John Parkinson

The agency licensed the new indication for Sanofi’s Adacel (Tetanus Toxoid, Reduced Diphtheria Toxoid and Acellular Pertussis Vaccine, Adsorbed [Tdap]) shot for immunization during the third trimester of pregnancy.

Research will focus on new technologies for early diagnosis of severe illnesses resulting from SARS-CoV-2 infection.

The company is moving forward with vaccines to address respiratory and latent viruses as well as oncology.

The investigational antiviral showed the potential of another therapy that could benefit this patient population that is at risk for hospitalization and death.

Newer diagnostic technologies can play a role in identifying specific bacterium, decrease the time to optimal therapy, and offer the possibility of better outcomes.

Central Ohio has seen 82 pediatric cases since November, and more than a third of children infected have been hospitalized.

Developed by Sanofi and AstraZeneca, the single-dose long-acting antibody was designed to help protect all infants from birth through their first respiratory syncytial virus (RSV) season.

A new Infectious Diseases Society of America (IDSA) board member and vice president offers some insights on the leadership’s goals and direction for 2023.

The company’s vaccine candidate, MenABCWY, which is indicated for adolescents was given a Prescription Drug User Fee Act (PDUFA) goal date for later this year.

One clinician offers some insights on the RSV surge witnessed last year and the prospective benefits of having a maternal vaccine to protect newborns from this virus.

A look back on some of the significant discussions with clinicians, researchers, and infectious disease stakeholders.

The new recommendation from the organization believes it will help avoid delays in patient care.

Virax Biolabs has developed a T-cell testing platform to develop an immune risk profile against viral threats.

This therapy is the first of a new class of antiretrovirals, and it is indicated for people with multi-drug resistance, intolerance, or safety considerations.

Roche’s Actemra is the first FDA approved monoclonal antibody to be used for COVID-19.

The committee will meet on January 26 to discuss whether and how the composition for primary doses of the currently available COVID-19 vaccines should be modified.

In a new CDC report, these immunizations aid against emergency department and urgent care encounters in immunocompetent adults.

The New Drug Application (NDA) for the company’s investigational therapy, Olorofim, looks to serve an unmet medical need in this treatment space.

The Centers for Disease Control and Prevention (CDC) is looking into the possibility of this rare group of infections emerging.

A new CDC report highlights another health-related area where interruptions occurred due to the pandemic, but data suggests both improved rapidly.

TP-05, a novel, oral therapeutic recently reported topline results from its phase 1 study.

A large health system saw a reduction of 40% and 70% respectively when the antiviral was prescribed.

A single-dose of acoziborole could simplify the treatment of this fatal infection.

A new report looked at mortality over a 2 ½ year period, and the epidemiology of who was most affected.

Postural orthostatic tachycardia syndrome (POTS) is happening in people post-virus as well as within a 90-day period post-vaccination.

The Wistar Institute’s research on DNA-encoded SARs-CoV-2 monoclonal antibodies (DMAbs) allowed it to advance to clinical trials. One researcher explains how it differs from the mRNA platform.

With an already overwhelming respiratory virus season with RSV and influenza, the hope is to prevent COVID-19 with these vaccines available to younger pediatric populations.

A clinician offers insight into what he sees in terms of these therapies and the need to get more information to those providers in the field as well as access to them.

With the proliferation of therapies for skin and soft tissue infections (SSTIs), a clinician discusses how providers can appropriately find the balance between these novel therapies, the existing treatment guidelines, and stewardship.

A clinician has a novel approach to patient conversations around this topic to determine if they want to assess if their penicillin allergies truly present a problem for treatment.