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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.

Panoramica dello studio

Stato

Reclutamento

Descrizione dettagliata

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.

Tipo di studio

Interventistico

Iscrizione (Stimato)

36

Fase

  • Prima fase 1

Contatti e Sedi

Questa sezione fornisce i recapiti di coloro che conducono lo studio e informazioni su dove viene condotto lo studio.

Contatto studio

Backup dei contatti dello studio

  • Nome: LI NING Vice President of Cancer Hospital, Chinese Academy of Medical, Doctorate
  • Numero di telefono: +86-10-87788495
  • Email: cancergcp@163.com

Luoghi di studio

      • Beijing, Cina, 100021
        • Reclutamento
        • No.17 Panjiayuan Nanli, Chaoyang District, Beijing
        • Contatto:

Criteri di partecipazione

I ricercatori cercano persone che corrispondano a una certa descrizione, chiamata criteri di ammissibilità. Alcuni esempi di questi criteri sono le condizioni generali di salute di una persona o trattamenti precedenti.

Criteri di ammissibilità

Età idonea allo studio

  • Adulto
  • Adulto più anziano

Accetta volontari sani

No

Descrizione

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.

Piano di studio

Questa sezione fornisce i dettagli del piano di studio, compreso il modo in cui lo studio è progettato e ciò che lo studio sta misurando.

Come è strutturato lo studio?

Dettagli di progettazione

  • Scopo principale: Trattamento
  • Assegnazione: Non randomizzato
  • Modello interventistico: Assegnazione sequenziale
  • Mascheramento: Nessuno (etichetta aperta)

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: 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.
Sperimentale: 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.

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Incidence and characteristics of AE/SAE
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Objective Response Rate (ORR)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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)
Lasso di tempo: 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.

Collaboratori e investigatori

Qui è dove troverai le persone e le organizzazioni coinvolte in questo studio.

Investigatori

  • Direttore dello studio: Shuhang Wang, NCC, CICAMS

Studiare le date dei record

Queste date tengono traccia dell'avanzamento della registrazione dello studio e dell'invio dei risultati di sintesi a ClinicalTrials.gov. I record degli studi e i risultati riportati vengono esaminati dalla National Library of Medicine (NLM) per assicurarsi che soddisfino specifici standard di controllo della qualità prima di essere pubblicati sul sito Web pubblico.

Studia le date principali

Inizio studio (Effettivo)

27 novembre 2025

Completamento primario (Stimato)

9 ottobre 2026

Completamento dello studio (Stimato)

30 dicembre 2026

Date di iscrizione allo studio

Primo inviato

28 marzo 2026

Primo inviato che soddisfa i criteri di controllo qualità

24 agosto 2026

Primo Inserito (Effettivo)

28 agosto 2026

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

28 agosto 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

24 agosto 2026

Ultimo verificato

1 luglio 2026

Maggiori informazioni

Termini relativi a questo studio

Piano per i dati dei singoli partecipanti (IPD)

Hai intenzione di condividere i dati dei singoli partecipanti (IPD)?

NO

Informazioni su farmaci e dispositivi, documenti di studio

Studia un prodotto farmaceutico regolamentato dalla FDA degli Stati Uniti

No

Studia un dispositivo regolamentato dalla FDA degli Stati Uniti

No

prodotto fabbricato ed esportato dagli Stati Uniti

No

Queste informazioni sono state recuperate direttamente dal sito web clinicaltrials.gov senza alcuna modifica. In caso di richieste di modifica, rimozione o aggiornamento dei dettagli dello studio, contattare register@clinicaltrials.gov. Non appena verrà implementata una modifica su clinicaltrials.gov, questa verrà aggiornata automaticamente anche sul nostro sito web .

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