William Kaplan retweeted
Am I understanding this correctly?
$NWBO can potentially save lives in the US and all over the world, but because certain market participants stand to lose big if the stock price takes off, it gives the appearance that they're interfering in some way.
$NWBO ❤️ Braelyn is fighting brain cancer and must travel across an ocean for treatment. If you’re able, please consider helping her family cover the cost of her next trip to London.
Every donation helps. If you can’t contribute, sharing her mom’s message below is another meaningful way to support Braelyn. ❤️ @peterjkostis @greta @DrOz
William Kaplan retweeted
🇺🇸❤️ WE MET PRESIDENT TRUMP TONIGHT! ❤️🇺🇸
What an extraordinary evening for our family!
Tonight, Braelyn, Ben, and I had the incredible opportunity to meet President Trump at the rally in Pendleton, South Carolina!
We had only about 20–30 seconds with him, and I knew I needed to make every second count.
I introduced him to Braelyn and thanked him for telling Dr. Oz about her brain cancer story.
I explained that Braelyn had been diagnosed with glioblastoma, the deadliest type of brain tumor, but that today she is CANCER-FREE after receiving DCVax-L, a personalized cancer vaccine developed right here in America!
Yet we must travel all the way to England for her ongoing treatments because we cannot access it here in the United States.
Then something pretty cool happened!
President Trump turned to one of his staffers and instructed them to get me in touch with Dr. Oz!
I also expressed my hope that we could connect with Secretary Kennedy.
As our brief time together came to an end, I made one final appeal:
“Please help bring this American-made treatment back home to America.”
President Trump was incredibly gracious to our family and very kind to Braelyn. We are so grateful for the opportunity to speak with him!
Earlier in the evening, I was also able to give a member of his staff a detailed packet about Braelyn’s journey, DCVax-L, and the obstacles American patients face in accessing promising investigational treatments.
Now we are praying that the connection with Dr. Oz comes through!
Three years ago, Braelyn was given just months to live. Today, she’s 19, attending college, and her latest MRI shows NO EVIDENCE OF DISEASE RECURRENCE!
Tonight, we had the opportunity to bring her story directly to the President of the United States. ❤️
My prayer is that this opens the door to a much bigger conversation—one that could change the future for countless American cancer patients.
📸 We were not permitted to bring our phones into the private meeting with President Trump, so we couldn’t take our own pictures with him. His staff took an official photograph of us together, which we’re told will be emailed to us. I can’t wait to share it! In the meantime, here are some pictures from our unforgettable evening.
Thank you to EVERYONE who helped make tonight possible and to all of you who continue to share Braelyn’s story. You helped us get this far, and we’re not stopping now! ❤️🙏
@realDonaldTrump @DrOzCMS @WhiteHouse
#DCVaxForBraelyn #DCVax
William Kaplan retweeted
$nwbo @alphavestcap
hankmanhub
Tuesday, October 20, 2026 6:18:27 PM
The meeting between Braelyn Hollensbe and President Donald Trump is scheduled to happen on Wednesday, October 21, 2026, in the "click line" (VIP photo line) at a midterm election campaign rally. [1, 2]
Meeting Location & Details
• Venue: The meeting will take place at Clemson University's T. Ed Garrison Arena, which is physically located in nearby Pendleton, South Carolina. [1, 2]
• Timeline: The rally doors open at 3:30 PM, pre-events begin at 5:30 PM, and President Trump is scheduled to address the crowd at 7:00 PM. Braelyn and her family were officially invited to sit in the VIP section and meet the president directly. [1, 2]
Summary of Press & Media Reports
The upcoming meeting and the advocacy surrounding Braelyn's case have been documented across several reports:
1. Rasmussen Reports Commentary: An October 20, 2026, piece authored by economist Stephen Moore highlighted Braelyn's battle with glioblastoma and her use of the experimental vaccine DCVax-L. The report details her family's struggle with FDA regulatory barriers, which has forced them to fly to London for treatments, and outlines a challenge to federal authorities to reform domestic access to advanced immunotherapies. [1, 2]
2. Local Campaign Coverage: Media outlets like FOX Carolina and the SC Daily Gazette confirmed the official logistics of the Republican National Committee-hosted rally in Pendleton/Clemson, where Trump is appearing to support U.S. Senator Darline Graham. [1, 2, 3]
3. Family and Independent Investor Outlets: Public updates compiled by market and policy watchdogs such as Alpha Vest Capital confirmed that the 19-year-old and her mother, Amanda Hollensbe, accepted the invitation to meet Trump at the rally to directly discuss U.S. treatment barriers. Amanda Hollensbe also publicly shared on X that the meeting invitation was finalized on October 20, noting they live just ten minutes away from the venue. [1, 2, 3]
William Kaplan retweeted
$NWBO #DCVax #DCVaxForBraelyn #GBM #PresidentTrump
𝗗𝗖𝗩𝗮𝘅-𝗟, 𝗕𝗿𝗮𝗲𝗹𝘆𝗻 𝗮𝗻𝗱 𝗦𝘁𝗲𝗽𝗵𝗲𝗻 𝗠𝗼𝗼𝗿𝗲’𝘀 𝗰𝗵𝗮𝗹𝗹𝗲𝗻𝗴𝗲 𝘁𝗼 𝘁𝗵𝗲 𝗙𝗗𝗔.
Stephen Moore is calling for Americans to gain access to promising cancer treatments at home. The patient in his Rasmussen Reports column is Braelyn. Her treatment is DCVax-L.
Her vaccine has already been made. Her family still travels from South Carolina to London to receive it. The deeper policy connection is in what Moore had already written.
In February, Moore and health economist Tomas Philipson valued the years cancer takes. In May, their FDA-reform report named glioblastoma and proposed preparing regulatory review, manufacturing and coverage together. In October, Moore put a young woman’s face on that agenda.
𝗠𝗿. 𝗣𝗿𝗲𝘀𝗶𝗱𝗲𝗻𝘁, @POTUS @realDonaldTrump @DrOzCMS @WhiteHouse: 𝘄𝗲 𝗮𝗿𝗲 𝗮𝘀𝗸𝗶𝗻𝗴 𝗳𝗼𝗿 𝘁𝗵𝗿𝗲𝗲 𝗮𝗰𝘁𝗶𝗼𝗻𝘀.
1. Establish immediate U.S. compassionate-use access to DCVax-L for eligible patients, with the manufacturer and clinical centers ready to deliver it.
2. Establish a product-specific Plausible Mechanism Pathway for DCVax-L, connecting biological function, clinical outcomes and manufacturing quality.
3. Prioritize DCVax-L for a Commissioner’s National Priority Voucher, with the clinical and manufacturing submission ready for expedited review.
The Plausible Mechanism Pathway addresses how certain individualized therapies build an evidence case. The Commissioner’s National Priority Voucher program addresses review speed. The manufacturer, clinic and payment arrangements determine whether a decision becomes a dose.
𝗧𝗵𝗲 𝗿𝗲𝘃𝗼𝗹𝘂𝘁𝗶𝗼𝗻𝗮𝗿𝘆 𝗰𝗵𝗮𝗻𝗴𝗲 𝗶𝘀 𝗺𝗼𝘃𝗶𝗻𝗴 𝘁𝗵𝗲 𝘄𝗼𝗿𝗸 𝗼𝗳 𝗮𝘀𝘀𝗲𝗺𝗯𝗹𝗶𝗻𝗴 𝗮𝗰𝗰𝗲𝘀𝘀 𝗼𝘂𝘁 𝗼𝗳 𝘁𝗵𝗲 𝗵𝗼𝘂𝘀𝗲𝗵𝗼𝗹𝗱 𝗮𝗻𝗱 𝗶𝗻𝘁𝗼 𝘁𝗵𝗲 𝗶𝗻𝘀𝘁𝗶𝘁𝘂𝘁𝗶𝗼𝗻𝘀 𝗲𝗾𝘂𝗶𝗽𝗽𝗲𝗱 𝘁𝗼 𝗽𝗿𝗼𝘃𝗶𝗱𝗲 𝗶𝘁.
The illustrated article follows Braelyn’s story, the MRI timeline her family shared after surgery and the first three DCVax-L doses, and the reforms needed to bring treatment home.
𝗛𝗲𝗿 𝘃𝗮𝗰𝗰𝗶𝗻𝗲 𝗵𝗮𝘀 𝗮𝗹𝗿𝗲𝗮𝗱𝘆 𝗯𝗲𝗲𝗻 𝗺𝗮𝗱𝗲. 𝗦𝗵𝗲 𝘀𝗵𝗼𝘂𝗹𝗱 𝗻𝗼𝘁 𝗵𝗮𝘃𝗲 𝘁𝗼 𝗰𝗿𝗼𝘀𝘀 𝗮𝗻 𝗼𝗰𝗲𝗮𝗻 𝘁𝗼 𝗿𝗲𝗰𝗲𝗶𝘃𝗲 𝗶𝘁.
@FDA @FDADrugs @HHSGov @CMSGov @MHRAgovuk
Full illustrated analysis:
X article:
xitter.cf/andrewcaravello/status…
Reddit:
reddit.com/r/NWBO/comments/1…
LinkedIn:
linkedin.com/pulse/dcvax-l-b…
xitter.cf/HollensbeAmanda/status…
That’s my girl! My beautiful, amazing, warrior daughter, Braelyn! She make me so proud.
#DCvaxForBraelyn
share.google/YU3eB2mWD8ZZqHd…
William Kaplan retweeted
🚨🚨FAILS TO DELIVER ILLEGAL NAKED SHORTING HOW THE SHELL GAME WORKS
This is not just one bad actor it is criminal syndicate working together to rig the stock market.
Loopholes have loopholes.
Only Bona Fide Market Maker have a special exemption to sell shares they don't own. However this doesn't mean they never have to deliver. It is supposed to be temporary to keep the stock market moving smoothly.
But these Market Makers are renting out their exemption so anyone willing to pay. So they can sell shares they don't own.
Instead of them being temporary fails to deliver they create a system that hides the fails to deliver and resets the clock.
THE NEVER ENDING SHELL GAME‼️
William Kaplan retweeted
Treatments not cures b/c chemo profits are so large for Big Pharma. Add in counterfeit naked short sellers in cahoots with Big Pharma to try to bk companies like $NWBO out of biz. It's a corrupt RACKET. End the corruption @POTUS People as waking up.
xitter.cf/kshaughnessy2/status/2…
$NWBO
A video letter to President @realDonaldTrump
@HollensbeBrae is the young woman whose Glioblastoma story you recently shared with @DrOzCMS.
Braelyn and her parents live ten minutes from Wednesday’s campaign stop in Clemson and would like to meet you.
“Today she’s 19 years old, attending college, living her life - and her latest MRI shows no evidence of disease.”
Braelyn receives DCVax-L, a promising personalized cancer vaccine developed by American scientists (@NorthwestBio).
But she can’t get it in the U.S. Her family has to travel back and forth to England for compassionate use.
“For three years I fought to save my daughter‘s life and along the way I’ve discovered just how difficult it is for American patients to access promising investigational treatments - even when those treatments were developed right here in their own country.
We need to ask some very serious questions about the barriers facing smaller biotechnology companies, the influence of the pharmaceutical industry, and why patients are left waiting while promising treatments navigate years of regulatory hurdles…
…You signed right-to-try into law and I tremendously appreciate what that legislation was intended to accomplish, but I’ve learned firsthand that having the right to request a treatment doesn’t necessarily mean a patient can actually obtain it…
An American family shouldn’t have to cross an ocean to receive a promising cancer treatment developed by American scientists…”
— @HollensbeAmanda
William Kaplan retweeted
Replying to @RoyalJD11 @MHRAgovuk
UK regulators approved toxic CAR-T treatments on open label single arm trials.
If these unusual standards are required for nontoxic DCVax then put it in writing instead of hiding metrics & blaming the trial sponsor $NWBO.
Replying to @peterjkostis @Siobhain_Mc
Peter, I have been asking @MHRAgovuk about the delay in evaluating $NWBO.
They only offer self-serving answers while being opaque on their own performance & the evaluation process.
Patients require an expeditious evaluation not posturing from MPs and Whitehall.
William Kaplan retweeted
$nwbo Anthony Chalmers has publicly criticized DCVax-L and has disclosed paid pharma relationships, including GSK, while leading a UK brain-cancer review. To avoid even the appearance of bias, he should recuse himself from any NWBO/DCVax-L discussions!!
William Kaplan retweeted
📣📣THIS IS ONE OF THE MOST IMPORTANT VIDEOS THAT GIVES A GLIMPSE OF THE CORRUPT SYSTEM 🙈🙉🙊
FINRA SRO Self Regulatory Organization
Collects fines for criminal activity but instead of giving the money to the victims it goes into their general fund to pay salaries.
FINRA'S GENERAL FUND IS
2 BILLION DOLLARS
I can't believe he admitted this in the Congressional hearing.
FINRA has some very shady activities that are being exposed. But for some reason they have immunity.
So basically they can do what ever they want and answer to NO ONE
REVOKE FINRA IMMUNITY ‼️
William Kaplan retweeted
Dear Secretary Bessent @SecScottBessent,
My name is Everett Stern. In 2010 I was a compliance officer at @HSBC. From a back office in New Castle, Delaware, I watched billions of dollars move to drug cartels, sanctioned regimes, and terrorist organizations. The enemies of the United States. I documented it, I escalated it, and when the bank would not act, I took it to the @FBI, the @CIA, and eventually the @SECGov.
The result was a $1.92 billion settlement. At the time, it was one of the largest in American history. It was also about five weeks of the bank’s profit. Not one banker was charged. Not one went to prison.
I paid a different price. I lost my career, my savings, and my place in the industry I had trained for. I was blacklisted. Every door in American finance closed at once. I slept on a camping cot in a 300 square foot apartment because I could not afford a bed, and I waited tables at @PFChangs to eat. I tell you this not for sympathy, but so you understand that I know exactly what it costs to do the right thing in American finance, and exactly how little the system does in return.
I made that sacrifice because I believed it would change something.
Yesterday, your department fined @BankofAmerica $1.2 billion for failing to report more than $5 billion in suspicious transactions, some of it tied by your own findings to Chinese laundering networks, narcotics, and the southwest border, alongside 475 apparent sanctions violations touching Russia, Iran, and global terrorism. The bank admitted it willfully violated the Bank Secrecy Act.
Fourteen years after HSBC. A bank with “America” in its name. And once again, not one individual charged.
Secretary Bessent, I want to say plainly what I believe you already know. The fines are not working.
A fine is paid by shareholders, absorbed by the balance sheet, and forgotten by the next earnings call. Bank of America reported earnings this morning. Nobody who set the alert thresholds, nobody who decided the 2024 cease and desist could wait, nobody who chose the backlog over the law will lose a single thing they value. Their lives are untouched. That is the entire reason the behavior repeats.
This is money laundering. This is blood money. Money that reaches a cartel buys fentanyl that kills Americans. Money that reaches a terrorist organization buys the next attack. This country has fought a war on drugs and a war on terror for decades, at enormous cost in lives and treasure, and all the while we have allowed the financing to flow through institutions we charter and regulate. Cut off the money and we win. We have never seriously tried.
There is also a question of equal justice that I cannot let go.
Before I walked into the FBI building to report HSBC, I stopped in front of the Great Seal on the wall and read the words engraved beneath it: “Justice is the defense of our liberty.” I believed that. I still want to. But every day in this country, people go to prison for crimes that are nothing next to moving money for the people who want Americans dead. A suit, a title, and a corporate badge should not be a shield from the consequences that apply to everyone else. If a street dealer goes to prison for what he sells, the banker who moved the cartel’s money should be standing next to him.
I also want to raise something that is rarely said in these conversations. Why has no one inside Bank of America come forward the way I did? The answer is that everyone in American banking knows what happened to me, and to the whistleblowers who came after. The last person who spoke up is the only policy anyone believes. That is a culture problem, and it starts with leadership, in the banks and in the agencies that regulate them.
This is not a political issue. It has spanned administrations of both parties. It is a national security issue, and I am asking you to treat it as one.
Three things would change the math overnight.
Refer individuals for criminal prosecution. Not the analyst in the queue. The executives who set the thresholds and chose the risk. One banker in handcuffs would do more than every fine in Treasury’s history combined.
End “too big to jail.” An institution cannot be too big to fail and too big to jail at the same time. If it is the first, it must be held to a higher standard, not a lower one.
And if Bank of America will not act as America’s bank, review its charter. A national charter is a privilege granted on behalf of the American people. It should be conditioned on not moving money for the people trying to kill them.
Secretary Bessent, you said yesterday that these actions send a clear message that even the biggest institutions are not above the law. With respect, the institution was never the problem. The people inside it are above the law, and they know it. Until that changes, I will keep writing letters like this one, and the next bank will keep paying the next fine.
I gave up everything I had to stop this. I am asking you to use the power you have to finish it.
Respectfully,
Everett A. Stern
HSBC Whistleblower
Founder and Intelligence Director, Tactical Rabbit
William Kaplan retweeted
NorthWest Biotherapeutics Inc : Tsunami is coming. .The fundamental s... investorshub.advfn.com/board… via @Investors_Hub $nwbo
$NWBO it seems some brokers turned off the buy button. Can you report back on your broker? The company will call to ask why.
William Kaplan retweeted
🙉🙈🙊 SEC ZERO INTEGRITY AGENCY
We are not the only ones that have zero respect for the SEC.
The SEC has made it perfectly clear they are not protecting investors. Which is wild as that is actually their job.
If they had done their job the markets wouldn't be in this mess.
They don't know how to fix it because it is out of control.
SEC WE CAN'T FIX IT SO WE WILL IGNORE IT‼️
Replying to @SecKennedy
@SecKennedy
$NWBO
@peterjkostis
@kshaughnessy2
@parkerici
How much longer will the FDA remain silent on the $NWBO platform for solid tumors?
At least post another pic of flags..saying Americans shouldn’t have to travel overseas for medical treatment.. like @HollensbeAmanda
27,000 dead per day globally from solid tumors..
Replying to @JR31415926535
I started finding more long-term survivors.
This was probably the biggest change in my thinking.@ThomasOwenMcCa1 wasn’t alone.
Brad Silver received DCVax-L in one of the earliest trials after being diagnosed with GBM in his early 30s. He’s now a 23-year survivor.
Jamil Newirth was diagnosed at 32 and given approximately 17 months to live. He received UCLA’s personalized dendritic-cell vaccine and was profiled by UCLA more than a decade later, alive and thriving.
Sarah Rigby was diagnosed with GBM in 2011 and has been documented more than 15 years later as a long-term DCVax patient.
Nigel French was diagnosed with GBM in 2015, entered the DCVax-L trial at King’s College Hospital and was subsequently documented in long-term remission.
Kat Charles was diagnosed with grade 4 GBM in 2013 and at one point was told she had only three months to live. She later obtained a personalized dendritic-cell vaccine and continued receiving maintenance booster injections. More than a decade later, hers remains an extraordinary long-term-survivor story.
And I found other early UCLA dendritic-cell-vaccine survivors, including Jennifer Sugioka, Elijah Luyten and Gallia Kistler.
Suddenly Thomas didn’t look like one isolated anomaly anymore.
I was finding a group of people who had received this type of dendritic-cell vaccine and experienced extraordinary survival — 10 years, 12 years, 20-plus years — including patients with many years without recurrence.
And there is something especially important about these early survivors:
Many of them didn’t receive Hiltonol.
Some were treated years before the later UCLA study combining dendritic-cell vaccination with poly-ICLC.
In other words, the extraordinary long-term survivors already existed before these newer combinations were being used.
And that made the newer research even more exciting to me.
If some patients became 10-, 15- and even 20-plus-year survivors with the earlier vaccine approaches, what might be possible if researchers can now strengthen that immune response even further?
That’s the question that gives me hope.
Then came Marnix Bosch’s July 3, 2026 presentation.
At the British Neuro-Oncology Society meeting, Bosch presented new analyses using individual-patient data that hadn’t been available for the original Phase III analysis.
Researchers were now able to match DCVax patients much more precisely with patients from three randomized GBM trials based on important prognostic characteristics.
Across several propensity-score-matching approaches, the estimated survival advantage associated with DCVax-L was 3.4 to 6.3 months, rather than the original 2.8 months. Other statistical approaches produced similar results.
Their overall conclusion was that the original analysis had likely underestimated the survival benefit associated with DCVax-L.
Was that encouraging to me?
Absolutely.
But I want to be honest: an extra handful of months still isn’t what gives me hope.
Whether the median advantage is three months or six months, I don’t want six extra months for my daughter.
I want her to live a long, full life.
What the newer analysis did was strengthen my confidence that DCVax has a real treatment effect and that its original benefit may have been underestimated.
But my hope comes from the long tail.
At five years, 13% of newly diagnosed GBM patients receiving DCVax were alive compared with 5.7% of the external controls — more than double.
And now I know of some of the people represented by that tail.
Brad.
Thomas.
Jamil.
Sarah.
Nigel.
Kat.
Jennifer.
Elijah.
Gallia.
Those are the people I think about.
William Kaplan retweeted
$NWBO
Could license and access land on the same day?
@andrewcaravello asks what if the nearly three years DCVax-L has been before the UK regulator also includes the NHS payment work that used to start only after a licence?
$NWBO #DCVax #DCVaxForBraelyn
𝗧𝗛𝗘 𝗦𝗘𝗖𝗢𝗡𝗗 𝗖𝗟𝗢𝗖𝗞
𝗪𝗵𝗮𝘁 𝗶𝗳 𝘄𝗲 𝗵𝗮𝘃𝗲 𝗯𝗲𝗲𝗻 𝗺𝗲𝗮𝘀𝘂𝗿𝗶𝗻𝗴 𝘁𝗵𝗲 𝗗𝗖𝗩𝗮𝘅-𝗟 “𝗱𝗲𝗹𝗮𝘆” 𝗮𝗴𝗮𝗶𝗻𝘀𝘁 𝘁𝗵𝗲 𝘄𝗿𝗼𝗻𝗴 𝗳𝗶𝗻𝗶𝘀𝗵 𝗹𝗶𝗻𝗲?
DCVax-L’s UK Marketing Authorisation Application was submitted on December 20, 2023.
Today marks 1,016 calendar days.
The obvious question has always been:
“Why is MHRA taking so long?”
I think there may be a better one.
𝗪𝗵𝗮𝘁 𝗶𝗳 𝗮 𝘀𝗲𝗰𝗼𝗻𝗱 𝗰𝗹𝗼𝗰𝗸 𝗵𝗮𝘀 𝗯𝗲𝗲𝗻 𝗿𝘂𝗻𝗻𝗶𝗻𝗴 𝗯𝗲𝘀𝗶𝗱𝗲 𝘁𝗵𝗲 𝗳𝗶𝗿𝘀𝘁?
Under the traditional UK model, the process was largely sequential:
𝗠𝗛𝗥𝗔 𝗿𝗲𝘃𝗶𝗲𝘄
↓
𝗠𝗮𝗿𝗸𝗲𝘁𝗶𝗻𝗴 𝗮𝘂𝘁𝗵𝗼𝗿𝗶𝘀𝗮𝘁𝗶𝗼𝗻
↓
𝗡𝗜𝗖𝗘 𝗮𝗽𝗽𝗿𝗮𝗶𝘀𝗮𝗹
↓
𝗡𝗜𝗖𝗘 𝗴𝘂𝗶𝗱𝗮𝗻𝗰𝗲
↓
𝗡𝗛𝗦 𝗳𝘂𝗻𝗱𝗶𝗻𝗴 𝗮𝗻𝗱 𝗮𝗰𝗰𝗲𝘀𝘀
Approval was never the same thing as access.
NICE says there has typically been about a 90-day gap between MHRA marketing authorisation and NICE guidance.
The new MHRA-NICE Aligned Pathway is specifically designed to remove that gap.
Instead of running the clocks one after another, Britain can now run them in parallel.
𝗠𝗛𝗥𝗔 𝗿𝗲𝘃𝗶𝗲𝘄
↕
𝗡𝗜𝗖𝗘 𝗮𝗽𝗽𝗿𝗮𝗶𝘀𝗮𝗹
↓
𝗟𝗶𝗰𝗲𝗻𝗰𝗲 + 𝗡𝗜𝗖𝗘 𝗴𝘂𝗶𝗱𝗮𝗻𝗰𝗲
↓
𝗔 𝘀𝗵𝗼𝗿𝘁𝗲𝗿 𝗿𝗼𝗮𝗱 𝘁𝗼 𝗳𝘂𝗻𝗱𝗲𝗱 𝗡𝗛𝗦 𝗮𝗰𝗰𝗲𝘀𝘀
NICE can now hold appraisal committee meetings before marketing authorisation. It can publish draft guidance before authorisation. It can even complete final draft guidance before MHRA makes its decision, with the recommendation conditional upon the licence ultimately being granted.
For medicines that remain on schedule, the stated objective is simultaneous publication of the MHRA licence and NICE guidance.
The government estimates this can remove 3 to 6 months from the journey to patients.
𝗕𝘂𝘁 𝗵𝗲𝗿𝗲 𝗶𝘀 𝘄𝗵𝗲𝗿𝗲 𝗗𝗖𝗩𝗮𝘅-𝗟 𝗯𝗲𝗰𝗼𝗺𝗲𝘀 𝗽𝗮𝗿𝘁𝗶𝗰𝘂𝗹𝗮𝗿𝗹𝘆 𝗶𝗻𝘁𝗲𝗿𝗲𝘀𝘁𝗶𝗻𝗴.
The second clock did not suddenly appear in 2026.
𝗕𝘆 𝗦𝗲𝗽𝘁𝗲𝗺𝗯𝗲𝗿 𝟮𝟬𝟮𝟰, 𝗡𝗼𝗿𝘁𝗵𝘄𝗲𝘀𝘁 𝗕𝗶𝗼𝘁𝗵𝗲𝗿𝗮𝗽𝗲𝘂𝘁𝗶𝗰𝘀 𝘄𝗮𝘀 𝗮𝗹𝗿𝗲𝗮𝗱𝘆 𝘄𝗼𝗿𝗸𝗶𝗻𝗴 𝗼𝗻 𝗿𝗲𝗶𝗺𝗯𝘂𝗿𝘀𝗲𝗺𝗲𝗻𝘁.
The company disclosed that it had selected specialized reimbursement consultants, executed contracts, and begun the first stage of the process.
That work included health economics and outcomes analyses, analysis of the clinical landscape, engagement with experts and stakeholders, and other preparations necessary for reimbursement review.
That is not theory.
That is Northwest telling us that while one process was occurring at MHRA, another process was already being built around what happens 𝗮𝗳𝘁𝗲𝗿 regulatory approval.
And there was already infrastructure connecting those worlds.
MHRA’s Operational Information Sharing system allows an applicant, with consent, to let MHRA share administrative information with NICE and NHS England, including the regulatory route, submission date, estimated MHRA decision date, and ultimately the actual decision.
The stated purpose is to allow the health system to prepare its own processes more efficiently and reduce avoidable delays in patient access.
We do not know publicly whether Northwest provided that consent.
But the channel exists.
And DCVax-L was not arriving at NICE as a new product.
It already had 𝗜𝗗𝟴𝟯𝟲.
NICE had referred the topic years earlier, conducted scope work, consulted stakeholders, and invited the company into the appraisal process.
In fact, in the 2018 ID836 scope documents, NICE was already stating that it aimed to publish guidance on cancer drugs within 90 days of marketing authorisation.
So the regulatory and reimbursement tracks around DCVax-L have a much longer history than the current aligned pathway.
Then the public chronology becomes very interesting.
𝗔𝗽𝗿𝗶𝗹 𝟮𝟴, 𝟮𝟬𝟮𝟱.
The UK government tells Parliament that NICE aims, wherever possible, to issue recommendations close to the time of MHRA licensing.
Then it confirms something specific to DCVax-L:
NICE is already in discussions with the manufacturer about a potential appraisal, subject to licensing.
That is important.
It means the NICE clock was publicly visible months before the formal aligned pathway opened.
𝗢𝗰𝘁𝗼𝗯𝗲𝗿 𝟭𝟬, 𝟮𝟬𝟮𝟱.
MHRA and NICE open the aligned pathway to early adopters six months ahead of schedule.
And they specifically invite companies whose products already have NICE technology appraisals scheduled to contact NICE if their medicine may be suitable.
DCVax-L already had exactly that kind of NICE history through ID836.
The new system offers priority NICE scheduling and coordinates licensing and value assessment so the decisions can be published together.
This does not automatically move an existing product onto the pathway.
The company has to participate.
We do not have public proof that Northwest did.
But DCVax-L clearly sits inside the category NICE was actively seeking.
𝗗𝗲𝗰𝗲𝗺𝗯𝗲𝗿 𝟴, 𝟮𝟬𝟮𝟱.
The government makes another unusually specific statement about DCVax-L:
The application “is not affected by any historical backlogs.”
Then it again confirms that NICE is in discussions with Northwest Biotherapeutics about a potential appraisal subject to licensing.
Whatever is consuming the time, the UK government has therefore specifically told us what it is not.
It is not simply the old MHRA backlog.
𝗠𝗮𝗿𝗰𝗵 𝟭𝟴, 𝟮𝟬𝟮𝟲.
The government repeats that DCVax-L remains under MHRA assessment and again states that NICE aims to issue recommendations close to licensing and is discussing a potential DCVax-L appraisal with Northwest.
𝗔𝗽𝗿𝗶𝗹 𝟮𝟬𝟮𝟲.
The aligned pathway becomes fully operational.
At essentially the same time, another variable changes.
NICE raises the standard cost-effectiveness range from £20,000 to £30,000 per QALY to £25,000 to £35,000 per QALY.
And critically, NICE says the new thresholds apply not just to future appraisals, but also to technology appraisals already underway.
For a personalized living-cell therapy with an unusual upfront manufacturing cost structure, that change is potentially material.
It does not guarantee a favorable NICE decision.
But it unquestionably changes the economic framework within which an appraisal occurring today would be judged.
𝗝𝘂𝗹𝘆 𝟮𝟬𝟮𝟲.
Northwest presents new individual-patient-level survival analyses at BNOS using propensity score matching and inverse probability weighting against external randomized-trial controls.
The analyses were performed by independent statisticians and produced results broadly consistent across multiple comparator datasets and analytical approaches.
Those methods are also highly relevant to health technology assessment because they address one of the central problems with external controls: balancing measured confounders between treated patients and comparison populations.
That does not establish that the BNOS analyses were created for NICE.
But the same evidence can plainly matter to both clocks.
𝗦𝗲𝗽𝘁𝗲𝗺𝗯𝗲𝗿 𝟮𝟴, 𝟮𝟬𝟮𝟲.
I wrote directly to MHRA asking about the extraordinarily long DCVax-L process.
MHRA responded that it is:
“working actively on this application”
and is:
“progressing this application as rapidly as possible and in collaboration with the company.”
MHRA also specifically directed me to NICE’s DCVax-L appraisal, ID836.
That does not prove DCVax-L is on the aligned pathway.
But it establishes something important at the very end of this timeline.
𝗧𝗵𝗶𝘀 𝗶𝘀 𝗻𝗼𝘁 𝗮 𝗱𝗲𝗮𝗱 𝗮𝗽𝗽𝗹𝗶𝗰𝗮𝘁𝗶𝗼𝗻 𝘀𝗶𝘁𝘁𝗶𝗻𝗴 𝗶𝗻 𝗮 𝗾𝘂𝗲𝘂𝗲.
MHRA says it is actively working on it, rapidly, and in collaboration with Northwest.
Two days later, on 𝗦𝗲𝗽𝘁𝗲𝗺𝗯𝗲𝗿 𝟯𝟬, NICE published its latest report on the aligned pathway.
NICE disclosed that 90 topics across 49 therapeutic areas have now been scheduled, including products from both multinational companies and smaller and medium-sized enterprises.
The names are not disclosed publicly.
MHRA and NICE aligned pathway- how it's working in practice
And this is perhaps the most important structural fact of all.
NICE now says openly that it works with MHRA so that final guidance can be published at the same time as marketing authorisation when companies can meet the required timings.
Companies are asked to keep UK PharmaScan current, update both organizations on regulatory plans, and permit operational and planning information to be shared between NICE and MHRA.
That is not two agencies independently happening to finish around the same time.
𝗧𝗵𝗮𝘁 𝗶𝘀 𝗮 𝘀𝘆𝘀𝘁𝗲𝗺 𝗯𝘂𝗶𝗹𝘁 𝘁𝗼 𝘀𝘆𝗻𝗰𝗵𝗿𝗼𝗻𝗶𝘇𝗲 𝘁𝘄𝗼 𝗰𝗹𝗼𝗰𝗸𝘀.
And that brings me to the thesis.
𝗧𝗵𝗲 𝗠𝗛𝗥𝗔-𝗡𝗜𝗖𝗘 𝗔𝗹𝗶𝗴𝗻𝗲𝗱 𝗣𝗮𝘁𝗵𝘄𝗮𝘆 𝗱𝗶𝗱 𝗻𝗼𝘁 𝗰𝗮𝘂𝘀𝗲 𝘁𝗵𝗲 𝟭,𝟬𝟭𝟲-𝗱𝗮𝘆 𝗗𝗖𝗩𝗮𝘅-𝗟 𝗿𝗲𝘃𝗶𝗲𝘄.
It could not have.
The application had already been under review for nearly two years when the early-adopter phase began.
And I have found no evidence that MHRA completed its scientific review and deliberately placed an otherwise-ready licence on a shelf waiting for NICE.
That is not how the aligned pathway is designed.
𝗕𝘂𝘁 𝘁𝗵𝗮𝘁 𝗺𝗮𝘆 𝗯𝗲 𝘁𝗵𝗲 𝘄𝗿𝗼𝗻𝗴 𝘄𝗮𝘆 𝘁𝗼 𝘁𝗵𝗶𝗻𝗸 𝗮𝗯𝗼𝘂𝘁 𝘁𝗵𝗲 𝗱𝗲𝗹𝗮𝘆.
The more interesting possibility is that the value of the remaining time changed.
If NICE appraisal preparation, health-economic work, reimbursement planning, regulatory information sharing, manufacturing readiness, and NHS access planning are occurring during the MHRA review, then every additional calendar month before the visible licensing decision is not necessarily another month added to the ultimate patient-access timeline.
Some of that work is time that the old system would have forced everyone to spend 𝗮𝗳𝘁𝗲𝗿 approval.
That is why simply counting days to an MHRA announcement may now tell only half the story.
𝗧𝘄𝗼 𝗰𝗹𝗼𝗰𝗸𝘀.
𝗦𝗮𝗺𝗲 𝗰𝗮𝗹𝗲𝗻𝗱𝗮𝗿.
And for DCVax-L, this distinction could matter far more than it would for an ordinary pill.
Northwest itself says DCVax-L is a personalized living-cell product with substantial manufacturing costs incurred upfront, specialized distribution requirements, and potentially complex reimbursement arrangements. The company explicitly warns that obtaining workable reimbursement will be essential to commercialization.
For a therapy like this, a licence alone solves only part of the problem.
The real finish line is not:
𝗖𝗔𝗡 𝗪𝗘 𝗦𝗘𝗟𝗟 𝗜𝗧?
It is:
𝗖𝗔𝗡 𝗧𝗛𝗘 𝗡𝗛𝗦 𝗣𝗔𝗬 𝗙𝗢𝗥 𝗜𝗧, 𝗖𝗢𝗠𝗠𝗜𝗦𝗦𝗜𝗢𝗡 𝗜𝗧, 𝗔𝗡𝗗 𝗗𝗘𝗟𝗜𝗩𝗘𝗥 𝗜𝗧?
Because once NICE recommends a medicine, the NHS is normally legally required to fund it within three months of final guidance.
So compare the two outcomes:
𝗢𝗟𝗗 𝗙𝗜𝗡𝗜𝗦𝗛
Licence
↓
NICE appraisal
↓
Guidance
↓
Funding
𝗡𝗘𝗪 𝗙𝗜𝗡𝗜𝗦𝗛
Licence + NICE guidance
↓
Funding
That is a very different endpoint.
𝗡𝗼𝘁 𝗷𝘂𝘀𝘁 𝗽𝗲𝗿𝗺𝗶𝘀𝘀𝗶𝗼𝗻 𝘁𝗼 𝘀𝗲𝗹𝗹.
𝗔 𝗽𝗮𝘁𝗵 𝘁𝗼 𝗯𝗲 𝗽𝗮𝗶𝗱.
𝗡𝗼𝘁 𝗷𝘂𝘀𝘁 𝗮𝗽𝗽𝗿𝗼𝘃𝗮𝗹.
𝗔𝗰𝗰𝗲𝘀𝘀.
𝗛𝗢𝗪 𝗧𝗢 𝗧𝗘𝗦𝗧 𝗧𝗛𝗘 𝗧𝗛𝗘𝗦𝗜𝗦
This remains a hypothesis.
I cannot find public evidence proving that DCVax-L is one of the 90 topics scheduled through the aligned pathway.
An old NICE appraisal does not automatically migrate into the new pathway.
Northwest would have had to engage with the process.
And NICE explicitly acknowledges that some complex products may use alternate scheduling, with committee consideration occurring only after marketing authorisation.
So there are two versions.
𝗧𝗛𝗘 𝗦𝗧𝗥𝗢𝗡𝗚 𝗩𝗘𝗥𝗦𝗜𝗢𝗡
DCVax-L is formally proceeding through aligned scheduling, and NICE activity becomes visible before MHRA authorisation, potentially allowing NICE guidance to land with the licence.
𝗧𝗛𝗘 𝗪𝗘𝗔𝗞𝗘𝗥 𝗩𝗘𝗥𝗦𝗜𝗢𝗡
The licence arrives first, but NICE follows unusually quickly because substantial appraisal and reimbursement preparation has already occurred behind it.
Either way, the place to watch is:
𝗜𝗗𝟴𝟯𝟲.
It remains listed by NICE as “In development” with publication timing TBC.
If substantive NICE activity appears before MHRA approval, the strong version becomes much more compelling.
If MHRA approves DCVax-L and ID836 then remains dormant for months, this thesis loses much of its force.
But after following the evidence from the company, Parliament, MHRA and NICE, I no longer think the most revealing question is:
“Why has MHRA taken 1,016 days?”
I think it is this:
𝗛𝗢𝗪 𝗠𝗨𝗖𝗛 𝗢𝗙 𝗪𝗛𝗔𝗧 𝗖𝗢𝗠𝗘𝗦 𝗔𝗙𝗧𝗘𝗥 𝗔𝗣𝗣𝗥𝗢𝗩𝗔𝗟 𝗛𝗔𝗦 𝗔𝗟𝗥𝗘𝗔𝗗𝗬 𝗛𝗔𝗣𝗣𝗘𝗡𝗘𝗗?
𝗧𝗵𝗮𝘁 𝗶𝘀 𝘁𝗵𝗲 𝘀𝗲𝗰𝗼𝗻𝗱 𝗰𝗹𝗼𝗰𝗸.
Long $NWBO.
𝗔 𝗵𝘆𝗽𝗼𝘁𝗵𝗲𝘀𝗶𝘀. 𝗡𝗼𝘁 𝗮 𝗽𝗿𝗲𝗱𝗶𝗰𝘁𝗶𝗼𝗻.

































