28
Participants
Start Date
December 1, 2025
Primary Completion Date
December 1, 2027
Study Completion Date
February 1, 2028
QL1706, nab-paclitaxel, carboplatin
Participants will receive QL1706 (5 mg/kg, IV, day 1) in combination with nab-paclitaxel (260 mg/m², IV, day 1) and carboplatin (AUC=4-5, IV, day 1) every 21 days for 4-6 cycles. Dose adjustments may be made based on clinical judgment. Patients who do not experience disease progression or intolerable toxicity will proceed to maintenance therapy with QL1706 (5 mg/kg, IV, day 1) every 21 days. Treatment will continue until disease progression, unacceptable toxicity, consent withdrawal, investigator decision, loss to follow-up, death, or meeting other protocol-defined criteria for discontinuation. The maximum duration of QL1706 treatment is 24 months, after which continuation will be at the investigator's discretion based on individual benefit-risk assessment.
National Cancer Center/National Clinical Research Center for Cancer/Cancer Hospital, Beijing
Hebei Medical University Fourth Hospital
OTHER
Peking University Cancer Hospital & Institute
OTHER
Zhijie Wang
OTHER