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Pfizer Global Regulatory Affairs
Pfizer Inc.
400 Arcola Road Collegeville, PA 19426
Global Product Developm ent
30July2021
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 26 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 ’s26July2021 Information Request to
Pfizer, received via email fromLaura Gottschalk, PhD (CBER). The reques t isregarding the
addition of a table to the BLAregarding the disposition of participants in safet y populations
who experienced pregnancy . TheResponse to CB ER26July2021 Information Request
RegardingDisposition of Participants in Safety Population swho Experienced Pregnancy is
provided inModule 1.11.3.
Should you have any questions re garding this submission, or re quireadditionalinformation,
pleasecontact me vi aphone at 215-280-5503; vi a facsimile at 845-474-3500; or via e-m ail at
elisa.hark [email protected].
Sincerely,
FDA-CBER-2021-5683-0950144
Marion Gru ber, Ph.D. , Director Page2of 2
BLA125742 30July 2021
Pfizer Confidential
Page 2ElisaHarkins
Global Regulatory Lead
Global Regulatory Affairs –Vaccines
CC: Ramac handra S. Naik, Ph.D.
FDA-CBER-2021-5683-0950145