- ICH GCP
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- Klinische Studie NCT05009836
Klinische Studie zu Savolitinib + Osimertinib zur Behandlung von EGFRm+/MET+ lokal fortgeschrittenem oder metastasiertem NSCLC (SANOVO)
Eine multizentrische, randomisierte, doppelblinde klinische Phase-III-Studie zur Bewertung der Wirksamkeit und Sicherheit von Savolitinib + Osimertinib im Vergleich zu Placebo + Osimertinib als Erstlinientherapie für Patienten mit EGFRm+/MET+ NSCLC
A Phase III Clinical Study on Savolitinib Combined with Osimertinib in Treatment of EGFRm+/MET+ Locally Advanced or Metastatic Non-small Cell Lung Cancer
Studienübersicht
Status
Bedingungen
Intervention / Behandlung
Detaillierte Beschreibung
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
Studientyp
Einschreibung (Geschätzt)
Phase
- Phase 3
Kontakte und Standorte
Studienorte
-
-
-
Guangzhou, China
- Guangdong General Hospital
-
-
Teilnahmekriterien
Zulassungskriterien
Studienberechtigtes Alter
Akzeptiert gesunde Freiwillige
Studienberechtigte Geschlechter
Beschreibung
Inclusion Criteria:
- Fully aware of this study and voluntary to sign the informed consent form, and being willing and able to comply with the study procedure;
- Age ≥ 18
- 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;
- Carrying two common EGFR mutations clearly related with the sensitivity to EGFR-TKI (i.e., exon 19 deletion, and L858R) and c-MET overexpression
- Having measurable lesions (in accordance with RECIST 1.1 criteria);
- ECOG Performance Status score 0 or 1, or Karnofsky score ≥80;
- Survival is expected to exceed 12 weeks;
- No any previous systematic antitumor therapy for advanced/metastatic disease;
- adequate bone marrow reserve or organ function
- 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;
- 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
- Being able to take or swallow the drug orally.
Exclusion Criteria:
- Previous treatment with EGFR inhibitors or MET inhibitors;
- Currently having other malignant tumors, or having other infiltrating malignant tumors in the past 5 years;
- 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;
- 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;
- 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;
- Currently receiving the potent CYP3A4 inducers or potent CYP1A2 inhibitors within two weeks prior to the start of study treatment;
- Having not been sufficiently recovered from the toxicity and/or complication resulting from any interventional measure prior to the start of treatment;
- Clinically significant active infection, including but not limited to tuberculosis, human immunodeficiency virus (HIV) infection (positive HIV1/2 antibody);
- Active hepatitis B, or active hepatitis C;
- Acute myocardial infarction, unstable angina pectoris, stroke or transient ischemic attack;
- Uncontrollable hypertension despite the use of drugs,
- Mean resting corrected QT interval (QTcF) or Any important abnormality in rhythm;
- 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;
- Any important abnormality in rhythm
- Presence of meningeal metastasis, spinal cord compression or active brain metastasis prior to the start of study treatment.
- Known allergy to the active or inactive ingredient of Savolitinib or Osimertinib;
- 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;
- Having participated in other drug clinical trials and received the study drug within 3 weeks prior to the start of study treatment;
- Known allergy to the active or inactive ingredient of Savolitinib or Osimertinib;
- Previous history of interstitial lung diseases, drug-induced interstitial lung diseases, radiation pneumonitis requiring glucocorticoid therapy and any active interstitial lung diseases;
- Pregnant and lactating women;
- 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.
- History of cirrhosis of any etiology and clinical stage; or other severe liver disease or chronic disease with severe liver involvement.
Studienplan
Wie ist die Studie aufgebaut?
Designdetails
- Hauptzweck: Behandlung
- Zuteilung: Zufällig
- Interventionsmodell: Parallele Zuordnung
- Maskierung: Vervierfachen
Waffen und Interventionen
Teilnehmergruppe / Arm |
Intervention / Behandlung |
|---|---|
|
Experimental: 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
Andere Namen:
Osimertinib 80 mg QD orally |
|
Placebo-Komparator: 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 |
Was misst die Studie?
Primäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
PFS
Zeitfenster: 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
|
Sekundäre Ergebnismessungen
Ergebnis Maßnahme |
Maßnahmenbeschreibung |
Zeitfenster |
|---|---|---|
|
Safety and tolerability
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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)
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
Zeitfenster: 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
|
Mitarbeiter und Ermittler
Sponsor
Ermittler
- Hauptermittler: Yilong Wu, MD, Guangdong Provincial People's Hospital
Studienaufzeichnungsdaten
Haupttermine studieren
Studienbeginn (Tatsächlich)
Primärer Abschluss (Geschätzt)
Studienabschluss (Geschätzt)
Studienanmeldedaten
Zuerst eingereicht
Zuerst eingereicht, das die QC-Kriterien erfüllt hat
Zuerst gepostet (Tatsächlich)
Studienaufzeichnungsaktualisierungen
Letztes Update gepostet (Tatsächlich)
Letztes eingereichtes Update, das die QC-Kriterien erfüllt
Zuletzt verifiziert
Mehr Informationen
Begriffe im Zusammenhang mit dieser Studie
Zusätzliche relevante MeSH-Bedingungen
- Neubildungen nach Standort
- Neubildungen
- Erkrankungen der Atemwege
- Lungenkrankheit
- Neubildungen der Atemwege
- Thoraxneoplasmen
- Lungentumoren
- Karzinom, bronchogen
- Bronchiale Neubildungen
- Karzinom, nicht-kleinzellige Lunge
- Osimertinib
- 1- (1- (Imidazo (1,2-A) Pyridin-6-yl)-Ethyl) -6- (1-Methyl-1H-Pyrazol-4-yl) -1H- (1,2,3) Triazolo (4,5-b) -Pyrazin
Andere Studien-ID-Nummern
- 2020-504-00CH4
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