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Dear Rayilyn,

I perfectly understand your current situation. Although I have been 
trained as MD, I have never treated patients since I am engaged 100% in 
PD research. I am in close contact with the Spanish association of 
Parkinson's disease, and I strongly feel that one of my obligations is 
to explain the patients what's going on in PD research. I know that it 
is fustrating to see that anything new has arrived in the past few 
years, besides some minor improvements in dopamine-replacement therapies 
(if I am right, a phase 2 trial testing an inhaled preparation of 
levodopa is going to start soon in US). When attending scientific 
meetings, the overall feeling is that everybody is always moving around 
the same topics, without any real new improvement or any real new ideas 
to follow. In this regard, gene-based therapies such as ProSavin at 
least represent something different. I cannot anticipate how long will 
it take to see these new arrivals fully available in the market as a 
therapeutic tool. Nevertheless, I still thinking that approaches this 
kind at least represent something different, and I am sure that this is 
a right step in the right direction. In the past two years my group has 
received some EU funding to start testing different approaches of gene 
therapy for manipulating basal ganglia circuits. We are using 
MPTP-treated monkeys since these represent the best animal model 
available so far, and working with monkeys speeds up the time required 
to start testing new tools in humans suffering from PD. I can give you 
my word that we are working very hard trying to generate the expected 
results asap. We have just started several experiments, all very risky 
approaches, and therefore I cannot anticipate any final result. 
Nevertheless, you can be sure that the situation of PD patients always 
is very well represented in my mind at all times.

I know that it is not easy to be optimistic in the current scenario. 
However, my personal feeling is that testing some new research avenues 
has just been started. There is too much pressure to go traslational, 
and to start testing new approaches in patients asap. This pressure 
implies that some promising things enter clinical trials too early, and 
therefore it is fustrating to see that most of these new therapies 
failed in clinical trials. Just simply remember the failures of GDNF and 
nurturin. These are very good examples of promising things that failed 
because by the time these get tested in humans, we knew very little 
about their function. For instance, by the time in which GDNF entered 
phases 1-2 (the "Kentucky" and "Bristol" trials), we didn't knew too 
much about the neurobiology of GDNF. Researches we have to deal with 
this pressure, that's life. However, my feeling is that we cannot 
generate any solid expectances for PD patients without a clear 
proof-of-principle. As I have mentioned before, some failures we have 
seen in the past easily rank within this category of things being tested 
too early.

According to the published results from ProSavin, this might not be seen 
as the way to go. My opinion is just the opposite. Although I will have 
been delighted to see a better clinical outcome, the important argument 
of ProSavin is that approaches this kind at least opens new vistas in PD 
research. I can perfectly understand that you are tired of getting worse 
and waiting. I just can tell you that everything that me -and many 
others- we are currently doing is done bearing in mind at all times the 
clinical situation of thousands of PD patients. You are our main 
motivation, and this is how things should be. Of course I cannot promise 
any miracle, just a tireless effort in PD research, every day.

All the best and have a nice day, Jose L. Lanciego

Rayilyn Brown escribió:
> Jose
>
> I've had PD 18 years, have gotten worse, am 78 years old and fear at 
> the present pace of research will not live long enough to benefit from 
> any of the 'promising" treatments on the horizon.  I'm tired of 
> getting worse and waiting.  But then I'm anemic, maybe that’s it.
>
> -----Original Message----- From: José Luis Lanciego
> Sent: Tuesday, January 21, 2014 3:06 AM
> To: [log in to unmask]
> Subject: Re: ProSavin gene therapy
>
> Dear Rayilyn,
>
> I guess this is not discouraging at all. Although this is a preliminary
> study, my feeling is that ProSavin represents a right step in the right
> direction. A number of gene therapy experiments are currently undergoing
> and we will see what's coming out in the next few years. Indeed, this
> approach -and few more under experimental implementation- is something
> different, e.g., it is not based on dopamine-replacement strategies. My
> laboratory -as many others- strongly feels that many new arrivals can be
> expected from gene therapy experiments, with the ultimate goal of using
> gene therapy tools to manipulate basal ganglia circuits. Compared to
> cell therapies, gene therapy seems to be a much more feasible and
> realistic strategy.
>
> All the best and have a nice day, Jose L. Lanciego
>
> Rayilyn Brown escribió:
>> discouraging isn't it?
>>
>> -----Original Message----- From: Nic Marais
>> Sent: Saturday, January 18, 2014 12:29 AM
>> To: [log in to unmask]
>> Subject: Re: ProSavin gene therapy
>>
>> When you read the Viartis notification, it does not look as positive as
>> this article...
>>
>> http://www.viartis.net/parkinsons.disease/news/140113.htm
>>
>> Nic 61/19
>>
>>
>> On 17 January 2014 21:18, Rayilyn Brown <[log in to unmask]> wrote:
>>
>>> http://www.domain-b.com/technology/Health_Medicine/20140115_patients.html 
>>>
>>>
>>> Ray
>>> Rayilyn
>>> Past Director AZNPF
>>> Arizona Chapter National Parkinson Foundation
>>>
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