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This is the REAL timeline for HM


#1

Sometime in 2008, Aderans expects to make an announcement of the development by scientists at Intercytex of a viable experimental protocol for a workable HM procedure that may be approximately five years away from the stage where preparations can be made for a possible project in 2009 that will lead hair scientists in Japan to tell us that within five years from some date to be announced then, we will hear of the development of a potential ICX-TRC protocol that has been successful in some rats and that will become reality in about five years after the approval of the first Phase II application for human clinical tests that will be filed by Intercytex research scientists within five years from the planned announcement by Dr. Washenik that five years from the time of the first FDA application for Phase III clinical trials of the most promising experimental HM procedure, set to take place nearly five years after Aderans Research Institute files reports of its continuiing research studies on mice by scientists and developed by doctors into future laboratory protocols scheduled for the first quarter of 2010 that some hair experts expect to be completed five years after the preliminary license is granted and regulatory applications are filed for the last of the Phase II clinical trials which clinical researchers at Intercytex expect will be approved for human testing by scientists such as Dr. Fuchs, which, many knowledgeable doctors suggest, may produce a potential cure for MPB in most laboratory animals within five years of certain developments by Dr. Cotsarelis and Dr. Kemp, that British research scientists expect might become reality five years after the beginning of the regulatory review process for the next formal application that is expected to be submitted by Bosley’s researchers about five years from the announcement by doctors and clinical scientists that in five years the subsequent application for the next Phase of animal testing of a preliminary, experimental HM procedure that will take five years to be researched and developed by doctors and clinical research scientists into hair-growth protocols that may be nearly completed by researchers and finished five years after the preliminary license is granted and secondary applications are filed for the second round of Phase II clinical trials that will be conducted for human testing and which some doctors at Intercytex say might produce a cure for MPB in mice within a five-year period of a predicted announcement that scientists will find a possible solution to these problems within the space of about five years and could discover a viable form of HM that will be developed by Aderans in Japan approximately five years from the phase that will be completed five years from the date on which some scientists will likely tell us that in about five years, many experts anticipate hearing the annoucement of a new procedure that will become reality five years after the approval of the preliminary FDA application that might be filed within five years from the announcement by research scientists that in approximately five years from the second official application by laboratory doctors for Phase I human safety trials of an experimental procedure that will take around five years to be researched by clinical doctors and scientists at ARI and developed into predicted experimental human protocols that potentially will be finished five years after the licenses are granted and regulatory applications for the subsequent Phase III clinical trials are accepted, an FDA application for a new protocol for HM in humans will be filed after additional laboratory testing on animal subjects that will produce a cure for MPB in some laboratory rats within five years of predicted developments that will become reality nearly five years after HM testing on mice in advance of approval of the FDA application that will be filed by doctors and laboratory researchers within five years from a 2010 announcement by ICX researchers will be made, that in an approximately five-year space of time, the second application to conduct additional animal testing of an experimental HM procedure that will take five years to be researched and developed by research doctors into amended protocols that will be finished five years after the license is granted and applications for the next round of Phase II clinical trials to be conducted by laboratory doctors and research scientists on human subjects in 2011 that experts say will produce a potential cure for MPB within five years of an announcement by Dr. Gho that five years later a workable HM process will be approximately five years away from the stage where in five years doctors will tell us that the approval of a viable HM procedure will be at hand in about five years from the time we will hear predictions of developments that some researchers and experts say a viable HM process will become reality five years after the approval of the next FDA clinical trials application that may be filed by Aderans research scientists within five years from the announcement by the FDA that in five years the 2012 applications for Phase II clinical trials of a new experimental protocol that will take five years to be researched and developed by ICX scientists into clinical protocols for testing on rats that will be finished five years after the preliminary license is granted and applications for renewed Phase II clinical trials which scientists predict will be conducted for human testing by Bosley that potentially will produce a cure for MPB in mice are made which experts say within another five years of expected developments that will become reality five years after the approval of animal testing in preparation for the second amended FDA application of a newly-developed experimental procedure that some doctors say may be filed within five years from the announcement by researchers that in about five years the third amended FDA application for Phase I human clinical trials of a workable HM procedure that will take five years to be researched by doctors and developed into new clinical HM protocols that will be nearly completed nearly five years after the first preliminary FDA approval is granted and applications for renewed animal testing in Japan for the approval of a viable HM protocol that will be researched for the next expected round of testing on human subjects that may produce a potential cure for MPB based on research by Dr. Fuchs within five years of an announcement by Dr. Kemp and other research doctors that within five more years of testing a possible cure for MPB in 2009 that will be ready approximately five years before the step where in early 2012 clinical scientists working with Dr. Washenik will tell us that in about five years we will hear of laboratory developments regarding HM that some experts may say will become reality almost five years after the completion of the final FDA approval process for the application to approve human clinical trials that will be filed within an additional five years from the announcement by scientific researchers at Intercytex that in around five years the next amended application for renewed Phase I safety trials of a possible new experimental procedure that will take five years for predicted human testing to develop into a viable HM procedure to be researched and developed into preliminary protocols that will be finished by laboratory doctors five years after the license is granted and the amended second applications for the Phase II clinical trials will be conducted for human testing that some experts like Dr. Washenik predict will produce a cure for MPB in rats within five years of developments that will become reality five years after the approval of Intercytex’s subsequent FDA application that will be filed within five years from the announcement by research doctors that in five years after the start of the approval process of the next application by Dr. Washenik for Phase II clinical trials of a new experimental protocol based on research by Aderans doctors that will take five years to be researched and developed by doctors into research protocols that will be nearly completed five years after the subsequent preliminary license is granted and applications for the next Phase III clinical trials in England may be taken to conduct possible human testing by Intercytex that some research-doctors say might produce a cure for MPB sometime after 2011 or within five years of a newly-developed experimental procedure performed on mice and destined to be part of laboratory protocol around 2008 that may be finished by Intercytex’s research doctors five years after the preliminary approval is granted and applications for the Phase II clinical trials for the final approval of a viable HM procedure for rats that will be potentially approved for Intercytex’s final human testing in Japan and which some scientists expect might produce a possible cure for MPB within five years of an announcement by Intercytex researchers that before the end of five years a workable HM procedure based on early research by Dr. Gho that will be approximately five years away from the stage where Intercytex scientists in England will tell us that in about five years we will hear of new developments that some researchers say might become reality in the UK five years after the approval of the final applications that will be filed by Dr. Cotsarelis and Aderans clinical scientists within about five years from the announcement by the FDA that within five more years the third amended FDA application for Phase III clinical trials by Bosley of a workable HM procedure for humans that Dr. Washenik says will take five years to be researched and developed by clinical doctors into workable protocols that will be almost finished five years after the final license is granted and new applications for the Phase II clinical trials will be filed to permit human testing by Dr. Kemp that some experts predict will produce a viable cure for MPB in rats within five years after developments that most research doctors at ICX will say may become a reality around five years after the approval by the FDA of an application that will be filed by ARI’s laboratory researchers within five years from the announcement of a potentially viable HM protocol by Aderans clinical researchers who within five years after completing the final amended application process for secondary Phase II human clinical trials by Dr. Washenik of a viable HM procedure or an experimental human clinical procedure that will be performed in 2010 and will be reviewed and researched by doctor-researchers in Japan into viable protocols that some scientists tell us may be developed and completed in 2012 or five years after the last preliminary FDA approval is granted and the final applications for Intercytex’s Phase III clinical trials are approved by the MHRA, which within five years will very likely result in the approval and marketing of a viable HM procedure for use on humans.


#2

What a useless thread…


#3

paragraphs…

help folks read:-)


#4

…TheRealGame…I know youre frustrated. Here is where we stand.

We now have seen a couple of pics of phase one.

We are waiting to see if the first phase two trial in humans is successful. 6 men were shot up in large balding areas, and one square centimeter of completely bald scalp what shot up with 100 injects.

WE will KNOW ALOT about ICX’s product when the test is over and results are released. This will happen some time before the new year according to ICX (second half of 07).

If its “all good”, we might expect HM in the next few years beacause they would obviously have a working product, already proven safe. If its not…it really may take a several years. Thats where we are at. In a way, if they have bad results, the forum might look like a ghostown for a few years as it will become a transplant discussion form mainly.

If the tests fail badly…you will be right. It would probably be more than five years, and I’ll quit following it altogether and proceed as if it may never happen. Im personally waiting on it before making any moves “up there”, hence my interests in it.


#5

» …TheRealGame…I know youre frustrated. Here is where we
» stand.
»
»
»
» We now have seen a couple of pics of phase one.
»
»
» We are waiting to see if the first phase two trial in humans is
» successful. 6 men were shot up in large balding areas, and one square
» centimeter of completely bald scalp what shot up with 100 injects.
»
»
» WE will KNOW ALOT about ICX’s product when the test is over and results
» are released. This will happen some time before the new year according to
» ICX (second half of 07).
»
»
» If its “all good”, we might expect HM in the next few years beacause they
» would obviously have a working product, already proven safe. If its
» not…it really may take a several years. Thats where we are
» at. In a way, if they have bad results, the forum might look like a
» ghostown for a few years as it will become a transplant discussion form
» mainly.
»
»
»
» If the tests fail badly…you will be right. It would
» probably be more than five years, and I’ll quit following it altogether
» and proceed as if it may never happen. Im personally waiting on it before
» making any moves “up there”, hence my interests in it.

The pieces of info they have released have been released in such a way that it doesn’t raise or dampen people’s expectations.This leads me to believe that they still have many unanswered questions themselves.It’s very hard to come to a conclusion when there is so much mystery surrounding a product

I don’t think people truly recognise just how vulnerable hm is & this vulnerability worries me.It will only take 1 person from the trials to sink hm forever.If just 1 person showed signs of any form of cancer,the scare mongering will begin & this technology will be forever lost.The cancer may not even be a result of the injections but it will be enough to scare the public & do allot of damage to ICX’s reputation.
ICX can go from saviour to pariah overnight.
We have put all our hope in a product that is vulnerable to so many things.


#6

» The pieces of info they have released have been released in such a way
» that it doesn’t raise or dampen people’s expectations.This leads me to
» believe that they still have many unanswered questions themselves.It’s
» very hard to come to a conclusion when there is so much mystery
» surrounding a product
»
» I don’t think people truly recognise just how vulnerable hm is & this
» vulnerability worries me.It will only take 1 person from the trials to
» sink hm forever.If just 1 person showed signs of any form of cancer,the
» scare mongering will begin & this technology will be forever lost.The
» cancer may not even be a result of the injections but it will be enough to
» scare the public & do allot of damage to ICX’s reputation.
» ICX can go from saviour to pariah overnight.
» We have put all our hope in a product that is vulnerable to so many
» things.

i thought phase I cleared this cancer possibility up?


#7

why is everybody so obsessed with the game that they take the time to register similar names just to rant??? somebody needs some attention or a hug.


#8

Kemp injected this stuff into his own head… I don’t think the risk for cancer is high if he was willing to do that…


#9

What about the rats that they injected this stuff into? They didn’t get cancer in their trials did they? Didn’t they have human skin on the backs of rats? If there were cancer, they would have seen it on the skin on the rats…


#10

sheeesh !