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BioWorld - Saturday, March 28, 2026
Home » Topics » Science » Drug design, drug delivery and technologies

Drug design, drug delivery and technologies
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Non-Hodgkin lymphoma cells in the blood flow

Enzyme degrader could avoid drug resistance in B-cell cancers

Feb. 9, 2024
By Mar de Miguel
Bruton tyrosine kinase (BTK) enzyme inhibitors used to treat B-cell cancers, including chronic lymphocytic leukemia and non-Hodgkin lymphoma, also produce resistance by causing mutations in the protein. Now, a study on the BTK degrader NX-2127 showed the compound could be effective in eliminating BTK regardless of its mutations.
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Excitatory synapse, glutamate binds to the NMDA receptor. Calcium ions (yellow) are transported through the postsynaptic membrane.
Neurology/Psychiatric

Interaction inhibitor blocks toxic effect of glutamate in ALS

Feb. 9, 2024
By Mar de Miguel
The discovery of a complex formed by two types of ion channels in neurons has allowed researchers from Heidelberg University to develop an inhibitor that stopped motor neuron degeneration in amyotrophic lateral sclerosis (ALS) in mouse models and human brain organoids.
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Non-Hodgkin lymphoma cells in the blood flow
Cancer

Enzyme degrader could avoid drug resistance in B-cell cancers

Feb. 8, 2024
By Mar de Miguel
Bruton tyrosine kinase (BTK) enzyme inhibitors used to treat B-cell cancers, including chronic lymphocytic leukemia (CLL) and non-Hodgkin lymphoma, also produce resistance by causing mutations in the protein. Now, a study on the BTK degrader NX-2127 showed the compound could be effective in eliminating BTK regardless of its mutations.
Read More
Spyglass intraocular drug delivery
Patents

Spyglass strengthens IP for intraocular drug delivery platform

Feb. 7, 2024
By Simon Kerton
Spyglass Ophthalmics Inc. is seeking patent protection for intraocular drug delivery devices and methods of delivering therapeutic agents to the eye. The methods include implanting an intraocular implant into the eye and adjacent to a fluid-permeable membrane of the patient’s eye.
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Concept art for adeno-associated viral-based gene therapy.
Drug Design, Drug Delivery & Technologies

New regulatory playbook to guide AAV gene therapy development for rare diseases

Feb. 7, 2024
The Foundation for the National Institutes of Health (FNIH) has announced the online publication of the first playbook designed to help accelerate the development of adeno-associated virus (AAV) gene therapies for rare diseases.
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Lab mouse
Drug Design, Drug Delivery & Technologies

Consortium to research alternatives to animal testing

Feb. 2, 2024
The European Chemicals Agency (ECHA) has contracted a consortium to conduct scientific studies on the reliability and relevance of new approach methodologies (NAMs) as alternatives to animal testing and to promote the use of such methods in the future.
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Drug Design, Drug Delivery & Technologies

Invitae partners with Bridgebio to advance genetics-based drug discovery for rare diseases

Jan. 31, 2024
Invitae Corp. has entered into a partnership with Bridgebio Pharma Inc. to advance genetics-based drug discovery for rare diseases. The goal of the collaboration is to generate new insights focused on genetic modifiers and the discovery of novel therapeutic targets for rare diseases and other unmet medical needs.
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Senescent cells (blue)
Drug Design, Drug Delivery & Technologies

CAR T cells could slow aging by eliminating senescent cells

Jan. 31, 2024
By Mar de Miguel
CAR T cells could be repurposed to target senescent cells and delay the effect of aging. A study by scientists at Cold Spring Harbor Laboratory showed how to design them and demonstrated the advantages of this therapy in mice. “We only gave one dose, and we could have benefits [for] really long periods of time,” lead author Corina Amor told BioWorld.
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Accumulation of nanorobots in a bladder tumor by microscopy.
Drug Design, Drug Delivery & Technologies

Self-propelled nanobots can deliver drugs to bladder, other tumors

Jan. 29, 2024
By Coia Dulsat
Researchers from the Institute for Bioengineering of Catalonia (IBEC) and collaborators have successfully treated bladder tumors in mice using urease-powered nanobots. The testing consisted of the administration of 18F-nanorobots to tumor-bearing mice divided into four groups depending on tumor volumes using a group of non-tumor-bearing mice as control. Importantly, the therapy remained in the bladder with only a very small proportion of radioactivity seen in other organs. The results were published in Nature Nanotechnology on Jan. 15, 2024.
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Drug Design, Drug Delivery & Technologies

Genedit and Genentech collaborate on nanoparticle delivery for nucleic acid-based medicines

Jan. 26, 2024
Genedit Inc. has entered into a multiyear collaboration and license agreement with Genentech Inc., a member of the Roche Group, to use Genedit's Nanogalaxy platform to discover and develop novel hydrophilic nanoparticles to deliver Genentech's nucleic acid-based medicines for treatment of autoimmune disease.
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