Comparison of the Pathological Effect Between 2 and 4 Cycles Neoadjuvant CAPOX for Low/Intermediate Risk II/III Rectal Cancer

PHASE3Active, not recruitingINTERVENTIONAL
Enrollment

554

Participants

Timeline

Start Date

August 26, 2021

Primary Completion Date

October 1, 2024

Study Completion Date

December 1, 2027

Conditions
Rectal CancerNeoadjuvant Chemotherapy
Interventions
DRUG

Capox chemotherapy

oxaliplatin: 130 mg/m2 iv d 1, capecitabine: 1000 mg/m2 bid d 1-14, repeated at 3 week intervals

Trial Locations (4)

214104

Genecast Biotechnology Co., Ltd, Wuxi

610000

the Third People'S Hospital of Chengdu, Chengdu

West China Hospital, Chengdu

Unknown

The Third Affiliated Hospital of Kunming Medical University, Kunming

Sponsors
All Listed Sponsors
collaborator

The Third People's Hospital of Chengdu

OTHER

collaborator

Chengdu Fifth People's Hospital

OTHER

collaborator

Peking Union Medical College

OTHER

collaborator

Peking University Cancer Hospital & Institute

OTHER

collaborator

Sun Yat-sen University

OTHER

collaborator

Second Affiliated Hospital, School of Medicine, Zhejiang University

OTHER

collaborator

Yunnan Cancer Hospital

OTHER

collaborator

The First Affiliated Hospital of Zhengzhou University

OTHER

collaborator

The Affiliated Hospital Of Guizhou Medical University

OTHER

collaborator

Sichuan Provincial People's Hospital

OTHER

collaborator

Nanchong Central Hospital

OTHER_GOV

collaborator

Dazhou Central Hospital

OTHER

collaborator

Leshan People's Hospital

UNKNOWN

collaborator

GeneCast Biotechnology Co., Ltd.

INDUSTRY

lead

West China Hospital

OTHER

NCT04922853 - Comparison of the Pathological Effect Between 2 and 4 Cycles Neoadjuvant CAPOX for Low/Intermediate Risk II/III Rectal Cancer | Biotech Hunter | Biotech Hunter