A Phase Ib/II Clinical Study on AK112 Combined or Not Combined With AK119 in pMMR/MSS Colorectal Cancer
- Sponsor
- Akeso
- Study ID
- NCT05846867
- Phase
- PHASE1/PHASE2
- Status
- Active Not Recruiting
Conditions
Eligibility Criteria
- Sex
- ALL
- Age
- 18 Years - N/A
- Healthy Volunteers
- Not accepted
Interventions
- AK119 — DRUGAK119 IV every 2 weeks.intravenous infusion
- AK112 — DRUGAK112 IV every 2 weeks.intravenous infusion
- Oxaliplatin — DRUGOxaliplatin: 85mg/m2, intravenous infusion
- Irinotecan — DRUGIrinotecan 180mg/m2, intravenous infusion
- Calcium folinate — DRUGCalcium folinate: 400mg/m2, intravenous infusion
- Fluorouracil — DRUGFluorouracil 400mg/m2, intravenous injection
Study Details
This is an open label, multicenter Phase Ib/II clinical study on the efficacy and safety of AK119 and AK112 in combination with or without chemotherapy, and AK112 monotherapy in pMMR/MSS CRC
Key Dates
- Start date
- May 8, 2023
- Status verified
- Mar 2026
- Primary completion
- May 8, 2026
- Completion
- Aug 11, 2026
Study Design
- Enrollment
- 170 participants (estimated)
- Allocation
- NON_RANDOMIZED
- Intervention model
- SEQUENTIAL
- Primary purpose
- TREATMENT
Arms
- Experimental: AK119 20mg/kg+ AK112 20mg/kgSubjects will receive AK119 plus AK112 via intravenously (IV) Q2W, up to 2 years
- Experimental: AK119 40mg/kg+ AK112 20mg/kgSubjects will receive AK119 plus AK112 via intravenously (IV) Q2W, up to 2 years
- Experimental: AK119 + AK112 20mg/kg +mFOLFOX6Subjects will receive AK119 and AK112 plus mFOLFOX6 via intravenously (IV)Q2W, up to 12 cycles. Afterward, AK119 and AK112 will continue to be treated up to 2 years.
- Experimental: AK119 + AK112 20mg/kg +FOLFIRISubjects will receive AK119 and AK112 plus FOLFIRI via intravenously (IV)Q2W, up to 12 cycles. Afterward, AK119 and AK112 will continue to be treated up to 2 years.
- Experimental: AK112 20mg/kgSubjects will receive AK112 via intravenously (IV) Q2W, up to 2 years
Primary Outcome Measure
Objective response rate (ORR) [ Time Frame: Up to 2 years ]
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