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BioWorld - Saturday, April 11, 2026
Home » Topics » Regulatory » Patents

Patents
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Skin, tissue layer illustration
Dermatologic

Forendo Pharma Oy synthesizes new AKR1C3 and/or prostaglandin F2-alpha synthase inhibitors

Nov. 28, 2022
Forendo Pharma Oy has presented aldo-keto reductase family 1 member C3 (AKR1C3) and/or prostaglandin F2-α synthase inhibitors reported to be useful for the treatment of acne, cancer, alopecia, obesity, chronic obstructive pulmonary disease, dysmenorrhea, endometriosis and polycystic ovary syndrome, among others.
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Cancer

Chengdu Easton Biopharmaceuticals discovers new BRD4-targeting PROTACs

Nov. 25, 2022
Chengdu Easton Biopharmaceuticals Co. Ltd. has described proteolysis targeting chimera (PROTAC) compounds comprising a cereblon (CRBN) ligand binding moiety covalently bound to a bromodomain-containing protein 4 (BRD4; HUNK1)-targeting moiety through a linker.
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Endocrine/Metabolic

Genescience presents new GHSR agonists for growth hormone deficiency

Nov. 25, 2022
Genescience Pharmaceuticals Co. Ltd. has divulged indoline-containing spiro derivatives acting as growth hormone secretagogue receptor (GHSR) agonists reported to be useful for the treatment of growth hormone deficiency.
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Cancer

Bionova Pharmaceuticals describes new BTK inhibitors

Nov. 25, 2022
Bionova Pharmaceuticals Ltd. has identified heteroaromatic carboxamide compounds acting as Bruton tyrosine kinase (BTK) and BTK (C481S mutant) inhibitors reported to be useful for the treatment of asthma, cancer, graft-vs.-host disease, inflammatory bowel disease, psoriasis, thrombotic thrombocytopenic purpura, rheumatoid arthritis and autoimmune thyroiditis, among others.
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Cancer

Beigene divulges new EGFR mutant-targeting PROTACs for cancer

Nov. 25, 2022
Beigene Co. Ltd. has synthesized proteolysis targeting chimera (PROTAC) compounds comprising a cereblon (CRBN) E3 ubiquitin ligase-binding moiety covalently linked to an EGFR (mutant)-targeting moiety via linker.
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Cancer

Chinese researchers patent new GTPase KRAS (G12D mutant) inhibitors for cancer

Nov. 25, 2022
Zhejiang Hisun Pharmaceutical Co. Ltd. and Shanghai Aryl Pharmtech Co. Ltd. have identified heterocyclic derivatives acting as GTPase KRAS (G12D mutant) inhibitors reported to be useful for the treatment of cancer.
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Cancer

Constellation Pharmaceuticals discovers new TREX1 inhibitors for cancer

Nov. 24, 2022
Constellation Pharmaceuticals Inc. has described three-prime repair exonuclease 1 (TREX1) inhibitors reported to be useful for the treatment of cancer.
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Musculoskeletal

Janssen Pharmaceutica presents new NLRP3 inflammasome inhibitors

Nov. 24, 2022
Janssen Pharmaceutica NV has divulged NLRP3 inflammasome inhibitors reported to be useful for the treatment of osteoarthritis, cancer, nonalcoholic steatohepatitis (NASH), skin lesion, sarcoidosis, as well as cardiovascular, metabolic and Alzheimer's diseases, among others.
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Immune

Ocean University of China describes new PDE4 and/or PDE10A inhibitors for allergy

Nov. 24, 2022
Ocean University of China has identified novel benzotropone derivatives acting as phosphodiesterase 4 (PDE4) and/or cAMP and cAMP-inhibited cGMP 3ʹ,5ʹ-cyclic phosphodiesterase 10A (PDE10A) inhibitors reported to be useful for the treatment of allergy, inflammatory, neurological and cardiovascular diseases.
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Immuno-oncology

Chinese researchers divulge new ADCs targeting nectin-4 for cancer

Nov. 24, 2022
Jiangsu Mabwell Health Pharmaceutical R&D Co. Ltd. and Mabwell (Shanghai) Bioscience Co. Ltd. have synthesized antibody-drug conjugates (ADCs) consisting of antibodies targeting nectin-4 covalently linked to cytotoxic drugs through a linker reported to be useful for treatment of cancer.
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