This website is intended for healthcare professionals only

Trending Topic

Female breast anatomy glowing orange, 3d Medical illustration, women's health
12 mins

Trending Topic

Developed by Touch
Mark CompleteCompleted
BookmarkBookmarked
Aqsa Jawaid Siddiqui, Aamir Sikandar Kazi, Ghina Shamim Shamsi

Tuberculous mastitis (TM) is a rare chronic granulomatous disease predominantly caused by Mycobacterium tuberculosis.1 TM accounts for less than 0.1% of all breast diseases worldwide, whereas it is more common in endemic regions (3–4.5%).2,3 TM is more prevalent in the reproductive age group, especially during the lactation period, when patients are more susceptible since the […]

Michael Ison, IDWeek 2022: Respiratory syncytial virus (RSV) prefusion F protein candidate vaccine RSVPreF3 OA – Ongoing phase 3 study results

4 mins
Share
Facebook
X (formerly Twitter)
LinkedIn
Via Email
Mark CompleteCompleted
BookmarkBookmarked
Copy LinkLink Copied
Published Online: Nov 4th 2022

Respiratory syncytial virus (RSV) presents a significant disease burden in older adults, with no approved vaccines to protect against RSV. In this touchINFECTIOUS DISEASES interview, we met with Prof. Michael Ison (Northwestern University Feinberg School of Medicine, Chicago, IL, USA) to discuss the findings from an ongoing phase 3 study investigating vaccine efficacy of the AS01E-adjuvanted prefusion F protein candidate vaccine, RSVPreF3 OA,  in adults ≥ 60 years of age (NCT04886596).

The abstract entitled: ‘Respiratory Syncytial Virus (RSV) Prefusion F Protein Candidate Vaccine (RSVPreF3 OA) is Efficacious in Adults ≥ 60 Years of Age‘ (Abstract #LB745)’ was presented at IDWeek 2022, 19-23 October 2022.

Interviews available in this series:

Respiratory syncytial virus (RSV) – Health burden and current vaccine candidates

Highlights from IDWeek 2022

Questions: Michael Ison receives grant/research support from GSK.

  1. Could you tell us a little about the prefusion F protein candidate vaccine (RSVPreF3 OA)? (0:14)
  2. What were the methodology and eligibility criteria of your study evaluating RSVOreF3 OA? (0:56)
  3. What were the efficacy and safety findings of the study? (1:46)
  4. What will be the next steps in the clinical development of RSVOreF3 OA? (2:57)

Disclosures: Michael Ison receives grant/research support from GSK.

Support: Interview and filming supported by Touch Medical Media. Interview conducted by Katey Gabrysch.

Filmed as a highlight of IDWeek 2022

Share
Facebook
X (formerly Twitter)
LinkedIn
Via Email
Mark CompleteCompleted
BookmarkBookmarked
Copy LinkLink Copied
Close Popup