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Studio clinico su Savolitinib + Osimertinib nel trattamento del NSCLC EGFRm+/MET+ localmente avanzato o metastatico (SANOVO)

17 settembre 2026 aggiornato da: Hutchmed

Uno studio clinico multicentrico, randomizzato, in doppio cieco, di fase III per valutare l'efficacia e la sicurezza di Savolitinib + Osimertinib rispetto al placebo + Osimertinib come terapia di prima linea per i pazienti con NSCLC EGFRm+/MET+

A Phase III Clinical Study on Savolitinib Combined with Osimertinib in Treatment of EGFRm+/MET+ Locally Advanced or Metastatic Non-small Cell Lung Cancer

Panoramica dello studio

Stato

Attivo, non reclutante

Condizioni

Intervento / Trattamento

Descrizione dettagliata

A Multicenter, Randomized, Double-blind, Phase III Clinical Study to Evaluate the Efficacy and Safety of Savolitinib Combined with Osimertinib versus Placebo Combined with Osimertinib as the First-line Therapy for Patients with EGFRm+/MET+ Locally Advanced or Metastatic Non-small Cell Lung Cancer

Tipo di studio

Interventistico

Iscrizione (Stimato)

412

Fase

  • Fase 3

Contatti e Sedi

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

Luoghi di studio

      • Guangzhou, Cina
        • Guangdong General Hospital

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

18 anni e precedenti (Adulto, Adulto più anziano)

Accetta volontari sani

No

Sessi ammissibili allo studio

Tutto

Descrizione

Inclusion Criteria:

  1. Fully aware of this study and voluntary to sign the informed consent form, and being willing and able to comply with the study procedure;
  2. Age ≥ 18
  3. In accordance with the Eighth Edition of TNM Staging of Lung Cancer by the International Association for the Study of Lung Cancer and American Joint Committee on Cancer, and patients with histologically or cytologically confirmed unresectable locally advanced (stage ⅢB/ⅢC), metastatic or recurrent (stage IV) NSCLC who are not suitable for radical concurrent chemoradiotherapy;
  4. Carrying two common EGFR mutations clearly related with the sensitivity to EGFR-TKI (i.e., exon 19 deletion, and L858R) and c-MET overexpression
  5. Having measurable lesions (in accordance with RECIST 1.1 criteria);
  6. ECOG Performance Status score 0 or 1, or Karnofsky score ≥80;
  7. Survival is expected to exceed 12 weeks;
  8. No any previous systematic antitumor therapy for advanced/metastatic disease;
  9. adequate bone marrow reserve or organ function
  10. Female patients of childbearing potential must agree to use effective contraceptive methods from screening period to 6 weeks after discontinuation of the study drug , and agree not to donate ova (oocytes) for reproductive purposes during this period;
  11. Male patients whose sexual partners are women of childbearing potential must use condoms during sexual intercourse during the study and within 6 months after discontinuation of study drug
  12. Being able to take or swallow the drug orally.

Exclusion Criteria:

  1. Previous treatment with EGFR inhibitors or MET inhibitors;
  2. Currently having other malignant tumors, or having other infiltrating malignant tumors in the past 5 years;
  3. Antitumor therapy within 2 weeks prior to the start of study treatment, including hormone therapy, biotherapy, immunotherapy or the traditional Chinese medicine for antitumor indication;
  4. Having received extensive radiotherapy (including radionuclide therapy, e.g., Sr-89) within 4 weeks prior to the start of study treatment or palliative local radiotherapy within one week prior to the start of study treatment, or the above adverse reactions of radiotherapy did not recover;
  5. Having received a major surgery within 4 weeks prior to the start of study treatment or a minor surgery (except biopsy, and venous catheterization) within one week prior to the start of study treatment;
  6. Currently receiving the potent CYP3A4 inducers or potent CYP1A2 inhibitors within two weeks prior to the start of study treatment;
  7. Having not been sufficiently recovered from the toxicity and/or complication resulting from any interventional measure prior to the start of treatment;
  8. Clinically significant active infection, including but not limited to tuberculosis, human immunodeficiency virus (HIV) infection (positive HIV1/2 antibody);
  9. Active hepatitis B, or active hepatitis C;
  10. Acute myocardial infarction, unstable angina pectoris, stroke or transient ischemic attack;
  11. Uncontrollable hypertension despite the use of drugs,
  12. Mean resting corrected QT interval (QTcF) or Any important abnormality in rhythm;
  13. Patients whose known cancerous thrombus or deep vein thrombosis are stable for ≥2 weeks after receiving treatment with low molecular weight heparin (LMWH) or analogues with similar efficacy can be enrolled;
  14. Any important abnormality in rhythm
  15. Presence of meningeal metastasis, spinal cord compression or active brain metastasis prior to the start of study treatment.
  16. Known allergy to the active or inactive ingredient of Savolitinib or Osimertinib;
  17. Lack of compliance with participation in this clinical study or inability to comply with the limitations and requirements of the study, as judged by investigators;
  18. Having participated in other drug clinical trials and received the study drug within 3 weeks prior to the start of study treatment;
  19. Known allergy to the active or inactive ingredient of Savolitinib or Osimertinib;
  20. Previous history of interstitial lung diseases, drug-induced interstitial lung diseases, radiation pneumonitis requiring glucocorticoid therapy and any active interstitial lung diseases;
  21. Pregnant and lactating women;
  22. Any other disease, metabolic abnormality, physical examination abnormality or laboratory examination abnormality, certain disease or state, based on which there is a reason to suspect that the subject is not suitable for the study drug, or one condition that will affect intepretaton of the study results or put the subject at high risk.
  23. History of cirrhosis of any etiology and clinical stage; or other severe liver disease or chronic disease with severe liver involvement.

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: Randomizzato
  • Modello interventistico: Assegnazione parallela
  • Mascheramento: Quadruplicare

Armi e interventi

Gruppo di partecipanti / Arm
Intervento / Trattamento
Sperimentale: Savolitinib + Osimertinib

Savolitinib 600 mg or 400 mg daily (including 600/400 mg QD or 300/200 mg BID) orally+ Osimertinib 80 mg QD orally ( every 3 weeks)

Savolitinib 600 mg or 400 mg daily (including 600/400 mg QD or 300/200 mg BID) orally

Altri nomi:
  • HMPL-504

Osimertinib 80 mg QD orally

Comparatore placebo: Placebo + Osimertinib

Placebo 600 mg or 400 mg daily (including 600/400 mg QD or 300/200 mg BID) orally+ Osimertinib 80 mg QD orally ( every 3 weeks)

Osimertinib 80 mg QD orally

Placebo 600 mg or 400 mg daily (including 600/400 mg QD or 300/200 mg BID) orally

Cosa sta misurando lo studio?

Misure di risultato primarie

Misura del risultato
Misura Descrizione
Lasso di tempo
PFS
Lasso di tempo: 17 months after the last patient enrolled

Progression-free survival (PFS) using Investigator assessment as defined by Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1)

17 months after the last patient enrolled

Misure di risultato secondarie

Misura del risultato
Misura Descrizione
Lasso di tempo
Safety and tolerability
Lasso di tempo: 17 months after the last patient enrolled

Incidence and nature of treatment emergent adverse events (TEAE), the other safety variables including physical examination, vital signs and laboratory examinations

17 months after the last patient enrolled
The objective response rate of the tumor (ORR)
Lasso di tempo: 17 months after the last patient enrolled

the incidence of confirmed complete response or partial response

17 months after the last patient enrolled
The disease control rate (DCR)
Lasso di tempo: 17 months after the last patient enrolled

the incidence of complete response, partial response and stable disease

17 months after the last patient enrolled
Duration of Response (DoR)
Lasso di tempo: 17 months after the last patient enrolled

the duration between the date the criteria for complete response or partial response was first measured (first record shall prevail) and the date of disease recurrence or progression as objectively recorded

17 months after the last patient enrolled
Overall survival (OS)
Lasso di tempo: 17 months after the last patient enrolled

the time from the date of randomization to the date of death (all causes)

17 months after the last patient enrolled
PFS
Lasso di tempo: 17 months after the last patient enrolled

PFS evaluated by the IRC and investigators in the MET-amplified set

17 months after the last patient enrolled
PFS
Lasso di tempo: 17 months after the last patient enrolled

Progression-free survival (PFS) using IRC as defined by Response Evaluation Criteria in Solid Tumors version 1.1 (RECIST 1.1)

17 months after the last patient enrolled
Development of diagnostic technology
Lasso di tempo: 17 months after the last patient enrolled

The residual samples may be used for development of MET Companion Diagnostics (CDx)

17 months after the last patient enrolled

Collaboratori e investigatori

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

Sponsor

Investigatori

  • Investigatore principale: Yilong Wu, MD, Guangdong Provincial People's Hospital

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)

6 settembre 2021

Completamento primario (Stimato)

30 maggio 2028

Completamento dello studio (Stimato)

30 maggio 2028

Date di iscrizione allo studio

Primo inviato

30 luglio 2021

Primo inviato che soddisfa i criteri di controllo qualità

16 agosto 2021

Primo Inserito (Effettivo)

18 agosto 2021

Aggiornamenti dei record di studio

Ultimo aggiornamento pubblicato (Effettivo)

22 settembre 2026

Ultimo aggiornamento inviato che soddisfa i criteri QC

17 settembre 2026

Ultimo verificato

1 settembre 2026

Maggiori informazioni

Termini relativi a questo studio

Altri numeri di identificazione dello studio

  • 2020-504-00CH4

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

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 .