On Sunday, April 20th 2025, starting 8:30am GMT, there will be maintenance work that will involve the website being unavailable during parts of the day. We apologize for any inconvenience this may cause and appreciate your understanding.
We noted you are experiencing viewing problems
-
Check with your IT department that JWPlatform, JWPlayer and Amazon AWS & CloudFront are not being blocked by your network. The relevant domains are *.jwplatform.com, *.jwpsrv.com, *.jwpcdn.com, jwpltx.com, jwpsrv.a.ssl.fastly.net, *.amazonaws.com and *.cloudfront.net. The relevant ports are 80 and 443.
-
Check the following talk links to see which ones work correctly:
Auto Mode
HTTP Progressive Download Send us your results from the above test links at access@hstalks.com and we will contact you with further advice on troubleshooting your viewing problems. -
No luck yet? More tips for troubleshooting viewing issues
-
Contact HST Support access@hstalks.com
-
Please review our troubleshooting guide for tips and advice on resolving your viewing problems.
-
For additional help, please don't hesitate to contact HST support access@hstalks.com
We hope you have enjoyed this limited-length demo
This is a limited length demo talk; you may
login or
review methods of
obtaining more access.
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 April 19, 2025, 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.