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Max Gelman

@MaxGelman

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Reporting on pharma and biotech, @endpts. Baseball fan, Northwestern alum. Email: [email protected]

Joined May 2011
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@MaxGelman
Max Gelman
11 months
Neumora fail: First Phase 3 for depression drug is an unequivocal miss. The company is still running two other identical Phase 3 trials, @ky_lahucik has the latest. $NMRA -79% https://t.co/MFdJpOjqC9
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endpoints.news
Neuroscience drug developer Neumora Therapeutics released highly anticipated results from the first of three Phase 3 trials for its experimental major depression drug, saying Thursday that navacapr...
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@MaxGelman
Max Gelman
11 months
FDA approved Vertex's "vanza triple" formulation for cystic fibrosis, and new mutations for Trikafta. Both come with boxed warnings
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news.vrtx.com
- Approximately 300 more people with cystic fibrosis in the U.S. are now eligible for a medicine that treats the underlying cause of their disease for the first time - BOSTON --(BUSINESS WIRE)--Dec....
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@ByLizC
Elizabeth Cairns
11 months
Now updated and with new version of the chart! $NVO $LLY $VKTX $RHHBY
@endpts
Endpoints News
11 months
BREAKING: Novo Nordisk's CagriSema fails to hit 25% weightloss benchmark in Phase 3 readout. Novo’s stock $NVO crashed by as much as 26% pre-market Friday. https://t.co/koSAVi3xd7
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@RLCscienceboss
Ryan Cross the Science Boss
1 year
This will be one to watch. Sorriso says it has figured out how to make an orally-administered antibody, and is claiming success in Phase 1b study in ulcerative colitis. @MaxGelman has the details for @endpts -
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endpoints.news
A private startup from Salt Lake City aiming to develop oral antibodies says it has succeeded in an early trial, a potentially significant scientific advancement in a world where systemic ...
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@MaxGelman
Max Gelman
1 year
Sarepta has a long & controversial history of getting Duchenne drugs OK’d w/accelerated approval. Now it will try in more rare diseases. "We will apply that same focus and creative energy and patient-mission approach to these therapies," the CEO said. https://t.co/Eogl6UgnKh
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endpoints.news
Sarepta Therapeutics and Arrowhead Pharmaceuticals teamed up on an siRNA partnership that has one of the biggest promises of biobucks in recent years.
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@MaxGelman
Max Gelman
1 year
The FDA has approved BridgeBio's rare heart disease drug, notably including mortality on the label. BridgeBio will brand the drug as Attruby, and it will cost about $245K per year. $BBIO https://t.co/lOJfkM1yLD
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endpoints.news
The FDA approved BridgeBio’s ​​acoramidis in a rare, genetic heart disease that’s expected to become an intense area of market competition, and a broad label will give it a near-immediate boost...
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@MaxGelman
Max Gelman
1 year
Re-upping my piece from last week on a potential FDA commissioner under an RFK Jr.-led HHS
@MaxGelman
Max Gelman
1 year
Biotech industry worries over potential for RFK Jr. ally as FDA pick https://t.co/H6iXZYc9iJ
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@ky_lahucik
Kyle LaHucik
1 year
Evergreen reminder to always double check who you’re emailing before hitting send Ex-Pfizer CFO emailed CEO Albert Bourla over the weekend. The message was blank. But the “to” field included a rep for activist Starboard From @ArmstrongDrew @maxonwifi https://t.co/Z6p5IRWcGq
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endpoints.news
The message over the weekend to Pfizer’s CEO Albert Bourla was blank. But it contained a warning nonetheless. It came from his former CFO Frank D’Amelio. While there was no ...
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@Nicole_DeFeudis
Nicole DeFeudis
1 year
This year’s Women in Biopharma R&D report is dedicated to Natalie Grover, who launched the project with @AmberTongPW in 2019 while they were working at Endpoints. We’re proud to continue their tradition of honoring 20 exceptional women leaders. https://t.co/g7aeAVvPGl
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endpoints.news
Dedicated to the memory of Natalie Grover, who co-created the Women in Biopharma R&D special report while she was a reporter at Endpoints from 2018-2020. Natalie passed away earlier ...
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