines with cumulative dose exceeding 360 mg/m^2doxorubicin equivalent; b. LVEF once dropped to < 40% during prior anti-HER2 drug therapy, or symptomatic CHF occurred;
- 4. History of other malignancies within 3 years before randomization/first dose or concurrent active malignancies (except cured localized tumors such as basal cell carcinoma of the skin, squamous cell carcinoma of the skin, superficial bladder cancer, carcinoma in situ of the prostate, carcinoma in situ of the cervix, carcinoma in situ of the breast, etc., which are allowed to enroll);
- 5. Untreated (including those detected during screening period) or unstable brain parenchymal metastasis, spinal cord metastasis or compression, carcinomatous meningitis. Subjects with treated stable brain metastases may be considered for enrollment (Note: refers to participants who have received local brain treatment, whose symptoms are stable, imaging tests show stability for at least 28 days before randomization/first dose, no evidence of progressive brain edema, and no need for glucocorticoids or other symptom control measures);
- 6. Adverse reactions from prior anti-tumor therapy have not recovered to CTCAE 6.0 grade ≤ 1 (except for toxicities such as alopecia that researchers judge to have no safety risk);
- 7. Major surgery within 28 days before randomization/first dose, or planned to undergo systemic or local tumor resection during the study period;
- 8. History of severe bleeding risk (e.g., gastrointestinal varices) or bleeding diathesis, any gastrointestinal bleeding or other bleeding of ≥ CTCAE grade 2 within 28 days before randomization/first dose; Abdominal fistula, gastrointestinal perforation or abdominal abscess within 6 months before randomization/first dose;
9. History of severe cardiovascular disease, including but not limited to:
- Acute coronary syndrome within 6 months before randomization/first dose;
- Stroke or transient ischemic attack within 6 months before randomization/first dose;
- Pulmonary embolism or deep vein thrombosis within 3 months before randomization/first dose (intermuscular vein thrombosis may be enrolled if assessed as low risk by researchers);
- CHF with NYHA functional classification ≥ II;
- Documented history of cardiomyopathy that has not currently recovered;
- Pericarditis;
- Severe arrhythmia, such as ventricular arrhythmia requiring clinical intervention, II-III degree atrioventricular block, etc.;
- Baseline average QTcF > 450 ms (calculated using Fridericia formula), or history or family history of long QT syndrome;
- Uncontrolled hypertension (defined as persistent systolic blood pressure ≥ 150 mmHg and/or diastolic blood pressure ≥ 100 mmHg despite antihypertensive medication);
- 10. Presence of non-infectious lung disease/pneumonia requiring treatment at randomization/first dose, or history of interstitial lung disease/pneumonia requiring glucocorticoid treatment during prior anti-tumor therapy;
- 11. Active bacterial, fungal or viral infection within 14 days before randomization/first dose (defined as requiring intravenous anti-bacterial, anti-fungal or anti-viral drug therapy). Individuals receiving prophylactic anti-infective therapy without clinical manifestations of active infection may be considered for enrollment;
- 12. Active hepatitis B or hepatitis C, defined as HBsAg positive and HBV DNA > 2000 IU/mL for active hepatitis B; defined as HCV-Ab positive and HCV RNA > ULN for active hepatitis C;
- 13. History of immunodeficiency or positive HIV antibody test during screening;
- 14. Use of strong CYP3A4 inducers or inhibitors, OATP1B1 or OATP1B3 inhibitors before randomization/first dose (within 5 half-lives of inducer or inhibitor) or need to use such drugs during study treatment;
- 15. Known or suspected hypersensitivity to the study drug or its components;
- 16. Lactating women;
- 17. Presence of other conditions that may interfere with participants' participation in study procedures, not in line with participants' maximum benefit from participating in the study, or affect study results: such as history of mental illness, drug abuse or substance abuse, any other clinically significant disease or condition, etc.
研究計画
研究はどのように設計されていますか?
デザインの詳細
- 主な目的:処理
- 割り当て:なし
- 介入モデル:単一グループの割り当て
- マスキング:なし(オープンラベル)
武器と介入
参加者グループ / アーム |
介入・治療 |
|---|---|
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実験的:SYS6023 in combination with KN026
Patients with advanced breast cancer receiving SYS6023 in combination with KN026 treatment.
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SYS6023は、静脈内注入を介して投与されるHER3を標的とする新規抗体薬物コンジュゲート(ADC)です。
KN026 is an antibody targeting HER2, administered via intravenous infusion.
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この研究は何を測定していますか?
主要な結果の測定
結果測定 |
時間枠 |
|---|---|
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客観的奏効率 (ORR)
時間枠:最長約3年
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最長約3年
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The incidence of dose-limiting toxicity (DLT)
時間枠:At the end of Cycle 1 (each cycle is 21 days).
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At the end of Cycle 1 (each cycle is 21 days).
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Frequency and severity of AEs and SAEs (according to NCI-CTCAE 6.0);
時間枠:Baseline up to 28 days post last dose, Up to approximately 3 years
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Baseline up to 28 days post last dose, Up to approximately 3 years
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Recommended Phase 2 Dose(RP2D)
時間枠:Up to approximately 3 years
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Up to approximately 3 years
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二次結果の測定
結果測定 |
時間枠 |
|---|---|
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全生存期間 (OS)
時間枠:最長約3年
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最長約3年
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反応期間 (DoR)
時間枠:最長約3年
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最長約3年
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疾病制御率 (DCR)
時間枠:最長約3年
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最長約3年
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無増悪生存期間 (PFS)
時間枠:最長約3年
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最長約3年
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Maximum Plasma Concentration( Cmax)
時間枠:Up to approximately 3 years
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Up to approximately 3 years
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Time to Maximum Plasma Concentration (Tmax)
時間枠:Up to approximately 3 years
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Up to approximately 3 years
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Area Under the Serum Concentration Time Curve ( AUC)
時間枠:Up to approximately 3 years
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Up to approximately 3 years
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Elimination half-life (t1/2)
時間枠:Up to approximately 3 years
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Up to approximately 3 years
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Anti-Drug Antibody(ADA)
時間枠:Up to approximately 3 years
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Up to approximately 3 years
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Expression level of tumor markers
時間枠:Up to approximately 3 years
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Up to approximately 3 years
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Plasma drug concentration
時間枠:Up to approximately 3 years
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Up to approximately 3 years
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協力者と研究者
捜査官
- 主任研究者:Qingyuan Zhang, M.D.、Affiliated Tumor Hospital of Harbin
研究記録日
主要日程の研究
研究開始 (実際)
一次修了 (推定)
研究の完了 (推定)
試験登録日
最初に提出
QC基準を満たした最初の提出物
最初の投稿 (実際)
学習記録の更新
投稿された最後の更新 (実際)
QC基準を満たした最後の更新が送信されました
最終確認日
詳しくは
本研究に関する用語
その他の研究ID番号
- SYS6023-002
個々の参加者データ (IPD) の計画
個々の参加者データ (IPD) を共有する予定はありますか?
医薬品およびデバイス情報、研究文書
米国FDA規制医薬品の研究
米国FDA規制機器製品の研究
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