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BioWorld - Tuesday, July 14, 2026
Home » Topics » Disease categories and therapies » Infection

Infection
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TechnoPhage identifies therapeutic antibody for COVID-19

Oct. 18, 2021

VX-01, a humanized antibody with protective effects against murine mucormycosis

Oct. 18, 2021

Roche discloses new compounds for E. coli infections

Oct. 18, 2021

NLS reports preclinical data on NLS-4 for long COVID

Oct. 15, 2021

Medshine Discovery discovers HBV cccDNA formation inhibitors

Oct. 15, 2021
Bacteria in petri dishes

Potent selective pan-serotype dengue inhibitor developed

Oct. 13, 2021
By John Fox
Blocking the interaction between two dengue virus (DENV) nonstructural proteins, NS3 and NS4B, with a newly developed small-molecule inhibitor resulted in potent antiviral activity in mouse models, according to an international collaborative study led by scientists at the University of Leuven (KU Leuven), CD3 the Centre for Drug Design and Discovery in Leuven, and Janssen Pharmaceutica in Beerse, Belgium.
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Preclinical data support use of ibrexafungerp to treat mucormycosis

Oct. 13, 2021

NV-CoV-2 effective against SARS-CoV-2 in standard cell culture pseudovirion assay

Oct. 13, 2021

Potent selective pan-serotype dengue inhibitor developed

Oct. 13, 2021
FDA sign

Maribavir gets adcom approval, but Takeda’s work just beginning

Oct. 12, 2021
By Mari Serebrov
If the FDA follows the advice of its Antimicrobial Drugs Advisory Committee, Takeda Pharmaceutical Co. Ltd.’s antiviral drug, maribavir, will become the first drug approved in the U.S. to treat resistant or refractory cytomegalovirus infection and disease in both solid organ and hematopoietic stem cell transplant recipients. The committee voted 17-0 that the overall benefit-risk assessment favors the use of maribavir for transplant patients with refractory CMV infections both with and without genotypic resistance to the four antivirals currently used off-label to treat the infections – ganciclovir, valganciclovir, foscarnet and cidofovir.
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