CI

At a glance

ClinicalIndex Comparison Record
Phase 2Not Yet Recruiting· 120 target
Drug / intervention
QL1706 +1 moredrug
Likely dose
QL1706 5mg/kgfrom record
Structured eligibility isn't available for this trial yet — see the full criteria in the Eligibility tab below.

Standardized by ClinicalIndex from the ClinicalTrials.gov record · verify against the source.

Search/NCT07636226
NCT07636226Phase 2Not Yet Recruiting

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

Sun Yat-sen University·interventional·Posted Jun 9, 2026·Updated Jun 9, 2026

In Brief

A Phase 2 clinical trial evaluating QL1706 and Anlotinib for Small Cell Lung Cancer. Not yet recruiting, targeting 120 participants.

Detailed Summary

This is a multicenter, open-label, randomized controlled phase II/III study evaluating the efficacy and safety of QL1706 in combination with anlotinib as later-line treatment in patients with advanced lung cancer.

Study Details

Study Typeinterventional
Allocation--
Masking--
Primary Purpose--
Countries--
Collaborators--

Timeline

Phase 2Not Yet Recruiting
2027202820292030
First PostedJun 9, 2026
Enrollment StartJul 30, 2026
Primary CompletionDec 30, 2028
Study CompletionDec 30, 2029
TodayJul 1, 2026
Enrollment to primary: 2.4 yearsPosted 22 days agoPrimary completion in 2.5 years

Arms & Interventions

cohort 1experimental

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.

Drug: QL1706Drug: Anlotinib
cohort 2active_comparator

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.

Drug: Anlotinib
cohort 3experimental

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.

Drug: QL1706Drug: Anlotinib
cohort 4active_comparator

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.

Drug: Anlotinib

Interventions

QL1706drug

Every 3 weeks, 5mg/kg of QL1706 is administered intravenously until the disease progresses.

Anlotinibdrug

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.