Our latest survey of #biopharma professionals on #DigitalTransformation in the industry uncovered a hype-actual adoption gap.
Get the full industry report at https://t.co/xZJqIJbLID
#AI
CAR-T changed blood cancer care.
Solid and brain tumors are a different challenge: cells must reach, penetrate, and survive inside a physical tumor mass.
🔗 See the 3 barriers in the way, free with sign-in: https://t.co/Hx92Ab3WQd
#BioPharm#CARTCells#Oncology
One company’s reason to walk away is another’s opportunity.
When Big Pharma drops a drug candidate, smaller developers are often the ones who pick it up, but a second chance isn’t a guarantee.
Get the free FAQ here➡️ https://t.co/10ueVMeiKU
#BioPharm#DrugDevelopment
Drug developers are increasingly treating their suppliers as strategic partners.
Meeta Gulyani of @Ecolab on why that’s changing & where biomanufacturing is headed next.
📽️ Hear the trends shaping bioprocessing https://t.co/LPK49A0Fdr
#BioProcessing
Can AI predict which drug molecules fit platform formulations? AI-guided formulation development depends on high-quality data and stability outcomes, says @pfizer's Dr Johnson at #PharmSci360.
🎥 Learn more: https://t.co/zhua07Kbzo
#AIinDrugDevelopment#FormulationScience
In today's The BioPharm Brief: New clinical data highlight ADCs in cancer and CAR T-cell therapy for multiple sclerosis, including survival gains, modest benefit, and safety risks.
🎧 Listen: https://t.co/gbxL3cxaaF
#DrugDevelopment#CARTCellTherapy
Would your bispecific program hold up in a tech transfer tomorrow? Mispaired species and aggregation cut yield and investor confidence.
How to catch them early, with FUJIFILM Biotechnologies: https://t.co/dJVpYEtscw
Cell therapy developers are pivoting from ex vivo to in vivo CAR-T.
A 2026 review projects in vivo could cut treatment-course costs by 50% or more. Still a projection.
🔗 What in vivo still has to prove (free sign-in): https://t.co/nLSLvWPxz6
#BioPharm#CellTherapy
Can we trust agentic AI for risk assessment? Traceable evidence, transparent decisions, and verifiable outcomes are essential.
🎥 Learn more from Insilica CEO Thomas Luechtefeld ahead of @AAPSComms#PharmSci360: https://t.co/uHsLJH8dln
#AgenticAI#DrugDevelopment
How can biomarker testing improve access to targeted cancer therapies? @bmsnews’s Dr @n8pennell explains key barriers in precision oncology, from tissue collection to patient education.
🎥 Learn more: https://t.co/FA5mio208o
#PrecisionOncology#BiomarkerTesting#CancerResearch
At #ACG2026, @Odyssey_Tx is presenting a phase 2a trial design evaluating oral RIPK2 inhibitor OD-001 plus vedolizumab in moderate-to-severe UC. Topline induction results are expected in H2 2027.
👉 Read now: https://t.co/Dl2Zu2PjvQ
#UlcerativeColitis#DrugDevelopment
On today's podcast, The BioPharm Brief covers AL050 for Parkinson disease, a rare kidney disease partnership, VK2735 obesity dosing strategies, and phase 3 lymphoma data for epcoritamab + R-CHOP.
🎧 Listen now: https://t.co/q0Y9zJgIXg
#Biopharma#DrugDevelopment#ClinicalTrials
@genentech secured worldwide rights to @AlectorTx’s investigational AL050, a brain-penetrant GCase enzyme replacement therapy for Parkinson disease. The therapy targets GCase deficiency and neurodegeneration.
👉 Read more: https://t.co/UTFugwnrcZ
#Parkinsons#DrugDevelopment
Our latest podcast covers new obesity data for survodutide, expanded biosimilar capacity, an FDA review delay tied to facility remediation, and longer-term litifilimab data. 🎧 Listen to the latest episode: https://t.co/GWjgN1xbBk
#Biopharma#DrugDevelopment#ClinicalTrials
How does peptide length affect drug development and influence its regulation? Hear what LumaLex Law's Dustin Robinson has to say.
👉 Watch the full interview to learn more: https://t.co/w4FkPZujKE
#PeptideDrugs#DrugDevelopment#Biopharmaceuticals