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$SGMO Sangamo Therapeutics Launches #Auction Process for Clinical-Stage Chronic Neuropathic Pain Program
#NAV1_7 #epigenetic #editing
expected to be #completed in Q4 of 2026
SFN 180k patients in US
peripheral neuropathies 40M
ST-503 received #FastTrack
investor.sangamo.com/news-re…
Phoenix Biotech retweeted
‼️🔥🇫🇷 𝗔𝗟𝗘𝗥𝗧𝗘 𝗜𝗡𝗙𝗢 — La situation DÉGÉNÈRE à Paris : des policiers se retrouvent piégés et PRENNENT FEU après avoir reçu des cocktails Molotov.
Phoenix Biotech retweeted
🇫🇷 Things got ugly in Paris tonight as what looks like a Molotov cocktail was thrown at riot police
Around 70,000 people marched through the city, and in the footage it's a total mess, with fire and smoke everywhere.
Weeks of protests, and France still isn't calming down.
Halloween in Paris got scary for real.
Writer: Daniyal
Phoenix Biotech retweeted
🚨 RIOTERS BURN AMERICAN AND ISRAELI FLAGS IN LYON, FRANCE
Far-left and Islamist rioters in Lyon, France, are setting American and Israeli flags on fire amid demonstrations.
According to i24NEWS, demonstrators trampled and burned the flags atop a tram shelter while a crowd applauded and chanted “Israël assassin” (“Israel is a murderer”).
Phoenix Biotech retweeted
$PGEN $INO Inovio has to run a placebo-controlled confirmatory trial it has not designed or started, fund it on a balance sheet that until tonight had about a quarter of cash, and recruit patients to a placebo arm now that the drug is available on prescription.
And the FDA’s published efficacy figure is 27% with no surgery in year one, in the enriched subgroup, from an open-label 32-patient study. Precigen’s (PGEN) is about 51% complete response as the powered primary of a registrational trial, which the agency accepted as proof of benefit rather than a predictor of it.
Precigen $pgen overreaction to the $ino news. Their drug was not approved like Precigen’s is. Inovio still has work to do 👇
“The agency based this accelerated approval on clinical trial data showing Voceryq helps reduce the frequency of surgical procedures required to remove growths in adult patients with RRP — an intermediate clinical endpoint reasonably likely to predict clinical benefit. The accelerated approval pathway allows the FDA to approve drugs or biologics for serious or life-threatening conditions based on an effect on a surrogate or intermediate clinical endpoint reasonably likely to predict clinical benefit. The manufacturer must conduct post-approval clinical trials to verify and describe Voceryq’s clinical benefit.”
Phoenix Biotech retweeted
'We Fear These People': Scandal Erupts After Berlin 'Left Party' Mayoral Candidate Admits Concerns Over Islamists zerohedge.com/political/we-f…
Phoenix Biotech retweeted
WOW $PGEN Precigen Receives FDA #Platform Technology #Designation for AdenoVerse Platform
investors.precigen.com/news-…
Phoenix Biotech retweeted
$SGMO
Positive ST-920 update! $PTCT confirms BLA submission completion expected in Q4 2026, with potential launch in 2027. PTC paid $111M upfront, plus up to $100M in FDA approval milestones ($80M accelerated + $20M full approval). Successful approval could boost Sangamo’s bankruptcy estate and potential recovery for $SGMOQ shareholders.
Phoenix Biotech retweeted
ST-920 Fabry disease BLA submission expected to be completed in Q4 2026
$PTCT $SGMO $SGMOQ
ir.ptcbio.com/news-releases/…
Phoenix Biotech retweeted
$INO Because Precigen's Papzimeos has already successfully come to market, the FDA flagged that a viable therapy for RRP technically already exists. This means Inovio may no longer meet the strict legal requirements for an "accelerated" review pathway. [1, 2]
Phoenix Biotech retweeted
Replying to @Biotech2051
Phoenix Biotech retweeted
Replying to @BiotechAnalysst
$BMRN instead of grabbing the $SGMO Fabry GT ..
today buying into "HM15421/GC1134A designed to #extend half-life and #improve stability relative to currently available #enzyme #replacement therapies, supporting subcutaneous dosing."
$70M upfront $405M milestones
🤦🏽♂️ 🤷🏽♂️
Phoenix Biotech retweeted
Replying to @ShortSeller
$SGMOQ being the highest conviction idea is a bold statement. You and @CoachClayton424 remain my absolute go-to authorities for market insights.



















