- ICH GCP
- Registre américain des essais cliniques
- Essai clinique NCT07636226
QL1706 Plus Anlotinib as a Later-line Treatment for Patients With Advanced Lung Cancer
A Multicenter, Open-label, Randomized Controlled Phase II/III Study Evaluating the Efficacy and Safety of QL1706 in Combination With Anlotinib as a Later-line Treatment for Patients With Advanced Lung Cancer
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
Type d'étude
Inscription (Estimé)
Phase
- Phase 2
- Phase 3
Contacts et emplacements
Coordonnées de l'étude
- Nom: Yan Huang, MD
- E-mail: huangyan@sysucc.org.cn
Sauvegarde des contacts de l'étude
- Nom: Li Zhang, MD
- Numéro de téléphone: +86-20-87343289
- E-mail: zhangli@sysucc.org.cn
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
- Adulte
- Adulte plus âgé
Accepte les volontaires sains
La description
Inclusion Criteria:
1. Male or female patients aged 18 years and above, up to 80 years old. 2. Small cell lung cancer or lung squamous cell carcinoma confirmed by tissue or pathological examination.
3. Requires previous treatment with platinum-based drugs. 4. Requires previous treatment with PD-1/PD-L1 drugs. 5. Patients must have received at least 2 lines of treatment, no more than 3 lines of treatment.
6. Confirmed as small cell lung cancer by histological examination. 7. Able to provide informed consent and comply with the trial protocol. 8. According to RECIST 1.1 standards, there are measurable lesions (CT scan). 9. Expected lifespan ≥ 12 weeks. 10. ECOG performance status 0-1. 11. Patients must have adequate organ and bone marrow functions, defined as follows:
- Absolute neutrophil count ≥ 1,500/mcL
- Platelet count > 90,000/mcL
- Hemoglobin ≥ 9 g/dL (allowing for Hgb transfusion)
- Creatinine ≤ 1.5 × ULN
- Total bilirubin ≤ 1.5 mg/dL or ≤ 26 μmol/L
- If there is liver metastasis, AST (SGOT) / ALT (SGPT) ≤ 5 × ULN; if there is no liver metastasis, ≤ 2.5 × ULN
Albumin ≥ 2.5 g/dL 12. Patients are allowed to receive palliative radiotherapy (such as radiotherapy after brain metastasis), provided that there are measurable target lesions in the radiation field of the patient.
13. Able to go to the research center to ensure that patients complete all research-related appointments.
14. Pregnant women and male partners of pregnant women must agree to take adequate contraceptive measures (hormonal or barrier methods; abstinence) before entering the study, during the study, and within 90 days after completing the study (hormonal or barrier methods; abstinence). If a woman becomes pregnant during the study or suspects she is pregnant, she should immediately inform the attending doctor.
Note: Pregnant women are defined as any woman meeting the following criteria (regardless of sexual orientation, whether tubal ligation has been performed or being single):
- No hysterectomy or bilateral oophorectomy;
No natural menopause for at least 12 consecutive months (i.e., any time during the previous 12 months there was menstruation).
Exclusion Criteria:
1. Patients with symptomatic central nervous system metastases, or those with unstable neurological symptoms requiring an increase in the dosage of corticosteroids.
2. Presence of another primary malignant tumor (excluding cervical carcinoma in situ or skin basal cell carcinoma).
3. The patient has a clinically significant disease that affects their participation in this study, including but not limited to: active or uncontrolled infection, SARS-CoV-2 infection, immunodeficiency, hepatitis B, hepatitis C, uncontrolled diabetes, uncontrolled hypertension, symptomatic congestive heart failure, unstable angina pectoris, myocardial infarction within the past 6 months, uncontrolled arrhythmia, QTc interval prolongation > 450 ms or a mental illness/socioeconomic condition that limits their compliance with the study requirements.
4. Previous use of CTLA-4 monotherapy or combination antibodies containing CTLA-4.
5. Previous treatment with anti-angiogenic drugs. 6. Presence of uncontrolled or symptomatic pleural or pericardial effusion, etc.
7. Uncontrolled or clinically significant third-space effusion. 8. Severe adverse reactions occurred during previous immunotherapy, and the investigator considers it unsuitable for re-administration of immunotherapy.
9. Any condition that may interfere with the subject's participation in the study or the evaluation of the study results.
10. Receiving major surgery within 30 days before the first day of the study. 11. Currently using or expected to use within 14 days before the first administration of drugs or foods known to be potent CYP3A4/5 inhibitors or CYP3A4/5 inducers (such as grapefruit juice or grapefruit/grapefruit-related citrus fruits (such as oranges, grapefruits), ketoconazole, miconazole, itraconazole, voriconazole, posaconazole, clarithromycin, telithromycin, indinavir, saquanavir, ritonavir, nelfinavir, amprenavir, fosamprenavir, nefazodone, lopinavir, ritonavir), and applying these drugs locally (such as 2% ketoconazole cream is allowed);
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Objectif principal: Traitement
- Répartition: Randomisé
- Modèle interventionnel: Affectation parallèle
- Masquage: Aucun (étiquette ouverte)
Armes et Interventions
Groupe de participants / Bras |
Intervention / Traitement |
|---|---|
|
Expérimental: cohort 1
Cohort 1 includes patients with advanced SCLC who have received at least 2 lines of treatment but no more than 3 lines of treatment in the past.
|
Every 3 weeks, 5mg/kg of QL1706 is administered intravenously until the disease progresses.
10mg Anlotinib is administered orally.
It is given daily for the first 14 days, then stopped for 7 days.
A 3-week period constitutes one cycle, and this process continues until the disease progresses.
|
|
Comparateur actif: cohort 2
Cohort 2 includes patients with advanced SCLC who have received at least 2 lines of treatment but no more than 3 lines of treatment in the past.
|
10mg Anlotinib is administered orally.
It is given daily for the first 14 days, then stopped for 7 days.
A 3-week period constitutes one cycle, and this process continues until the disease progresses.
|
|
Expérimental: cohort 3
Cohort 3 includes patients with advanced lung squamous cell carcinoma who have received at least 2 lines of treatment but no more than 3 lines of treatment in the past.
|
Every 3 weeks, 5mg/kg of QL1706 is administered intravenously until the disease progresses.
10mg Anlotinib is administered orally.
It is given daily for the first 14 days, then stopped for 7 days.
A 3-week period constitutes one cycle, and this process continues until the disease progresses.
|
|
Comparateur actif: cohort 4
Cohort 4 includes patients with advanced lung squamous cell carcinoma who have received at least 2 lines of treatment but no more than 3 lines of treatment in the past.
|
10mg Anlotinib is administered orally.
It is given daily for the first 14 days, then stopped for 7 days.
A 3-week period constitutes one cycle, and this process continues until the disease progresses.
|
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
OS
Délai: From date of first study treatment to date of death from any cause, assessed up to approximately 36 months
|
Overall survival (OS), defined as the time from first study treatment to death from any cause.
|
From date of first study treatment to date of death from any cause, assessed up to approximately 36 months
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
PFS
Délai: From date of first study treatment to the date of first documented disease progression or date of death from any cause, whichever occurs first, assessed up to approximately 36 months.
|
Progression-free survival (PFS) is defined as the time from the first trial treatment to disease progression or death due to any cause (whichever occurs first).
|
From date of first study treatment to the date of first documented disease progression or date of death from any cause, whichever occurs first, assessed up to approximately 36 months.
|
|
DCR
Délai: From first study treatment to disease progression or initiation of new anti-tumor therapy, assessed up to approximately 36 months
|
Disease Control Rate (DCR), the proportion of patients achieving the best overall therapeutic response of CR, PR or SD
|
From first study treatment to disease progression or initiation of new anti-tumor therapy, assessed up to approximately 36 months
|
|
12-months OS rate
Délai: From date of first study treatment to date of death from any cause, assessed up to 12 months
|
The 12-month overall survival rate is defined as the proportion of patients who remain alive 12 months after the first trial treatment.
|
From date of first study treatment to date of death from any cause, assessed up to 12 months
|
|
Adverse Events
Délai: From signing of informed consent through 90 days after the last dose of study treatment or initiation of new anti-tumor therapy, whichever occurs first.
|
Incidence and severity of adverse events (AEs), graded according to the National Cancer Institute Common Terminology Criteria for Adverse Events (NCI-CTCAE) version 5.0.
Relationship to study treatment (QL1706 and/or anlotinib) is assessed by the investigator.
|
From signing of informed consent through 90 days after the last dose of study treatment or initiation of new anti-tumor therapy, whichever occurs first.
|
Collaborateurs et enquêteurs
Parrainer
Les enquêteurs
- Chercheur principal: Li Zhang, Sun Yat-sen University
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Estimé)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- SL-B2025-731-02
Plan pour les données individuelles des participants (IPD)
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Description du régime IPD
Informations sur les médicaments et les dispositifs, documents d'étude
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