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1.
Future Microbiol ; 15: 389-400, 2020 04.
Article in English | MEDLINE | ID: mdl-32166967

ABSTRACT

Brincidofovir (BCV) is a lipid conjugate of cidofovir with good oral bioavailability, enabling optimal intracellular levels of the active drug. Lower rates of nephrotoxicity and myelotoxicity make it a favorable alternative. Despite a greater safety profile among pediatric hematopoietic cell transplant recipients, the oral formulation has been associated with increased gastrointestinal toxicity in adult hematopoietic cell transplant recipients. Oral BCV continues to be developed as a countermeasure against smallpox, while a potentially safer intravenous preparation has been out licensed to another company. BCV has demonstrated great in vitro potency against double-stranded DNA viruses, especially adenovirus. Because of its importance for immunocompromised patients, this review aims to evaluate BCV's clinical and safety profile to support its continued development.


Subject(s)
Adenovirus Infections, Human/drug therapy , Antiviral Agents , Cytosine/analogs & derivatives , DNA Virus Infections/drug therapy , DNA Viruses/drug effects , Organophosphonates , Adenovirus Infections, Human/virology , Animals , Antiviral Agents/adverse effects , Antiviral Agents/pharmacokinetics , Antiviral Agents/pharmacology , Antiviral Agents/therapeutic use , Clinical Trials as Topic , Cytosine/adverse effects , Cytosine/pharmacokinetics , Cytosine/pharmacology , Cytosine/therapeutic use , DNA Virus Infections/virology , Humans , Immunocompromised Host , Organophosphonates/adverse effects , Organophosphonates/pharmacokinetics , Organophosphonates/pharmacology , Organophosphonates/therapeutic use
3.
San Juan, P.R; U.P.R., R.C.M., Escuela Graduada de Salud P£blica, Depto. de Bioestad¡stica y Epidemiolog¡a; 2005. 106 p gr ficas, tablas:col.
Thesis | Puerto Rico | ID: por-45352
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