A Study to Access Efficacy and Safety of P1101 in Chinese PV Patients Who Are Intolerant or Resistance to HU

PHASE2Active, not recruitingINTERVENTIONAL
Enrollment

49

Participants

Timeline

Start Date

October 8, 2021

Primary Completion Date

September 7, 2022

Study Completion Date

July 31, 2027

Conditions
Polycythemia Vera
Interventions
DRUG

Ropeginterferon alfa-2b

Initial dose of 250 µg at Week 0, a medium dose of 350 µg at Week 2, a target dose of 500 µg at Week 4, and a maintenance dose of 500 µg until Week 52.

Trial Locations (14)

Unknown

Peking Union Medical College Hospital, Beijing

Xiangya Hospital Central South University, Changsha

The First Affiliated Hospital of Chongqing Medical Universit, Chongqing

Nanfang Hospital affiliated to Southern Medical University, Guangzhou

Anhui Provincial Hospital, Hefei

Huashan Hospital affiliated to Fudan University, Shanghai

Ruijin Hospital affiliated to Shanghai Jiaotong University, Shanghai

Shenzhen Second People's Hospital, Shenzhen

The First Affiliated Hospital of Soochow University, Suzhou

Institute of Hematology &Blood Diseases Hospital ,Chinese Academy of medical science & Peking Union Medical College, Tianjin

The Second Hospital of Tianjin Medical University, Tianjin

Zhongnan Hospital affiliated to Wuhan University, Wuhan

The First Affiliated Hospital Zhejiang University of Medicine, Zhejiang

Henan Cancer Hospital, Zhengzhou

Sponsors

Lead Sponsor

All Listed Sponsors
lead

PharmaEssentia

INDUSTRY

NCT05485948 - A Study to Access Efficacy and Safety of P1101 in Chinese PV Patients Who Are Intolerant or Resistance to HU | Biotech Hunter | Biotech Hunter