I’m happy to announce that @ionispharma has entered a licensing agreement with @cwru to translate a new treatment approach for Pelizaeus-Merzbacher disease (https://t.co/HlnnehjSKT) to patients suffering from this severe neurological disease.
This has quietly been a miracle month in medicine.
In the last 5 weeks we’ve got news on:
- retatrutide, the triple agonist GLP-1 from Lilly, basically melting fat and body-wide inflammation at record levels
- RevMed’s new pancreatic cancer drug showing unprecedented abilities to extend life
- small trial of a one-and-done PCSK9 gene editing therapy for slashing LDL cholesterol
- Mayo’s AI-assisted radiology showing vastly improved cancer detection
- this new therapy for metastatic solid tumors
This stuff is at varying levels of evidence. Retatrutide is ~100% on its way, other stuff needs more clinical trial data. But put it together and we’re maybe on the verge of majorly reducing the mortality of heart disease and cancer, the two leading causes of death in America.
Excited and deeply honored to be selected as a Heed Ophthalmic Foundation Fellow. Thankful to the incredible mentors, collaborators, and colleagues who have shaped my training and research journey. Looking forward to continuing work at the intersection of vitreoretinal surgery, translational science, and emerging gene and cell therapies.
https://t.co/lZgNr5W1Hu
https://t.co/e5DylFW01v
Across nearly 100k participants in randomized, placebo controlled GLP1-1 drug trials the rate of NAION was equivalent between drug and placebo. This is the highest quality data that we have currently and hopefully it puts this issue to rest.
@fdzmurillo@RockBolig This is fake news. Across more than 10000+ patients no hepatic safety signals were observed. Perhaps you’re thinking about the three patients with liver enzyme elevations secondary to gallbladder disease in their obesity trial?
I can't believe @sensible__med retweeted this horrible take. It demonstrates how little appreciation the sensible med crew has for basic biology.
The desmoplastic stroma of PDAC is so dense that no biologic drug can penetrate. PDAC learned to hijack every immune suppression mechanism - CAFs, MDSCs, TAMs, Tregs. Immune checkpoint inhibitors have ZERO effect on PDAC.
This is the perfect example of medical nihilism!
🚨 BREAKING: $HIMS HAS REMOVED ALL META ADS CONTAINING "SAME ACTIVE INGREDIENT AS WEGOVY" FOR ITS NEW COMPOUNDED GLP-1 PILL
The below ad was live as of yesterday. I just checked the Meta Ads library and it is nowhere to be found.
It was always surprising that Hims included that phrase in its press release and Meta ads, given the FDA's September letter specifically asked them not to use it.
From conversations I've had today, it sounds like this is what rankled Makary and caused the tweet last night. The ads have officially been taken down, and neither of the two remaining GLP-1 pill ads contains the problematic "same active ingredient" line.
Good news.
@DrEricDing Eric. Hims was attempting to sell oral semaglutide (illegal) with a completely unproven/untested delivery vehicle (also illegal). Hims produces nothing novel and gets to free ride the innovations of others. Hopefully their executives go to prison.
$HIMS -- Removing oral sema from mkt was not a choice. They were staring down the barrel of a preliminary injunction.
Now that the government has established HIMS as a bad actor, the dominos probably keep falling...I'm not a lawyer, but this is pretty much an admission of guilt:
(i) FDA sent HIMS a warning letter in Sept'25.
(ii) HIMS ignores the letter and launches oral semaglutide (with unapproved absorption tech + misleading marketing).
(iii) This passes the 'Willfulness Test' which opens HIMS up to CRIMINAL prosecution under FDCA.
The highest profile cases of criminal FDCA violations resulted in multi-billion $ fines.
Let’s be very clear here because I see a lot of confusion on the timeline.
$HIMS halting sales of their compounded semaglutide pill today is a step in the right direction.
But it does not fix the bigger problem.
Yesterday, the HHS General Counsel explicitly referred $HIMS to the DOJ. The referral wasn't just for FDA violations. It specifically cited Title 18 provisions.
If you don't speak legal, let me translate.
Title 18 = The Federal Criminal Code.
This takes the conversation from "regulatory slap on the wrist" to potential criminal territory. We are talking about the code that covers:
1. Healthcare Fraud. If there was intent to deceive regulators or consumers.
2. Mail/Wire Fraud. If misleading marketing was used to ship products.
3. Product Tampering. If the pills were misrepresented as FDA-approved equivalents (like Wegovy).
Stopping sales today might mitigate future risk, but the DOJ investigation is retroactive. They are looking at what has already happened.
If prosecutors find evidence of willful misconduct, like knowingly distributing misbranded drugs after the shortage ended, an apology isn't going to cut it.
This is no longer just a civil matter. It’s a criminal probe.
Hope this helps.
NFA, DYOR.
@SteelCBlues@RepLuna The FDA did bring regulatory action against many compounders for selling adulterated GLP1s. But the entire issue is moot now because there are no shortages of GLP1s so it’s illegal for any compounder to sell these Chinese made products, even if they were pure (which they are not)