RecruitingPHASE1, PHASE2NCT05987449
A Study to Evaluate the Safety, Tolerability, Pharmacokinetics, Pharmacodynamics, and Efficacy of NXT007 in Persons With Severe or Moderate Hemophilia A
Studying Hemophilia
Last synced from ClinicalTrials.gov
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Clinical trial records are synced from ClinicalTrials.gov through automated extraction.
Report missing dataKey facts
- Sponsor
- Hoffmann-La Roche
- Principal Investigator
- Clinical TrialsHoffmann-La Roche
- Intervention
- NXT007(drug)
- Enrollment
- 60 enrolled
- Eligibility
- 2-59 years · MALE
- Timeline
- 2023 – 2030
Study locations (13)
- UC Davis Cancer Center, Sacramento, California, United States
- Georgetown Uni Medical Center, Washington D.C., District of Columbia, United States
- Indiana Hemophilia & Thrombosis center, Indianapolis, Indiana, United States
- University of Iowa Hospitals and Clnics Dept of Pediatrics, Iowa City, Iowa, United States
- British Columbia Children's Hospital, Vancouver, British Columbia, Canada
- Hamilton Health Sciences Corporation, Hamilton, Ontario, Canada
- Istituto Clinico Humanitas, Rozzano (MI), Lombardy, Italy
- Auckland Cancer Trial Centre, Auckland, New Zealand
- Uniwersyteckie Centrum Kliniczne, Gda?sk, Poland
- Instytut Hematologii i Transfuzjologii, Warsaw, Poland
- Hospital Sant Joan de Deu, Esplugues de Llobregat, Barcelona, Spain
- Hospital Universitario la Paz, Madrid, Spain
- Hospital Regional Universitario Carlos Haya, Málaga, Spain
Primary source
Recruitment status, site addresses, contacts, and full eligibility criteria can change between syncs. Always verify with the trial team before planning travel or treatment.
Open NCT05987449 on ClinicalTrials.govOther trials for Hemophilia
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