Last updated: 11/07/2018 10:12:39
PGx: Genotypic analysis of baseline and nadir HCV patient samples from the HBI115040 Phase I clinical trial
Clinicaltrials.gov ID
Not applicable
EudraCT ID
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EU CT Number
Not applicable
Trial status
Study complete
Study complete
Trial overview
Official title: PGx: Genotypic analysis of baseline and nadir HCV patient samples from the HBI115040 Phase I clinical trial
Trial description: PGx: Genotypic analysis of baseline and nadir HCV patient samples from the HBI115040 Phase I clinical trial
Primary purpose:
Not applicable
Trial design:
Not applicable
Masking:
Not applicable
Allocation:
Not applicable
Primary outcomes:
Not applicable
Secondary outcomes:
Not applicable
Interventions:
Not applicable
Enrollment:
Not applicable
Primary completion date:
Not applicable
Observational study model:
Not applicable
Time perspective:
Not applicable
Clinical publications:
David Wilfret, Jill Walker, Christian Voitenleitner, Sharon Baptiste-Brown, Mark Lovern, Joseph Kim, Kimberly Adkison, Amanda Mathis, Lee Moss, Daniel Lee, Lou Yu, Jianjun Gan, Brad Shotwell, Andrew Spaltenstein.A Randomized, Double Blind, Dose Escalation, Fusion, First Time in Human Study to Assess the Safety, Tolerability, Pharmacokinetics, and Antiviral Activity of Single Doses of GSK2485852 in Chronically Infected Hepatitis C Subjects.Clin Pharmacol Drug Devel.2014;3(6):439-448
Inclusion and exclusion criteria
Trial location(s)
This study does not involve prospective enrollment of participants.
Study documents
Clinical study report
Available language(s): English
Scientific result summary
Available language(s): English
If you wish to request for full study report, please contact - [email protected]
Results overview
Not applicable
Recruitment status
Study complete
Actual primary completion date
Not applicable
Actual study completion date
2011-08-06
Plain language summaries
Plain language summaries of clinical trial results for Phase 2-4 clinical trials that were initiated on or after January 2022 will be posted by GSK within one year following study completion.
Additional information about the trial
Not applicable
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