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NCT05914610Toborzás még nem indult3. fázis

Envollizumab Combined With Fruquintinib and SOX Versus SOX for Conversion Therapy in Advanced Gastric Cancer

Envollizumab Combined With Fruquintinib and SOX Versus SOX for Conversion Therapy in Her-2 Negative Unresectable Locally Advanced Gastric Cancer: a National Multicenter Randomized Controlled Study

Forrás: ClinicalTrials.gov · Utoljára frissítve: 2023. aug. 25. · Több mint 12 hónapja nem frissült - kérdezd meg a helyszínt, nyitott-e még

Következő lépések

Rövid összefoglaló (regiszter, angolul)

To investigate the clinical efficacy and safety of envollizumab combined with fruquintinib and SOX versus SOX in conversion therapy for patients with Her-2 negative, unresectable locally advanced gastric cancer.

Állapot (regiszter)
Toborzás még nem indult
Fázis (regiszter)
3. fázis
Vizsgálattípus
Beavatkozással járó
Résztvevők száma
100 (tervezett)
Első benyújtás
2023. máj. 27.
Kezdés
2023. szept. 1.
Elsődleges befejezés
2025. júl. 30.
Fő szponzor
Fujian Medical University
NCT-szám
NCT05914610

Mit vállalsz

  • Vizsgálat típusa: Beavatkozással járó · 3. fázis
  • Tervezett résztvevők: 100
  • 2023. szept. 1. és az elsődleges befejezés (2025. júl. 30.) között
  • Nincs megadott helyszín, ország nélkül
  • Vizitek és vizsgálatok: kérdezd a vizsgálat csapatát, a regiszter nem sorolja fel őket

A(z) ClinicalTrials.gov regisztermezőiből összeállítva. A vizsgálat felépítését írja le.

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Korábbi kezelés

  • Live vaccine was administered within 4 weeks prior to enrolling or possibly during the study period
  • Had an active autoimmune disease or a history of autoimmune disease within 4 weeks prior to enrollment
  • Patients with significant evidence or history of bleeding tendency within 3 months prior to enrollment (bleeding within 3 months >30 mL, hematemesis, black stool, blood in stool), hemoptysis (within 4 weeks >5 mL fresh blood) or a thromboembolic event (including stroke and/or transient ischemic attack) within 12 months

Más betegség

  • Patients with allergies or suspected allergies to study drugs or similar drugs
  • Other malignancies in the past 5 years, except basal cell or squamous cell carcinoma of the skin after radical surgery, or carcinoma in situ of the cervix
  • Patient has any current disease or condition that affects drug absorption, or the patient is unable to take the drug orally
  • The blood pressure of patients with hypertension cannot be reduced to the normal range by the one antihypertensive drugs (systolic pressure ≥150 mmHg, diastolic pressure ≥100 mmHg) or hard to controled by two or more antihypertensive drugs
  • The patient currently has gastrointestinal diseases such as active gastric and duodenal ulcers, ulcerative colitis, or active bleeding from unresectosed tumors, or other conditions determined by researchers that may cause gastrointestinal bleeding or perforation
  • Active or uncontrolled severe infection (≥CTCAE grade 2 infection)

Laborértékek

  • Cardiovascular disease of significant clinical significance, including but not limited to acute myocardial infarction, severe/unstable angina, or coronary artery bypass grafting within 6 months prior to enrollment; New York Heart Association (NYHA) Grades for Congestive Heart Failure more than class II ; Ventricular arrhythmias requiring medical treatment; An electrocardiogram (ECG) showed a QT c interval ≥480 milliseconds
  • A history of human immunodeficiency virus (HIV) infection or clinically significant liver disease, including viral hepatitis [active HBV infection must be ruled out as a known carrier of hepatitis B virus (HBV), i.e. positive HBV DNA (>1×104 copies /mL or >2000 IU/ml); known hepatitis C virus infection (HCV) and HCV RNA positive (>1×103 copies /mL), or other hepatitis, cirrhosis]

Egyéb

  • Imaging or intraoperative exploration found patients with peritoneum, liver, lung and other distant metastases
  • Confirmed HER-2 positive patients
  • Past recipients of allogeneic bone marrow transplants or organ transplants
  • Patients are positive of urine protein (urine protein detection 2+ or above, or 24 hours urine protein quantitative >1.0g)
  • The researchers consider those who were not suitable for inclusion

Kiket keres a vizsgálat

  • Age: 18-75 years of age;
  • Pathological (including histological or cytological) confirmation of gastric adenocarcinoma;
  • Before surgery, CT/MRI, PET-CT, if necessary, laparoscopic exploration to determine the clinical stage of T4bN0M0 and TanyN2-3M0, and determined by researchers that the local advanced patients can not be resectable;
  • At least one measurable detected by CT examination in accordance with the RECIST1.1
  • ECOG#Eastern Cooperative Oncology Group#PS#Performance Status#:0-1 scores;
  • The expected survival time is more than 3 months
  • The main organ function is normal, which should meet the following criteria:
    • #1#blood routine examination standards should be met#no blood transfusion within 14 days#
    • a.HB≥ 100g/L b. WBC≥3×109/L c. ANC≥1.5×109/L d. PLT≥100×109/L #2#biochemical examination shall comply with the following criteria#
    • BIL#1.5 normal upper limit ULN
    • ALT and AST#2.5 ULN
    • Cr≤1 ULN#CCR#creatinine clearance rate##60ml/min(Cockcroft Gault formula)
  • Women of childbearing age must have a pregnancy test in 7 days before entering the group (in serum), and the results were negative, and willing to use appropriate contraception during the study period and the last 8 weeks after giving drug test; men should have the surgical sterilization, or adopt the appropriate contraceptive methods during the test and the last 8 weeks after giving drug test#
  • No other clinical studies were conducted before and during the treatment
  • Participants is willing to participate in this study, sign the informed consent, have good compliance, cooperate with follow-up

Életkor a regiszterben: 18 év – 75 év · Nem: nők és férfiak · Egészséges önkénteseket nem fogad

A teljes feltétellista: ClinicalTrials.gov

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