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SYNBIO.INTEL
DNAGinkgo+PlatformTWSTTwist+SynthesisABSIAbsci+AIDesignCRSPCRISPR Therapeutics+EditBEAMBeam+BaseEditNTLAIntellia+InVivoCRBUCaribou+CellTherapyRXRXRecursion+AIILMNIllumina+SeqEDITEditas+GeneFUND.YTD2025$17.3B.Raised

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Real-time intelligence on synbio and synbio funding, regulatory milestones, deployments, and policy.

Jun 26, 2026RESEARCH

MUC16 CAR-T Cuts Bladder Tumor Growth via Catheter

MUC16-targeting CAR T cells delivered via catheter controlled bladder tumors in mice, opening a local delivery route for solid tumor CAR-T.

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Jun 23, 2026BREAKING

Serapha Raises $230M Around China Gene-Editing Asset

Serapha closes $230M debut round built around a Chinese-originated gene-editing candidate, one of 2026's largest synbio therapy raises.

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Jun 8, 2026DEEP DIVE

AI Designs Caffeine-Based Molecular Switch for Cell Control

Researchers use AI to engineer caffeine as a reversible off-switch for gene circuits and CAR-T cells

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Jun 5, 2026RESEARCH

TRIM Platform Stacks 3+ Crop Traits via Twin Prime Editing

New genome engineering platform combines prime editing with knockouts for efficient multi-trait crop development

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Jun 4, 2026RESEARCH

D&D-seq Maps DNA-Protein Contacts at Single-Cell Resolution

New method uses base editor-nanobody fusions to record DNA-protein interactions in individual cells

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Jun 4, 2026BREAKING

NTLA Surges 35% on Phase 3 Gene Editing Readout Anticipation

NTLA jumps 35% overnight as investors position ahead of first Phase 3 CRISPR therapy data expected this quarter

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Jun 3, 2026BREAKING

Lilly Licenses Ascidian Gene Editing Tech for Kidney Disease

Eli Lilly secures exclusive licensing deal with Ascidian for gene editing platform targeting kidney diseases

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Jun 3, 2026BREAKING

Lundbeck Partners with Cradle for AI Protein Design Platform

Danish pharma giant Lundbeck teams with AI protein design startup Cradle to accelerate drug discovery programs

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May 28, 2026BREAKING

YolTech Raises $70M Series B for CRISPR Therapies in China

Chinese gene editing startup secures major funding to advance CRISPR therapeutic pipeline

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May 28, 2026RESEARCH

PRINCE System Enables Reversible Gene Editing with Small Molecules

New CRISPR system allows researchers to turn gene editing on and off with small molecules

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May 21, 2026BREAKING

Off-Shelf Gene Editing Shows 85% Efficacy in Sickle Cell Primates

Primate study demonstrates 85% editing efficiency using allogeneic approach, potentially eliminating patient-specific manufacturing

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May 21, 2026MARKET

Precision BioSciences Misses Q1 Earnings Amid Gene Editing Volatility

DTIL platform company reports revenue shortfall as gene editing sector faces investor skepticism

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May 20, 2026RESEARCH

RNA Motifs Boost Prime Editing Efficiency 4x in New Study

Engineered RNA-stabilizing motifs quadruple prime editing success rates through directed evolution approach

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May 20, 2026MARKET

In Vivo Gene Editing Market Hits $37.75B by 2032

In vivo gene editing market projected to reach $37.75 billion by 2032, driven by CRISPR advances and clinical successes

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May 19, 2026BREAKING

Precision BioSciences ECUR-506 Trial Data Sparks Investor Interest

Precision BioSciences gains attention following new ECUR-506 trial data, highlighting ARCUS platform capabilities in allogeneic CAR-T

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May 14, 2026RESEARCH

MD Anderson CAR-T Therapy Enters Phase I for Solid Tumors

UT MD Anderson's novel CAR-T approach targets solid tumor challenges with enhanced persistence and trafficking capabilities.

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May 14, 2026BREAKING

Editas EDIT-401 Achieves 90% LDL-C Reduction in 6-Month NHP Study

Single-dose base editor achieves sustained cholesterol reduction in non-human primates with 6-month durability data

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May 14, 2026BREAKING

Melazyme Raises $2M for Melanin and Sweet Proteins

Perfect Day alumni launch Melazyme with $2M seed round targeting melanin biosynthesis and alternative sweetener production

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May 13, 2026RESEARCH

Pichia Pastoris Cell-Free System Cuts Protein Production Costs

New yeast-based cell-free expression system promises significant cost reductions for therapeutic protein manufacturing

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May 13, 2026BREAKING

Gene Editing Extends Epilepsy Mouse Survival by 400%

CRISPR correction of SCN1A mutations dramatically improves survival in Dravet syndrome mouse model

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