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Printable Handouts
Navigable Slide Index
- Introduction
- Transmission of MDR in primary HIV-1 infection
- IQ and the genetic barrier
- E-184V study
- E-184V study design
- Results: 3TC alone vs. treatment interruption
- Lamivudine activity as MDR HIV-1 infection therapy
- Characteristics of study subjects at entry
- Presence of 184V mutation in the absence of 3TC
- Level of viral load in the absence of 3TC
- Partial treatment interruptions (change in viral load)
- Phenotypic sensitivity to Tipranavir
- Phenotypic resistance of multi-PI-resistant isolates
- TPV resist studies (1)
- TPV resist studies (2)
- TPV resist studies (3)
- Efficacy of TMC125
- Time to virological failure
- MONARK trial
- MONARK trial results: HIV RNA levels
- SPREAD trial: transmitted drug resistance
- Transmitted drug resistance over time
- MK-0518: potent activity of integrase inhibitor
- MK-0518 vs. EFV: HIV RNA levels
- Potential benefits of MVC (entry inhibitor)
- Phase II trial of efficacy and safety of vicriviroc
- Summary
Topics Covered
- Drug resistance in HIV disease can occur for each drug used in therapy
- Drug resistant forms of HIV can be sexually transmitted
- Drug resistance can be selected by antiviral drugs
- HIV mutations can interact with one another to affect phenotype
- Newer drugs in each class can work against resistant forms of HIV
- New drug classes continue to be developed
Links
Series:
Categories:
Therapeutic Areas:
Talk Citation
Wainberg, M. (2007, October 1). What to do in therapy in the face of HIV drug resistance? [Video file]. In The Biomedical & Life Sciences Collection, Henry Stewart Talks. Retrieved December 3, 2024, from https://doi.org/10.69645/XJNT9019.Export Citation (RIS)
Publication History
Financial Disclosures
- Prof. Mark Wainberg has not informed HSTalks of any commercial/financial relationship that it is appropriate to disclose.