Efficacy and Safety of AK104 (PD-1/CTLA-4 Bispecial Antibody) Combined With Chemotherapy for Neoadjuvant Treatment of Advanced Ovarian Cancer

PHASE3Not yet recruitingINTERVENTIONAL
Enrollment

100

Participants

Timeline

Start Date

October 1, 2024

Primary Completion Date

October 31, 2027

Study Completion Date

October 31, 2030

Conditions
Advanced Ovarian CancerAK104(PD-1/CTLA-4 Bispecial Antibody)ChemotherapyEfficacySafety
Interventions
DRUG

AK104

The study treatment was followed by a 3-week treatment cycle. The dosing time window is ±3 days. Within 72 hours before each dosing cycle, subjects are required to complete various examinations, including vital signs, physical examination, laboratory examination, and physical status score, to evaluate the safety and tolerability of continued treatment.

All Listed Sponsors
lead

Anhui Provincial Hospital

OTHER_GOV

NCT06542549 - Efficacy and Safety of AK104 (PD-1/CTLA-4 Bispecial Antibody) Combined With Chemotherapy for Neoadjuvant Treatment of Advanced Ovarian Cancer | Biotech Hunter | Biotech Hunter