George Lee

609 posts

George Lee

George Lee

@TinMarkProd

Katılım Mart 2026
65 Takip Edilen17 Takipçiler
George Lee retweetledi
George Lee retweetledi
George Lee retweetledi
canoebrookbl
canoebrookbl@canoebrookbl·
FDA Advisory Committees: More Transparency Needed on Policies for Making Conflict of Interest Determinations. Must disclose all AV TIES. AV-MM-VP AXIS. gao.gov/products/gao-2…
English
0
1
2
84
George Lee retweetledi
KL (for HD)
KL (for HD)@CommonSense3241·
Fight the FDA - HD community must come together. A phase 3 placebo trial is twisted and nonsensical when the phase 2 results has shown 75% slowing of disease progression. If they don’t reconsider or President Trump does not fire FDA commissioner Makary, we make our voices heard during the midterms. MAHA is turning out to be a massive disappointment, we need to make our collective 200,000 voices heard. @SenRonJohnson @SenRickScott @SenateAging @SusieWiles @WSJ @StevenCheung47 @Scavino47 @KushDesai47 @FDA_KyleD @mkratsios47 @BeckyQuick @HDSA_SF @FDACDERDirector @DrMakaryFDA @LauraLoomer @WSJopinion @l_e_whyte @bariweiss @60Minutes
English
0
2
2
18
George Lee retweetledi
KL (for HD)
KL (for HD)@CommonSense3241·
@SenRonJohnson - please hold the FDA accountable. Huntington’s disease affects 41,000 Americans and 200,000 carry the gene. The HD community is incensed by the cruelty of Prasad and Makary demanding a placebo trial for AMT-130. We are mobilizing and will make our voices heard. @BeckyQuick @andrewrsorkin @SenRickScott @LauraLoomer @WSJ @WSJopinion @60Minutes @SenRandPaul @SenBillCassidy @bariweiss @SecKennedy @CNBC @foxandfriends
English
0
2
2
10
George Lee
George Lee@TinMarkProd·
@FDACDERDirector @US_FDA @FDACDERDirector - I genuinely hope in the post-Prasad FDA, that CBER is willing to show regulatory flexibility towards AMT-130 for Huntington’s disease patients. It is unconscionable that the FDA would delay a promising therapy for our loved ones for a placebo trial. @BeckyQuick
English
0
1
2
20
Tracy Beth Høeg, MD, PhD
Tracy Beth Høeg, MD, PhD@FDACDERDirector·
The @US_FDA CDER just approved a new treatment for Hunter Syndrome. I discuss what Hunter Syndrome is, the data the approval was based on, the post marketing requirement and what this means for families who have children with the disease. For more info👇 fda.gov/news-events/pr…
English
18
13
57
13.3K
George Lee retweetledi
KL (for HD)
KL (for HD)@CommonSense3241·
@HDSA & Huntington’s disease community - We must continue putting maximum pressure on the FDA. Continue to reach out to our members of Congress, the White House, and friends and family. This disease affects too many Americans and loved ones for the FDA to treat us like this. Judgement day is coming and sooner or later @DrMakaryFDA, @VPrasadMDMPH, @FDACDERDirector - will be forced to testify to Congress and the American people. They must be held accountable.
English
1
4
8
183
George Lee retweetledi
Dr. Toonces, MD, PhD
Dr. Toonces, MD, PhD@toonces4280·
The Q2 Type B meeting between uniQure and the FDA will be the most important conversation about Huntington's disease in a generation. New CBER leadership. New political pressure from Sen. Johnson's investigation. 48-month data coming this summer. The question isn't whether AMT-130 works. p = .003 answered that. The question is whether the FDA's new leadership is willing to evaluate the data honestly, without the baggage of the last regime. 48,000 families are watching. $QURE #HuntingtonsDisease #AMT130
English
2
15
58
10.3K
George Lee retweetledi
KL (for HD)
KL (for HD)@CommonSense3241·
@SecKennedy - The FDA cannot keep rejecting life saving therapies for Americans suffering from rare diseases. The agency has lost public trust. The Huntington’s disease community cannot wait another 5 years for a twisted Prasad-mandated phase 3 trial. Our loved ones do not have the luxury of time and we cannot stand for this. @SenRonJohnson @RonJohnsonWI @SenRickScott @LauraLoomer @BeckyQuick @andrewrsorkin @CNBC @WSJ @WSJopinion @l_e_whyte @SusieWiles @StevenCheung47 @KushDesai47 @FDA_KyleD @FDACDERDirector @mkratsios47 @bariweiss @MariaBartiromo
English
0
2
3
29
George Lee retweetledi
KL (for HD)
KL (for HD)@CommonSense3241·
Congress now must force Makary, Prasad, and Hoeg to testify in front of Congress and the American people for rejecting numerous therapies for Americans suffering from rare diseases. President Trump must replace Makary and change the leadership at the FDA. The agency has been decimated and has lost all public trust. @SenRonJohnson @RonJohnsonWI @SenRickScott @BeckyQuick @MariaBartiromo @KushDesai47 @FDA_KyleD @StevenCheung47 @SusieWiles @WhiteHouse @bariweiss @FrankLuntz @SenBillCassidy @LauraLoomer @WSJ
English
0
2
2
13
George Lee retweetledi
KL (for HD)
KL (for HD)@CommonSense3241·
@SenRonJohnson @RonJohnsonWI - please force Makary, Prasad, and others at the FDA to testify in front of Congress and the American people. The FDA has lost public trust and numerous career scientists have left since the Commissioner took over. The Huntington’s disease community cannot wait another 5 years for a twisted phase 3 placebo trial on what should be an accelerated approval with a confirmatory trial. This is utterly cruel and we will not stand for this. @SenateAging @WhiteHouse @SenRickScott @SenBillCassidy @SenGillibrand @SusieWiles @StevenCheung47 @Scavino47 @FDA_KyleD @KushDesai47 @mkratsios47 @BeckyQuick @andrewrsorkin @bariweiss @LauraLoomer @MariaBartiromo @FoxNews @foxandfriends @60Minutes @CBSNews
English
0
2
2
29
George Lee
George Lee@TinMarkProd·
@StevenCheung47 Steven - please help the Huntington’s disease community - the FDA is rejecting a life saving therapy for us. We are being called “the swamp” by @AndrewNixonHHS . President Trump should be taking credit for the first ever disease slowing drug for this terrible disease. Please help
English
0
2
2
12