General Replicel/Shiseido News

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  • lacazette
    Senior Member
    • May 2015
    • 396

    #76
    Originally posted by Arieux
    Yesterday they replied on their Facebook to one of the desparate users' posts:



    So they confirmed starting phase II this year again. Maybe they want to start it before World Hair Congress to avoid embarassing questions about their delays?
    Well if they aren't lying about that "even soon via Sisheido", that sounds good as Sisheido could have temporary approval before phase 3. Fingers crossed

    Comment

    • FearTheLoss
      Senior Member
      • Dec 2012
      • 1589

      #77
      Shiseido's trial is really the only one that matters in my opinion. They have the power to get it approved during phase II and bring it to the market the quickest. It will be interesting to see how it goes.

      Comment

      • Eric5
        Member
        • Jan 2015
        • 38

        #78
        Well someone better hurry the hell up because we need hair and the longer they wait the less customers they are gonna have because once this generation completely loses their hair they are gonna say screw it I'm already bald I'm not gonna pay for some expensive procedure

        Comment

        • Folliman
          Junior Member
          • Jun 2015
          • 4

          #79
          I want to see pictures of the results so bad...

          Comment

          • TooMuchHairWontKillYou
            Senior Member
            • Apr 2015
            • 104

            #80
            5 Questions with David Hall


            "The regeneration of chronically injured tendon, the natural rejuvenation of the extra-cellular matrix under the dermis of those with aging or sun-damaged skin, and the regrowth of hair for those people suffering from pattern baldness"

            Comment

            • efedrez
              Senior Member
              • May 2013
              • 168

              #81
              I'm not sure if it has been published before but replicel answered a question about their phase 2 trial on their facebook page.

              "Yes, our phase 2 trial start date has been pushed off many times; however we believe the reasons for us doing so are in the stakeholder’s best interests. When we completed our phase 1 trial it was with the anticipation that we would almost immediately apply to commence a larger phase 2 trial but a significant manufacturing issue that was out of our control conspired to prevent that from happening. GE pulled the growth media off the market that we had always used to grow the dermal sheath cup cells (the basis of RCH-01). When Lonza tried to reproduce the same media it did not work, so we had to go back to the R&D bench and essentially recreate a media that would give us the same product. We tried many different formulas and even after that was accomplished we then had to conduct all the validation runs and testing to gather the data needed to prove to the regulators that it was materially the same product we had tested in phase 1 -- a prerequisite for them to consider an application for a phase 2 trial (rather than having to go back and repeat phase 1). This has taken an incredible amount of work but it is now almost complete. In the meantime, we took advantage of this opportunity to improve other aspects of the manufacturing in order to optimize the product/process robustness, minimize product failures, better define the product specifications, etc. We also began to work on developing other more proprietary media solutions such as serum-free media and animal-free media which we anticipate will add future value to the product. We have also worked on optimizing cell recovery from the original tissue biopsy. In the end, we believe the RCH-01 that we expect to use for next-phase clinical testing both in Japan and Germany is in biologic terms the same product but is a more commercially viable product because of the various process optimizations we conduct. We continuing to invest in manufacturing optimization of RCH-01 and our other cell-based products with the aim of bringing any improvements possible such as abbreviating manufacturing time, increasing cell yield, lowering production costs, etc. With this said, we should be able to file our clinical trial application with German regulators before the end of this year, and expect Shiseido to announce the start of their trial this year as well."

              Comment

              • brocktherock
                Senior Member
                • Dec 2013
                • 205

                #82
                These delays do get annoying but they are literally the only company that has given us news updates, timelines, expectations and answers email questions. I don't think they are just goofing around.

                Comment

                • runrunrun
                  Junior Member
                  • Feb 2015
                  • 17

                  #83
                  Guys Replicel updated new PPT files in their facebook homepage.

                  Comment

                  • Arieux
                    Member
                    • Jun 2015
                    • 86

                    #84
                    This is their updated presentation from Mesa: http://replicel.com/wp-content/uploa...n-Oct-2015.pdf

                    Note:
                    • Shiseido manufacturing and clinical trial in Japan: (...) Trial expected to readout late 2017 with potential to predicate a market approval
                    application

                    Comment

                    • TooMuchHairWontKillYou
                      Senior Member
                      • Apr 2015
                      • 104

                      #85
                      Shiiiet now they're saying they will conduct phase 2 in 2015/2016. In 2016 they will say 2016/2017 and so on...

                      Comment

                      • Sogeking
                        Senior Member
                        • Feb 2011
                        • 497

                        #86
                        Originally posted by Arieux
                        This is their updated presentation from Mesa: http://replicel.com/wp-content/uploa...n-Oct-2015.pdf

                        Note:
                        they are still aiming for 2018 on the market.Hopefully it will be more effective than Replicel Phase 1.

                        Comment

                        • Renee
                          Senior Member
                          • Jul 2015
                          • 196

                          #87
                          Their chief medical officer Rolf Hoffman filed a new patent, don't know what that means though!

                          The present invention relates to a method for isolating hair follicle mesenchymal stem cells and to the use thereof for therapy and prophylaxis as well as for cosmetic treatments.

                          Comment

                          • lacazette
                            Senior Member
                            • May 2015
                            • 396

                            #88
                            Thanks Arieux, it's good to have update


                            May 2014 Shiseido
                            opened new cell
                            -
                            processing facility; PMDA certified 2015

                            Tech transfer & comparability/validation runs completed 2015

                            Clinical protocol under ASRM (clinical research pathway) currently in review by
                            MHLW


                            Trial expected to readout late 2017 with potential to predicate a market approval
                            application


                            Can't wait for their trial to begin, if 2016, their 2018 market timeline will finally become a real concrete option

                            Again it's incredible how japan regenerative medecine system is an insane benediction for us, it cut 7/10 years in timeline. just imagine if it doesn't exist o0 we would depressly talk about 2022/2025 as the shorter possibility if everything would go well

                            Now with japan, any company who would come out with a strong protocol is one phase away for possible marketing ( as they explained the timeline between preclinical and commercialisation now is 2/3 years ( safety phase/prediction efficiency, approval administration, GMP manufacturing), unlike the 7/10 years that would be needed in the old approval system

                            Comment

                            • hellouser
                              Senior Member
                              • May 2012
                              • 4423

                              #89
                              Originally posted by lacazette
                              Thanks Arieux, it's good to have update


                              May 2014 Shiseido
                              opened new cell
                              -
                              processing facility; PMDA certified 2015

                              Tech transfer & comparability/validation runs completed 2015

                              Clinical protocol under ASRM (clinical research pathway) currently in review by
                              MHLW


                              Trial expected to readout late 2017 with potential to predicate a market approval
                              application


                              Can't wait for their trial to begin, if 2016, their 2018 market timeline will finally become a real concrete option

                              Again it's incredible how japan regenerative medecine system is an insane benediction for us, it cut 7/10 years in timeline. just imagine if it doesn't exist o0 we would depressly talk about 2022/2025 as the shorter possibility if everything would go well

                              Now with japan, any company who would come out with a strong protocol is one phase away for possible marketing ( as they explained the timeline between preclinical and commercialisation now is 2/3 years ( safety phase/prediction efficiency, approval administration, GMP manufacturing), unlike the 7/10 years that would be needed in the old approval system
                              Hey Lacazette,

                              Is there anything you'd want to ask the guys at Replicel during the Hair Congress next month?

                              Comment

                              • ShookOnes
                                Senior Member
                                • Jun 2014
                                • 213

                                #90
                                So from phase 1 regrowth was garbage but anyone know if participants lost hair? Freezing hairloss would be a cure asbi just had a 1600 fue..

                                Comment

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