I do not know a thing about this Texas medical research company but go to http://www.ophidia.com/RNAviruses.html . There have been rumors for some time that "venoms" have HIV inhibitor properties. And this Australian Taipan snake venom isolate HIV Inhibitor medicine they have had success with is a proof. The worlds most deadly snake. Which has many many competitors throughout world habitats for that claim. The advantages of venom with HIV inhibitor properties can be contrasted to todays HIV non venom Inhibitor medicines as follows: Venoms in nature, a function of, work by going into the lymph system and killing or immobilizing. Todays HIV Inhibitor medicines, all non venom, can not go into the lymph system with efficiency. And much of the HIV is in the lymph system.                                                                                         It is the body HIV virus infected T 4 white blood cells dormant or semi dormant in the Lymph System, these in the lymph system HIV infected T 4 cells that will produce in the future "HIV virus for the HIV virus" as strange as it may seem, that are the reason today there is no cure for HIV. They can not be gotten to in their lymph system citadel by current HIV medicines. Instead there is only decades of viral reproduction suppression by continual administration of currently used HIV Inhibitor medicines that work in suppressing HIV virus efficiently only outside of the lymph system in the blood stream, not within the lymph system.                                                                                        That is, the HIV infected person at this time can not be told "Treatment is over with. We have killed all the HIV not in the lymph system and we have killed enough in the lymph system that the body natural defenses can handle and kill it as it wakes up from dormancy". Because todays HIV medicines can not efficiently kill HIV in the lymph system (all who have been stuck by HIV infected needles in hospitals but who have not seroconverted to HIV+ status have a quantity of HIV dormant in their lymph system, some of the dormant HIV remaining in the lymph system for years - but the quantity of HIV virus in the lymph system is limited to where the body natural defenses can handle it, meaning killing it all as it wakes up from its dormancy and begins to multiply).                                                                         When the quantity of HIV virus infecting human T-4 white blood cells in the lymph system is a quantity more than the persons natural system can handle that person seroconverts to HIV+. If a person seroconverts to HIV+ it will happen within a few weeks to months of being initially HIV infected.                                                                            There may be "unstable reaction" at certain times by some persons to venom - consider honey bee venom as it is not easy to produce a pure serum non synthesized isolate from a venom serum or any serum (to mention a non synthesized isolate). And we do not know the reaction of venom HIV Inhibitor natural or synthesized isolates (a synthesized isolate is what Ophidia has produced) in the lymph system and beyond. There must be testing on primates. We do know that people can survive pure natural venom serum in the lymph system and beyond without permanent damage.                                                                                 To reiterate I do not know anything at all about this Texas company nor its Taipan venom isolate HIV Inhibitor medicine product. But I do know it has been rumored about for a long time that the oldest medicine on earth - and perhaps the most dangerous - may in the end provide the only HIV cure, as venom mainly spreads via the lymph system - where the problem with HIV today exists. HIV inhibitor medicines principally are efficient in the bloodstream and have no problem gettin rid of HIV in the blood stream. It would seem to be a long way off even if venom is a cure. But the possibility of now a real cure on the horizon is a good reason among a number of reasons to get on current HIV Inhibitor medicines early and clog up the lymph system as minimally as possible with dormant HIV, and keep the immune system strong.                                                                                    HIV infection would have been cured a half decade ago with modern HIV Protease and HIV Reverse Transcriptase medicines except that these modern HIV medicines can not enter the lymph system efficiently, thus the lymph system remaining a breeding grounds for new HIV virus.                                                                                   A hypothesis answer to statistics that have encouraged in recent past years a belief or hope that the HIV cure can be effected by current HIV Inhibitor medicines is that when current HIV Inhibitor medicines are administered great drops in HIV viral load are observed in both blood HIV viral load and HIV lymph node viral load. Yet most HIV infected T 4 white blood cells do not remain dormant in the lymph system long before rewakening and returning to the blood stream. And it is this phenomena of rewakening and returning to the blood stream - that in reality most HIV is in actuality destroyed in the blood stream by HIV Inhibitor medicines and not in the lymph system where current HIV medicines are inefficient. As they universally fail to destroy enough HIV virus in the lymph system to prevent HIV Virus from reproducing itself. In contrast these same in current use HIV Inhibitor medicines in the blood stream reduce HIV virus to where it can no longer be found or measured (this not the case in the lymph system). To reiterate a venom isolate HIV Inhibitor medicine should destroy HIV mainly in the lymph system as venom is efficient in the lymph system, whereas current HIV Inhibitor medicines are efficent in the blood stream. For more explanation go or return to my homepage http://www.nylicsocialworkeramazonas.com/