Program Director, Clinical R&D

Rare diseases treated or studied

Based on trial PI assignments and publication topics.

• Congenital fibrinogen deficiency→
• Alpha-1-antitrypsin deficiency→
• Hemophilia B→
• Hereditary angioedema with C1Inh deficiency→
• Primary immunodeficiency→
• Von Willebrand disease→
• Hereditary angioedema with normal C1Inh→
• Congenital factor XIII deficiency→

Clinical trials (12)

• NCT00945906
• NCT00168103
• NCT00883090
• NCT00885742
• NCT01224808
• NCT00496262
• NCT00751621
• NCT00670007
• NCT00916656
• NCT00803101
• NCT00941616
• NCT01213446

Verify independently

• ClinicalTrials.gov PI search for Program Director, Clinical R&D

Other specialists for Congenital fibrinogen deficiency

Peers ranked by clinical-trial PI role, publications, and verification quality.

• Cristina Solomon, MD
  Octapharma
• Niki A. Ottenhof, MD, PhD
  Erasmus Medical Center
• Caroline van der Marel, MD, PhD
  Erasmus Medical Center
• Program Director
  CSL Behring
• Claudia Djambas Khayat, MD
  Hôtel Dieu de France, Dept. of Pediatrics
• Sigurd Knaub, PhD
  Octapharma
• Alessandro Casini, MD
  University Hospitals of Geneva
• Niels Rahe-Meyer, Prof.
  Franziskus Hospital, Bielefeld

See all specialists for Congenital fibrinogen deficiency →