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Pfizer Documents (PHMPT/FDA)

Pfizer Bla Submission

Pfizer 16 Plus Documents

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Pfizer Global Regulatory Affairs
Pfizer Inc.
400 Arcola Road Collegeville, PA 19426
Global Product Developm ent
02 August 2021
Marion Gruber, Ph.D.
Director
Office of Vaccines Research and Review 
Food and Drug Administration
Center for Bi ologics Evaluation and Research
DocumentControl Center
10903 New Hampshire Avenue
WO71, G112
Silver Spring, MD 20993 -0002THIS DOCUMENT CONTAINS CONFIDENTIAL 
AND/OR TRADE SECRET INFORMATION 
THAT IS DISCLOSED ONLY IN CONNECTION 
WITH THE LICENSING AND/OR 
REGISTRATION OF PRODUCTS FOR PFIZER
INC OR ITS AFFILIATED COMPANIES.  THIS 
DOCUMENT SHOULD NOT BE DISCLOSED OR 
USED, IN WHOLE OR IN PART, FOR ANY 
OTHER PURPOSE WITHOUT THE PRIOR 
WRITTEN CONSENT OF PFIZER INC.
Re:BLA 125742
COVID-19 mRNA Vaccine ( BNT162/PF-07302048)
Response to 29 Ju ly2021 Information Request
Dear Dr. Gruber ,
Reference is made to the Biologics License Applicatio n (BLA) submitted 19 May 2021 for 
the COVID -19 mRNA Vaccine (BNT162/PF -07302048) developed by  BioNTech and Pfizer
under BB -IND19736 for the prevention of COVID -19caused by  SARS-CoV-2in 
individuals ≥16 years of age.
The purpose of thissubmission is to respond to CBER ’s29July2021 Information Request to 
Pfizer, received via email fromLaura Gottschalk, PhD (CBER). The requests arefor the 
provision of the analyses presented in Table 7 (page 116) of the Summary  of Clinical Safety  
for the following age groups: 1) 16 through 55 years, 2) 56 years and older of the 6 month 
CSR for S tudy C4591001 . TheResponse to CBER 29July2021Information Request for 
Study C4591001 is provided in Module 1.11.3.
Should you have any questions re garding this submission, or re quireadditionalinformation, 
pleasecontact me vi aphone at 215-280-5503; via facsimile at 845-474-3500; or via e-m ail at 
elisa.hark [email protected] .
Sincerely,
FDA-CBER-2021-5683-0950165
Marion Gru ber, Ph.D. , Director Page2of 2
BLA125742 2 August 2021
Pfizer Confid ential
Page 2ElisaHarkins
Global Regulatory Lead
Global Regulatory Affairs –Vaccines
CC: Ramac handra S. Naik, Ph.D.
FDA-CBER-2021-5683-0950166