Resumen de: WO2026006524A2
The present invention provides, in part, cationic lipid compounds of Formulae (I), (II), (III), (IV), (V), or (VI) or a pharmaceutically acceptable salt thereof. The compounds provided herein can be useful for delivery and expression of mRNA and encoded protein, e.g., as a component of liposomal delivery vehicle, and accordingly can be useful for treating various diseases, disorders and conditions, such as those associated with deficiency of one or more proteins.
Resumen de: WO2026003770A1
A formulation for nutraceutical and/or pharmaceutical use based on protein nanoparticles is described, including a bioactive compound chosen from hydroxytyrosol, tyrosol, olive phenolic compounds, and mixtures thereof, and a zein protein matrix stabilized with sodium deoxycholate.
Resumen de: WO2026005944A1
A compound having the structure (I) is provided. The compound is useful as a therapeutic agent in the form of a lipoplex, or in a form of a polyplex, in a form of a lipid nanoparticle, or in a form of a liposome, or in a form of a micelle, or in a form of an emulsion including a drug, vaccine, oligonucleotide, antibody, enzyme, protein, small molecule, or nucleotide.
Resumen de: WO2026006617A1
The present invention relates to lyophilized and frozen pharmaceutical formulations comprising a nucleic acid (NA)-lipid nanoparticle (LNP) particle, wherein the NA-LNP particle comprises a nucleic acid encapsulated in the lipid nanoparticle, wherein the formulation further comprises an excipient comprising a lyoprotectant or cryoprotectant and a buffer, and wherein the lyoprotectant or cryoprotectant is a polyvinylpyrrolidone (PVP) or a polyethylene glycol (PEG). Methods of making the lyophilized and frozen formulations are also provided.
Resumen de: WO2026002313A1
A system and method are disclosed for the production of drug delivery vesicles formed from hydroxyapatite (Ca10(PO4)6(OH)2), called apasomes, using a microfluidic device. The device comprises a first inlet with a bifurcated tube and a second inlet with an inlet tube. Hydroxyapatite nanoparticles and, optionally, therapeutic agents suspended in a second fluid are introduced into the device via the second inlet, while a miscible first fluid is introduced via the first inlet. The two fluids are combined at a mixing point within the device and the combination fluid travels through an elongate tube before exiting the device. Shear forces cause self-assembly of vesicles, the size of which can be modified by adjusting the flow rates, the shapes and dimensions of the tube, and the composition of the fluids. The method may also include refluxing, filtration and drying steps to enable scalable production of customizable drug delivery vesicles for therapeutic applications.
Resumen de: WO2026003403A1
It is provided a novel lipid of formula (I) or a pharmaceutically acceptable salt thereof, or a stereoisomer of any one of them, and a nanoparticle comprising the ionizable lipid, particularly as encapsulating agent, optionally comprising a molecule or a pharmaceutically active inside. It is also provided a lipid nanoparticle or a pharmaceutical composition comprising thereof for use in medicine, and the use of the lipid nanoparticles as encapsulating agents. Formula (I)
Resumen de: WO2026003373A1
The present invention provides lipids of Formula (I) to (IX) or subformulae thereof, or pharmaceutically acceptable salts thereof. Said lipids can be useful for the delivery and expression of mRNA and encoded protein, e.g. as a component of liposomal delivery vehicles, and accordingly can be useful for treating various diseases, disorders, and conditions, such as those associated with deficiency of one or more proteins. Compositions comprising lipid compounds of Formulae (I) to (X) and subformulae thereof, and mRNA encoding a peptide or protein may be administered to subjects in need thereof intranasally.
Resumen de: WO2026002534A1
The present invention refers to the use of novel polyoxyalkylene based block copolymers in particles or in medical devices, wherein the particles comprise at least one novel polyoxyalkylene based block copolymer and preferably at least one active agent.
Resumen de: WO2026003582A2
The disclosure provides for lipids that may be formulated in a delivery vehicle to facilitate the encapsulation of a wide range of single or multiple payloads including therapeutic, theragnostic, preventive, prophylactic, pre-emptive, and diagnostic agents, such as, without limitation, nucleic acids (e.g., RNA or DNA), proteins, peptides, and small molecule active pharmaceutical ingredients (APIs). Methods of delivering and/or producing a polypeptide of interest in a cell are also provided.
Nº publicación: WO2026005041A1 02/01/2026
Solicitante:
RADIONANO THERAPEUTICS INC [JP]
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Resumen de: WO2026005041A1
The present invention provides a neutron capture therapy agent with a superior therapeutic effect. The present invention provides modified boron carbide nanoparticle powder with a suitable particle diameter for polyglycerol-functionalized boron carbide, capable of producing a boron neutron capture therapy (BNCT) agent that exhibits high accumulation efficiency in tumors and excellent therapeutic efficacy, with the surface of the boron carbide nanoparticles not coated with graphite.