125742 0 20219002.P0

Pfizer Documents (PHMPT/FDA)

Pfizer Bla Submission

Pfizer 16 Plus Documents

18

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Page 1of 13Reason for Submission
܆For Release
…For Surveilla nce
܈For Licensing Action*
STN:  125742_0
…Corrected Protocol
Date : 16 Aug 21
Subject: Electronic Protocol Signature Page
License No.:  2229
Company Name: Pharmacia & Upjohn Company LLC for BioNTech Manufacturing GmbH
Pharmacia & Upjohn Company LLC for BioNTech Manufacturing GmbH hereby submits the 
following lot as an electronic submission by Electronic Submissions Gateway (ESG).  All test 
conducted on this lot are reported and pass specifications as required.
Proper name of product 
Electronic Protocol
STN Lot Number Lot Type          Filename
125742_0 FE3592    FC     20219002.P0
Sample Status
… Sample Not Required
… Sample Submitted with Protocol
܈ Sample Previous Submitted:       16-Aug-2021
Virus Verification
Software Name: Symantec Web Security Service
Company Name: Symantec Version: 7.2.1
Date of Definitions: 16-Aug-2021 Date of Scan: 16-Aug-2021
I certify that the submission is virus-free.
The approximate file size of this submission is 1.25MB.
Comments:
N/A
Signature of Authorized Official
Printed Name and Title of Signatory Title
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bcf9b9f3-dcbe-4cfe-a38a-d0dfba6a6f4c16 Aug 2021 17:03:036-0400
REASON: I approve this document.
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FDA-CBER-2021-5683-1149974
Page 2of 13cc: STN 125742-0/ 2229/FC
Lot Number: FE3592
License Name of Product: COVID-19 mRNA Vaccine (nucleoside modified)
Manufacturer Name: Pharmacia & Upjohn Company LLC for BioNTech Manufacturing GmbH
Ma nufacturer Address: 7000 Portage Rd., Ka lamazoo, MI 49001 USA
Trade name: COMIRNATY
Da te of Manufacturing: 30-Jun-2021 Expira tion Date: 30-Nov-2021
Fill Information 
Container Type: Vial Volume per container: 0.45mL
Approved Storage Period: 6 months Storage Temperature: -90°C to -60°C
Number of containers manufactured:
Number of Dosesper
container:6
Number of containers for release:
Volume of singlehuman dose: 30μg/DoseStartDate of periodof
Validity:Date of 
Manufacture
All tests conducted on this lot are reported and pass specifications as required.
Signature: Date:
Title:     
Electronic Protocol # - 20219002.P0
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bcf9b9f3-dcbe-4cfe-a38a-d0dfba6a6f4c16 Aug 2021 17:03:036-0400
REASON: I approve this document.
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FDA-CBER-2021-5683-1149975
 
Page 3 of 13 
   
 
 
cc: STN 125742-0/ 2229/FC 
 
   Lot Number: FE3592  
 
License Name of Product: COVID-19 mRNA Vaccine (nucleoside modified)  
 
Manufacturing Site:  Pha rmacia & Upjohn Company LLC, 7000 Portage Rd., Ka lamazoo, MIC 49001 USA 
 Date of Manufacture:  30-Jun-2021 Date of Expiry:  30-Nov-2021 
 
Date of Fill:  30-Jun-2021  
 Product Information :  
 
COMPONENTS 
 
Component 
Description Batch Number Date of 
Manuf. Manufacture Site Quantity Target 
Concentration 
BNT162b2 Drug Substance
 Pfizer  
BNT162b2 Drug 
Substance  Pfizer  
LNP Fabrication Pharmacia & 
Upjohn Company 
LLC 
Formulated Bulk 
Batch  30-Jun- 2021 Pharmacia & 
Upjohn Company 
LLC 
 
 
 
 
 
  
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Page 4 of 13 
 cc: STN 125742-0/ 2229/FC 
 
Lot Number: FE3592 
 
License Name of Product: COVID-19 mRNA Vaccine (nucleoside modified)  
 
 
Table 1. Filled Vaccine Quality Control Tests 
 
Test Test Method  Specification  Date of Test  Result  
Appear ance  Appear ance (Visual) White to off-white 
suspension MEETS TEST  
Appea rance (Visible 
Particulates)  Appearance (ParticlesMay contain white to off-
white opa que amorphous
pa rticles MEETS TEST  
Subvisible Particles Subvisible Particulate 
Matter  
 
pH  6.9 - 7.9 
Osmolality Osmome try   mOsmol/kg 
LNP Size Dynamic Light 
Scattering (DLS)  nm 
LNP Polydispersity Dynamic Light 
Scattering (DLS)  
RNA Encapsulation Fluorescence assay % 
RNA content Fluorescence assay  mg/mL 
ALC- 0315 content HPLC-CAD   mg/mL 
ALC- 0159 content HPLC-CAD   mg/mL 
DSPC content HPLC-CAD   mg/mL 
Cholesterol content HPLC-CAD   mg/mL 
Vial content  Container Content Not less than mL 
Lipid identities HPLC-CAD  Retention times 
consistent with 
references (ALC -0315, 
ALC -0159, Cholesterol, 
DSPC) Positive 
 
  
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FDA-CBER-2021-5683-1149977
 
Page 5 of 13 
 cc: STN 125742-0/ 2229/FC 
 
Lot Number: FE3592  
License Name of Product: COVID-19 mRNA Vaccine (nucleoside modified)  
 
 
Table 1 (Continued)  Filled Vaccine Quality Control Tests 
 
Test Test Method  Specification  Date of Test  Result  
Identity of encoded 
RNA sequence RT-PCR Identity confirmed  Positive 
In Vitro Expression Cell-based Flow 
Cytometry % Cells Positive  
RNA Integrity  Ca pilla ry Gel 
Electrophoresis % intact RNA  
Ba cteria l Endotoxin Endotoxin (LAL)  EU/mL  
Abbreviations:   LNP = Lipid nanoparticles; CAD = charged aerosol detector; RT-PCR = re
polymerase chain reaction; LAL = Limulus amebocyte lysate; EU = endotoxin unit 
  
Filled Vaccine Quality Control Tests (cont.) 
 
Sterility  
Method:   Type:  Fina l Container 
Container:  Sterility-   
Date  On Test  Medium/Temperature  Date  Off Test  Specification  Test Result  
No growth observed No growth observed 
No growth observed No growth observed 
 
  
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Page 6 of 13 
  
 
cc: STN 125742-0/ 2229/FC 
 
Lot Number: FE3592  
License Name of Product: COVID-19 mRNA Vaccine (nucleoside modified)  
 
 
Filled Vaccine Quality Control Tests (Continued) 
 
 
Lipid Identity 
 
Specification                  Limit              Result    _____Pass_ ________ 
 
Lipid Standard 
Retention 
Times (RT) Sample 
Retention Time 
ALC -0315 content  
ALC -0159 content  
DSPC content  
Cholesterol content  
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
 
  
 
 
 
 
 
 
 
 
 
 
 
 
 
 
  
 
 
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FDA-CBER-2021-5683-1149979
 
Page 7 of 13 
  
 
 
 
 
Lot Number: FE3592  
License Name of Product: COVID-19 mRNA Vaccine (nucleoside modified)  
 
 
Filled Vaccine Quality Control Tests (Continued) 
 
 
RNA encapsulation and content test 
 
 
Test date                                              
 
Test method                ____ TM8940A             
  
 
Specification:  RNA Encapsulation             Result    ___  
 
Specification:  Content RNA Content    mg/mL  Result ___  
 
 
Sample/Control Acceptance Criteria  
Result 
R2 for Standard A  
R2 for Standard B  
Total RNA (mg/mL)  
 
Enca psulated RNA (mg/mL)  
 
 
 
 
 
  
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Page 8 of 13 
  
cc: STN 125742-0/ 2229/FC 
 
Lot Number: FE3592  
License Name of Product: COVID-19 mRNA Vaccine (nucleoside modified)  
 
 
Filled Vaccine Quality Control Tests (Continued) 
 
 
Identity of encoded RNA sequence test 
 
 
Test method                __RT-PCR_________ 
 
Test date                                             
 
Specification                 Identity confirmed              Result    Positive   
     
   
Sample/Control Lot number Replicate Ct value Acceptance 
criteria Pass/Fail 
DP Sample 
  
FE3592  1 Pass 
2 
3 
Positive PCR Control 
  
 1 Pass 
2 
3 
Positive  
Control 
 PF-
07302048-
DP-RM 
 1 Pass 
2 
3 
Negative PCR Control 
 NA 1 Pass 
2 
3 
Negative  
Control  NA 1 Pass 
2 
3 
 
 
 
 
 
  
 
 
 
 
 
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FDA-CBER-2021-5683-1149981
 
Page 9 of 13 
  
 
cc: STN 125742-0/ 2229/FC 
 
Lot Number: FE3592  
License Name of Product: COVID-19 mRNA Vaccine (nucleoside modified)  
 
 
Filled Vaccine Quality Control Tests (Continued) 
 
In Vitro Expression Assay 
 
 
Test date                                            
 Test method                _____LAB-3 8621  
 
Specification                  cells positive                
      
 
 
 Acceptance Criteria  
Result 
 Lot number   
Positive Control lot number   
% cell via bility 
Average Number of Cells Counted for Sample 
 Test Result (% positive cells)  
 
 
  
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Page 10 of 13 
  
 
cc: S
TN 125742-0/ 2229/FC 
 
Lot Number: FE3592  
License Name of Product: COVID-19 mRNA Vaccine (nucleoside modified)  
Filled Vaccine Quality Control Tests (Continued) 
 
 
Limulus Amebocyte Lysate Test 
 
Ca
lculations or additional comments  
 N/A 
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FDA-CBER-2021-5683-1149983
 
Page 11 of 13 
 cc: STN 125742-0/ 2229/FC 
 
Lot Number: FE3592  
License Name of Product: COVID-19 mRNA Vaccine (nucleoside modified)  
 
 
BNT162b2 Drug Substance  
 
Lot Number:    
 
Date of Manufacture:     Date of Expiry:    
 
Storage Temperature: - 25˚C to - 15˚C Approved Storage Period:  months  
 
Consumed Quantity:   
 
Table 1. Drug Substance Quality Control Tests 
Test Test Method  Specification  Date of Test  Result  
Clarity Appearance (Clarity) 
Colora tion Appear ance 
(Coloration) 
pH  
Content (RNA 
Concentration) UV Spectroscopy  
Identity of Encoded 
RNA Sequence RT-PCR 
RNA Integrity  Ca pilla ry Gel 
Electrophoresis 
5’- Cap RP-HPLC  
Poly(A) Tail  ddPCR
Residual DNA Template qPCR 
Residual dsRNA Immunoblot 
Ba cteria l Endotoxin Endotoxin (LAL) 
Bioburden Bioburden  
Abbreviations:   NTU = Nephelometric Turbidity Units; B = brown; RT-PCR = reverse transcription polymerase 
chain reaction; ddP CR = droplet digital PCR; qPCR = quantitative PCR; dsRNA = double stranded RNA;  
LAL = Limulus amebocyte lysate; EU = endotoxin unit; CFU = colony forming unit 
 
 
  
 
 
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Page 12 of 13 
 cc: STN 125742-0/ 2229/FC 
 
Lot Number: FE3592  
License Name of Product: COVID-19 mRNA Vaccine (nucleoside modified)  
 
 
BNT162b2 Drug Substance  
 
Lot Number:     
 
Date of Manufacture:    Date of Expiry:  
 
Storage Temperature: - 25˚C to - 15˚C Approved Storage Period:  months  
 
Consumed Quantity:   
 
Table 1. Drug Substance Quality Control Tests 
Test Test Method  Specification  Date of Test  Result  
Clarity Appearance (Clarity)
Colora tion Appear ance 
(Coloration) 
pH  
Content (RNA 
Concentration) UV Spectroscopy  
Identity of Encoded 
RNA Sequence RT-PCR 
RNA Integrity  Ca pilla ry Gel 
Electrophoresis 
5’- Cap RP-HPLC  
Poly(A) Tail  ddPCR
Residual DNA Template qPCR 
Residual dsRNA Immunoblot 
Ba cteria l Endotoxin Endotoxin (LAL) 
Bioburden Bioburden  
Abbreviations:   NTU = Nephelometric Turbidity
chain reaction; ddP CR = droplet digital PCR; qPCR = quantitative PCR; dsRNA = double stranded RNA;  
LAL = Limulus amebocyte lysate; EU = endotoxin unit; CFU = colony forming unit 
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FDA-CBER-2021-5683-1149985
Genealogy Flowchart
Page 13of 13Prepared By: Approved By: 
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REASON: I approve this document.
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REASON: I approve this document.
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FDA-CBER-2021-5683-1149986
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Untitled 
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FDA-CBER-2021-5683-1149988
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FDA-CBER-2021-5683-1149989
FE3592 Replicates 1-3 
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FDA-CBER-2021-5683-1149990
 
  
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FDA-CBER-2021-5683-1149991