Phase 3 trial to evaluate the safety, tolerability, and immunogenicity of V114, a 15-valent pneumococcal conjugate vaccine, followed by 23-valent pneumococcal polysaccharide vaccine 6 months later, in at-risk adults 18–49 years of age (PNEU-DAY): A subgroup analysis by baseline risk factors

Author:

Hammitt Laura L.1,Quinn Dean2,Janczewska Ewa3,Pasquel Francisco J.4,Tytus Richard5,Reddy K. Rajender6,Abarca Katia7,Khaertynova Ilsiyar M.8,Dagan Ron9,Dawson Rachel10,McCauley Jennifer10,Shekar Tulin10,Fu Wei10,Pedley Alison10,Sterling Tina10,Tamms Gretchen10,Musey Luwy10,Buchwald Ulrike K.10

Affiliation:

1. International Health, Johns Hopkins Bloomberg School of Public Health, Baltimore, MD, USA

2. P3 Research, Wellington Clinical Trial Research Unit, Wellington, New Zealand

3. The School of Health Sciences in Bytom, Medical University of Silesia, Bytom, Poland

4. Division of Endocrinology, Metabolism, and Lipids, Department of Medicine, Emory University School of Medicine, Atlanta, GA, USA

5. Family Medicine, McMaster University, Ontario, Canada

6. Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA

7. Escuela de Medicina, Pontificia Universidad Catolica de Chile, Santiago, Chile

8. Department of Infectious Diseases, Kazan State Medical Academy, Kazan, Russia

9. The Shraga Segal Department of Microbiology, Immunology and Genetics, Faculty of Health Sciences of the Ben-Gurion University of the Negev, Beer-Sheva, Israel

10. Merck & Co., Inc., Rahway, NJ, USA

Funder

Merck Sharp & Dohme LLC, a subsidiary of Merck & Co., Inc., Rahway, NJ, USA

Publisher

Informa UK Limited

Subject

Pharmacology,Immunology,Immunology and Allergy

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