Announcement

Collapse
No announcement yet.

Lemtrada anyone?

Collapse
X
 
  • Filter
  • Time
  • Show
Clear All
new posts

    Lemtrada anyone?

    I just came back from my appt at MS Clinic in Worcester. She talked to me about Lemtrada. It is currently being used in Europe and Australia with great results for both remitting relapsing MS and Secondary Progressive. FDA had rejected it previously because not enough long term data, but they are reviewing it again with a decision expected in November. She feels confident enough about it that she sent me for MRI.

    What does anyone know about this? I guess my heart condition is not an issue.
    ~Susan
    Be the person your dog thinks you are

    #2
    Originally posted by ssusan View Post
    I just came back from my appt at MS Clinic in Worcester. She talked to me about Lemtrada. It is currently being used in Europe and Australia with great results for both remitting relapsing MS and Secondary Progressive. FDA had rejected it previously because not enough long term data, but they are reviewing it again with a decision expected in November. She feels confident enough about it that she sent me for MRI.

    What does anyone know about this? I guess my heart condition is not an issue.
    ~Susan
    If you're not already aware of this, it might be something to consider:

    Only registered and activated users can see links., Click Here To Register...
    SPMS diagnosed 1980. Avonex 2001-2004. Copaxone 2006-2009. Glatopa (glatiramer acetate = Copaxone) 12/20 - 3/19/24.

    Comment


      #3
      Originally posted by agate View Post
      If you're not already aware of this, it might be something to consider:

      Only registered and activated users can see links., Click Here To Register...
      This is Copaxone not Lemtrada...right?
      Last edited by SalpalSally; 09-23-2014, 01:29 PM.
      Love, Sally


      "The best way out is always through". Robert Frost






      Comment


        #4
        Originally posted by SalpalSally View Post
        This is Copaxone not Lemtrada...right?
        Copaxone's generic name is glatiramer acetate. Lemtrada is also known as alemtuzumab or Campath.

        The scorecard for this game is a bit confusing!
        SPMS diagnosed 1980. Avonex 2001-2004. Copaxone 2006-2009. Glatopa (glatiramer acetate = Copaxone) 12/20 - 3/19/24.

        Comment


          #5
          It ends in -mab so it's a monoclonal antibody. I think that means that PML is a possible side effect. :-(

          ANN
          There comes a time when silence is betrayal.- MLK

          Comment


            #6
            Oh, Campath, yes I was thinking Copath. Thanks.
            Last edited by SalpalSally; 09-23-2014, 05:57 PM.
            Love, Sally


            "The best way out is always through". Robert Frost






            Comment


              #7
              Just to muddy things up a bit more, Copaxone began as Copolymer-2, known as Cop-2....
              SPMS diagnosed 1980. Avonex 2001-2004. Copaxone 2006-2009. Glatopa (glatiramer acetate = Copaxone) 12/20 - 3/19/24.

              Comment


                #8
                I was close..LOL
                Love, Sally


                "The best way out is always through". Robert Frost






                Comment


                  #9
                  Is Lemtrada Campath? Damn. Do the do this name game thing on purpose to stay convoluted. I know that when it goes from research to the drug company the name changes. Confused-nah, not me?
                  Be the person your dog thinks you are

                  Comment


                    #10
                    I just asked doc. Yes, it is Campath. She said the PML risk is only for Leukemia patients.
                    Be the person your dog thinks you are

                    Comment


                      #11
                      There have been no cases of PML in MS patents on any drug other than Tysabri although some lupus patients on CellCept have been diagnosed with PML. The FDA nixed Lemtrada a year ago and asked for another phase III trial using it against placebo...an ethical no no in later stage MS. You at least want your subjects to be on something to modify the disease whether it is the trial med or another proven med. All of a sudden, Genzyme is rallying again and hiring nurses to be part of their patient education call center team so it looks like there may be another attempt to get it approved for MS.

                      Comment


                        #12
                        I take rituxan which is Rituximab. You are correct Ann and I do test positive for the JCvirus but they have a test now to determine your relative risk which is helpful in making decisions.
                        Linda~~~~

                        Be the kind of woman that when your feet hit the floor each morning the devil says:"Oh Crap, She's up!"..

                        Comment


                          #13
                          Actually a few people on rituxan have developed PML. Risk is low but my neuro worries
                          Linda~~~~

                          Be the kind of woman that when your feet hit the floor each morning the devil says:"Oh Crap, She's up!"..

                          Comment


                            #14
                            Originally posted by Cherie View Post
                            There have been no cases of PML in MS patents on any drug other than Tysabri although some lupus patients on CellCept have been diagnosed with PML. The FDA nixed Lemtrada a year ago and asked for another phase III trial using it against placebo...an ethical no no in later stage MS. You at least want your subjects to be on something to modify the disease whether it is the trial med or another proven med. All of a sudden, Genzyme is rallying again and hiring nurses to be part of their patient education call center team so it looks like there may be another attempt to get it approved for MS.
                            Cherie,
                            There have been few but some PML cases with Rituximab. There is always a low level of concern because we took that blood test that determined my odds were on the low end.

                            The leukemia patients you mentioned...is that because they were taking a much higher dosage of cellcept than we would be taking? A friend of mine was taking Rituxan for non- Hodgkin's lymphoma and he was on a much higher dosage than I take so I was thinking that the dosage increases the odds.

                            Glad to see your posts again You were missed when you were not posting frequently for a short time span!
                            Linda~~~~

                            Be the kind of woman that when your feet hit the floor each morning the devil says:"Oh Crap, She's up!"..

                            Comment

                            Working...
                            X