CI

At a glance

ClinicalIndex Comparison Record
Phase 2Recruiting· 143 target
Drug / intervention
mFOLFOXIRI + Cadonilimab +3 moredrug
Likely dose
mFOLFOXIRI + Cadonilimab 6mg/kgfrom record
Key inclusion· 8
  • Age 18-70 years
  • Histologically confirmed colorectal adenocarcinoma
  • ECOG performance status 0-1
  • Colon cancer: T3>5mm or T4 by contrast-enhanced CT, no distant metastasis
Key exclusion· 20
  • Obstruction, active bleeding, perforation requiring emergency surgery or stent placement
  • Active, known or suspected autoimmune disease (with specific exceptions listed)
  • HIV infection or AIDS
  • Untreated active hepatitis B (HBV-DNA ≥500 IU/ml) or C, or co-infection

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

Search/NCT05571644
NCT05571644Phase 2RecruitingUpdate OverdueUpdated 11mo ago · Completion was 6mo ago
Enrollment Stalled
Update Overdue

Neoadjuvant Treatment With mFOLFOXIRI Plus Cadonilimab (AK104) Versus mFOLFOX6 Alone in Locally Advanced Colorectal Cancer: a Randomized Control Phase II Study (OPTICAL-2)

Sun Yat-sen University·interventional·Posted Oct 7, 2022·Updated Jul 23, 2025

In Brief

A Phase 2 clinical trial evaluating mFOLFOXIRI + Cadonilimab, mFOLFOX6, and 2 other interventions for Colorectal Cancer. Currently recruiting, targeting 143 participants across 1 site.

Signals

Enrollment appears stalled

Detailed Summary

Neoadjuvant chemoradiotherapy (CRT) followed by total mesenteric excision (TME) and adjuvant chemotherapy was the standard of treatment for locally advanced rectal cancer (LARC) in the past two decades. The main obstacles for improving survival benefit of LARC was distant metastasis. Recently, total neoadjuvant therapy (TNT) had been recommended as new preferred option for LARC. Induction chemotherapy with FOLFOXIRI followed by CRT or short-course radiotherapy followed by FOLFOX chemotherapy had improved survival benefit for LARC. Neoadjuvant immunotherapy had also been explored in pMMR patients with CRC. In the NICHE trial, neoadjuvant therapy with 2 dose of nivolumab and 1 dose of ipilimumab led to 29% of pathological response and 13% of pCR. Cadonilimab (AK104) was a PD-1/CTLA-4 bi-specific antibody. Here, we tried to explore the efficacy of Neoadjuvant Treatment With mFOLFOXIRI with or without Cadonilimab (AK104) Versus mFOLFOX6 in LARC.

Study Details

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

Timeline

Phase 2Recruiting
20232024202520262027
First PostedOct 7, 2022
Enrollment StartJul 10, 2023
Primary CompletionDec 31, 2025
Study CompletionAug 15, 2027
TodayJul 1, 2026
Enrollment to primary: 2.5 yearsPosted 3.7 years ago

Interventions

mFOLFOXIRI + Cadonilimabdrug

Cadonilimab(AK104)6mg/kg, intravenous d for 60 minutes, followed by mFOLFOXIRI (oxaliplatin 85 mg/m2, irinotecan 150 mg/m2, and folinic acid 400 mg/m2 followed by 5-fluorouracil 2400mg/m2 as a 46-hour continuous infusion on day 1) every 2 weeks for 6 cycles before surgery

mFOLFOX6drug

mFOLFOX6 (oxaliplatin 85 mg/m2, and folinic acid 400 mg/m2 followed by bolus 5-fluorouracil 400 mg/m2 and 5-fluorouracil 2400mg/m2 as a 46-hour continuous infusion on day 1) every 2 weeks for 6 cycels before surgery

mFOLFOXIRIdrug

mFOLFOXIRI (oxaliplatin 85 mg/m2, irinotecan 150 mg/m2, and folinic acid 400 mg/m2 followed by 5-fluorouracil 2400mg/m2 as a 46-hour continuous infusion on day 1) every 2 weeks for 6 cycles before surgery

mFOLFOXIRI+AK104+fruquintinibdrug

Cadonilimab(AK104)6mg/kg, intravenous d for 60 minutes, followed by mFOLFOXIRI (oxaliplatin 85 mg/m2, irinotecan 150 mg/m2, and folinic acid 400 mg/m2 followed by 5-fluorouracil 2400mg/m2 as a 46-hour continuous infusion on day 1) every 2 weeks for 6 cycles, and fruquintinib (3mg Qd, D1-21, Q4W for 3 months) before surgery