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Protease Inhibitors

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Willem,

I remember that post about protease inhibitors well...I even researched it after

you posted the information. I believe that the answer just might lie in the use

of these protease inhibitors...but it will takes years before they will be

available to us. They are so cautious over the use of new drugs that often

everyone with the disease has died off before the " cure " is released for

use...it's probably all part of the masterplan to help the pharmaceuticals keep

their patents on the older, less effective treatments.

It is fortunate that you live in a country that is not as controlled by greed as

this country seems to be. You had access to the peg long before those of us in

the states has access to it too if I remember correctly.

Tatezi <who is way behind in mail>

protease inhibitors

Hi gang.Some three months ago I wrote about these inhibitors,I was the first

to mangene them maby claudine too but I don.t count her as a member,she.s Chief

Executive.In this mail I stated that in trials conducted in Geno Type 1

relapsers the viral load was reduced, in 24hrs, to a level that only a very

sensitive test could detect the virus.If you use Google you can read more about

them,also type AASLD,there was a conference in Bosten,1 Nov.2002,where they also

discussed the protease Inhibitors.I think our Chief -Chief -Executive Doc.

attended this meeting also.Maby he could comment.So there.s light on the end of

the tunnel for people who do not respond to the classic treatment inwhich the

virus is not directly aimed.Willem.

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  • 1 month later...
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If that be the case, it could be too late for many of us... :(

Princess

Protease Inhibitors

They are studying many different protease inhibitors and anti-

fibrotic meds for us. Keep in mind that unless we can get into a

study, it will be 5-10 yrs before these things are available to us.

If these companies are just now being allowed to study them, it's

possible it may be even 3 yrs before they get to the Human Study

stage.

These are the drugs of the future for us. Protease Inhibitors have

been used for HIV for quite some time and work real well with their

immune system problems. The few that have been looked at for HCV have

not done so well so far.

It's good news to see the FDA allowing more studies to be done on

more of these new drugs. The drug makers always tout the word " cure "

when trying out their newest toys so be careful with that one!

LeighAnn

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Thanks everybody, for all the great information! I was just so surprised to

hear about this on the news, and they only give you like, 30 seconds of

information. I remembered thinking after I heard about it, I'd better be

verrrrry good to my liver for the next 10 or so years until this stuff is

available.

Marilyn

Protease Inhibitors

They are studying many different protease inhibitors and anti-

fibrotic meds for us. Keep in mind that unless we can get into a

study, it will be 5-10 yrs before these things are available to us.

If these companies are just now being allowed to study them, it's

possible it may be even 3 yrs before they get to the Human Study

stage.

These are the drugs of the future for us. Protease Inhibitors have

been used for HIV for quite some time and work real well with their

immune system problems. The few that have been looked at for HCV have

not done so well so far.

It's good news to see the FDA allowing more studies to be done on

more of these new drugs. The drug makers always tout the word " cure "

when trying out their newest toys so be careful with that one!

LeighAnn

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  • 1 month later...
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Thanks for passing this info along, Willem...I'll give it to my friend who

is dead set against doing peg.

Liefs

Tatezi

protease inhibitors

> HI.In Dec.2003 a trial is starting in the Academic Medical Centre(AMC) in

Amsterdam with protease inhibitors for Hep.C.The person to contact is

Dr.Remkes.

>

>

>

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Thanks for passing this info along, Willem...I'll give it to my friend who

is dead set against doing peg.

Liefs

Tatezi

protease inhibitors

> HI.In Dec.2003 a trial is starting in the Academic Medical Centre(AMC) in

Amsterdam with protease inhibitors for Hep.C.The person to contact is

Dr.Remkes.

>

>

>

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Thanks for this, Pam. I'll pass it along to my friend.

Tatezi

protease inhibitors

>

>

> Hi

> Have been lurking for a couple of years. Something is wrong when I try to

> email I always get them back. Why I get all the emails from the list but

> can't talk to the list I don't know. Some might call it an ironic twist

of

> fate.

> But I do have some info about protease inhibitors. I go to the Liver

Center

> at Beth Israel Hospital in Boston MA. (Just finished 49 weeks of

Peg-Intron

> in April. Virus came rushing back after being off 1 month. But I am in

> good shape) After the Nov. 2002 conference I asked about them. BI is one

> of the study sites in the US. They were going to start trials in Feb.

Then

> they got postponed until spring. Then they got postponed indefinitely. I

> asked why and they said there were " safety issues " What they told me was

> some(one?) of the monkeys died. A very big issue indeed! I asked again at

> my last appointment. It was a little more important to me now that I am a

> non-responder. They said probably in the fall.

> By the way, the state of Massachusetts paid for every cent of my treatment

> without a murmur. Except for the Procrit, because that was a study so it

> was free. I once figured out that the cost of treatment was more money

than

> I had ever made annually in my life.

> I suggest that everyone move to Massachusetts for treatment.

>

> Pam in New England

>

> PS finally read the returned email. All I had to do was turn off the html

> format.

>

> _________________________________________________________________

> MSN 8 helps eliminate e-mail viruses. Get 2 months FREE*.

> http://join.msn.com/?page=features/virus

>

>

>

>

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Guest guest

Thanks for this, Pam. I'll pass it along to my friend.

Tatezi

protease inhibitors

>

>

> Hi

> Have been lurking for a couple of years. Something is wrong when I try to

> email I always get them back. Why I get all the emails from the list but

> can't talk to the list I don't know. Some might call it an ironic twist

of

> fate.

> But I do have some info about protease inhibitors. I go to the Liver

Center

> at Beth Israel Hospital in Boston MA. (Just finished 49 weeks of

Peg-Intron

> in April. Virus came rushing back after being off 1 month. But I am in

> good shape) After the Nov. 2002 conference I asked about them. BI is one

> of the study sites in the US. They were going to start trials in Feb.

Then

> they got postponed until spring. Then they got postponed indefinitely. I

> asked why and they said there were " safety issues " What they told me was

> some(one?) of the monkeys died. A very big issue indeed! I asked again at

> my last appointment. It was a little more important to me now that I am a

> non-responder. They said probably in the fall.

> By the way, the state of Massachusetts paid for every cent of my treatment

> without a murmur. Except for the Procrit, because that was a study so it

> was free. I once figured out that the cost of treatment was more money

than

> I had ever made annually in my life.

> I suggest that everyone move to Massachusetts for treatment.

>

> Pam in New England

>

> PS finally read the returned email. All I had to do was turn off the html

> format.

>

> _________________________________________________________________

> MSN 8 helps eliminate e-mail viruses. Get 2 months FREE*.

> http://join.msn.com/?page=features/virus

>

>

>

>

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  • 6 years later...
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