Top Tweets for #BlueBirdBio
$CABA — Valye Company Analysis #celltherapy #KitePharma #bluebirdbio #Sangamo
In Q2 2026, Cabaletta Bio initiated a registrational clinical trial for rese-cel targeting dermatomyositis and anti-synthetase syndrome, marking a pivotal step toward potential regulatory approval. The company is also scaling manufacturing
Key points:
• Cabaletta Bio initiated a registrational trial for rese-cel in dermatomyositis and anti-synthetase syndrome in December 2025, advancing toward pivotal clinical data.
• Multiple Phase 1/2 trials of rese-cel continue across autoimmune indications including systemic lupus erythematosus, systemic sclerosis, generalized myasthenia gravis, and pemphigus vulgaris.
• The company is scaling manufacturing using the automated Cell Shuttle platform from Cellares, aiming to produce therapy for thousands of patients annually with lower capital investment.
• As of June 30, 2026, Cabaletta Bio held $225.1 million in cash and equivalents and maintained a current ratio of 5.79, reflecting strong liquidity to fund clinical and manufacturing activities.
• No clinical trials have been completed and no product revenues have been generated, highlighting ongoing clinical and regulatory risks.
🟠 The technology works, but the business model doesn’t. If gene therapy can’t scale profitably, who funds the next breakthrough?
#biotech #genetherapy #stock #BluebirdBio
🟧Bluebird Bio Plunges on Buyout, as Gene Therapy’s Woes Grow
https://t.co/osaoUhQ2rt
#biotech #genetherapy #stock #BluebirdBio
bluebird bio reveals new and updated data from LYFGENIA (lovotobegligene autotemcel, or lovo-cel) gene therapy for patients with sickle cell disease who have a history of vaso-occlusive events $BLUE, #bluebirdbio https://t.co/kE94ZT6FSv
@statnews I hope they overcome their economic crisis by helping more patients and that one day they reach Europe and the rest of the world, ruining your shorts. Have a nice day!
#blue #bluebirdbio
$BLUE $PFE $HTGC #BlueBirdBio #BioTech #SickleCell #Mergers #Acquisitions #Disease #Drugs #RateCutEnvironment #SmallCaps $XBI $IBB $SPY $QQQ $IWM $IWN
$HTGC Loan Agreement with
$BLUE $BlueBirdBio via MileStone payouts.
Renegotiated certain terms of its loan agreement with Hercules Capital, Inc. $HTGC and is eligible to receive two future tranches totaling $50 million.
contingent upon achievement of patient start and product delivery milestones and completion of additional financing.
$BalanceSheet
Cash Position: $193M
Cash Runway into Q2 2025 with two MileStone payouts of $50M by 2024 year end if it meets its 2024 guidance.
$BLUE #BioTech #SickleCell #Medicaid #BlueBirdBio #MergersAndAcquisitions Consolidating price action.
1 hour & 4 hour. $BLUE $PFE
$SPY $QQQ $IBB $XBI $IWM $IWN
$PFE Pfizer bought Oxbryta, also known as voxelotor, as part of its $5.4B buyout of Global Blood Therapeutics in 2022.
$PFE said on Wednesday it was withdrawing its #SickleCell disease treatment Oxbryta from all markets where it is approved,
citing risks of a painful complication & deaths.
https://t.co/MQ8JFms9cR
#Notes
Pfizer $PFE has been exploring other treatments for sickle cell disease, but with the withdrawal of Oxbryta (voxelotor), the immediate options within their portfolio are limited.
Oxbryta was the only drug $PFE had in the #SickleCell Space.
$BLUE #BlueBirdBio Updates.
Current as of August 14, 2024:
1. #2024Guidance
The Company anticipates approximately 85 patient starts (cell collections) in 2024 combined across its portfolio of three FDA approved therapies
👉LYFGENIA: Approved for #SickleCell
ZYNTEGLO: Approved for the treatment of beta-thalassemia in patients who require regular blood transfusions.
SKYSONA: Approved for the treatment of cerebral adrenoleukodystrophy (CALD), a rare neurological disorder affecting boys.
2. #SickleCell
Successfully completed manufacturing and release testing for first commercial LYFGENIA patient and the first infusion is being scheduled.
3.
Rapid acceleration projected for ZYNTEGLO following the recent approval of additional manufacturing capacity.
https://t.co/b8RVg0cYk2

$BLUE #BioTech #SickleCell #Medicaid #BlueBirdBio #MergersAndAcquisitions Consolidating price action.
1 hour & 4 hour. $BLUE $PFE
$SPY $QQQ $IBB $XBI $IWM $IWN
$PFE Pfizer bought Oxbryta, also known as voxelotor, as part of its $5.4B buyout of Global Blood Therapeutics in 2022.
$PFE said on Wednesday it was withdrawing its #SickleCell disease treatment Oxbryta from all markets where it is approved,
citing risks of a painful complication & deaths.
https://t.co/MQ8JFms9cR
#Notes
Pfizer $PFE has been exploring other treatments for sickle cell disease, but with the withdrawal of Oxbryta (voxelotor), the immediate options within their portfolio are limited.
Oxbryta was the only drug $PFE had in the #SickleCell Space.
$BLUE #BlueBirdBio Updates.
Current as of August 14, 2024:
1. #2024Guidance
The Company anticipates approximately 85 patient starts (cell collections) in 2024 combined across its portfolio of three FDA approved therapies
👉LYFGENIA: Approved for #SickleCell
ZYNTEGLO: Approved for the treatment of beta-thalassemia in patients who require regular blood transfusions.
SKYSONA: Approved for the treatment of cerebral adrenoleukodystrophy (CALD), a rare neurological disorder affecting boys.
2. #SickleCell
Successfully completed manufacturing and release testing for first commercial LYFGENIA patient and the first infusion is being scheduled.
3.
Rapid acceleration projected for ZYNTEGLO following the recent approval of additional manufacturing capacity.
https://t.co/b8RVg0cYk2

$BLUE Updates!
$XBI $IBB $IWM $IWN $SER $RSLS $BFRG $TBIO $CTOR $VTGN $CRBU $SRRK $ATRA $ARQT $VERU
In march, $BLUE sold off on accounting errors.
$BLUE had to restate its financials for 2022 and 2023, Q1 & Q2 2024, after finding several accounting errors.
#Update
$BLUE has completed the restatement of its consolidated financial statements for the year ended:
2022
1) December 31, 2022, and for each of the first three quarters of 2022.
2023
2) filed its Annual Report on Form 10-K for the year ended December 31, 2023 (the “2023 Form 10-K”)
2024 Q1
3) restated information, and Form 10-Q for the quarter ended March 31, 2024 (the “Q1 2024 Form 10-Q”) with the Securities and Exchange Commission (“SEC”).
#Note
The restatements had NO IMPACT on the Company’s CASH position or REVENUE.
2024 Q2
4) $BLUE is currently working on Q2 2024 restatement, and is working expeditiously to complete this filing.
https://t.co/sePneEW1OK
#FurtherUpdates
$BLUE will be having a meeting of stockholders on November 6, 2024.
The company will be voting on:
👇
A) the approval of named executive officer compensation
(Prop 1)
B) the approval of an amendment to our Amended and Restated Certificate of Incorporation. (Prop 2)
👉C) to provide for the exculpation of officers for certain breaches of fiduciary duty**** (Prop 3)
👉D) Incorporation to effect a reverse stock split of our common stock at a ratio ranging from any whole number between 1-for-15 and 1-for-20, as determined by our Board of Directors (Prop 4)
E) the approval of an amendment and restatement of our 2023 Incentive Award Plan
(Prop 5)
F) increase the number of shares of our common stock authorized for issuance thereunder ("Proposal 5"),
G) the ratification of the appointment of Ernst & Young LLP as our independent registered public accounting firm for the fiscal year ending December 31, 2024. (Prop 6)
https://t.co/m5zKv6d6lx
About a month after reporting it’s had a tough time starting enough patients on its treatments, bluebird bio announced it will lay off about 25% of its employees, over half of whom work in R&D.
https://t.co/iauMN8MiDQ
#layoffs #bluebirdbio
Could $EDIT be the biggest winner of $CRSP $BLUE DUEL! But NOW #bluebirdbio incredible run is finally HEADED out to 10s of thousands patients drastically reducing healthcare needs and making co. PROFITABLE! WIN WIN 🥇
$BLUE #biotech with decades of r&D, 3 approved transformative #gene therapies that cure trades @ $3, below 5% off not so distant highs! how would you value startups in ph 1/2 days from INN? $ 0?!
#bluebirdBIO treating just 1000 patients (1% of population) - is $2-3B alone!
$BLUE Some if not most "physicians and patients maybe more comfortable with Bluebird #Lyfgenia - vector technology which dates back to 1990s!", #FDA black box label potentially quite deceiving here! Today was a HUGE opportunity to BUY sub $3 #BluebirdBio on $MS upgrade! $EDIT win
Tough road ahead for Bluebird Bio $BLUE despite FDA approval for sickle cell therapy https://t.co/SjwDpIEVE6 via @brittanytrang $VRTX $CRSP
US FDA to delay decision on Bristol Myers-2seventy bio cancer therapy https://t.co/QPsgYQxGaY
#usfda #bristolmyerssquibbb #ristolmyerssquibbnews #2seventybio #bloodcancertherapy #abecma #multiplemyeloma #bluebirdbio #healthnews #mednews #medicalnews #medicaldialogues #medtwitter
If approved, #exacell by #Vertex would be d first #genetherapy with #CRISPR gene-editing technique to treat sickle cell disease. By Dec. 20, F.D.A. will decide on a second gene therapy for sickle cell by #BluebirdBio. LT follow up >15y is a must @NYTimes https://t.co/iwI4BihVKO
Is $BLUE CAR-T and #genetherapy pioneer worth only a fraction of all investments pre- and post-2013 IPO, and the value of their three approved treatments?
Just how short sighed current market is. #Bluebirdbio cos clearly high single/low double $B’s market cap co. $IBB #crispr
$BLUE ready for light. Q1 submission&approval of #LovoCel 2trigger substantial re-evaluation of market cap: #1 now with 3 approved drugs #bluebirdbio platform & technology is VALIDATED #2 comparative to $CRSP CTX-001 huge upward stock revision has2be made:
https://t.co/0zI9WCsMzD
$BLUE's in Downtrend: Moving Average Convergence Divergence (MACD) Histogram just turned negative. View odds for this and other indicators: https://t.co/BxXO7IRkQu #bluebirdbio

While advances have been made in sickle cell disease, companies such as @GraphiteBio, @bluebirdbio, @VertexPharma and @editasmed have loftier ambitions.
#GraphiteBio #bluebirdbio #VertexPharma #EditasMedicine #BioSpace
https://t.co/212QpWrYXj
bluebird bio Receives FDA Accelerated Approval for SKYSONA®(elivaldogene autotemcel)Gene Therapy for Early, Active Cerebral Adrenoleukodystrophy (CALD)
#bluebirdbio #CALD #Skysona #Elivaldogeneautotemcel #USFoodandDrugAdministration #FDA #Drug #NewProduct #DATA

The @US_FDAis heading into fall with a few new Prescription Drug User Fee Act dates. Here's a look at this week's upcoming action.
#FDA #PDUFA #FDAUpdates #bluebirdbio #Biotech #BioSpace
https://t.co/6yKHbddWES
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