AFX3772
Phase 2- Indications
- Pneumococcal disease, Pneumonia, Meningitis, Sepsis
Company intelligence / Profile preview
In adult Phase I/II clinical trials, their lead vaccine candidate AFX3772 was well tolerated and demonstrated good immune responses compared to the current standard of care. The FDA granted Breakthrough Therapy designation for AFX3772 in July 2021 to prevent S. pneumoniae invasive disease and pneumonia in adults 50 years and above. Phase III preparations were underway as of 2022, and Phase II clinical trials for pediatric use started in June 2022[1][4].
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