x-propagation

335 posts

x-propagation

x-propagation

@unknown_tester_

xprop

Katılım Kasım 2025
138 Takip Edilen17 Takipçiler
Seedy19
Seedy19@seedy19tron·
I’m no expert but could this be front running a potential oil supply overload? Iran and Russia sanctions get eased in the coming days , we’ve seen this regime likes to get a feeler of headlines before executing and easing of restrictions on both came up this week. Oil eases up, bond market takes a breather from circuit breaking territory and hopefully selfishly fuelled by good data at ASCO , a couple M&As and Q2 remaining positive catalysts $xbi out performs. The other clean explanation is someone with conviction that the Iran war premium is overstated and headlines will deescalate, which gets you to the same trade without assuming mnpi.
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Seedy19
Seedy19@seedy19tron·
@DominickCampag I’m very confident. Hard to put a number on it as so many variables but I get 33-35% when running the numbers
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TraderNick
TraderNick@RealTradingNick·
Haven’t heard anything regarding $abvx from @unemon1 for hours, are you ok my friend?
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“paula”
“paula”@paularambles·
ottomaxxing
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Sehaj
Sehaj@SehajFund·
$NKTR January 2028 70c is selling at $33. Doesn’t seem like a terrible bet that the stock trades well above $103 by then
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Rep. Jake Auchincloss 🟧
Rep. Jake Auchincloss 🟧@RepAuchincloss·
Good, he’s gone. But now the hard work starts. The next commissioner must improve management & morale, toss out the illegal CNPV & rebuild the guardrails to political interference, and launch a clinical trials abundance agenda in concert with Congress.
Rep. Jake Auchincloss 🟧@RepAuchincloss

🧵Earlier this week, I questioned RFK Jr. on Marty Makary’s incompetent leadership of the FDA. RFK Jr. could not defend Marty Makary. The commissioner needs to be fired. Here’s why:

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x-propagation
x-propagation@unknown_tester_·
@MaartenDik oh thanks for that. Didn’t click your link just the one uniqure pr sent out which did have the aggregate
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mike
mike@mike98572986·
$clpt I don’t care what anyone says here, Clearpoint just got super de-risked, this is a huge moment.
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Clippy
Clippy@AB1001_disciple·
I'm going to be at the fourth day closing in on a 3.5k cal deficit on 1.5mg oral wegovy and there's not been a single time where I've been been hungry
Hated Moats Investor@HatedMoats

🚨 NOVO'S HIGHER-DOSE LOOKS A LOT MORE COMPETITIVE $NVO just got a much-needed obesity headline. The News Novo Nordisk presented new STEP UP analyses at ECO showing that early responders to Wegovy 7.2 mg lost 27.7% of body weight by week 72. Across the full trial, semaglutide 7.2 mg delivered 20.7% average weight loss, versus 17.5% for Wegovy 2.4 mg and 2.4% for placebo. Novo also reported that 84% of the weight loss came from fat mass, with muscle function preserved in a smaller MRI sub-study. My Take This is a positive update and Novo needed this. The market has increasingly framed obesity as “ $LLY has the better drug, Novo is playing defence.” These data do not erase that narrative per se, but they do weaken it. High-dose Wegovy gives Novo a stronger efficacy story, narrows the gap versus next-gen competitors, and helps address one of the big concerns around GLP-1 weight loss,which is muscle loss. That said, the 27.7% figure is from early responders, not the whole population. The more important number is still the full-trial 20.7% average loss. Verdict: Bullish Not thesis-changing on its own, but clearly supportive. Which still helps, considering the current sentiment. In my view, this strengthens Novo’s obesity franchise and gives the company a better answer to the “Wegovy is falling behind” narrative. Novo is still under pressure, but this is exactly the kind of data it needs now.

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dough
dough@semodough·
$NKTR Jefferies Base Case, $150, +80% • US peak adjusted (55% POS) sales in AD: ~$1.9B • US peak adjusted (55% POS) sales in AA: ~$1.3B • Pipeline value: $100M • Price target: $150. Upside case $208
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Vamsi Aribindi
Vamsi Aribindi@aribindi·
@bijans The objections weren't BS. Huntington's is notorious for placebo effect false positive studies. The melanoma drug, meant to be used in combo with nivo, needed to be compared to nivolimab placebo because nivo is known to work all on its own.
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Bijan Salehizadeh
Bijan Salehizadeh@bijans·
So let me get this straight - this FDA 1) won’t approve life saving melanoma and Huntington’s disease drugs based on BS objections related to control groups that would not be ethical 2) blocks large study showing exquisite safety of COVID vaccines which Trump drove via Warp Speed and 3) will allow certain peptides with zero human data to be prescribed? BTW I’m all for people injecting peptides if they want to if they are safe. But I’m also all for not sabotaging cancer and rare disease patients and not censoring well run studies.
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Houman David Hemmati, MD, PhD
Houman David Hemmati, MD, PhD@houmanhemmati·
To every rare disease patient and every family who loves them: When you’re told “you have a rare disease,” it can feel almost insulting. Because to you, it is not rare at all — it is your whole life. Every single day. Every hope. Every fight. This is why the FDA works so hard — and so smart — to evaluate these therapies with the highest standards of safety and efficacy. So that promising treatments can give patients and their doctors a real fighting chance. You deserve nothing less. ❤️
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Eric
Eric@StockDaddy6597·
As a reminder, the commissioner went on CNBC in March and dragged $QURE illegally by abusing MNPI. He needs to be investigated immediately, and someone needs to drug test him if he can’t remember high profile cases from 6 months ago. @RepAuchincloss @DC_Draino @RickSantorum
CP2@LuckyPenguin10

FDA Commissioner Makary just went on national TV and blatantly lied regarding $QURE AMT-130 decision: "was before my time, the FDA said no." The FDA is in a state of disarray because it has a leadership problem — and Huntington disease patients and the broader rare disease community are suffering because of it. In case @DrMakaryFDA needs a refresher... here's the timeline of events that *all* took place under him: > Nov 2025: FDA reverses year-old agreement with uniQure on external control pathway [1] > Jan 2026: FDA formally rejects the approach in a Type A meeting [2] > Mar 2026: FDA demands a sham surgery-controlled P3 trial [3] > Mar 2026: A senior FDA official calls AMT-130 a "failed product" on a media briefing [4] The CBER Director who oversaw all of this was Vinay Prasad, appointed by Makary in May 2025. [5] His deputy, Katherine Szarama, drafted Arnold Ventures' formal FDA comment letters arguing against the exact regulatory pathway that was then reversed for AMT-130 [6]. She was hired by Prasad in October 2025 [7]. Last week, Makary promoted her to Acting CBER Director [8]. Cc @SaraGonzalesTX @DC_Draino@SenGillibrand | @lukaske @SenRickScott | @ClareLattanze @SenRonJohnson | @GraceCarnathan @RepAuchincloss | @GeorginaBurros @RickSantorum | @mattbeynon

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DesertDweller_ROAR_4_A_CURE_4_HD
DesertDweller_ROAR_4_A_CURE_4_HD@DesertDweller93·
Something to consider with @uniQure_NV $QURE AMT130 FDA meetings. It was at Type B meetings that the FDA previously aligned with QURE for BLA filing. The first meeting was described by Matt as being so good that they "almost fell off their chairs" from the FDA reaction. Today we received word that a Type B meeting has been scheduled, ostensibly for path forward on P3. We know @VPrasadMDMPH is out. While his replacement has not been named, there COULD BE a chance that those who will be in attendance at the next meeting might go back to original alignment that was agreed to and allow them to file BLA on existing data. How likely is this scenario? No idea but until last November, how likely was it that the FDA would go back on their word? First screenshot is from this week's proxy filing showing that they had 3 prior Type B meetings where they had alignment. 2nd screenshot is Matt describing reaction of FDA officials at the first Type B meeting from the Guggenheim conference 02/05/2025. With Prasad gone, will sanity return to the FDA? Come on Congress, start the investigations NOW. @SenRonJohnson @SenRickScott @RepAuchincloss @houmanhemmati @adamfeuerstein @l_e_whyte @temple_west @laurencurehd @JRenz0418 @rachelreising96 @BeckyQuick @MariaBartiromo @bradloncar @docrodwong @LuckyPenguin10 @SECGov @johnarnold @DrMakaryFDA @VPrasadMDMPH @POTUS @SenateAging @SenBillCassidy @SenRandPaul @WhiteHouse @SusieWiles @StevenCheung47 @StevenCheung @Scavino47 @PressSec @SecKennedy @MariaBartiromo @RickSantorum @FoxNews @bariweiss @60Minutes @CNBC @WSJopinion @WSJ @statnews @BillAckman @Loftus @MartinShkreli
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x-propagation
x-propagation@unknown_tester_·
@mahesh_shenai @mike98572986 @RickSantorum @POTUS coming from same guy who is saying CNPV is transformative when its basically just a way for commissioner to give favors to big pharma. You, MM, VP, and arnold ventures are all jerking each other off
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〽️ahesh Shenai, 〽️D
〽️ahesh Shenai, 〽️D@mahesh_shenai·
We can look at each of the drugs on the merits. Some decisions may be liminal, but not irrational. If you are talking about $qure, for example, I have gone through the publicly available (company published) data, and I have several critical/technical questions. Its not as clearcut as some of the louder voices would have you believe. Open to hear more, and there is probably more data behind the scenes- objectivity is key. ClearPoint brain surgery (one of my specialties) is not trivial or risk free, so rigor should be welcomed, and the bar a bit higher.
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Rick Santorum
Rick Santorum@RickSantorum·
.⁦@POTUS⁩ this did not happen in DJT’s first term. He appointed great leaders who put patients and families first getting treatments and cures out in record time. It is time to clean house and appoint people who follow the DJT’s vision. foxnews.com/opinion/son-te…
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