Study to Nivolumab Following Preoperative Chemoradiotherapy

PHASE1/PHASE2UnknownINTERVENTIONAL
Enrollment

90

Participants

Timeline

Start Date

October 31, 2016

Primary Completion Date

December 31, 2021

Study Completion Date

August 31, 2022

Conditions
Cancer of Rectum
Interventions
DRUG

Nivolumab

Capecitabine:Dose of 1650mg/m2,14days, Radiation:45Gy/25 fractions, Nivolumab :240mg on day1 of each cycle, Surgical therapy:The resection (LAR), intersphincteric resection (ISR), or abdominoperineal resection (APR).

DRUG

Ipilimumab

For only Cohort D,1 mg/kg at six-week intervals

Trial Locations (3)

Unknown

RECRUITING

National Cancer Center Hospital East, Kashiwa

RECRUITING

Hokkaido University, Sapporo

RECRUITING

Osaka National Hospital, Osaka

Sponsors
All Listed Sponsors
collaborator

Ono Pharmaceutical Co. Ltd

INDUSTRY

lead

Takayuki Yoshino

OTHER

NCT02948348 - Study to Nivolumab Following Preoperative Chemoradiotherapy | Biotech Hunter | Biotech Hunter