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BioWorld - Tuesday, March 10, 2026
Home » Sanofi SA

Articles Tagged with ''Sanofi SA''

Cancer

Sanofi divulges new SERDs

March 20, 2024
Sanofi SA has synthesized compounds acting as selective estrogen receptor degradation inducers (SERDs) reported to be useful for the treatment of cancer, endometriosis, osteoporosis, benign prostatic hyperplasia and inflammatory disorders.
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Immuno-oncology

Sanofi’s trispecific MAb outperfoms conventional T-cell-engaging bispecific antibodies

March 1, 2024
T-cell-engaging antibodies (TCEs) are synthetic molecules that redirect T cells to bind to the antigens on the surface of cancer cells to promote tumor elimination. In the case of multiple myeloma (MM), the approvals of anti-CD38 monoclonal antibodies (MAbs), chimeric antigen receptor T-cell therapies (CAR T) targeting B-cell maturation antigen (BCMA) or, more recently, bispecific TCEs represent great advances, but some patients still relapse after treatment.
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FDA Approved stamp

Takeda quickly follows Sanofi-Regeneron with esophagitis approval

Feb. 20, 2024
By Lee Landenberger
Less than a month after the U.S. FDA approved Sanofi SA and Regeneron Pharmaceuticals Inc.’s bestseller Dupixent (dupilumab) for treating eosinophilic esophagitis in children ages 1 to 11, the agency has approved Takeda Pharmaceutical Co. Ltd.’s Eohilia (budesonide oral suspension) for the same indication but for an older group.
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Cancer

Sanofi discloses MAPK7 inhibitors for cancer

Feb. 19, 2024
A Sanofi SA patent describes imidazopyridine compounds acting as mitogen-activated protein kinase 7 (MAPK7; ERK5) inhibitors and reported to be useful for the treatment of cancer.
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Another ALS defeat as Denali, Sanofi disclose phase II miss

Feb. 16, 2024
By Jennifer Boggs
Getting a drug successfully through clinical development in amyotrophic lateral sclerosis (ALS) continues to be an elusive task, with Denali Therapeutics Inc. and partner Sanofi SA reporting the latest failure in the progressive neurodegenerative disease.
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FDA Approved stamp

Takeda quickly follows Sanofi-Regeneron with esophagitis approval

Feb. 12, 2024
By Lee Landenberger
Less than a month after the U.S. FDA approved Sanofi SA and Regeneron Pharmaceuticals Inc.’s bestseller Dupixent (dupilumab) for treating eosinophilic esophagitis in children ages 1 to 11, the agency has approved Takeda Pharmaceutical Co. Ltd.’s Eohilia (budesonide oral suspension) for the same indication but for an older group.
Read More
Dollar sign dropper and test tube
Immune

Sanofi invests in Graviton Bioscience with eye on ROCK2 inhibitors

Feb. 2, 2024
Graviton Bioscience Corp. has announced a strategic investment from Sanofi SA. Under the agreement, Sanofi receives a right of first negotiation to license compounds across various indications, including immunological and metabolic syndrome indications.
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Gastrointestinal

Sanofi divulges new IL-23 receptor antagonists

Jan. 30, 2024
Sanofi SA has synthesized cyclic peptides acting as IL-23 receptor (IL-23R) antagonists reported to be useful for the treatment of psoriasis, Crohn’s disease, ulcerative colitis, psoriatic arthritis and hidradenitis suppurativa.
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Inflammatory

Synthekine and Sanofi collaborate on IL-10 receptor agonists for inflammatory diseases

Jan. 30, 2024
Synthekine Inc. has established a worldwide collaboration with Sanofi SA to develop and commercialize IL-10 receptor agonists for the treatment of inflammatory diseases.
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Dupixent

US FDA clears Dupixent for children with eosinophilic esophagitis

Jan. 26, 2024
By Karen Carey
Becoming the first treatment for children ages 1 to 11 with eosinophilic esophagitis (EE), Sanofi SA and Regeneron Pharmaceuticals Inc.’s IL-4/IL-13 inhibitor Dupixent (dupilumab) was cleared by the U.S. FDA on Jan. 25.
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