Bio Stocks™
@BioStocks
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Investor/trader focused primarily in the biopharma sector. Tweets are not investment advice and are not recommendations of any kind.
Toronto
Joined February 2010
Just realized, I celebrate my 15th Twitterversary this month. Back then, I never imagined this app would become a second home. What started as a place to share ideas has grown into so much more. This platform has allowed me to share biotech insights, bounce ideas, and learn
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Lots of failed studies end up stat sig when you selectively exclude patients. Lol
$NKTR REZOLVE-AA Phase 2b Study of Rezpegaldesleukin Establishes Proof-of-Concept in Patients with Severe-to-Very-Severe Alopecia Areata https://t.co/RhAHtCUQmy
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$PVLA Granted FDA Fast Track Designation for QTORIN 3.9% Rapamycin Anhydrous Gel for the Treatment of Angiokeratomas
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$NKTR primary endpoint narrowly missed statistical significance with the mean percent SALT reduction at Week 36 of 28.2% for the 24 µg/kg rezpegaldesleukin arm, 30.3% for the 18 µg/kg rezpegaldesleukin arm, and 11.2% for placebo (p=0.186 and p=0.121, respectively)
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$NKTR data from the patients ongoing in the 16-week treatment extension will be available in early Q2
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Did you know that asphalt is recycled? Here's how.
tristateinfrastructurenews.com
Did you know that asphalt is recycled? Here's how.
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$NKTR achieved target product profile on the primary endpoint, with a mean percent reduction in SALT score at 36 weeks of 28.2% in the 24 µg/kg arm versus 11.2% in placebo Mean percent reduction in SALT scores at 36 weeks was 30% for both treatment arms versus 6% for placebo,
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$NKTR REZOLVE-AA Phase 2b Study of Rezpegaldesleukin Establishes Proof-of-Concept in Patients with Severe-to-Very-Severe Alopecia Areata https://t.co/A20HrV2aRJ
prnewswire.com
Achieved target product profile on the primary endpoint, with a mean percent reduction in SALT score at 36 weeks of 28.2% in the 24 µg/kg arm versus 11.2% in...
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$ADAG Announces FDA Fast Track Designation for Muzastotug (ADG126)
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Experience comfortable reading with lenses designed to reduce blue-light exposure and enhance visual clarity. The dual-focus design supports both near and mid-distance viewing, helping you read and work with ease throughout the day.
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$ALDX PDUFA extended for Reproxalap NDA. 03/16/26 https://t.co/KS84a3PWcp
businesswire.com
Aldeyra Therapeutics, Inc. (Nasdaq: ALDX) (Aldeyra), a biotechnology company devoted to discovering and developing innovative therapies designed to treat imm...
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$ABVX cash and equivalents of EUR 590M ($693M), with a cash runway into Q4'27
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$GUTS Announces Call of Tranche A Warrants Tied to August 2025 Public Offering. Holders will have until December 30 to exercise Tranche A Warrants at $1.05 per share, enabling up to $17.9M in potential gross proceeds https://t.co/Fd0nmtElL5
globenewswire.com
Holders will have until December 30, 2025 to exercise Tranche A Warrants at $1.05 per share, enabling up to $17.9 million in potential gross proceeds...
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$IMNM Announces Positive Topline Results from Phase 3 RINGSIDE Trial of Varegacestat in Patients with Desmoid Tumors Trial met primary endpoint with varegacestat significantly improving PFS vs. placebo (hazard ratio = 0.16, p<0.0001) Trial also met all key secondary endpoints,
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$VNDA Submits BLA for Imsidolimab for the Treatment of Generalized Pustular Psoriasis
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$KYTX Announces Positive Topline Data from Registrational KYSA-8 Trial of Miv-cel in Stiff Person Syndrome. Miv-cel achieved statistically significant clinical benefit across all primary and secondary endpoints, reversing disability and eliminating immunotherapies after a single
ir.kyvernatx.com
Landmark results could pave the way for miv-cel to become the first FDA-approved CAR T-cell therapy for autoimmune disease; Company on track to submit BLA for stiff person syndrome in 1H 2026 ...
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