A Phase Ⅲa Study of Genetically Modified Recombinant Human Interleukin-11

PHASE3CompletedINTERVENTIONAL
Enrollment

62

Participants

Timeline

Start Date

March 31, 2015

Primary Completion Date

August 31, 2017

Study Completion Date

August 31, 2017

Conditions
Chemotherapy-induced Thrombocytopenia
Interventions
DRUG

NL201

mIL-11:5μg/kg,subcutaneous administration once daily for 10 days,beginning 24 h after chemotherapy;

DRUG

NL201

mIL-11:7.5μg/kg,subcutaneous administration once daily for 10 days,beginning 24 h after chemotherapy;

DRUG

NL201

The optimal dosing dose NL201,subcutaneous administration once daily for 10 days,beginning 24 h after chemotherapy.

DRUG

rhIL-11

rhIL-11(25μg/kg),subcutaneous administration once daily for 10 days,beginning 24 h after chemotherapy.

Trial Locations (5)

200032

Fudan University Shanghai Cancer Center, Shanghai

Unknown

Beijing Cancer Hospital, Beijing

The Third Affiliated Hospital of Harbin Medical University, Harbin

The First Hospital of Jilin University, Changchun

Tianjin Medical University Cancer Institute and Hospital, Tianjin

All Listed Sponsors
lead

Beijing Northland Biotech. Co., Ltd.

INDUSTRY

NCT01663441 - A Phase Ⅲa Study of Genetically Modified Recombinant Human Interleukin-11 | Biotech Hunter | Biotech Hunter