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Johnson & Johnson (JNJ.US) submits regulatory application to FDA for antibody therapy for moderate to severe active ulcerative colitis

Market IntelSunday, Nov 24, 2024 4:10 am ET

1min read

JCI --

Johnson & Johnson (JNJ.US) announced that it has submitted a supplemental Biologics License Application (sBLA) to the US FDA seeking approval of its anti-IL-23 antibody Tremfya (guselkumab) as a subcutaneous (SC) induction regimen for the treatment of adults with moderate to severe active ulcerative colitis (UC).

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rbrar33

11/24

Tremfya's approval could boost JNJ stock nicely

SpirituallyAwareDev

11/24

Ulcerative colitis sufferers need options. Guselkumab might just be the magic bullet they've been waiting for. 🚀

Outrageous-Rate-4080

11/24

Riding $JNJ wave; long term hold for me

TeslaCoin1000000

11/24

Could J&J be onto the next big biotech win? Watch how this rollercoaster might affect $JNJ long-term.

Anklebreakers10

11/24

Tremfya's approval would solidify JNJ's foothold in IBD space. Wonder how $TSLA plays into this picture.

tempestlight

11/24

J&J's Tremfya could be a game-changer for UC

themagicalpanda

11/24

Could see JNJ leveraging Tremfya into UC opening more doors. With their track record, it's almost like they're guaranteeing a green light from the FDA. Keep an eye on how the market reacts. This one feels like a solid long-term hold for me.

notbutterface

11/24

Biotech breakthroughs are wild to watch, who's in? 🚀

Direct_Name_2996

11/24

New meds for UC? More potential for pharma plays

VirtualLife76

11/24

With JNJ's drug pipeline, could we see a shift from dividend focus to growth focus? Time to reassess my holdings?

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