autologous assassin 🇺🇸🇨🇱⚜️🏴‍☠️

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autologous assassin 🇺🇸🇨🇱⚜️🏴‍☠️

autologous assassin 🇺🇸🇨🇱⚜️🏴‍☠️

@DCVaxDefender

$NWBO shareholder. not economic, financial, or legal advice. professional phagocyte. geriatric millennial. semi retired. #whodat

Houston, TX Tham gia Mart 2024
251 Đang theo dõi451 Người theo dõi
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autologous assassin 🇺🇸🇨🇱⚜️🏴‍☠️
@wesstreeting @Keir_Starmer @CommonsHealth @Siobhain_Mc @zubirahmed @DrScottArthurMP @mimsdavies @johnmcdonnellMP @libdemdaisy @NadiaWhittomeMP @helenhayes_ How many more will die before @MHRAgovuk approves DCVax? Let's look at the absolute, undeniable math of this delay. Glioblastoma (GBM) is a universally fatal death sentence. The clock does not stop for patients because bureaucrats are pushing paper. THE MATH OF INACTION: Baseline: approximately 3,200 people die from Glioblastoma in the UK every single year. Daily Toll: That is 266 deaths per month. 9 people die every single day. Manufacturing Milestone: UK GMP manufacturing for DCVax was approved March 20, 2023. That was nearly 36 months ago. Review Period: The official application was submitted in December 2023. Regulators have been sitting on this for 27 months. Death Toll: During the 27 months this application has been under review, 7,200 people have died. If you start the clock from when manufacturing was cleared, we are looking at nearly 9,600 dead. THE FACTS: The trial produced statistically and clinically significant results measuring who actually lived and died after receiving DCVax. There are no serious side effects. It is incredibly nontoxic compared to treatments already approved by MHRA. Manufacturing was approved March 20, 2023. It is profoundly unethical and completely immoral to withhold a safe, proven, statistically significant treatment from terminal patients who are dying at a rate of approximately 9 per day. No more analysis. No more meetings. Enough is enough. #ApproveDCVaxNow! jamanetwork.com/journals/jamao… nwbio.com/northwest-biot… nwbio.com/northwest-biot…
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David Nola
David Nola@DavidMora·
“New Orleans makes it possible to go to Europe without ever leaving the United States.” – Franklin D. Roosevelt 🇫🇷⚜️🇪🇸 #ExchangePlace #NewOrleans
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kristen shaughnessy
kristen shaughnessy@kshaughnessy2·
$NWBO The six market maker defendants named in $NWBO spoofing lawsuit don’t want to hand over the trading data They are trying all sorts of delay tactics. “…Meanwhile, even though NWBO has produced 3,466 documents, no Defendant has produced more than 350 documents. Despite this, Defendants have harassed NWBO with frivolous discovery requests requiring unnecessary burden and expense to contest….” Courtesy: @hoffmann6383
Hoffmann@hoffmann6383

NWBO Spoofing Lawsuit - Joint Status Report $NWBO The Case: Northwest Biotherapeutics, Inc v. Canaccord Genuity LLC, 1:22-cv-10185, (S.D.N.Y.) The Docket: courtlistener.com/docket/6657959… On May 4th the parties in the above action submitted a joint status report advising the Court as to the status of discovery. Both the Defendants and NWBO submitted their own updates within the same letter. The status report contains the typical back and forth bickering. ➡️Defendants state that they are nearly complete with discovery “Defendants’ productions are complete or substantially complete.” ➡️Defendants point the finger at $NWBO for failing to agree on search terms “As of the date of this filing, NWBO has still refused to provide string-by-string hit counts for the terms Defendants proposed in February (even though NWBO confirmed it has run them).” ➡️Defendants object to $NWBO’s 150-day extension request “NWBO had agreed to produce documents responsive to several categories of Defendants’ RFPs in September 2025. Ex. A at 23. Eight months later, it has not done so—and nothing in NWBO’s request for an additional 150 days explains how more time would cure what NWBO has made no effort to accomplish.” ➡️Third-Party Discovery "On May 1, 2026, NWBO filed a letter motion seeking a protective order regarding a subpoena that Citadel Securities served on Joshua Mitts in September 2025." ➡️$NWBO points the finger at Defendants for the discovery delays “The current discovery schedule has been strained by Defendants’ repeated, prolonged, and dilatory discovery disputes.” “The Parties have continued to negotiate and work through numerous discovery issues. But discovery has been mired in disputes largely occasioned or prolonged by Defendants’ conduct.” ➡️$NWBO points at the Defendants’ meager productions to date "Meanwhile, even though NWBO has produced 3,466 documents, no Defendant has produced more than 350 documents. Despite this, Defendants have harassed NWBO with frivolous discovery requests requiring unnecessary burden and expense to contest. NWBO addresses these requests in further detail its motion to extend the case management schedule, which will be filed today." “Moreover, Defendants have limited their data productions to specific days in the relevant period, with some producing only the minutes surrounding the events alleged in the complaint. Additionally, there are inconsistencies between Defendants’ trading data, suggesting curated and incomplete productions.” ➡️My takeaway Citadel, et. al, is attempting to produce minimal documents while running out the discovery clock. $NWBO needs to pick up the pace so they get the documents that are needed. The Court's ruling on $NWBO's 150-day discovery extension along with $NWBO's protective order for Joshua Mitts will be important decisions by the Court.

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Michael Bigger
Michael Bigger@biggercapital·
@US_FDA Head lying to the American public on national TV unreal. Now we have Arnold Ventures’ Shawarma running CBER …. after being appointed by Quackery who was funded by Arnold. WTF am I missing? $QURE
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Ray Dalio
Ray Dalio@RayDalio·
I LOVE and highly recommend the New Orleans Jazz and Heritage Festival. I love festivals – in fact, I’m a bit of a festival addict – and I am addicted to this one (I have been coming to it for 33 years) because of the music, the food, and the vibe at the festival. All around, the festival in New Orleans is extraordinary. I recommend that you put it on your bucket list.
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ATLnsider
ATLnsider@ATLnsider·
Thanks for posting this information.Type-1 polarized alpha DC vaccines are a significant complement to $NWBO #DCVax dendritic cell vaccine platform technology. All of this adds to the tremendous franchise value of these assets. Dr. Pawel Kalinski is a valuable addition to NWBio:
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Peter Davis@peter_brit

#dcvax $nwbo #gbm Latest Pawel Kalinski co-authored article:- Type 1-polarized DC immunotherapeutic contains heterogeneous populations with IL-12p70 production restricted to a rare subset: May 02, 2026 "Heterogeneity within αDC1 preparations may underlie inconsistent clinical trial outcomes, and identification of associated surface proteins provides a prospective strategy for subcluster enrichment to enhance DC release criteria and patient stratification for optimized therapeutic efficacy" Gemini AI Analysis: The bioRxiv preprint (DePuyt et al., 2026) titled "Type 1-polarized DC immunotherapeutic contains heterogeneous populations with IL-12p70 production restricted to a rare subset" provides critical insights into the alpha DC1 platform, which is the core technology Northwest Biotherapeutics (NWBO) in-licensed through its deal with Dr. Pawel Kalinski and the University of Pittsburgh/Roswell Park.The paper is highly relevant to NWBO because it identifies why clinical responses to dendritic cell (DC) therapies can be inconsistent and offers a technological "upgrade" to the DCVax platform to ensure higher potency. 1. Synergy with DCVax Platform Technology The DCVax-L platform traditionally uses a standard maturation process for dendritic cells. The synergy here lies in the transition from standard DCs to alpha DC1 (Alpha-type-1 polarized DCs). Potency Enhancement: The paper demonstrates that alpha DC1s are significantly superior to standard "PGE2-DCs" in producing IL-12p70. IL-12p70 is the "holy grail" cytokine for cancer vaccines because it is essential for priming cytotoxic T-lymphocytes (CTLs) that actually kill tumors. Precision Manufacturing: The study uses single-cell multiomics to show that even within alpha DC1 preparations, there is a "rare subset" of cells responsible for most of the IL-12p70 production. This identifies specific surface markers that NWBO can use to enrich the most potent cells during the manufacturing of DCVax, potentially increasing the efficacy of the vaccine. 2. Relevance to the Kalinski/NWBO In-Licensing Deal This research serves as the scientific validation for the "Next-Gen" DCVax platform that NWBO secured in its licensing deal with Dr. Pawel Kalinski.Intellectual Property (IP): The paper explicitly mentions that Dr. Kalinski is an inventor on patents covering this platform and its "upgrade," which have been licensed to Northwest Bio. This confirms that NWBO owns the commercial rights to the specific "know-how" and methods described in the paper to produce high-IL-12 producing DCs. Overcoming "Non-Responders": A major hurdle for NWBO has been explaining why some patients respond to DCVax while others do not. This paper provides the answer: individual variability in the proportion of these "high-producer" DC subsets. By using the markers identified in this study (like Siglec-1/CD169), NWBO can move toward a more standardized, high-potency product. Combination Potential: The alpha DC1 cells described in the paper are shown to be highly responsive to CD40L (a helper signal). This supports NWBO’s strategy of combining DCVax with other agents (like Poly-ICLC or checkpoint inhibitors) to trigger that CD40L response, effectively "turning on" the IL-12 production once the vaccine is injected. In short, the paper provides the molecular "blueprint" for optimizing DCVax-L. It suggests that by selecting for specific sub-populations of dendritic cells identified through single-cell sequencing, NWBO can potentially manufacture a significantly more potent vaccine than the one used in the original Phase III trials. P. Kalinski has been an inventor on other patents covering specific application of available under aCC-BY 4.0 International license. was not certified by peer review) is the author/funder, who has granted bioRxiv a license to display the preprint in perpetuity. It is made bioRxiv preprint doi: doi.org/10.64898/2026.…; This version posted May 2, 2026. The copyright holder for this preprint (this platform and its upgrade) which have been licensed to Northwest Bio by the University of Pittsburgh and Roswell Park Comprehensive Cancer Center, and he is entitled to portions of the licensing fees and potential royalties collected by both institutions. P. Kalinski is a paid consultant for Northwest Bio. biorxiv.org/content/10.648…

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d_stock
d_stock@d_stock07734·
$NWBO I suppose Baker Brothers should know that Dr. Annalisa Jenkins joined $NWBO. I even think they might recommend Dr. Annalisa Jenkins to LP. But I could be delusional. Non Executive Director Skye Bioscience Inc. · Self-employed Mar 2024 - Present · 2 yrs 3 mos San Diego County, California, United States · Remote Non Executive Director Mereo BioPharma · Contract Sep 2022 - Present · 3 yrs 9 mos London Area, United Kingdom President and CEO Dimension Therapeutics Sep 2014 - Nov 2017 · 3 yrs 3 mos Cambridge, MA Acquired by Ultragenyx fintel.io/so/us/rare/bak… Member of the Supervisory Board Prosensa BioMarin Nederland B.V. Aug 2014 - Oct 2015 · 1 yr 3 mos Leiden Acquired by Biomarin
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d_stock@d_stock07734

$NWBO Annalisa Jenkins was the CEO of Dimension Therapeutics, Inc and Baker Brothers were the institutional investors. It is a small world indeed!!! Annalisa Jenkins has a stunning resume and it seems like she is going to play a key role in further business operation after the MHRA approval. Hypothetical question: Assuming some big investors agreed on a memo about acquiring a certain percentage of 900m shares, should LP consult with those big investors about recruiting Annalisa Jenkins? Top women in biopharma 2015 fiercebiotech.com/special-report… Northwest Biotherapeutics Appoints Dr. Annalisa Jenkins As Strategic Adviser To Advance Dendritic Cell Cancer Vaccine Platform prnewswire.com/news-releases/… fintel.io/so/us/dmtx/bak…

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Clue Heywood
Clue Heywood@ClueHeywood·
Today’s plan is to hike New Orleans’s famous “Shia LeBeouf Trail,” which is all the dive bars with confirmed Shia sightings during Mardi Gras as he made his way east to his ultimate arrest at R Bar
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Playteaux
Playteaux@Playteaux1·
$1.4M in New Orleans
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kristen shaughnessy
kristen shaughnessy@kshaughnessy2·
@FlyEaglesFly529 I’m quite sure that post has to be included in discovery material VIRT must hand over. Let’s hope $NWBO lawyers see it.
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Polish Assassin2.0
Polish Assassin2.0@FlyEaglesFly529·
$NWBO @kshaughnessy2 I wonder if dirty Doug Cifu still thinks that the NWBO lawyers are "terrorists"? 😂🤦‍♂️
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autologous assassin 🇺🇸🇨🇱⚜️🏴‍☠️
Cantor Fitzgerald refused to be the next Bayer buying Monsanto. ​They looked at Canaccord's books, saw the $NWBO spoofing lawsuit, and realized they were about to inherit the financial equivalent of Glyphosate. Cantor put a gun to their head and forced them to purge that toxic liability. Possible an indemnification clause & escrow kept this live until settlement? youtu.be/ZC1Pdsppch4?si…
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kristen shaughnessy
kristen shaughnessy@kshaughnessy2·
$NWBO Northwest Biotherapeutics settles spoofing lawsuit against Canaccord What did Canaccord agree to disclose/give up to settle allegations of spoofing and manipulating the shares of a company developing a promising brain cancer treatment? The proposed settlement puts pressure on the other defendants- • Citadel Securities LLC • G1 Execution Services LLC • GTS Securities LLC • Instinet LLC • Lime Trading Corp. • Virtu Americas LLC Courtesy @SouthernDrive21 Thoughts @hoffmann6383?
SemperFITrader@SouthernDrive21

@hoffmann6383 $nwbo NWBO Just Dimissed the case against one of the defendents "Canaccord Genuity LLC" "NWBO has agreed to dismiss with prejudice all claims asserted against Canaccord in the above-captioned action, without costs to any party" That leaves CITADEL SECURITIES LLC, G1 EXECUTION SERVICES LLC, GTS SECURITIES LLC, INSTINET LLC, LIME TRADING CORP., and VIRTU AMERICAS LLC

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Andrew Caravello, DO
Andrew Caravello, DO@andrewcaravello·
🧬 7 of 9 women with triple-negative breast cancer had their tumors essentially erased. Zero immune-related adverse events. Compare that to Keytruda + chemo: 65%, but with autoimmune side effects that can be permanent — thyroid damage, adrenal failure, lung & liver inflammation. That’s the result $NWBO in-licensed platform just produced. Today (4/29), Pawel Kalinski explained why. It’s not luck. It’s molecular design. Cold tumors fail immunotherapy because there are no T cells inside to release. The αDC1 platform builds the missing instructor cells in a lab — supercharged dendritic cells that pump out IL-12 (the “go kill” signal) at 100x normal, and train T cells carrying both an antigen receptor AND stress-sensors. They recognize cancer even when it hides its identity. They spare healthy cells. The companion CKM regimen does the same thing as a drug given IV. The key ingredient is $AIM Ampligen (rintatolimod) — a TLR3 agonist that hits the immune accelerator without hitting the inflammation switch. Standard poly-ICLC hits both. That’s why CKM works at full IV dose without the flu-like toxicity of other adjuvants. Bonus selectivity: tumors run elevated NF-kB. Healthy tissue doesn’t. CKM amplifies ONLY where cancer is. One catch — same-day dosing with checkpoint blockade is mandatory. 24h late = 20% gone. 5d late = no effect. Next-gen #DCVax-Direct integrates this on the #EDEN bioreactor. $NWBO controls the IP. Full transcript: investorshub.advfn.com/boards/read_ms…
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Marco
Marco@marcorasi1960·
Reflections, Gov Nicholls and Royal, New Orleans
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New York Post
New York Post@nypost·
Bombshell sex harassment suit against Lorna Hajdini, JPMorgan branded 'complete fabrication' as John Doe unmasked trib.al/lwsWCbT
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