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Tuesday, January 10, 2017 8:14:18 PM
From http://www.columbia.edu/itc/hs/medical/pathophys/id/2009/hivantiColor.pdf
FDA-approved Antiretroviral Classes
• Nucleoside reverse transcriptase inhibitors (NsRTIs)
• Nucleotide reverse transcriptase inhibitor (NtRTI)
• Non-nucleoside reverse transcriptase inhibitors (NNRTIs)
• Protease Inhibitors (PIs)
• Fusion inhibitor
• CCR5 antagonist
• Integrase inhibitor
![](http://investorshub.advfn.com/uimage/uploads/2017/1/10/ciajuScreen_Shot_2017-01-10_at_5.10.30_PM.png)
If you see the above pic, one can see why Pro 140 can replace HAART drugs to a large extent. Whether Pro 140 can completely replace HAART regimen in R5 strain patients--is a question for the investigation. That's what 300 patients P3 trial is for. Earlier, longs on this board discounted any criticism about Pro 140 resistance by saying it is all due to screening issues (this is the NONSENSE peddled on this board for very long). However, Pourhassen has given us an answer: CCR5 density and resistance are related. This is for the phase 3 to figure out: can increasing the dosage fix the resistance issues or not? To what extent, increasing the dosage can prevent resistance? Even if the dosage is increased to maximum, even if Pro 140 is injected twice a week, can we see resistance to Pro 140 drug. These are questions for P3. Will wait and see.
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