O+O Alpan LLC
Fairfax, Virginia 22152
0 studies enrolling now · 18 studies all time
What they study most
Antiphospholipid (aPL)-Positive, Asthma, Autoimmune Diseases, Common Variable Immune Deficiencies, Common Variable Immunodeficiency, Fabry Disease, Gaucher Disease, Hyper-IgM Syndrome, Hyperimmunoglobulin M Syndrome, Hypogammaglobulinemia, Inflammatory Diseases, Lysosomal Storage Disorders
Studies at this site
- A Study of Lebrikizumab in Participants With Uncontrolled Asthma Who Are on Inhaled Corticosteroids and a Second Controller Medication — Completed
- A Study Evaluating the Efficacy and Safety of Lebrikizumab in Adult Patients With Mild to Moderate Asthma — Completed
- A Study of Lebrikizumab in Adolescent Participants With Uncontrolled Asthma Who Are on Inhaled Corticosteroids and a Second Controller Medication — Stopped early
- Open Label Extension Study of 1 mg/kg Pegunigalsidase Alfa Every 2 Weeks in Patients With Fabry Disease — Completed
- Dose-ranging Study of PRX-102 in Adult Fabry Disease Patients — Completed
- Study of the Safety and Efficacy of PRX-102 Compared to Agalsidase Beta on Renal Function — Completed
- Safety Study of Replagal® Therapy in Children With Fabry Disease — Completed
- Extension Study of TKT028 Evaluating Safety and Clinical Outcomes of Replagal® in Adult Patients With Fabry Disease — Completed
- Pharmacokinetics, Pharmacodynamics And Safety Study Of Elelyso(tm) In Pediatric Subjects With Type 1 Gaucher Disease — Withdrawn before enrolling
- SRT in Comparison to ERT on Immune Aspects and Bone Involvement in Gaucher Disease — Status unconfirmed
- Longitudinal Cohort Study in Participants With Severe Asthma to Assess Biomarkers — Completed
- Pharmacokinetics (PK) and Safety of Subgam-VF in Primary Immunodeficiency Diseases — Completed
- A Study of the Efficacy and Safety of Omalizumab Through 48 Weeks in Participants With Chronic Idiopathic Urticaria — Completed
- A Study in Participants With Asthma Initiating Treatment With Omalizumab (Xolair) — Completed
- Phase IIa Trial of ALXN1007 for the Treatment of Non-criteria Manifestations of Antiphospholipid Syndrome — Stopped early
- Investigating Lysosomal Storage Diseases in Minority Groups — Status unconfirmed
- Investigation of Immune Disorders and Deficiencies — Status unconfirmed
- Bioequivalence Study to Evaluate the Pharmacokinetics, Safety, and Tolerability of Gammaplex® 10 and Gammaplex® 5% in Primary Immunodeficiency Diseases — Completed