genetic disorders
Showing 1 - 9 of 9
Whole Exome Sequencing and Whole Genome Sequencing for
Recruiting
- Non-immune Fetal Hydrops
- +2 more
- Whole Exome Sequencing
- Whole Genome Sequencing
-
Philadelphia, PennsylvaniaThomas Jefferson University
Jun 27, 2021
Genetic Disorders Trial in Portland (Whole Genome Sequencing, Carrier status testing)
Completed
- Genetic Disorders
- Whole Genome Sequencing
- Carrier status testing
-
Portland, OregonKaiser Permanente Northwest
Apr 8, 2019
Genetic Disorders, Hereditary Angioedema Trial in Leiden, Târgu-Mures (Recombinant Human C1 Inhibitor)
Completed
- Genetic Disorders
- Hereditary Angioedema
- Recombinant Human C1 Inhibitor
-
Leiden, Netherlands
- +1 more
Apr 3, 2018
Charcot-Marie-Tooth Disease, Hereditary Neuropathy With Liability to Pressure Palsies, Genetic Disorders Trial in France
Completed
- Charcot-Marie-Tooth Disease
- +2 more
- PXT3003 Low dose
- +3 more
-
Lille, France
- +5 more
Oct 19, 2017
Genetic Disorders Trial in Leiden (i.v. recombinant human C1 inhibitor)
Completed
- Genetic Disorders
- i.v. recombinant human C1 inhibitor
-
Leiden, NetherlandsFor information contact Sonja Visscher
Apr 24, 2013
Genetic Disorders Trial in Leiden (i.v. recombinant human C1 inhibitor)
Completed
- Genetic Disorders
- i.v. recombinant human C1 inhibitor
-
Leiden, NetherlandsFor information on sites in Europe, please contact Pharming Tech
Feb 21, 2013
Hereditary Angioedema, Angioneurotic Edema, Genetic Disorders Trial in Leiden, Tirgu Mures (recombinant human C1 inhibitor,
Completed
- Hereditary Angioedema
- +2 more
- recombinant human C1 inhibitor
- Placebo
-
Leiden, Netherlands
- +1 more
Sep 27, 2012
Genetic Disorders, Sickle Cell Anemia Trial in New York (Busulfan, Cyclophosphamide, BMD)
Completed
- Genetic Disorders
- Sickle Cell Anemia
- Busulfan, Cyclophosphamide, BMD
-
New York, New YorkMemorial Sloan-Kettering Cancer Center
Sep 10, 2008
Array-Based Comparative Genomic Hybridization System Using Whole
Unknown status
- Genetic Disorders
- (no location specified)
Jul 13, 2006