- ICH GCP
- Yhdysvaltain kliinisten tutkimusten rekisteri
- Kliininen tutkimus 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
Tutkimuksen yleiskatsaus
Tila
Interventio / Hoito
Yksityiskohtainen kuvaus
Opintotyyppi
Ilmoittautuminen (Arvioitu)
Vaihe
- Vaihe 2
- Vaihe 3
Yhteystiedot ja paikat
Opiskeluyhteys
- Nimi: Yan Huang, MD
- Sähköposti: huangyan@sysucc.org.cn
Tutki yhteystietojen varmuuskopiointi
- Nimi: Li Zhang, MD
- Puhelinnumero: +86-20-87343289
- Sähköposti: zhangli@sysucc.org.cn
Osallistumiskriteerit
Kelpoisuusvaatimukset
Opintokelpoiset iät
- Aikuinen
- Vanhempi Aikuinen
Hyväksyy terveitä vapaaehtoisia
Kuvaus
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);
Opintosuunnitelma
Miten tutkimus on suunniteltu?
Suunnittelun yksityiskohdat
- Ensisijainen käyttötarkoitus: Hoito
- Jako: Satunnaistettu
- Inventiomalli: Rinnakkaistehtävä
- Naamiointi: Ei mitään (avoin tarra)
Aseet ja interventiot
Osallistujaryhmä / Arm |
Interventio / Hoito |
|---|---|
|
Kokeellinen: 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.
|
|
Active Comparator: 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.
|
|
Kokeellinen: 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.
|
|
Active Comparator: 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.
|
Mitä tutkimuksessa mitataan?
Ensisijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
|
OS
Aikaikkuna: 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
|
Toissijaiset tulostoimenpiteet
Tulosmittaus |
Toimenpiteen kuvaus |
Aikaikkuna |
|---|---|---|
|
PFS
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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
Aikaikkuna: 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.
|
Yhteistyökumppanit ja tutkijat
Sponsori
Tutkijat
- Päätutkija: Li Zhang, Sun Yat-sen University
Opintojen ennätyspäivät
Opi tärkeimmät päivämäärät
Opiskelun aloitus (Arvioitu)
Ensisijainen valmistuminen (Arvioitu)
Opintojen valmistuminen (Arvioitu)
Opintoihin ilmoittautumispäivät
Ensimmäinen lähetetty
Ensimmäinen toimitettu, joka täytti QC-kriteerit
Ensimmäinen Lähetetty (Todellinen)
Tutkimustietojen päivitykset
Viimeisin päivitys julkaistu (Todellinen)
Viimeisin lähetetty päivitys, joka täytti QC-kriteerit
Viimeksi vahvistettu
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Avainsanat
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