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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

This is an open-label, dose-escalation and cohort expansion study to evaluate the safety and preliminary efficacy of YSCH-01 in subjects with pulmonary metastasis of advanced solid tumors and advanced non-small cell lung cancer by nebulized inhalation administration. This study is consisting of two phases: the dose escalation phase and the cohort expansion phase.

연구 개요

상세 설명

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.

연구 유형

중재적

등록 (추정된)

36

단계

  • 초기 1단계

연락처 및 위치

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연구 연락처

연구 연락처 백업

  • 이름: LI NING Vice President of Cancer Hospital, Chinese Academy of Medical, Doctorate
  • 전화번호: +86-10-87788495
  • 이메일: cancergcp@163.com

연구 장소

      • Beijing, 중국, 100021
        • 모병
        • No.17 Panjiayuan Nanli, Chaoyang District, Beijing
        • 연락하다:

참여기준

연구원은 적격성 기준이라는 특정 설명에 맞는 사람을 찾습니다. 이러한 기준의 몇 가지 예는 개인의 일반적인 건강 상태 또는 이전 치료입니다.

자격 기준

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설명

Inclusion Criteria:

  1. Subjects are able to understand and comply with protocol requirements, in the investigator's judgment.
  2. Subjects are willing to sign the informed consent form (ICF) before any study procedures are initiated.
  3. Male or female patients aged ≥18 years old and ≤75 years old.
  4. 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).
  5. Subjects with relapsed, refractory, or locally advanced lesions are eligible; subjects with curable or resectable lesions are not eligible.
  6. 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).
  7. Pulmonary function test: FEV1/expected FEV1 ≥50% and FVC ≥50% of expected value.
  8. Subjects have adequate hematologic, hepatic, renal, and coagulation function.
  9. 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.
  10. Women of childbearing potential must have a negative pregnancy test within 7 days before starting treatment.
  11. Subjects with an eastern cooperative oncology group (ECOG) score of 0-1 and an expected survival of at least 12 weeks.
  12. All adverse events (AEs) from prior treatment or surgery must have recovered to Grade 1 or baseline.

Exclusion Criteria:

  1. 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.
  2. 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.
  3. 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.
  4. 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.
  5. 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.
  6. 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.
  7. 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.
  8. 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.
  9. History of leptomeningeal disease.
  10. 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).
  11. The subject has a known allergy to any component of the study drug or immunotherapy.
  12. The subject has a past or current history of organ dysfunction.
  13. 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.
  14. 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.
  15. Current presence of uncontrolled pleural effusion, pericardial effusion, or ascites.
  16. The subject lacks legal capacity or has limited legal capacity and is unable to complete informed consent.
  17. 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.
  18. The subject has severe and uncontrolled disease or other conditions that may affect their participation in this study, as determined by the investigator.
  19. The subject is pregnant or breastfeeding.
  20. The subject receives any live vaccine during the screening period or treatment period.

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: 무작위화되지 않음
  • 중재 모델: 순차적 할당
  • 마스킹: 없음(오픈 라벨)

무기와 개입

참가자 그룹 / 팔
개입 / 치료
실험적: 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.
실험적: 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.

연구는 무엇을 측정합니까?

주요 결과 측정

결과 측정
측정값 설명
기간
Incidence and characteristics of AE/SAE
기간: 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)
기간: 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)
기간: 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

2차 결과 측정

결과 측정
측정값 설명
기간
Objective Response Rate (ORR)
기간: 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)
기간: 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:

  1. Subjects who were evaluated as SD, PR or CR during the study treatment;
  2. Subjects who were not PD and were excluded from the study, and after exclusion, did not receive other anti-tumor drug treatment, and whose tumors were evaluated as SD, PR or CR. (For subjects excluded due to non-PD, a tumor assessment will be conducted every 12 weeks until disease progression, initiation of new anti-cancer treatment, withdrawal of informed consent, death, or 12 months after the last study treatment administration, whichever occurs earlier.
The maximum estimated time for each subject to undergo tumor assessment is 30 months.
progression free survival (PFS)
기간: 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)
기간: 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.

공동 작업자 및 조사자

여기에서 이 연구와 관련된 사람과 조직을 찾을 수 있습니다.

수사관

  • 연구 책임자: Shuhang Wang, NCC, CICAMS

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 (실제)

2025년 11월 27일

기본 완료 (추정된)

2026년 10월 9일

연구 완료 (추정된)

2026년 12월 30일

연구 등록 날짜

최초 제출

2026년 3월 28일

QC 기준을 충족하는 최초 제출

2026년 8월 24일

처음 게시됨 (실제)

2026년 8월 28일

연구 기록 업데이트

마지막 업데이트 게시됨 (실제)

2026년 8월 28일

QC 기준을 충족하는 마지막 업데이트 제출

2026년 8월 24일

마지막으로 확인됨

2026년 7월 1일

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