Source:http://linkedlifedata.com/resource/pubmed/id/16518958
Switch to
Predicate | Object |
---|---|
rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
|
pubmed:dateCreated |
2006-3-7
|
pubmed:abstractText |
Albumin-interferon-alpha (IFN-alpha) is a novel 85.7-kDa recombinant protein consisting of IFN-alpha that is genetically fused to human serum albumin. In this Phase I/II, multicentre, open-label study, we evaluated the safety and tolerability, pharmacokinetics and pharmacodynamics of albumin-IFN-alpha in IFN-alpha-experienced patients with chronic hepatitis C. Albumin-IFN-alpha was administered in 22 escalating doses (7-900 microg) in a single injection or in two injections 14 days apart. In the 119 patients studied, there were no discontinuations because of adverse events, and albumin-IFN-alpha had a favourable safety profile at doses up to 900 microg. The most common adverse events were headache (56%), fatigue (52%), injection site erythema (38%), arthralgias (32%) and pyrexia (27%). Reduced clearance resulted in a mean elimination half-life of 159 h, which supports dosing at 2- to 4-week intervals. Induction of the IFN-specific gene OAS1 was maintained for > or = 28 days following a single injection of albumin-IFN-alpha at doses of > or = 40 microg. Dose-dependent antiviral activity was observed in this IFN-alpha-experienced study population. Antiviral activity of > or = 1.0-log reductions in HCV RNA was observed in 47% (37/78) of patients in the 120- to 900-microg cohorts and in 59% (16/27) in the 400- to 900-microg double-injection cohorts. These results support further clinical studies of albumin-IFN-alpha for the treatment of patients with chronic hepatitis C.
|
pubmed:language |
eng
|
pubmed:journal | |
pubmed:citationSubset |
IM
|
pubmed:chemical | |
pubmed:status |
MEDLINE
|
pubmed:issn |
1359-6535
|
pubmed:author |
pubmed-author:BalanVijayanV,
pubmed-author:DavisGary LGL,
pubmed-author:DicksonRolland CRC,
pubmed-author:EversonGregory TGT,
pubmed-author:FreimuthWilliam WWW,
pubmed-author:LambiaseLouis RLR,
pubmed-author:NelsonDavid RDR,
pubmed-author:NeumannAvidan UAU,
pubmed-author:OsbornBlaire LBL,
pubmed-author:PostAnthony BAB,
pubmed-author:RedfieldRobert RRR,
pubmed-author:SubramanianG ManiGM,
pubmed-author:SulkowskiMark SMS,
pubmed-author:WiesnerRusell HRH
|
pubmed:issnType |
Print
|
pubmed:volume |
11
|
pubmed:owner |
NLM
|
pubmed:authorsComplete |
Y
|
pubmed:pagination |
35-45
|
pubmed:meshHeading |
pubmed-meshheading:16518958-Adult,
pubmed-meshheading:16518958-Aged,
pubmed-meshheading:16518958-Antiviral Agents,
pubmed-meshheading:16518958-Dose-Response Relationship, Drug,
pubmed-meshheading:16518958-Female,
pubmed-meshheading:16518958-Hepatitis C, Chronic,
pubmed-meshheading:16518958-Humans,
pubmed-meshheading:16518958-Interferon-alpha,
pubmed-meshheading:16518958-Male,
pubmed-meshheading:16518958-Middle Aged,
pubmed-meshheading:16518958-Serum Albumin,
pubmed-meshheading:16518958-Treatment Outcome
|
pubmed:year |
2006
|
pubmed:articleTitle |
A Phase I/II study evaluating escalating doses of recombinant human albumin-interferon-alpha fusion protein in chronic hepatitis C patients who have failed previous interferon-alpha-based therapy.
|
pubmed:affiliation |
Mayo Clinic, Phoenix, AZ, USA. Balan.Vijayan@mayo.edu
|
pubmed:publicationType |
Journal Article,
Multicenter Study,
Clinical Trial, Phase II,
Clinical Trial, Phase I
|