YSCH-01 Via Nebulization in Pulmonary Metastasis of Advanced Solid Tumors and Non-small Cell Lung Cancer (NSCLC)
An Open-label, Single-center Study to Evaluate the Dose Escalation and Cohort Expansion of YSCH-01 in Subjects With Pulmonary Metastasis of Advanced Solid Tumors and Advanced Non-small Cell Lung Cancer by Nebulized Inhalation Administration
調査の概要
詳細な説明
In dose escalation phase, subjects with pulmonary metastasis of advanced solid tumors and advanced non-small cell lung cancer will be enrolled to receive YSCH-01 treatment by inhalation via nebulization. The "3+3" design will be adopted to explore the MTD and determine RP2D. Two dose groups will be established as follows:
Dose group 1: 2E+11 VP; Dose group 2: 4E+11 VP. All the subjects received a single dose of YSCH-01 treatment, followed by a 21-day DLT observation period. If no DLT occurred, the YSCH-01 will administered once a week thereafter until the investigator deemed that the subjects no longer benefited significantly, experienced intolerable toxicity, withdrew their informed consent, had disease progression, died, were lost to follow-up, or the investigator deemed that terminating the treatment was in the best interest of the subjects (whichever occurred first).
In cohort expansion phase, subjects will receive the optimal dose and administration schedule determined during the dose escalation phase. The cohort expansion phase further evaluated the safety and preliminary efficacy of YSCH-01 and planned to include 3 cohorts, with 10-30 subjects in each cohort.
研究の種類
入学 (推定)
段階
- 初期フェーズ 1
連絡先と場所
研究連絡先
- 名前:Shuhang Wang
- 電話番号:13552715820
- メール:snowflake201@gmail.com
研究連絡先のバックアップ
- 名前:LI NING Vice President of Cancer Hospital, Chinese Academy of Medical, Doctorate
- 電話番号:+86-10-87788495
- メール:cancergcp@163.com
研究場所
-
-
-
Beijing、中国、100021
- 募集
- No.17 Panjiayuan Nanli, Chaoyang District, Beijing
-
コンタクト:
-
-
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:
- Subjects are able to understand and comply with protocol requirements, in the investigator's judgment.
- Subjects are willing to sign the informed consent form (ICF) before any study procedures are initiated.
- Male or female patients aged ≥18 years old and ≤75 years old.
Dose escalation phase: Subjects with histologically or cytologically confirmed advanced unresectable/relapsed metastatic non-small cell lung cancer (NSCLC) or advanced solid tumors with lung metastases who have failed prior standard therapy, have no standard therapy or are not eligible for standard therapy.
Cohort expansion phase:
- Cohort 1: Subjects with advanced unresectable or metastatic NSCLC who have failed prior immunotherapy and/or platinum-based chemotherapy, including:
- Those with driver gene mutations positive for which no targeted therapy is approved;
- Those without driver gene mutations.
- Cohort 2: Subjects with histologically or cytologically confirmed relapsed sarcoma with lung metastases after surgical resection (lung metastases only).
- Cohort 3: Subjects with histologically or cytologically confirmed relapsed hepatocellular carcinoma (HCC), intrahepatic cholangiocarcinoma (ICC), or other sensitive tumors with lung metastases after surgical resection (lung metastases only).
- Subjects with relapsed, refractory, or locally advanced lesions are eligible; subjects with curable or resectable lesions are not eligible.
- Subjects must have at least one measurable lesion as defined by RECIST 1.1, i.e., non-lymph node lesions with a long diameter ≥10 mm or a lymph node lesion with a short diameter ≥15 mm on cross-sectional imaging (CT or MRI).
- Pulmonary function test: FEV1/expected FEV1 ≥50% and FVC ≥50% of expected value.
- Subjects have adequate hematologic, hepatic, renal, and coagulation function.
- Eligible subjects of childbearing potential (male and female) must agree to use reliable contraceptive methods during the study and for at least six months after the last dose.
- Women of childbearing potential must have a negative pregnancy test within 7 days before starting treatment.
- Subjects with an eastern cooperative oncology group (ECOG) score of 0-1 and an expected survival of at least 12 weeks.
- All adverse events (AEs) from prior treatment or surgery must have recovered to Grade 1 or baseline.
Exclusion Criteria:
- The subject has received chemotherapy or antibody therapy, molecular targeted therapy, hormone therapy, therapeutic or palliative radiotherapy within 21 days before the first dose, has received anti-tumor traditional Chinese medicine therapy within 1 week before the first dose, or has received immune checkpoint inhibitors (e.g., PD-1, PD-L1 monoclonal antibodies) within 42 days.
- The subject has experienced cardiac-related adverse reactions, or ≥Grade 3 immune-related adverse events (irAEs) or severe irAEs (excluding skin or endocrine irAEs that have recovered to Grade 1 or normal after treatment), or >Grade 2 cytokine release syndrome (CRS) from prior anti-tumor therapy.
- The subject has systemic diseases that are not stably controlled after treatment, such as diabetes, severe organic cardiovascular or cerebrovascular diseases, hypertension, second-degree or higher atrioventricular block, myocardial infarction within the past 6 months, or cerebral infarction within the past 6 months.
- The subject has uncontrolled infectious diseases, active hepatitis B (positive for anti-hepatitis B core (HBc) antibody and hepatitis B virus (HBV)-DNA > the lower limit of detection(LLOD) of the study center); active hepatitis C (positive for anti-hepatitis C virus (HCV) antibody and HCV RNA > LLOD); or positive for anti-human immunodeficiency virus (HIV)-1 or HIV-2 antibodies.
- The subject has uncontrolled active infection of ≥Grade 3 with significant clinical relevance according to the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE) v5.0.
- The subject has had other malignancies within the past 5 years, excluding basal cell or squamous cell carcinoma of the skin that has been cured by radical resection, or carcinoma in situ of the cervix.
- The subject has lesions located in high-risk positions (including those near the airways, major blood vessels, etc.) that may cause occlusion or compression due to tumor enlargement, or erosion into major vessels due to necrosis, or encasement of major vascular structures (e.g., pulmonary artery), or tumors adjacent to important neurovascular structures.
Known symptomatic, untreated, or active central nervous system (CNS) metastases. Subjects with asymptomatic and previously treated brain metastases may participate provided that:
- Imaging is stable, i.e., no evidence of disease progression on imaging during the screening period (note: imaging should be performed after local therapy for CNS);
- Clinically stable with no history of intracranial hemorrhage or spinal cord hemorrhage;
- Does not require steroid therapy for at least 14 days before the first dose of study treatment;
- Has not received stereotactic radiotherapy within 7 days before the first dose, whole-brain radiotherapy within 14 days before the first dose, or neurosurgery within 28 days before the first dose;
- Metastases are limited to the cerebellum or supratentorial region (i.e., no metastases to the midbrain, pons, medulla oblongata, or spinal cord);
- Must have measurable disease outside the CNS.
- History of leptomeningeal disease.
- The subject has active autoimmune disease or a history of autoimmune disease with potential for recurrence, such as ulcerative colitis, Crohn's disease, rheumatoid arthritis, systemic lupus erythematosus, autoimmune vasculitis, or granulomatosis with polyangiitis (Wegener's granulomatosis). Subjects with the following conditions are permitted: autoimmune hypothyroidism requiring only hormone replacement therapy; skin diseases not requiring systemic treatment (e.g., eczema involving <10% of body surface area).
- The subject has a known allergy to any component of the study drug or immunotherapy.
- The subject has a past or current history of organ dysfunction.
- The subject requires systemic corticosteroids (equivalent to >10 mg prednisone/day) within 14 days before enrollment or during the study period. Subjects are eligible for cohort enrollment in the following cases: topical (excluding inhaled) corticosteroid use, or short-term (≤7 days) use of glucocorticoids to prevent or treat non-autoimmune allergic conditions.
- History of pulmonary fibrosis, or current interstitial pneumonia, pneumoconiosis, chemical pneumonia, or other severe pulmonary function impairment, or conditions that make nebulized administration difficult due to prior medical history, such as asthma, airway obstruction, etc.
- Current presence of uncontrolled pleural effusion, pericardial effusion, or ascites.
- The subject lacks legal capacity or has limited legal capacity and is unable to complete informed consent.
- The subject has participated in another clinical trial of a drug or medical device within the previous 4 weeks or 5 half-lives, whichever is shorter.
- The subject has severe and uncontrolled disease or other conditions that may affect their participation in this study, as determined by the investigator.
- The subject is pregnant or breastfeeding.
- The subject receives any live vaccine during the screening period or treatment period.
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:非ランダム化
- 介入モデル:順次割り当て
- 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 |
|---|---|
|
実験的:YSCH-01 at Dose Level 1 (2.0×10¹¹ VP)
YSCH-01 is administered via nebulization inhalation at a dose of 2.0×10¹¹ VP per administration.
Following the first administration, there is a 21-day DLT observation period before the second dose.
Dosing is performed once weekly starting from the third administration.
|
YSCH-01, 2.0×10¹¹ VP, inhalation via nebulizer; the second administration is to be given 21 days after the first administration, and then once weekly thereafter.
YSCH-01, 4.0×10¹¹ VP, inhalation via nebulizer; the second administration is to be given 21 days after the first administration, and then once weekly thereafter.
|
|
実験的:YSCH-01 at Dose Level 2 (4.0×10¹¹ VP)
YSCH-01 is administered via nebulization inhalation at a dose of 4.0×10¹¹ VP per administration.
Following the first administration, there is a 21-day DLT observation period before the second dose.
Dosing is performed once weekly starting from the third administration.
|
YSCH-01, 2.0×10¹¹ VP, inhalation via nebulizer; the second administration is to be given 21 days after the first administration, and then once weekly thereafter.
YSCH-01, 4.0×10¹¹ VP, inhalation via nebulizer; the second administration is to be given 21 days after the first administration, and then once weekly thereafter.
|
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 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Incidence and characteristics of AE/SAE
時間枠:From the date of first dose up to 28 days after the date of last dose
|
Type, frequency, severity, and relationship to study treatment of AEs and SAEs assessed per NCI-CTCAE v5.0
|
From the date of first dose up to 28 days after the date of last dose
|
|
Incidence of Dose Limiting Toxicities (DLT)
時間枠:Within 21 days following the date of the first administration of YSCH-01
|
The proportion of subjects who experienced the defined DLT as per the protocol during the DLT observation period after receiving YSCH-01 treatment
|
Within 21 days following the date of the first administration of YSCH-01
|
|
Determine the maximum tolerated dose (if applicable)
時間枠:Within 21 days following the date of the first administration of YSCH-01
|
Maximum tolerated dose is defined as the highest dose level with a DLT incidence rate ≤ 1/6 per standard "3+3" dose escalation rules.
|
Within 21 days following the date of the first administration of YSCH-01
|
二次結果の測定
結果測定 |
メジャーの説明 |
時間枠 |
|---|---|---|
|
Objective Response Rate (ORR)
時間枠:The maximum estimated time for each subject to undergo tumor assessment is 30 months.
|
The proportion of subjects who achieved confirmed CR or PR during the period from the first dose up to 12 months following the last dose of study treatment, and who did not initiate any new anticancer therapy within 12 months after the last dose of study treatment.
Tumor assessments will be performed every 6 weeks after the first dose during treatment.
For subjects who discontinue study treatment without disease progression, tumor assessments will be conducted every 12 weeks thereafter until disease progression, initiation of new anticancer therapy, withdrawal of informed consent, death, or 12 months following the last dose of study treatment, whichever occurs first.
|
The maximum estimated time for each subject to undergo tumor assessment is 30 months.
|
|
Disease Control Rate (DCR)
時間枠:The maximum estimated time for each subject to undergo tumor assessment is 30 months.
|
The proportion of patients whose tumor assessment reached SD, PR or CR during the research process among the total number of enrolled patients; The patients whose tumor assessment reached SD, PR or CR include the following types:
|
The maximum estimated time for each subject to undergo tumor assessment is 30 months.
|
|
progression free survival (PFS)
時間枠:The maximum estimated time for each subject to undergo tumor assessment is 30 months.
|
The period from the first dose to the date of the first occurrence of disease progression or death due to any cause
|
The maximum estimated time for each subject to undergo tumor assessment is 30 months.
|
|
overall survival (OS)
時間枠:The maximum estimated time for each subject to undergo tumor assessment is 30 months.
|
The period from the time of the first dose to the date of death due to any cause by the subject
|
The maximum estimated time for each subject to undergo tumor assessment is 30 months.
|
協力者と研究者
捜査官
- スタディディレクター:Shuhang Wang、NCC, CICAMS
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
キーワード
追加の関連 MeSH 用語
その他の研究ID番号
- YSCH-01-IIT-CN001
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
米国で製造され、米国から輸出された製品。
この情報は、Web サイト clinicaltrials.gov から変更なしで直接取得したものです。研究の詳細を変更、削除、または更新するリクエストがある場合は、register@clinicaltrials.gov。 までご連絡ください。 clinicaltrials.gov に変更が加えられるとすぐに、ウェブサイトでも自動的に更新されます。