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NEJM Correspondence   Message List  
Reply | Forward Message #253 of 634 |
Re: NEJM Correspondence

From Lynne Murphy at MGH:

"Keep checking our website www.faustmanlab.org for updated
information. We will also be informing all individuals in our
database when the clinical trial is about to start. I think we are
planning for early 2008."

I believe this is for the BCG arm of the trial only. They have yet
to identify the second agent, to make this "cure" permanent.

Possibly another 10 to 15 years to identify the second agent?


--- In nathanfaustmantrials@yahoogroups.com, "imcimc1"
<curtieimc@...> wrote:
>
>
> Go the below website and lok on the right hand side
under "Contact" and
> it will give you information on who to contact about the trials.
>
> http://www.faustmanlab.org <http://www.faustmanlab.org>
>
>
>
>
> --- In nathanfaustmantrials@yahoogroups.com, "mjspicer51"
> <mjspicer51@> wrote:
> >
> > I am new to this group. I have been waiting for 20+ years to see
a
> > cure or a real hope of a cure...What is happening seems to be
faster
> > than the ADA who seems satisfied with the band aid of using
insulin
> > instead of finding a real cure. How do I get my name on the list
> > for the trials? I have two grandsons who I hope never have to
deal
> > with this desease personally. Thank you, would love to hear from
> > anyone on this situation --- In
> > nathanfaustmantrials@yahoogroups.com, "imcimc1" curtieimc@
> > wrote:
> > >
> > > They have to automate the process. They cannot monitor even a
> > small
> > > group of people effectively day after day during the trial
without
> > > automation. I would rather see this automation process get off
> > the
> > > ground now instead of after phase 1 of the trial is finished.
At
> > > least the are working with some kind of vision and greater
plan in
> > > mind. My fingers are crossed with this one.
> > >
> > > --- In nathanfaustmantrials@yahoogroups.com, "stilltypeone"
> > > <stilltypeone@> wrote:
> > > >
> > > > Sue, thanks for the info. I am still baffled that they chose
to
> > > > spend time and money on the automation process, when it may
be a
> > > > moot point.
> > > > If they can count T cells from hundreds of mice, can they
not do
> > > the
> > > > same for such a small sample of humans?
> > > >
> > > >
> > > > --- In nathanfaustmantrials@yahoogroups.com, Sue root
> > > > <susan_root@> wrote:
> > > > >
> > > > > The procedure to separate and count the targeted T cells
from
> > > > whole blood samples in humans takes 1 ½ days by hand. Seeing
> > that
> > > > they plan to ultimately take blood samples every other day
from
> > the
> > > > patients to monitor the effect, and they will plan to have 40
> > > > patients in the trial with controls, the automation will make
> > this
> > > > possible in a timely manner by decreasing the procedure to
only
> > > > about 6 hrs. More importantly, standardizing dosing in mice
is
> > much
> > > > less of an issue compared to humans, even if we're talking 40
> > people
> > > > > Even though the NOD mouse is the best known animal model
for
> > type
> > > > I diabetes, when dosing in mice, one doesn't have to deal
with
> > > > variables such as body weight. The groups of mice are born at
> > the
> > > > same time, are the same size, and develop diabetes roughly
the
> > same
> > > > time. Therefore, being able to standardize the dosing of BCG
in
> > a
> > > > group of humans with such variables, will be a key factor for
> > > > success.
> > > > > What we do know is that the NOD mice have the same 2
defects
> > > > found in humans with type I diabetes and the treatment that
Dr.
> > > > Faustman used targets and eliminates these defects.
> > > > >
> > > > >
> > > > > stilltypeone <stilltypeone@> wrote:
> > > > > Patsy, I think you are misunderstanding what I am
> > > > inferring.
> > > > > The point I am making is why spend so much time and money
on a
> > > > > automation process that, in the end may end up as useless.
> > Kind
> > > of
> > > > > like the "cart before the horse". Why not do the initial
trial
> > by
> > > > > hand, as the mouse trials were done. If sucessful, then
move
> > on
> > > to
> > > > > scale this up to a larger group trial.
> > > > > I would not expect death from BCG injections, as it is
used in
> > > > huge
> > > > > quantities for bladder cancer.
> > > > > The begining trial as I understand it will be 40
individuals.
> > I
> > > > > consider that "small". I realize that is a relative term.
> > > > > If asking questions is "grumbling" then I am guilty.
> > > > >
> > > > > --- In nathanfaustmantrials@yahoogroups.com, Patsy Van
Huyck
> > > > > <patsy@> wrote:
> > > > > >
> > > > > > The answer in short is because if a mouse dies, nobody
> > cares.
> > > > > Just
> > > > > > think if the "small human trial" was a failure either
due to
> > > > huge
> > > > > > complications or due to the lack of results. Do you think
> > that
> > > > > they
> > > > > > would just get to try again with another dose? The assay
is
> > > very
> > > > > > important so that the trial can be successful, and we can
> > then
> > > > > move to
> > > > > > the next stage.
> > > > > >
> > > > > > We all want the cure to have been in 2002, but dealing
with
> > the
> > > > > FDA is
> > > > > > tediously slow. Grumbling isn't going to get the research
> > done
> > > > > any more
> > > > > > quickly.
> > > > > >
> > > > > > Patsy
> > > > > >
> > > > > > >
> > > > > > > Re: NEJM Correspondence
> > > > > > >
> > > > >
> > > >
> > >
> >
<http://groups.yahoo.com/group/nathanfaustmantrials/message/245;_ylc=
> > > > >
> > > >
> > >
> >
X3oDMTJxMmg3MXB1BF9TAzk3MzU5NzE1BGdycElkAzE2NDEyMTQ1BGdycHNwSWQDMTcwN
> > > > >
> > > >
> > >
> >
TA2MTY2MgRtc2dJZAMyNDUEc2VjA2Rtc2cEc2xrA3Ztc2cEc3RpbWUDMTE3MDU4NDUyMQ
> > > > > -->
> > > > > > >
> > > > > > >
> > > > > > >
> > > > > > > Posted by: "stilltypeone" stilltypeone@
> > > > > > > <mailto:stilltypeone@?Subject=%20Re%3A%20NEJM%
> > > > > 20Correspondence>
> > > > > > > stilltypeone <http://profiles.yahoo.com/stilltypeone>
> > > > > > >
> > > > > > >
> > > > > > > Sat Feb 3, 2007 6:57 pm (PST)
> > > > > > >
> > > > > > > Sue, can we agree that these trials will not proceed
until
> > > > > > > the "automated assay" is completed?
> > > > > > > Did Faustman have this automated assay during the mouse
> > > trials?
> > > > > > > I am guessing the answer is no.
> > > > > > > So, why the need for automation for a small human
trial?
> > > > > >
> > > > >
> > > >
> > >
> >
>





Thu Mar 1, 2007 3:43 am

stilltypeone
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Forward
Message #253 of 634 |
Expand Messages Author Sort by Date

In the most recent edition of the New England Journal of Medicine (NEJM), a letter from Dr. Faustman written in response to a letter to the NEJM from Douglas...
Scott Strumello
sstrumello
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Jan 31, 2007
9:50 pm

What will be different in Dr. Faustman and Dr. Nathan's human clinical trial is that they will be using multiple dosing of BCG in humans at an increasing...
Sue root
susan_root
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Feb 1, 2007
7:44 pm

Sue, can we agree that these trials will not proceed until the "automated assay" is completed? Did Faustman have this automated assay during the mouse trials? ...
stilltypeone
Offline Send Email
Feb 4, 2007
2:57 am

The answer in short is because if a mouse dies, nobody cares. Just think if the "small human trial" was a failure either due to huge complications or due to...
Patsy Van Huyck
PatsyVanHuyck
Offline Send Email
Feb 4, 2007
4:36 pm

Patsy, I think you are misunderstanding what I am inferring. The point I am making is why spend so much time and money on a automation process that, in the end...
stilltypeone
Offline Send Email
Feb 8, 2007
1:52 pm

The procedure to separate and count the targeted T cells from whole blood samples in humans takes 1 ½ days by hand. Seeing that they plan to ultimately take...
Sue root
susan_root
Offline Send Email
Feb 8, 2007
7:12 pm

Sue, thanks for the info. I am still baffled that they chose to spend time and money on the automation process, when it may be a moot point. If they can count...
stilltypeone
Offline Send Email
Feb 13, 2007
2:38 am

They have to automate the process. They cannot monitor even a small group of people effectively day after day during the trial without automation. I would...
imcimc1
Offline Send Email
Feb 13, 2007
10:24 pm

I am new to this group. I have been waiting for 20+ years to see a cure or a real hope of a cure...What is happening seems to be faster than the ADA who seems...
mjspicer51
Offline Send Email
Feb 15, 2007
1:48 pm

Go the below website and lok on the right hand side under "Contact" and it will give you information on who to contact about the trials. ...
imcimc1
Offline Send Email
Feb 15, 2007
3:30 pm

From Lynne Murphy at MGH: "Keep checking our website www.faustmanlab.org for updated information. We will also be informing all individuals in our database...
stilltypeone
Offline Send Email
Mar 1, 2007
1:33 pm

If BCG is successful and safe, I would welcome taking it every day until the second agent is identified. We need a cure NOW. This is an absolutely miserable...
imcimc1
Offline Send Email
Mar 1, 2007
7:15 pm

Perhaps if BCG is successful in temporarily halting the autoimmune attack, then millions of the research money raised would start funnelling into the search...
rmccully2000
Online Now Send Email
Mar 2, 2007
8:58 pm

Forget about the fundraisers jumping on board at that point. IF BCG halts the autoimmune attach I would like to see the government step in an recognize that...
imcimc1
Offline Send Email
Mar 8, 2007
10:13 pm

What second agent? Are you talking about the second arm of the research, where they plan to add healthy tissue matching spleen cells? Patsy...
Patsy Van Huyck
PatsyVanHuyck
Offline Send Email
Mar 2, 2007
6:51 pm
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