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Another impressive result for the national priority voucher program. 54 days for a full FDA review! 🇺🇸

50,642 views • 6 months ago •via X (Twitter)

32 Comments

Bullish's profile picture
Bullish6 months ago

Of course—another Big Pharma therapy that isn’t a cancer cure, while countless patients suffer from chemo-induced lymphopenia that ANKTIVA could actually help reverse. But once again, @DrMakaryFDA is conveniently ignoring it. $IBRX

Dr. Marty Makary's profile picture
Dr. Marty Makary6 months ago

Read more:

dbien's profile picture
dbien6 months ago

We love the fact that you are ignoring people and request for Anktiva to be approved and you’re dandering around talking about cutting red tape… put your money where your mouth is @DrMakaryFDA

Macro First's profile picture
Macro First6 months ago

Building looks empty? where is everyone?

Chau Doan's profile picture
Chau Doan6 months ago

As you said: ‘If a trial result shows immediate promise for many Americans, why wait? Quote from your interview with CNBC: ‘… your career at Johns Hopkins as physician… break bad news, … it has an impact on your soul… ‘ My husband is a physician too - just like you and @DrPatrick - he always acts in the best interests of his patients. Please look into IL15 from Immunitybio and its trial results and approve it for cancer patients. Please give this company a voucher to expedite the review process. It would be a gift from heaven for cancer patients. When people are sick, especially with cancer, they are desperate seeking a cure or anything to extend their lives. Dr Makary, you have that power, please act on it. Please do not wait any longer. @ImmunityBio @DrPatrick

Rebel Warrior's profile picture
Rebel Warrior6 months ago

And Anktiva sits on the shelves because you requested additional information dragging it out longer while more people keep dying.

Dash_Man's profile picture
Dash_Man6 months ago

Did you clear your statement with Arnold Ventures? Here is a DOGE suggestion: subcontract the entire FDA to Arnold because they control you all anyway.

Rajesh's profile picture
Rajesh6 months ago

Need to get busy - ImmunityBio sBLA - Papillary (Bladder Cancer) coming up for a Yes/No Decision. Anything less than a Priority Review is a failure of the FDA. NCCN has given its blessings just this week.

Prof. Dollar's profile picture
Prof. Dollar6 months ago

Very impressive 👇😎

Special K's profile picture
Special K6 months ago

Seriously? We want the same for anktiva! It’s been under a stranglehold at the FDA for years! Anktiva ANKTIVA (((ANKTIVA)))

SC2436's profile picture
SC24366 months ago

Why is the building empty, Marty? And these selfie videos are creepy fyi

Chellee🌻🖤's profile picture
Chellee🌻🖤6 months ago

You’d rather people to be on medication’s to lose weight? What happened to Maha? What happened to taking the chemicals to the food? The red dyes glyphosate, we worry about Swedish fish and skittles with the candy, baby formula fluoride in the list goes on. Instead of taking care of some of those issues, also transforming America and educating them how to eat properly. In my day, there was a health class that you had to take later I studied nutrition. You know one of the big things that you could be doing is before these people or any other benefits they take a health class or online clap before they get the to make responsible food choices for their family it seems like an easy thing to do but instead you want millions and millions of dollars to go out for medication so people can be relied on medications. You are not even thinking about the health risks of the American people at all. The administration has completely left. The US down, the government has led us down and we are not happy. To push big Pharma, vaccines that hurt, injured and have killed. you turn away and sweep them under the rug. It’s absolutely appalling what has taken place in our administration. Trust science? Trust the government? Don’t think so… The government supposed to work for the people not the other way around. The government creates lost to protect themselves and not the people. It’s absolutely disgusting with their administration and our three letter agencies have done to the US and around the world.

Chris cote's profile picture
Chris cote6 months ago

Was it deramiocel? $capr

sarah mitchell's profile picture
sarah mitchell6 months ago

A huge unmet public health need is treatments for progressive ultra RARE diseases. Biotech has studied invested and conducted trials and 25 were rejected under you in the past year. Please show FLEXIBILITY and talk to patients and clinicians. These drugs work 🧬‼️💉❤️‍🩹

Todd A. Barvinek's profile picture
Todd A. Barvinek6 months ago

Anktiva now

Macro First's profile picture
Macro First6 months ago

And there it is. Selfie time.

Jeremy Renz's profile picture
Jeremy Renz6 months ago

I’m tired of seeing my family die. I’m tired of seeing my wife contemplate her existence. You are killing us by CHOICE. Approve AMT-130 to treat Huntingtons Disease!!! #murderer

Farmer Dan's profile picture
Farmer Dan6 months ago

Anktiva?!?

Paul Robinson's profile picture
Paul Robinson6 months ago

Encouraging to see faster timelines. Consistency across reviews would make a meaningful difference, especially for patients waiting on ImmunityBio and Anktiva

Ray's profile picture
Ray6 months ago

#makaryout

Rebel Warrior's profile picture
Rebel Warrior6 months ago

So now Macau has authorized Anktiva for all cancers, and you are doing what? @ImmunityBio .. So back to who has paid the people at the @US_FDA for all the big pharma cartel? First Saudi Arabia, EU in 27 countries, and now Macau, you’re not going to keep this genie in the bottle mush longer.

Thomas Murtagh's profile picture
Thomas Murtagh6 months ago

ANKTIVA

Piri Reis's profile picture
Piri Reis6 months ago

Fire this guy @WhiteHouse

George Smiley's profile picture
George Smiley6 months ago

Huntingtons

Dogs&Viruses's profile picture
Dogs&Viruses6 months ago

A janitor could have done that. It’s not an NCE.

Aunt Ne's profile picture
Aunt Ne6 months ago

@US_FDA Please help cancer patients get access to anything that has even the possibility of helping. The clock is ticking for so many

Spinoza did nothing wrong's profile picture
Spinoza did nothing wrong6 months ago

Please read this and get the FDA back on track with it's deadline missed regarding the citizens petition on #nurown #ALS patients do not have long to live and are being protected to death get regulations out of their way please.

Y. Stew's profile picture
Y. Stew6 months ago

Deramiocel needs to be next for approval. How long are you gonna wait? The DMD kids don’t have time.. the sooner they receive the therapy the better their lives will be. Why are you TAKING SO LONG??? Get it APPROVED

John Jacobus's profile picture
John Jacobus6 months ago

Priority should be getting NVG-291 available for every single SPINAL CORD INJURY patient . This will save healthcare billions. We need it NOW . It’s SAFE and EFFECTIVE 100% . Please release it so us human beings can recover and get back to work and rebuild our lives .

Adam Gafford's profile picture
Adam Gafford6 months ago

What about my vape? It would be nice if the FDA would look out for adults at least once!

Kimberly Coyne's profile picture
Kimberly Coyne6 months ago

@US_FDA Semdexa for sciatica would be nice. Can we see this drug expedited?

JLeonard's profile picture
JLeonard6 months ago

@BiotechAnalysst Vanity is one of the great seven

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