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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
23July2021
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 15 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 th e current document is to re spond to CBER ’s15 July2021 Information 
Request regarding PREA post -marketing commitment goal dates that was provided by
Captain MichaelSmith, PhD (CBER) to Pfizer via email. TheResponse to CBER ’s 15July
2021 Information Request regarding datasets is provided in Module 1.11.3. 
The present submission also provides the amended agreed Pediatric Study  Plan(Clean Copy
and Track Changes Copy) andRequest for Deferralof Pediatric Studies (Clean Copy  and 
Track Changes Copy )as requested b y CBER. These documents have been updated to include 
the addition of study  C4591023, a dose -finding safety  and effectiveness study  in infants less 
than 6 months of age .They willalso be submitted to B B-IND 19736.
Should you have any questions re garding this submission, or re quire additionalinformation, 
pleasecontact me vi aphone at 215-280-5503; via facsimile at 845-474-3500; or via e -mail at 
elisa.hark [email protected] .
FDA-CBER-2021-5683-0950089
Marion Gru ber, Ph.D. , Director Page2of 2
BLA125742 23July 2021
Pfizer Confid ential
Page 2Sincerely,
Elisa Harkins
Global Regulatory Lead
Global Regulatory Affairs –Vaccines
CC: Ramac handra S. Naik, Ph.D.
FDA-CBER-2021-5683-0950090