NCT07061535Toboroz2. fázis
Sintilimab Combined With Tafolecimab and Chemotherapy as First-Line Treatment for Extensive-Stage Small Cell Lung Cancer
Efficacy and Safety of Sintilimab Combined With Tafolecimab and Chemotherapy as First-Line Treatment for Extensive-Stage Small Cell Lung Cancer (STAR-SCLC):A Prospective, Single Arm Trial
Forrás: ClinicalTrials.gov · Utoljára frissítve: 2026. szept. 15.
Rövid összefoglaló (regiszter, angolul)
This is a single arm, multi-center clinical trial. The goal of this clinical trial is to evaluate the efficacy, safety and biomarkers of Tafolecimab combined with Sintilimab and Chemotherapy as first-line treatment for patients with extensive-stage small cell lung cancer (ES-SCLC). Tafolecimab is a recombinant fully humanized monoclonal antibody against proprotein convertase subtilisin/kexin type 9 (PCSK-9), which can reduce low-density lipoprotein-C levels and increase the expression level of major histocompatibility complex class I (MHC-I) on tumor cells. Sintilimab is a fully humanized IgG4 monoclonal antibody targeting programmed cell death protein 1 (PD-1).
- Állapot (regiszter)
- Toboroz
- Fázis (regiszter)
- 2. fázis
- Vizsgálattípus
- Beavatkozással járó
- Résztvevők száma
- 40 (tervezett)
- Első benyújtás
- 2025. júl. 2.
- Kezdés
- 2025. júl. 30.
- Elsődleges befejezés
- 2027. aug. 1.
- Fő szponzor
- Second Affiliated Hospital, Zhejiang University, School of Medicine
- Betegségek
- Tüdőrák
- NCT-szám
- NCT07061535
Mit vállalsz
- Vizsgálat típusa: Beavatkozással járó · 2. fázis
- Tervezett résztvevők: 40
- 2025. júl. 30. és az elsődleges befejezés (2027. aug. 1.) között
- 5 helyszín, 1 országban
- Vizitek és vizsgálatok: kérdezd a vizsgálat csapatát, a regiszter nem sorolja fel őket
A(z) ClinicalTrials.gov regisztermezőiből összeállítva. A vizsgálat felépítését írja le.
Ki nem vehet részt
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Korábbi kezelés
- Previously receiving systemic anti-tumor therapy for ES-SCLC;
- Receiving other investigational drugs or participated in other interventional clinical studies within 4 weeks before signing the informed consent form;
- Receiving systemic immunostimulant treatment within 4 weeks before enrollment;
- Severe chronic/active infections requiring systemic antibacterial, antifungal or antiviral treatment within 2 weeks before enrollment;
- Having a disease that requires systemic corticosteroids or other immunosuppressants to be treated within ≤14 days before enrollment;
- Using attenuated live vaccines, or planned to receive attenuated live vaccines within 28 days before enrollment;
- Toxicity caused by previous anti-cancer treatment has not recovered to baseline or stable state at the time of enrollment;
Más betegség
- Severe cardiovascular disease;
- Active hepatitis B virus (HBV)/ hepatitis C virus (HCV)/ human immunodeficiency virus (HIV) infection;
- Active autoimmune diseases, a history of interstitial lung disease, or other uncontrolled systemic diseases;
- Known to be allergic to Sintilimab or Tafolecimab or its excipients, having a history of severe allergic reaction to any monoclonal antibody, or having a history of allergy to cisplatin, carboplatin or etoposide;
Laborértékek
- Creatinine clearance rate < 60 mL/min (cisplatin) or < 45 mL/min (carboplatin)
Egyéb
- Combined SCLC (mixed SCLC and NSCLC histological types) or transformed SCLC confirmed by histological or cytological examination;
- Active central nervous system (CNS) metastases (asymptomatic patients with stable lesions allowed);
- Pregnancy or lactation;
- Requiring at least monthly or more frequent drainage of pleural and/or pericardial or peritoneal effusion;
- Uncontrolled or symptomatic hypercalcemia.
Kiket keres a vizsgálat
- Age ≥18 years, ECOG performance status 0-1;
- Histologically or cytologically confirmed extensive-stage small cell lung cancer (ES-SCLC) according to Veterans Administration Lung Study Group criteria;
- Previously not receiving systemic treatment for ES-SCLC;
- Greater than or equal to 1 measurable lesion exists according to RECIST v1.1;
- Expected survival >= 12 weeks;
- Adequate organ system functions (no blood transfusion or component blood use within 14 days before testing).
Életkor a regiszterben: 18 év – - · Nem: nők és férfiak · Egészséges önkénteseket nem fogad
Helyszínek (5)
Helyszínek a regiszter sorrendjében. Ha a profilodba mented a városodat, távolság szerint rendeződnek.
| Helyszín | Város | Ország | Helyszín állapota |
|---|---|---|---|
| Hunan Cancer Hospital(The Affiliated Cancer Hospital of Xiangya School of Medicine, Central South University | Changsha | Kína | Toborzás még nem indult |
| Second Affiliated Hospital, School of Medicine, Zhejiang University | Hangzhou | Kína | Toboroz |
| First Affiliated Hospital, School of Medicine, Zhejiang University | Hangzhou | Kína | Toboroz |
| Department of Thoracic Medical Oncology, Zhejiang Cancer Hospital, Hangzhou Institute of Medicine (HIM), Chinese Academy of Sciences | Hangzhou | Kína | Toboroz |
| Shandong Cancer Hospital and Institute, Shandong First Medical University and Shandong Academy of Medical Science | Jinan | Kína | Toboroz |
Ez az oldal tájékoztatás, nem orvosi tanács. Bármely vizsgálatról az orvosoddal beszélj.