Literature DB >> 7861020

The need for additional options in the treatment of human immunodeficiency virus infection.

P Volberding1.   

Abstract

Current therapy for human immunodeficiency virus (HIV) infection is inadequate to control the progression of the disease. Although existing nucleoside analogues, such as zidovudine, have clear benefits, they also have drawbacks, including toxicity and the possibility of drug resistance. In addition, the timing of therapy and the use of monotherapy versus combination therapy as initial treatment have not been definitively established. HIV drugs currently in development include newer nucleoside analogues, such as stavudine and lamivudine, nonnucleoside reverse transcriptase inhibitors, and protease inhibitors. The addition of these agents to the antiretroviral armamentarium will expand the treatment options available to clinicians who treat patients with HIV infection.

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Year:  1995        PMID: 7861020     DOI: 10.1093/infdis/171.supplement_2.s150

Source DB:  PubMed          Journal:  J Infect Dis        ISSN: 0022-1899            Impact factor:   5.226


  2 in total

1.  Human immunodeficiency virus type 1 drug susceptibility during zidovudine (AZT) monotherapy compared with AZT plus 2',3'-dideoxyinosine or AZT plus 2',3'-dideoxycytidine combination therapy. The protocol 34,225-02 Collaborative Group.

Authors:  B A Larder; A Kohli; S Bloor; S D Kemp; P R Harrigan; R T Schooley; J M Lange; K N Pennington; M H St Clair
Journal:  J Virol       Date:  1996-09       Impact factor: 5.103

2.  Randomized, controlled phase I/II, trial of combination therapy with delavirdine (U-90152S) and conventional nucleosides in human immunodeficiency virus type 1-infected patients.

Authors:  R T Davey; D G Chaitt; G F Reed; W W Freimuth; B R Herpin; J A Metcalf; P S Eastman; J Falloon; J A Kovacs; M A Polis; R E Walker; H Masur; J Boyle; S Coleman; S R Cox; L Wathen; C L Daenzer; H C Lane
Journal:  Antimicrob Agents Chemother       Date:  1996-07       Impact factor: 5.191

  2 in total

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