Rallying the troops.... we need to get together on this

dramamama

New member
Hi everyone~
I have some crazy news that I think we all need to be aware of as we go forward in our agreement to take the vertex drugs. I had become increasingly concerned about CFers getting sick and experiencing more exacerbations as the vertex drugs were being discontinued after Phase II trials. While the vertex scientists are not all doctors, some of them are and I feel and felt like they were completely falling away from one of the principal precepts of medical ethics taught to doctors: First, Do no harm. Yes, the drugs are life-changing in a positive way (a cure even) and, for this reason, are harmful when discontinued.
Because of this I contacted a top 25 Lobbyist in Washington to just see if there was anything he could do to help us atleast get the patients who are volunteering a pass to continue the drugs when the phase II trials end (seeing as there is no glaring safety concern). While he had never heard of this issue with CF patients, he was very aware with all going on with Vertex and CF. He graciously contacted the Deputy FDA commisioner and addressed our concern....
According to the Deputy FDA commisoner: there is no FDA law keeping these patients from receiving these drugs following Phase II trials!!!! WHAT??? VERTEX has complete control and authority to allow these patients access to these drugs. Now, keep in mind, that is not all of us, but can we not agree that our community should stand behind these patients who are agreeing to take these drugs!?
According to the LOBBYIST, he said we must all rally together and agree to NOT SIGN up for trials, unless it is written in the contract that the trial patient is able to remain on the drugs after Phase II ends. We have the power. Vertex needs us just like we need them.... They can't get paid unless we agree to be a part of this... it is ok to stand up for ourselves in this way....sometimes the boat needs to be rocked.
Along those same lines, there is a bill going through Congress right now with approval (they think) by October that will allow drugs that are life changing to have a very different course of review and trial period. It is called the Advancing Breakthrough Therapies for Patients Act.... Basically, this allows companies to expidite clinical trials so that patients can get access to drugs possibly after Phase II trials. The company will have to conduct phase III trials even while patients have access to the drugs. GUYS, IF THERE WAS EVER A TIME TO CALL YOUR CONGRESSMAN IT IS NOW. The ExPert Act is also important, but the other will allow drugs to reach us much more quickly.

And, Finally.... Do you know how powerful our words are?? One of the reasons that Vertex released interim results from the 770/809 Phase II trials was due to the fact patienst were blogging and Vertex could no longer control what information was being released. From the CFO of Vertex at the Deutesche Bank Securities Annual Healthcare Conference last week:
"The safety finding was very strong and we want to accelerate the program into a Phase III setting. For us to do that we have to talk to regulators both in the US and Europe.<strong> We have to talk to trial investigators, patients are now blogging regarding the results and there was a corporate concern here about information getting out of the company and not being in a controlled environment</strong>. That is what drove us to the announcement"
It is time to make our voices heard... They need us as much as we need them.
read about the BILL:
http://articles.chicagotribune.com/2012-05-09/news/sns-rt-drugs-breakthroughl1e8g8a89-20120509_1_cancer-drug-drug-regulators-approval-of-breakthrough-drugs
 

dramamama

New member
Hi everyone~
I have some crazy news that I think we all need to be aware of as we go forward in our agreement to take the vertex drugs. I had become increasingly concerned about CFers getting sick and experiencing more exacerbations as the vertex drugs were being discontinued after Phase II trials. While the vertex scientists are not all doctors, some of them are and I feel and felt like they were completely falling away from one of the principal precepts of medical ethics taught to doctors: First, Do no harm. Yes, the drugs are life-changing in a positive way (a cure even) and, for this reason, are harmful when discontinued.
Because of this I contacted a top 25 Lobbyist in Washington to just see if there was anything he could do to help us atleast get the patients who are volunteering a pass to continue the drugs when the phase II trials end (seeing as there is no glaring safety concern). While he had never heard of this issue with CF patients, he was very aware with all going on with Vertex and CF. He graciously contacted the Deputy FDA commisioner and addressed our concern....
According to the Deputy FDA commisoner: there is no FDA law keeping these patients from receiving these drugs following Phase II trials!!!! WHAT??? VERTEX has complete control and authority to allow these patients access to these drugs. Now, keep in mind, that is not all of us, but can we not agree that our community should stand behind these patients who are agreeing to take these drugs!?
According to the LOBBYIST, he said we must all rally together and agree to NOT SIGN up for trials, unless it is written in the contract that the trial patient is able to remain on the drugs after Phase II ends. We have the power. Vertex needs us just like we need them.... They can't get paid unless we agree to be a part of this... it is ok to stand up for ourselves in this way....sometimes the boat needs to be rocked.
Along those same lines, there is a bill going through Congress right now with approval (they think) by October that will allow drugs that are life changing to have a very different course of review and trial period. It is called the Advancing Breakthrough Therapies for Patients Act.... Basically, this allows companies to expidite clinical trials so that patients can get access to drugs possibly after Phase II trials. The company will have to conduct phase III trials even while patients have access to the drugs. GUYS, IF THERE WAS EVER A TIME TO CALL YOUR CONGRESSMAN IT IS NOW. The ExPert Act is also important, but the other will allow drugs to reach us much more quickly.

And, Finally.... Do you know how powerful our words are?? One of the reasons that Vertex released interim results from the 770/809 Phase II trials was due to the fact patienst were blogging and Vertex could no longer control what information was being released. From the CFO of Vertex at the Deutesche Bank Securities Annual Healthcare Conference last week:
"The safety finding was very strong and we want to accelerate the program into a Phase III setting. For us to do that we have to talk to regulators both in the US and Europe.<strong> We have to talk to trial investigators, patients are now blogging regarding the results and there was a corporate concern here about information getting out of the company and not being in a controlled environment</strong>. That is what drove us to the announcement"
It is time to make our voices heard... They need us as much as we need them.
read about the BILL:
http://articles.chicagotribune.com/2012-05-09/news/sns-rt-drugs-breakthroughl1e8g8a89-20120509_1_cancer-drug-drug-regulators-approval-of-breakthrough-drugs
 

dramamama

New member
Here is one way to easily email your Representatives regarding this legislation:<a href="http://www.opencongress.org/contact_congress_letters/new?bill=112-s2236&position=support" rel="nofollow nofollow" target="_blank"><span>http://<span>www.opencongress.org/<span>contact_congress_letters/<span>new?bill=112-s2236&position=support</a>Don't forget to personalize the message for greatest impact! This bill would help the CF community so much!

This is not the Experrt Act.... This will allow smaller trials and faster trials and help us gain access to the drugs faster...
 

dramamama

New member
Here is one way to easily email your Representatives regarding this legislation:<a href="http://www.opencongress.org/contact_congress_letters/new?bill=112-s2236&position=support" rel="nofollow nofollow" target="_blank"><span>http://<span>www.opencongress.org/<span>contact_congress_letters/<span>new?bill=112-s2236&position=support</a>Don't forget to personalize the message for greatest impact! This bill would help the CF community so much!

This is not the Experrt Act.... This will allow smaller trials and faster trials and help us gain access to the drugs faster...
 

rmotion

New member
Yeah we need to be proactive on this. It is so hard to get on a trial and if given a placebo is a risk.
I think if the drugs are reasonably safe then we should be on them. How many years have we waited for something. How many clinical trials have we been in over the years, too many. It is time we had some relief and hope from this disease!
 

rmotion

New member
Yeah we need to be proactive on this. It is so hard to get on a trial and if given a placebo is a risk.
I think if the drugs are reasonably safe then we should be on them. How many years have we waited for something. How many clinical trials have we been in over the years, too many. It is time we had some relief and hope from this disease!
 

musclemania70

New member
thank you for the link. I tried to complete the form, then it asked me to verify with an email confirmation, which I did, but it doesn't say if the letter got sent. Once i have a login, where do i go to send this letter?
 

musclemania70

New member
thank you for the link. I tried to complete the form, then it asked me to verify with an email confirmation, which I did, but it doesn't say if the letter got sent. Once i have a login, where do i go to send this letter?
 
P

petersymons

Guest
Im hoping vertex will make the drugs available to those who dont qualify for the trials and need them the most. My son has Fev of 30%, is colonised by cepacia, regularly coughs up blood, has cf related liver disease and visits the transplant team for that. He also has a hernia caused by the coughing that needs an operation. He doesn't qualify for the trials. there are plenty of people like him who want to enter trials but are to sick. Many of these people will die before the drugs are available. Im hoping vertex will offer people like Ben access to there drugs. The more pressure on vertex and the CF Foundation the better. I need to buy kalydeco, but cant afford it as Ben is Delta 508. Here in Australia we cant get the drugs if we arent G55d.
 
P

petersymons

Guest
Im hoping vertex will make the drugs available to those who dont qualify for the trials and need them the most. My son has Fev of 30%, is colonised by cepacia, regularly coughs up blood, has cf related liver disease and visits the transplant team for that. He also has a hernia caused by the coughing that needs an operation. He doesn't qualify for the trials. there are plenty of people like him who want to enter trials but are to sick. Many of these people will die before the drugs are available. Im hoping vertex will offer people like Ben access to there drugs. The more pressure on vertex and the CF Foundation the better. I need to buy kalydeco, but cant afford it as Ben is Delta 508. Here in Australia we cant get the drugs if we arent G55d.
 

saveferris2009

New member
Letter SENT! It was very easy.

I have to say, I missed this thread because it's tacked at the top of this forum. I rarely look at the top because it's usually the same threads for months upon months.

Maybe we should consider letting this thread float freely to attract more eyeballs?
 

saveferris2009

New member
Letter SENT! It was very easy.

I have to say, I missed this thread because it's tacked at the top of this forum. I rarely look at the top because it's usually the same threads for months upon months.

Maybe we should consider letting this thread float freely to attract more eyeballs?
 
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