A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Efficacy of NXT007 in Persons With Severe or Moderate Hemophilia A

PHASE1/PHASE2RecruitingINTERVENTIONAL
Enrollment

60

Participants

Timeline

Start Date

September 21, 2023

Primary Completion Date

June 16, 2030

Study Completion Date

June 16, 2030

Conditions
Hemophilia A
Interventions
DRUG

NXT007

Participants will receive NXT007 administered subcutaneously (SC), 2 loading doses once every two weeks (Q2W) followed by once every 4 weeks (Q4W) maintenance doses based on the schedule.

Trial Locations (12)

1023

RECRUITING

Auckland Cancer Trial Centre, Auckland

20007

WITHDRAWN

Georgetown Uni Medical Center, Washington D.C.

20089

RECRUITING

Istituto Clinico Humanitas, Rozzano (MI)

28046

RECRUITING

Hospital Universitario la Paz, Madrid

29010

ACTIVE_NOT_RECRUITING

Hospital Regional Universitario Carlos Haya, Málaga

46260

RECRUITING

Indiana Hemophilia & Thrombosis center, Indianapolis

52242

RECRUITING

University of Iowa Hospitals and Clnics Dept of Pediatrics, Iowa City

95817

RECRUITING

UC Davis Cancer Center, Sacramento

V6H 3N1

RECRUITING

British Columbia Children's Hospital, Vancouver

L8N 3Z5

RECRUITING

Hamilton Health Sciences Corporation, Hamilton

80-214

RECRUITING

Uniwersyteckie Centrum Kliniczne, Gda?sk

02-776

RECRUITING

Instytut Hematologii i Transfuzjologii, Warsaw

All Listed Sponsors
lead

Hoffmann-La Roche

INDUSTRY