Top Tweets for #VYVGART
Argenx’s Vyvgart sales jump in Q2 highlights strong demand and strategic execution. A solid signal for therapeutic potential and growth trajectory in autoimmune care. More details here: https://t.co/xCG3pTU316 #Argenx #Vyvgart #Biotech #Healthcare #Pharm… https://t.co/tuq15KkRdw
Report from Global Banking & Finance Review Argenx’s Vyvgart sales surge in Q2 signals strong demand for autoimmune therapies. Stay ahead with biotech insights, market trends, and growth strategies in pharma. #Biotech #Pharma #Healthcare #Vyvgart #Argenx… https://t.co/tuq15KkRdw
@markroseman Just found myself remarking that if the province fired just Bonnie Henry and Penny Ballem, they could probably fund #Vyvgart for about ten patients for a year. Instead our tax dollars get wasted while people die. 🙃 #bcpoli
Wow, just came across this article in the Prince George Citizen paper about a man with MG who's only getting #Vyvgart because he's got Alberta coverage. It says BC Pharmacare refuses to cover Vyvgart. Imagine if he'd had access immediately... https://t.co/3Fo9v5jLKw
Efgartigimod shows long-term benefit in Sjögren’s disease study in Phase 2 extension study. Phase 3 underway.
https://t.co/URlmQeo9xn
Just your regular reminder: I advocate for immunotherapy access for treatments like #IVIG + #Vyvgart (especially in Canada) because it’s effective, not because it’s accessible. I know it’s virtually impossible to access. It shouldn’t be like this. #Care4ComplexCanada
@lesiawaschuk @manruipa It is extremely difficult in Canada, and restricted to those who are very severe, refractory to symptom management meds, and have fairly overt symptoms (and preferably hard evidence) of progressive autonomic and small fiber neuropathy.
The label for #Vyvgart and Vyvgart Hytrulo was expanded by the @US_FDA to include treatment for adults with AChR– #gMG serotypes, such as MuSK+, LRP4+, and triple-seronegative disease.
https://t.co/TOipMCSfzK
@Argenxglobal @myastheniaorg @AANmember
I just learned about the "Right to Try Act". Why don't we have this in Canada?
This is EXACTLY what would give me access to the drugs that could save my life, since I don't qualify for the clinical trials. I deserve aid before #MAID! #Care4ComplexCanada
https://t.co/y1BG7pwHtK
🧠#FcRn inhibition is redrawing the #neuromuscular treatment map
Dr. Truyen (@luct_1 @argenxglobal) digs into new ADAPT OCULUS & ADAPT SERON data showing how #VYVGART is pushing into ocular MG, seronegative MG, & even treatment‑naïve #CIDP➡️https://t.co/IADt4ZOsB7
#MedTwitter
Phase 3 ADAPT SERON trial shows #Vyvgart treatment significantly improved MG-ADL scores in adults with AChR-Ab-negative generalized #myasthenia gravis. Data presented at #AANAM 2026.
https://t.co/ys6XBKNWA0
@AANmember #efgartigimod @argenxglobal #gMG

For adults with ocular #Myasthenia_gravis, treatment with #Vyvgart (#efgartigimod) demonstrated statistically significant improvement in patient-reported ocular symptoms. https://t.co/j3v5XgaDag
@MyastheniaOrg @NANOSTweets @AANmember @argenxglobal
#argenx $ARGX
#Vyvgart
FY25 omzet: ~$4,15mld (verwacht: $4,
13mld)
4Q25: $1,29mld (verw: 1,26mld)
#Doelen2026
4 fase 3-readouts (ocular MG 1Q, myositis 3Q, ITP & MMN 4Q)
seronegatieve gMG-launch YE26
Een katalysatorrijk jaar met pipeline-uitbreiding

I just put on the TV and saw the first ad for @argenxglobal’s self infused subcutaneous version of #Vyvgart, Hytrulo, being marketed for #CIDP.
It’s so hard knowing it’s been recommended to me and would probably be a miracle drug for my #NeuroSjogrens induced autoimmune Small Fiber + Autonomic Neuropathy, but because I don’t check the right boxes (and am not SSA positive since having Rituximab, which made me so sick) I can’t access it or even join the #Sjogrens clinical trials.
#Care4Complex = forever shut out of accessing care, due to not having textbook presentations or a more common disease.
I’m a pre-Covid post-viral complex illness/Dysautonomia + Neuro Sjogren’s patient (who also had a bad Covid infection), and due to the effectiveness but poor tolerance of #IVIG, for me and for any other LC people with post-viral Dysautonomia: #Vyvgart.
(For me, I’d want it in combo with Larazotide for my messed up gut, and anything else to clear chronic infections like perhaps Anktiva.)
My wish for 2026: ✨✨✨
As researchers like @JackHadfield14, @VirusesImmunity, @polybio, @OpenMedF, @dysclinic, and @PutrinoLab figure out the patient subsets, can we please rerun the @argenxglobal #Vyvgart trial (or have one with one of the alternative FcRN inhibitors like #Nipocalimab or #Rozanolixizumab)? 🙏
Autoimmune + post-viral SFN, #Dysautonomia, POTS, GI dysmotility, and (seronegative!) #NeuroSjogrens patients deserve a real chance at being treated with these wonderful new FcRN inhibitors that were designed specifically to replace IVIG for autoimmune diseases. We know these patients respond well to IVIG symptom wise, but typically tolerate it extremely poorly. A drug like Vyvgart could give me and so many like me another chance at life, and I believe the LC POTS trial failed due to the trial design, and not because it lacks promise for this group of patients. (It should also not be restricted to LC triggered POTS or SSA positive Sjogren’s - the reason why I cannot join the only trial in Canada!)
Complex patients who don’t check a single box (like SSA or AChR antibodies) must be allowed access to these lifesaving medications. Please let this be our year, before it is too late for so many more of us. I was on track for a trial at Stanford, and the clinic closed, and now I have no path forward, especially in Vancouver where all I can get is gaslighting and #MAID. I deserve a real chance, the treatments exist now, we all deserve a chance if our illness is treatable.
#Care4Complex
As we head into 2026, I want to explain why I’m more hopeful about making progress in ME/CFS and Long COVID with @amaticahealth than I have been about any single project (BC007, efgartigimod, nano-needle).
From my experience of hope rising & falling, & why Amatica is different.
#Vyvgart. Should it be tested in seronegative Sjogrens? About 50% w Neurosjogrens lack SSA. (Many also aren't dry when they get neurosjogrens.)
@NeuroSjogrens patients who are severely ill and often seronegative desperately need access - it is so hard to get IVIG and so many of us tolerate it very poorly, with unbearable side effects like frequent aseptic meningitis despite how it can help disease symptoms. The Sjogren’s #Vyvgart trials are going well so far, but seronegative patients are shut out as always. There are so many of us seriously suffering and dying preventable deaths. @argenxglobal Please help us. 🙏
@NeuroSjogrens patients who are severely ill and often seronegative desperately need access - it is so hard to get IVIG and so many of us tolerate it very poorly, with unbearable side effects like frequent aseptic meningitis despite how it can help disease symptoms. The Sjogren’s #Vyvgart trials are going well so far, but seronegative patients are shut out as always. There are so many of us seriously suffering and dying preventable deaths. @argenxglobal Please help us. 🙏
Video from a Norway ME patient who resumes normal life after success with #Daratumumab. It’s a drug also being trialled for #Sjogrens because it depletes nefarious antibodies in plasma. Similar idea to the #FcRN inhibitors like #Vyvgart which are more focused on IgG depletion (IgG is a component of plasma). Or to #IVIG which instead floods you with donor IgG from plasma.
These are all effective because they are targetting the disease causing antibodies - yet more proof that like Sjogren’s and autoimmune neuropathy or dysautonomia, ME in at least some people is driven by an autoimmune process. #Care4Complex
One of the Norwegian Daratumumab trial participants- who is in full remission - has shared some insights on Instagram
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