FDA Approves Radicava, First New ALS1 Therapy in 22 Years
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FDA Approves Radicava, First New ALS1 Therapy in 22 Years
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Re: FDA Approves Radicava, First New ALS1 Therapy in 22 Years
#2Re: FDA Approves Radicava, First New ALS1 Therapy in 22 Years
#3Re: FDA Approves Radicava, First New ALS1 Therapy in 22 Years
#4How does this works over there in US? Government or private insurance covers it?
Re: FDA Approves Radicava, First New ALS1 Therapy in 22 Years
#5How does this works over there in US? Government or private insurance covers it?
Re: FDA Approves Radicava, First New ALS1 Therapy in 22 Years
#6How does this works over there in US? Government or private insurance covers it?
Private insurance, unless you're on Medicare.
Re: FDA Approves Radicava, First New ALS1 Therapy in 22 Years
#7The stuff is called edaravone. Radicava is the name that was made up by some marketing intern.
Re: FDA Approves Radicava, First New ALS1 Therapy in 22 Years
#8Giving placebo to ALS patients? How is that allowed ? They should be able to tell already what is the course of a typical ALS patient without using such methods. For cancer drugs there are no placebo used since there is extensive survival data available to prove whether or not a drug actually makes any difference.
Re: FDA Approves Radicava, First New ALS1 Therapy in 22 Years
#9> Results from the six-month Japanese clinical trial — in which 137 patients were randomized to receive either Radicava or placebo Giving placebo to ALS patients? How is that allowed ? They should be able to tell already what is the course of a typical ALS patient without using such methods. For cancer drugs there are no placebo used since there is extensive survival data available to prove whether or not a drug actu…
>For cancer drugs there are no placebo used since there is extensive survival data available to prove whether or not a drug actually makes any difference.
Source, please?
Re: FDA Approves Radicava, First New ALS1 Therapy in 22 Years
#10I realize this doesn't add anything to the conversation, but as someone whose mom passed away from ALS, I welcome anything that can remotely improve this terrible disease. Watching her go from walking to barely able to lift a glass in six months was devastating and I'd have given much for 33% more able-bodied time with her.