ATTN Hair Restoration Surgeons: IF YOU OFFER HST, THEY WILL COME

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  • RichardDawkins
    Inactive
    • Jan 2011
    • 895

    #31
    JUST DO IT and the rest will come by ITSELF believe me.

    No its time to stand up for your hair and get this crap done.

    Btw would be nice if someone would then also post this link at hairsite because i am avoiding this site like the plague

    Comment

    • NeedHairASAP
      Senior Member
      • Jul 2011
      • 1408

      #32
      i'll try to do it some point this week


      if anybody has any suggestions of what should be included in the preamble-- make it known here

      Comment

      • RichardDawkins
        Inactive
        • Jan 2011
        • 895

        #33
        Thank you consider myself to owe you one for this

        Comment

        • nrj
          Junior Member
          • Dec 2011
          • 21

          #34
          Clinical Drug development:
          Clinical Drug Development is divided into four phases (or 5 if ‘phase ‘0’ is
          counted). At all stages patients are monitored for side effects and information
          on drug safety is gathered as a priority.

          Phase 0 is a transitional phase between the pre-clinical testing stage and full
          clinical trials. Sub-therapeutic doses are monitored for any unexpected effects.
          This ‘phase’ is most commonly used in development of chemotherapeutic
          agents for cancer treatment.

          Phase I is relatively small scale, usually involving around 20-80 healthy
          volunteers (often undergraduate students) and is concerned primarily with dose
          finding and tolerability. Volunteers are given progressively larger doses of drug
          until an effect is registered. Information gathered during phase I will allow
          estimates to be made of the amount of drug the body will tolerate without
          causing side effects and what side effects might occur. Several rounds of Phase
          I trials may occur for any given drug, in different countries and patient groups.

          Phase II trials are of medium size, involving 100-300 patient volunteers. At this
          stage the drug is tested for effectiveness against a specific disease which will
          be the intended ‘indication’ of the drug. Again, several phase II studies may be
          performed for a given drug.

          Phase III are large scale trials involving 1000-3000 patients where
          effectiveness is tested again and comparison is made with other treatments that
          are available. If a drug survives phase III then it may be registered and sold as
          a therapeutic agent.

          Transition through phases I, II and III takes about 6-10 years. Of 100 drugs
          entering phase I only a few, maybe 10, will survive to phase II and of these only
          1 or 2 will make it to phase III. If a drug makes it to phase III then it has a
          reasonable chance of success. The costs of drug discovery and development
          are enormous and most of the costs are incurred at phase III so companies
          have to be confident of a reasonable chance of success before allowing a drug
          candidate to proceed to this stage.

          From one of my lectures , Its a bit weird how these companies claim to finish trials with 3-4/2-3 years, i hope this is some kind of fast track that only applies in the us.

          Comment

          • DepressedByHairLoss
            Senior Member
            • Feb 2011
            • 854

            #35
            I don't agree with many aspects of that "Clinical Drug Development" piece. I don't agree with the long timeline that it supposedly takes for these drugs to reach the marketplace, the number of drugs that actually make it out of Phase I, II, etc., and several other things. With regards to Histogen, Replicel, and the rest of the hair loss drugs, I thankfully think that their trials will go much quicker since most of them (except for Aderans) are conducting them outside of North America so they don't need to be bogged down by many unnecessary FDA regulations and bureaucratic red tape.

            Comment

            • nrj
              Junior Member
              • Dec 2011
              • 21

              #36
              I think these are the rough guidlines in the uk.

              Comment

              • RichardDawkins
                Inactive
                • Jan 2011
                • 895

                #37
                Push again because shills are starting to write in the scam TRX2 thread which annoys me

                Comment

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