All Drug Development articles
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NewsBioLife patents effervescent oral peptide delivery platform targeting GLP-1 therapies
BioLife has been granted a US patent for its effervescent OralMatrix oral peptide delivery platform, with preclinical data showing measurable systemic semaglutide exposure and patent claims extending across six GLP-1 medicines.
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NewsWhole-genome sequencing delivers actionable biomarkers in 73 percent of cancer patients
A large real-world study published in Nature Medicine demonstrates that whole-genome sequencing can identify actionable biomarkers in nearly three-quarters of solid cancer patients within routine clinical practice, with findings that carry significant implications for precision drug development and biomarker-driven treatment strategies.
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NewsExperimental RNA drug reverses scleroderma signs in preclinical study
An experimental synthetic non-coding RNA drug has reversed signs of systemic sclerosis in patient-derived immune cells and mouse models, with researchers now preparing an IND application to the FDA.
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ArticleWhy more ribosomes can mean less protein in mRNA therapeutics
What happens when the cellular machinery making therapeutic proteins slows down? New research in Nature shows why translation speed could matter for the design of mRNA medicines.
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NewsGLP-1 drug semaglutide extends lifespan and slows ageing in older mice
A new NIH-funded study suggests the GLP-1 receptor agonist semaglutide may slow biological ageing and extend lifespan in older mice, raising the prospect that GLP-1 drugs could one day be developed as broad longevity-enhancing interventions.
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NewsOligonucleotide CDMO market set to triple to $11.14bn by 2031
The global oligonucleotide CDMO market is projected to nearly triple in value to USD 11.14 billion by 2031, driven by rising outsourcing demand as ASO and siRNA programmes advance through clinical and commercial development stages.
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NewsEngineered tRNAs and lipid nanoparticles target nonsense mutation cystic fibrosis
A preclinical study combining chemically modified suppressor tRNAs with inhaled lipid nanoparticles has restored functional CFTR protein production across bronchial epithelial cells, mouse models and patient-derived organoids, offering a potential new therapeutic strategy for nonsense mutation-driven cystic fibrosis.
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NewsNew LOX target discovery could help overcome chemotherapy-resistant breast cancer
A preclinical study has identified lysyl oxidase as an intracellular survival factor in triple-negative breast cancer, with researchers demonstrating that sequentially blocking LOX and a compensatory ferroptosis defence pathway significantly suppresses tumour growth without chemotherapy.
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ArticleSix assay requirements every researcher using NAMs should know
As NAMs become more widely used in drug discovery, assays must meet the demands of more complex models. Discover six requirements for reliable, reproducible and biologically meaningful data.
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NewsReview challenges one-size-fits-all approach to OSCC drug delivery
A new review published in the European Journal of Pharmaceutics and Biopharmaceutics argues that no single local drug-delivery formulation will suit every oral squamous cell carcinoma tumour, urging researchers to anchor development in clinical and biological context from the outset.
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NewsFirst-in-class drug targets ‘undruggable’ MYC in blood cancers
A first-in-class experimental drug has demonstrated preclinical activity against treatment-resistant blood cancers by exploiting a newly identified vulnerability between MYC and GSPT1, offering a potential route to one of oncology’s most elusive targets.
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ArticleHow AI-driven systems biology will reset the starting line for drug development
AI is making drug discovery faster, but can it make it more successful? Discover why combining AI with systems biology could help researchers tackle the biological complexity behind drug failure.
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ArticleWhy researchers are revisiting bisantrene decades after it was abandoned
An oncology drug abandoned decades ago is getting a second look, with new research uncovering a mechanism that could offer an alternative route to targeting MYC, one of cancer’s toughest targets.
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NewsNUS researchers identify molecular switch driving TNBC treatment resistance
Researchers at the National University of Singapore have identified DP103 as a potential molecular master switch sustaining tumour growth, cancer stem cells and treatment resistance in triple-negative breast cancer, with findings suggesting it could serve as a predictive biomarker for the investigational oral therapy RX-5902.
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NewsFirst multi-responsive foldamer-based gel offers new approach to controlled drug delivery
Researchers at the University of Birmingham have engineered a switchable gel built from synthetic foldamer molecules that responds to light, heat and acid — a platform with potential implications for controlled drug delivery and targeted therapeutic release.
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ArticleTargeting childhood myopia progression with 7-methylxanthine
Childhood myopia researcher Dr Klaus Trier explores how 7-methylxanthine targets scleral remodelling and axial elongation, and its potential to slow disease progression and reduce the risk of high myopia.
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NewsTissue chips target immunotherapy toxicity prediction without animal models
Researchers at the University of Rochester have developed human cell-based tissue chips designed to predict serious immunotherapy toxicities, including cytokine release syndrome, and have secured entry into the FDA’s ISTAND pilot programme.
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ArticleReducing drug development failures with human-relevant models and AI
Professor Joseph C. Wu of Stanford University explains how stem cells, human-relevant models and AI are helping researchers predict which drug candidates are most likely to succeed before clinical trials.
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NewsInsilico Medicine nominates AI-designed candidate for ocular diseases
Insilico Medicine has nominated ISM9077, an AI-designed small molecule targeting pathological inflammation, as its 32nd preclinical candidate since 2021, with potential applications across dry AMD, uveitis and dry eye disease.
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NewsWhat Google’s AI talent exodus could mean for future drug discovery
The departure of leading AI researchers from Google to found Discovery Loop raises important questions about the future direction of artificial intelligence in scientific research and drug development.