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NCT01059084

An Open-label Trial of the Effect of Valacyclovir on Plasma HIV-1 Levels Among HIV-1 Seropositive and HSV-1/2 Seronegative Persons

Withdrawn NA Last updated 4 December 2012
What this trial tests

NA trial testing Valacyclovir in HIV. Withdrawn.

Timeline
1 January 2010
Primary endpoint
1 December 2012
1 December 2012

Quick facts

Lead sponsorUniversity of Washington
PhaseNA
StatusWithdrawn
Study typeINTERVENTIONAL
Allocationna
Designsingle group
Maskingnone
Primary purposebasic science
Start date1 January 2010
Primary completion1 December 2012
Estimated completion1 December 2012

Drugs / interventions tested

Conditions studied

Sponsor

University of Washington

Who can join

18 and older, any sex, with HIV or HIV Infections. Patients with the condition only — healthy volunteers not accepted.

What's being measured

Primary outcomes are the specific endpoints the trial is designed to prove or disprove.

Sponsor's own description

The purpose of this study is to look at the effect of daily herpes medication, valacyclovir, on HIV levels in the blood in persons who are HIV positive and do not have oral or genital herpes.

Publications & conference data

1 peer-reviewed publication reference this trial (live from Europe PMC):

  1. Exploiting the anti-HIV-1 activity of acyclovir: suppression of primary and drug-resistant HIV isolates and potentiation of the activity by ribavirin.
    Vanpouille C, Lisco A, Introini A, Grivel JC, et al · · 2012 · cited 17× · PMID 22314523 · DOI 10.1128/aac.05986-11

Verify or expand the search:

Other trials of Valacyclovir

Trials testing the same drug.

Other recruiting trials for HIV

Currently open trials in the same condition.

Other University of Washington trials

Trials by the same sponsor.

Verify against primary sources

Data sources for this page

Drug Landscape aggregates and links these public records for informational use only. Always verify against the primary source before clinical or regulatory decisions. Canonical URL: https://druglandscape.com/trial/NCT01059084.

Primary sources · FDA · ClinicalTrials.gov · EMA · SEC EDGAR · ChEMBL · Wikidata · full sourcing