Usually the FDA must respond to an IND within 30 calendar days of receiving a complete application. The IND goes into effect 30 days after the FDA receives the application, and the study can begin 30 days after that IF it has been deemed “safe-to-proceed.”
November 6, 2026 at 5:08 PM
Usually the FDA must respond to an IND within 30 calendar days of receiving a complete application. The IND goes into effect 30 days after the FDA receives the application, and the study can begin 30 days after that IF it has been deemed “safe-to-proceed.”
You guys are good with Ghost Office right? Cuz a new org chart just dropped and hooker flouts office of Women’s heath is what? Fucking Gone! Merged with a few others under the new Office of Health Advancement. Which has no fucking staff!!!
www.fda.gov/about-fda/fd...
www.fda.gov/about-fda/fd...
November 6, 2026 at 5:32 PM
You guys are good with Ghost Office right? Cuz a new org chart just dropped and hooker flouts office of Women’s heath is what? Fucking Gone! Merged with a few others under the new Office of Health Advancement. Which has no fucking staff!!!
www.fda.gov/about-fda/fd...
www.fda.gov/about-fda/fd...
AES on Morning Joe yesterday made a point of saying, essentially, who says no to a law that makes the FDA make sure lettuce isn't covered in shit.
November 6, 2026 at 4:45 PM
AES on Morning Joe yesterday made a point of saying, essentially, who says no to a law that makes the FDA make sure lettuce isn't covered in shit.
Good morning ppl! The rats are jumping the fucking ship!!!
November 5, 2026 at 2:35 PM
Good morning ppl! The rats are jumping the fucking ship!!!
Just received word that the IND application for the bispecific monoclonal antibody targeting the Ebola virus (EBOV) glycoprotein I have been working on with my team for quite some time now has received a “safe-to-proceed” from the FDA.
This marks a huge milestone for us.
Today is a good day.
This marks a huge milestone for us.
Today is a good day.
November 6, 2026 at 5:00 PM
Just received word that the IND application for the bispecific monoclonal antibody targeting the Ebola virus (EBOV) glycoprotein I have been working on with my team for quite some time now has received a “safe-to-proceed” from the FDA.
This marks a huge milestone for us.
Today is a good day.
This marks a huge milestone for us.
Today is a good day.
Abolishing ICE. Medicare for all. Restoring CDC, DOJ, FDA, NIH independence
November 6, 2026 at 5:51 PM
Abolishing ICE. Medicare for all. Restoring CDC, DOJ, FDA, NIH independence
I’m still nervous about buying produce especially lettuce products after the explosive diarrhea summer we just had so I’m all in on El-Sayed’s ‘crap lettuce’ bill idea to restore the parts of the FDA & CDC gutted by Trump, RFK jr & DOGE.
El-Sayed: "The first 3 things we have to do is end this war -- we need a war powers resolution that brings war-making capacity back to Congress -- number 2, ending this tariff regime & war against Canada, but number 3, stopping the nuclear bomb that's about to go off in our healthcare system ... "
November 5, 2026 at 3:29 PM
I’m still nervous about buying produce especially lettuce products after the explosive diarrhea summer we just had so I’m all in on El-Sayed’s ‘crap lettuce’ bill idea to restore the parts of the FDA & CDC gutted by Trump, RFK jr & DOGE.
Breakthrough: FDA Approves First Drug Offering a 'Functional Cure' For Chronic Hepatitis B.
www.sciencealert.com/breakthrough...
www.sciencealert.com/breakthrough...
Breakthrough: FDA Approves First Drug Offering a 'Functional Cure' For Chronic Hepatitis B
There's new hope for the millions of people affected by chronic hepatitis B (CHB), a liver condition that can lead to cancer, scarring, or organ failure, and which is responsible for over a million de...
www.sciencealert.com
November 5, 2026 at 4:04 AM
Breakthrough: FDA Approves First Drug Offering a 'Functional Cure' For Chronic Hepatitis B.
www.sciencealert.com/breakthrough...
www.sciencealert.com/breakthrough...
i get nothing but the bleakest messages from friends in academia and cdc/fda. Just ruinous shit
This personally fucked up my life pretty badly through very direct second order effects , it would be nice to see someone pay.
November 5, 2026 at 1:01 PM
i get nothing but the bleakest messages from friends in academia and cdc/fda. Just ruinous shit
Blame the FDA.
Everytime I try to refill my Adderall it's out of stock.
November 7, 2026 at 3:06 AM
Blame the FDA.
For those who may not be aware, an Investigational New Drug (IND) Application is a request from a clinical study sponsor to the Food and Drug Administration (FDA) for permission to give an investigational drug or biological product to humans.
November 6, 2026 at 5:05 PM
For those who may not be aware, an Investigational New Drug (IND) Application is a request from a clinical study sponsor to the Food and Drug Administration (FDA) for permission to give an investigational drug or biological product to humans.
Thank you, I feel constantly like people are 'forgetting' the gutting of FDA, NIH, NSF, CDC, USAID
November 5, 2026 at 12:49 PM
Thank you, I feel constantly like people are 'forgetting' the gutting of FDA, NIH, NSF, CDC, USAID
Peptides are gaining attention, but access isn't the same as evidence. If you’re curious about one, ask:
Is it FDA-approved?
Do human trials show it works?
What are the risks?
Are safer alternatives available?
Who's overseeing your care?
Five questions worth asking before proceeding.
Is it FDA-approved?
Do human trials show it works?
What are the risks?
Are safer alternatives available?
Who's overseeing your care?
Five questions worth asking before proceeding.
November 6, 2026 at 2:15 AM
Peptides are gaining attention, but access isn't the same as evidence. If you’re curious about one, ask:
Is it FDA-approved?
Do human trials show it works?
What are the risks?
Are safer alternatives available?
Who's overseeing your care?
Five questions worth asking before proceeding.
Is it FDA-approved?
Do human trials show it works?
What are the risks?
Are safer alternatives available?
Who's overseeing your care?
Five questions worth asking before proceeding.
To-do list for Project 2029
1. Rejoin WHO
2. Fund Pan American Health Organization, USAID
3. Restore NSF, NIH, CDC, EPA, FDA to their former glory
4. Impeach RFK Jr & Russel Vought
5. Rescind Trump’s Executive Orders
6. Dissolve the Heritage Foundation
7. Regulations on AI
What else?
1. Rejoin WHO
2. Fund Pan American Health Organization, USAID
3. Restore NSF, NIH, CDC, EPA, FDA to their former glory
4. Impeach RFK Jr & Russel Vought
5. Rescind Trump’s Executive Orders
6. Dissolve the Heritage Foundation
7. Regulations on AI
What else?
November 7, 2026 at 1:48 AM
To-do list for Project 2029
1. Rejoin WHO
2. Fund Pan American Health Organization, USAID
3. Restore NSF, NIH, CDC, EPA, FDA to their former glory
4. Impeach RFK Jr & Russel Vought
5. Rescind Trump’s Executive Orders
6. Dissolve the Heritage Foundation
7. Regulations on AI
What else?
1. Rejoin WHO
2. Fund Pan American Health Organization, USAID
3. Restore NSF, NIH, CDC, EPA, FDA to their former glory
4. Impeach RFK Jr & Russel Vought
5. Rescind Trump’s Executive Orders
6. Dissolve the Heritage Foundation
7. Regulations on AI
What else?
The FDA gave tentative approval to make a generic version of a groundbreaking HIV prevention medicine, a key step in widening access for dozens of low- and middle-income countries. https://www.statnews.com/pharmalot/2026/11/02/lenacapavir-generic-version-approved-fda-hiv-prevention-dr-reddys/
FDA OKs generic HIV prevention shot, widening access for lower-income countries
The FDA has approved a generic HIV prevention shot, a key step in widening access for dozens of lower-income countries.
www.statnews.com
November 2, 2026 at 5:49 PM
The FDA gave tentative approval to make a generic version of a groundbreaking HIV prevention medicine, a key step in widening access for dozens of low- and middle-income countries. https://www.statnews.com/pharmalot/2026/11/02/lenacapavir-generic-version-approved-fda-hiv-prevention-dr-reddys/
I’m getting really tired of this.
www.newsweek.com/salmonella-o...
www.newsweek.com/salmonella-o...
Salmonella outbreak grows to 65 cases as FDA searches for source
The FDA has begun tracing a Salmonella Javiana outbreak as U.S. food-safety investigations this year have spanned lettuce, eggs and cheese.
www.newsweek.com
November 6, 2026 at 6:51 AM
I’m getting really tired of this.
www.newsweek.com/salmonella-o...
www.newsweek.com/salmonella-o...
That’s a tough question, given the state of our FDA 😆
November 5, 2026 at 9:08 PM
That’s a tough question, given the state of our FDA 😆
The FDA has approved a “functional cure” for chronic hepatitis B that suppresses the virus to undetectable levels in the blood.
Breakthrough: FDA Approves First Drug Offering a 'Functional Cure' For Chronic Hepatitis B
There's new hope for the millions of people affected by chronic hepatitis B (CHB), a liver condition that can lead to cancer, scarring, or organ failure, and which is responsible for over a million de...
www.sciencealert.com
November 5, 2026 at 4:25 AM
The FDA has approved a “functional cure” for chronic hepatitis B that suppresses the virus to undetectable levels in the blood.
In case you missed this.
Marshall purchased stock in obscure pharma company just before it secured key FDA approval
In the Senate, Marshall has oversight of the FDA
popular.info
November 3, 2026 at 12:44 AM
In case you missed this.
The US Food and Drug Administration (FDA) has granted tentative approval to a low-cost generic version of lenacapavir, a twice-yearly injection to prevent HIV.
www.attitude.co.uk/news/low-cos...
www.attitude.co.uk/news/low-cos...
Low-cost HIV prevention injection receives FDA approval for rollout in 120 countries
The US Food and Drug Administration (FDA) has granted tentative approval to a low-cost generic version of lenacapavir, a HIV prevention.
www.attitude.co.uk
November 6, 2026 at 5:00 AM
The US Food and Drug Administration (FDA) has granted tentative approval to a low-cost generic version of lenacapavir, a twice-yearly injection to prevent HIV.
www.attitude.co.uk/news/low-cos...
www.attitude.co.uk/news/low-cos...
This bill won't go anywhere but it is designed to ick people out about medication abortion.
Meanwhile, the FDA could soon force people to get pills by traveling to a clinic, not via telehealth @autonomynews.co
Meanwhile, the FDA could soon force people to get pills by traveling to a clinic, not via telehealth @autonomynews.co
FDA Lawyer Leaves Door Wide Open for Mifepristone Restrictions at Appeals Court Hearing
Louisiana made misleading claims about the safety of medication abortion, while the Justice Department sidestepped questions about whether the drug should remain available via telehealth.
www.autonomynews.co
November 6, 2026 at 10:43 PM
This bill won't go anywhere but it is designed to ick people out about medication abortion.
Meanwhile, the FDA could soon force people to get pills by traveling to a clinic, not via telehealth @autonomynews.co
Meanwhile, the FDA could soon force people to get pills by traveling to a clinic, not via telehealth @autonomynews.co
Sanders could use PDUFA negotiations to press for FDA, drug industry reforms https://www.statnews.com/2026/11/04/bernie-sanders-senate-help-key-role-pdufa-reauthorization/
Pharma critic Bernie Sanders is set to hold major sway over FDA funding bill
Sanders could use his role in crafting the bill to push for reforms.
www.statnews.com
November 4, 2026 at 9:50 PM
Sanders could use PDUFA negotiations to press for FDA, drug industry reforms https://www.statnews.com/2026/11/04/bernie-sanders-senate-help-key-role-pdufa-reauthorization/
Infuriating. RFKJr has spent years denouncing supposed conflicts of interest in FDA panels (conflicts which were usually imaginary and in any case always forbidden) and in 2025 fired a bunch of panelists for supposed C of I's--and then creates a new waiver system to legalize them,
SCOOP: Half of RFK Jr.'s appointees to the US Preventive Services Task Force were allowed to keep investments in pharmaceutical and other medical companies that make products affected by the task force's decisions, according to documents I reviewed.
RFK Jr.’s Appointees to Health Task Force Included Four Allowed to Keep Drug Stocks (Gift Article)
New members of the influential U.S. Preventive Services Task Force were given waivers to serve with financial conflicts.
www.nytimes.com
November 6, 2026 at 12:58 AM
Infuriating. RFKJr has spent years denouncing supposed conflicts of interest in FDA panels (conflicts which were usually imaginary and in any case always forbidden) and in 2025 fired a bunch of panelists for supposed C of I's--and then creates a new waiver system to legalize them,