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BioWorld - Sunday, July 12, 2026
Home » Topics » Disease categories and therapies » Infection

Infection
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Creative rendition of SARS-CoV-2 virus particles.
Infection

Recce-327 significantly reduces SARS-CoV-2 levels in hamsters

Oct. 19, 2022
Recce-327 (R-327) demonstrated significantly...
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Infection

Needle-free, spirulina-based malaria vaccine candidate shows efficacy in vivo

Oct. 19, 2022
Antibodies against PfCSP can block...
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Vials of monkeypox vaccine
Infection

Emergex synthesizes CD8+ T-cell adaptive vaccine for smallpox and monkeypox

Oct. 19, 2022
Emergex Vaccines Holding Ltd. has formulated...
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Coronavirus and antibodies
Drug Design, Drug Delivery & Technologies

Researchers develop DMAb platform for improved delivery of SARS-CoV-2 antibody-based therapeutics

Oct. 17, 2022
Anti-SARS-CoV-2 monoclonal antibody (MAb) pair COV2-2196 (tixagevimab, class I) and COV2-2130 (cilgavimab, class III) are human neutralizing Abs (nAbs) that target nonredundant, complementary epitopes within the receptor binding domain of SARS-CoV-2 spike protein (S-RBD).
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Creative rendition of SARS-CoV-2 virus particles.
Infection

Nanoviricides completes IND-enabling work for NV-CoV-2

Oct. 17, 2022
Nanoviricides Inc. has completed its IND-enabling preclinical drug development tasks pertaining to NV-CoV-2 for the treatment of SARS-CoV-2 infection and is working to prepare an IND application to submit to the FDA.
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Elderly person receiving shot

GSK posts strong results for RSV shot, as Pfizer prepares to file rival shot

Oct. 13, 2022
By Richard Staines
GSK plc has announced results from its respiratory syncytial virus (RSV) vaccine in older people that look stronger than those from its rival, Pfizer Inc., as the race to develop a first ever vaccine against the common respiratory disease heats up.
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‘SOFA’ so good: Inotrem’s nangibotide improves organ function in phase IIb septic shock study

Oct. 13, 2022
By Cormac Sheridan
A phase IIb trial of nangibotide in septic shock has demonstrated preliminary signs of efficacy in a subset of biomarker-defined patients and provided its developer, Inotrem SA, with a dataset that will inform the design of a registration program for the drug. Subject to agreement from regulatory agencies, the company aims to move the triggering receptor on myeloid cells 1 inhibitor into a first phase III trial in early 2024. “We should have a clearer picture by the beginning of the second next year,” CEO Sven Zimmermann told BioWorld.
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CSL’s Seqirus snags $30M contract with BARDA to develop pandemic avian flu vaccines

Oct. 11, 2022
By Tamra Sami
CSL Ltd. subsidiary Seqirus inked a $30.1 million deal with the U.S. Biomedical Advanced Research and Development Authority (BARDA) to develop and evaluate two influenza A subtype H2Nx (avian flu) vaccines in a phase I trial.
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CSL’s Seqirus snags $30M contract with BARDA to develop pandemic avian flu vaccines

Oct. 10, 2022
By Tamra Sami
CSL Ltd. subsidiary Seqirus inked a $30.1 million deal with the U.S. Biomedical Advanced Research and Development Authority (BARDA) to develop and evaluate two influenza A subtype H2Nx (avian flu) vaccines in a phase I trial.
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Influenza virus
Immune

A universal influenza vaccine candidate provides broad protection in young and aged mice

Oct. 10, 2022
Finding a vaccine that provides universal protection against seasonal influenza remains a public health priority. Although influenza neuraminidase (NA) undergoes slower antigenic changes than hemagglutinin (HA) and therefore constitutes a desirable vaccine target, NA standalone vaccination strategies present a limited breadth of NA immunity.
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