125742 S2 M2 drug product stability

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BNT162b2
2.3.P.8 Stability
PFIZER CONFIDENTIAL
Page 1TABLE OF CONTENTS
LIST OF TABLES ................................ ................................ ................................ ..................... 2
2.3.P.8. STABILITY ................................ ................................ ................................ .................. 3
2.3.P.8.1. Stability  Summary  and Conclusion ................................ ................................ ..3
2.3.P.8.1.1. Shelf L ife at Recommended Storage Temperature ............................. 3
2.3.P.8.1.2. Stability  Batches and Studies ................................ .............................. 3
2.3.P.8.1.3. Protocol for Testing at the Long Term Condition ( -90 to -60C).....10
2.3.P.8.1.4. Protocol of Testing at the Accelerated Condition ............................. 11
2.3.P.8.1.5. Protocol for Testing at the Thermal Stress Conditions ..................... 15
2.3.P.8.1.6. Summary  of Stability  Data ................................ ................................ 19
2.3.P.8.1.6.1. Summary  of Stability  Data at the Long Term 
Storage Condition ( -90 to -60C)................................ ..................... 19
2.3.P.8.1.7. Summary  of Stability  Data at the Accelerated Storage 
Condition ................................ ................................ ................................ .......... 20
2.3.P.8.1.8. Summary  of Stability  Data at the Thermal Stress Storage 
Conditions ................................ ................................ ................................ ........ 21
2.3.P.8.1.9. Summary  of Stability  Data at the Thermal Cy cling Storage 
Conditions ................................ ................................ ................................ ........ 21
2.3.P.8.1.10. Summary  of Photostability  Stability  in Drug Product Vials ........... 21
2.3.P.8.1.11. Shelf L ife and Conclusions ................................ ............................. 22
2.3.P.8.2. Post Approval Stability  Protocol and Stability  Commitment ........................ 23
2.3.P.8.3. Stability  Data ................................ ................................ ................................ ..23
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2.3.P.8 Stability
PFIZER CONFIDENTIAL
Page 2LIST OF TABLES
Table 2.3.P.8-1. Summary  of On -going Stability  Studies ................................ ..................... 5
Table 2.3.P.8-2. Protocol for BNT162b2 DP at the L ong Term Condition of  -90to -
60°C ................................ ................................ ................................ .......... 10
Table 2.3.P.8-3. Protocol for BNT162b2 Earl y Clinical and Non -clinical and 
Stability  DP at the Long Term Condition of -70 ± 10°C .......................... 11
Table 2.3.P.8-4. Protocol for BNT162b2 DP at the Accelerated Condition of -60 to 
-30°C................................ ................................ ................................ ......... 12
Table 2.3.P.8-5. Protocol for BNT162b2 DP at the Accelerated Condition of -40 
± 5°C................................ ................................ ................................ ......... 12
Table 2.3.P.8 -6. Protocol for BNT162b2 DP at the Accelerated Condition of -20 
± 5°C................................ ................................ ................................ ......... 13
Table 2.3.P.8 -7. Protocol BNT162b2 DP at the Accelerated Condition of 5 ± 3°C........... 14
Table2.3.P.8-8. Protocol for BNT162b2 DP Manufactured b y Polymun Scientific at 
the Accelerated Condition of 5 ± 3°C................................ ....................... 14
Table 2.3.P.8-9. Protocol for BNT162b2 DP at the Thermal Stress Condition of 25 ±
2°C/60 ± 5% RH................................ ................................ ....................... 15
Table 2.3.P.8-10. Protocol for BNT162b2 DP at the Thermal Stress Condition of 30 ± 
2°C/65 ± 5% RH................................ ................................ ....................... 16
Table 2.3.P.8 -11. Protocol for BNT162b2 DP at the Thermal Stress Condi tionof25 ± 
2°C ................................ ................................ ................................ ............ 16
Table 2.3.P.8 -12. Protocol for BNT162b2 Emergency  Suppl y DP Thermal Cycling 
Studies (L ots EK1768 and EJ1686) ................................ .......................... 17
Table 2.3.P.8 -13. Protocol for BNT162b2 PPQ DP Thermal Cy cling Studies (Lots 
EL8723, EN1195 and EL9266) ................................ ................................ 17
Table 2.3.P.8 -14. Protocol for BNT162b2 PPQ DP Thermal Cycling Studies 
(LotEL3249) ................................ ................................ ............................ 18
Table 2.3.P.8 -15. Protocol for BNT162b2 PPQ DP Thermal Cycling Studies 
(LotEK4242) ................................ ................................ ............................ 18
Table 2.3.P.8 -16. Protocol for BNT162b2 PPQ DP Thermal Cycling Studies 
(LotEL7834) ................................ ................................ ............................ 19
Table 2.3.P.8-17. Post-Approval Commercial Stability  Protocol for Drug Product 
Stored at - 90 to -60 °C................................ ................................ .............. 23
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Page 32.3.P.8. STABILITY
2.3.P.8.1. Stability Summary and Conclusion
2.3.P.8.1.1. Shelf Life at Recommended Storage Temperature
The initial commercial shelf life of the BNT162b2 drug product is 6 months when stored at 
the intended storage condition of -90 to -60 °C. The initial shelf life is based on the currentl y 
available data from stability  studies utilizing material from emergency  supply , process 
performance qualification, cl inical and one non -clinical lot of drug product. The stability  data 
generated to date on the emergency  supply  and process performance qualification lots also 
support an additional storage condition at -20 ± 5°C for up to 2 weeks, as well as short term 
storage at 5± 3°C for up to one month (within the 6 month shelf life). 
Drug product stability  lots, from multiple global manufacturing sites, have been enrolled in 
stability  programs and are being monitored in accordance with the approved protocols. All 
testing to date has been performed using anal ytical methodology  and phase appropriate 
specifications in place at time of testing. The analy tical procedures used in the stability  
programs were developed to monitor the composition, strength, purit y, safety and ge neral 
quality  attributes of the drug product.
In-use Period of Drug Product
The initial in -use period for the thawed, undiluted vial is room temperature for not more than 
2 hours  (Section 3.2.P.2.6 Compatibility ). Formal thermal cy cling stability  studies have been 
initiated on both emergency use lots and PPQ lots in order to further support the in -use 
period. Available data from these studies is provided in Section 3.2.P.8.3 Thermal Stress and 
Cycling. The in -use shelf life of undiluted and diluted vials i s defined in Section 3.2.P.2.6 
Compatibility .
2.3.P.8.1.2. Stability Batches and Studies 
The stability  program is designed to follow I CH guidelines for stability  of drug product (ICH 
Guideline Q1A: Stability Testing of New Drug Substances and Products; ICH Guideline 
Q5C: Quality  of Biotechnological Products, Stability  Testing of Biotechnological/Biological 
Products). To date, thirteen process performance qualification lots (with one additional PPQ 
lot being placed on a thermal cy cling stabilit y study onl y), eight emerg ency supply  lots, 
seven clinical lots and one non -clinical lot lots have been placed on stability and stored under 
long term, accelerated, and thermal stress conditions. The drug product lots placed on 
stability , to date, were packaged in commercial glass vials or glass vials representative of 
commercial packaging (for earl y non -clinical and clinical drug product studies).
Both the clinical and non -clinical drug product lots manufactured b y Polymun Scientific 
using the BNT162b2 construct are considered to b e predictive of the stability of the 
commercial materials based on comprehensive comparability  assessments performed during 
development. The emergency  suppl y lots were manufactured using the commercial process.
Therefore, the clinical and non- clinical drug product lots manufactured b y Polymun 
Scientific, as well as the emergency  supply  lots, are considered predictive of the stability  of 
the commercial materials.
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2.3.P.8 Stability
PFIZER CONFIDENTIAL
Page 4A summary  of all drug product lots on stability  studies and current available stability  data are
shown in Table 2.3.P.8-1. Stability  Summary  and Conclusion. At this time, stability  studies 
are on -going. Data from these studies will be used to confirm the initial s helf life of the drug 
product. Further information on confirmation and extension of the drug product shelf life is 
discussed in Section 3.2.P.8.1. Stability  Summary and Conclusion, Section 3.2.P.8.1.7 Shelf 
Life and Conclusions.
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Page 5Table 2.3.P.8-1. Summary of On -going Stability Studies 
Lot Number Stability Study Start Drug Product 
Batch UseStudy Type Storage Condition Data 
Available Study 
Status
EN6199
(Pfizer, Kalamazoo, 
Line Stability, Emergency 
Supplya, Process 
performance qualificationFebruary 2021 Long Term -90 to -60 C 1 month On-going
Accelerated -60 to -30 C Release On-going
Accelerated -20 5 C 1 month On-going
Accelerated 5 3 C 1 month On-going
EL3249 
(Pfizer, Kalamazoo, 
Line Stability, Clinical, 
Emergency Supplya, 
Process performance 
qualificationDecember 2020 Long Term -90 to -60 C 3month s On-going
Accelerated -20 5 C 3month s On-going
Accelerated 5 3 C 3month s On-going
Thermal Cycling Thermal Cycling: 1 week at -90 to 
-60°C , followed by 2 weeks at  - 20 ±
5 °C, 4 weeks at 2 to 8 °C and 1 week at 
25 ±2 °C/60 ±5% RH.8weeks Complete
EL9266
(Pfizer, Kalamazoo, Line Stability, Emergency 
Supplya, Process 
performance qualificationFebruary 2021 Thermal Cycling Thermal Cycling: Ultra frozen vials are 
placed at -20 ± 5 °C for 4 weeks and 
then moved to 2 to 8 °C for 12 weeks. 
Samples will be pulled for testing every 
2 weeks throughout protocol.8weeks On-going
EL9267
(Pfizer, Kalamazoo, 
Line Stability, Emergency 
Supplya, Process 
performance qualificationJanuary 2021 Long Term -90 to -60 C 1 month On-going
Accelerated -60 to -30 C Release On-going
Accelerated -20 5 C 1 month On-going
Accelerated 5 3 C 1 month On-going
EL3248 
(Pfizer, Kalamazoo, Line Stability, Clinical, 
Emergency Supplya, 
Process performance 
qualificationDecember 2020 Long Term -90 to -60 C 3month s On-going
Accelerated -20 5 C 3month s On-going
Accelerated 5 3 C 3month s On-going
Thermal Stress 25 2 C/ 60 5 % RH 1 month Complete
Thermal Stress 30 2 C/ 65 5 % RH 1 month Complete
EM4965 
(Polymun 
Scientific/Pfizer, Puurs)Stability, Emergency 
Supplya, Process 
performance qualificationFebruary 2021 Long Term -90 to -60 C 1 month On-going
Accelerated -60 to -30 C Release On-going
Accelerated -20 5 C 1 month On-going
Accelerated 5 3 C 1 month On-going
EL7834
(Polymun 
Scientific/Pfizer, PuursDecember 2020 Stability, 
Emergency 
Supplya, Process Long Term -90 to -60 C 3month s On-going
Accelerated -20 5 C 3month s On-going
Accelerated 5 3 C 3month s On-going
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(b) 
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PFIZER CONFIDENTIAL
Page 6Table 2.3.P.8-1. Summary of On -going Stability Studies 
Lot Number Stability Study Start Drug Product 
Batch UseStudy Type Storage Condition Data 
Available Study 
Status
performance 
qualificationThermal Cycling Thermal Cycling: 1 week at -90 to 
-60°C  followed by 4 weeks at -20 ±
5 °C and then 4 weeks at 2 to 8 °C. and 
1week at 25 ±2 °C/60 ±5% RH.10weeks Complete
Photostability Dark Control and Light Exposed Complete
EN1195
(mibe/Pfizer, Puurs)Stability, Emergency 
Supplya, Process 
performance qualificationMarch 2021 Long Term -90 to -60 C 1 month On-going
Accelerated -20 5 C 1 month On-going
Accelerated 5 3 C 1 month On-going
Thermal Cycling Thermal Cycling: Ultra frozen vials are 
placed at -20 ± 5 °C for 4 weeks and 
then moved to 2 to 8 °C for 12 weeks. 
Samples will be pulled for testing every 
2 weeks throughout protocol.6weeks On-going
EK4242
(mibe/Pfizer, Puurs)Stability, Emergency 
Supplya, Process 
performance qualificationDecember 2020 Long Term -90 to -60 C 3 months On-going
Accelerated -20 5 C 3 months On-going
Accelerated 5 3 C 3 months On-going
Thermal Cycling Thermal Cycling: 1 week at -90 to 
-60°C  followed by 4 weeks at 2 to 8 °C5 weeks Complete
EP2166
(Pfizer, Puurs)Stability, Emergency 
Supplya, Process 
performance qualificationJanuary 2021 Long Term -90 to -60 C 2 months On-going
Accelerated -20 5 C 2 months On-going
Accelerated 5 3 C 2 months On-going
EL8713
(Pfizer, Puurs)Stability, Emergency 
Supplya, Process 
performance qualificationJanuary 2021 Long Term -90 to -60 C 2 months On-going
Accelerated -20 5 C 2 months On-going
Accelerated 5 3 C 2 months On-going
EM6950
(Pfizer, Puurs)Stability, Emergency 
Supplya, Process 
performance qualificationJanuary 2021 Long Term -90 to -60 C 2 months On-going
Accelerated -60 to -30 C Release On-going
Accelerated -20 5 C 2 months On-going
Accelerated 5 3 C 2 months On-going
EL8723
(Pfizer, Puurs)Stability, Clinical, 
Emergency Supplya, 
Process performance 
qualificationJanuary 2021 Long Term -90 to -60 C 2 months On-going
Accelerated -60 to -30 C Release On-going
Accelerated -20 5 C 2 months On-going
Accelerated 5 3 C 2 months On-going
Thermal Stress 25 2 C/ 60 5 % RH 1 month Complete
Thermal Stress 30 2 C/ 65 5 % RH 1 month Complete
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PFIZER CONFIDENTIAL
Page 7Table 2.3.P.8-1. Summary of On -going Stability Studies 
Lot Number Stability Study Start Drug Product 
Batch UseStudy Type Storage Condition Data 
Available Study 
Status
Thermal Cycling Thermal Cycling: Ultra frozen vials are 
placed at -20 ± 5 °C for 4 weeks and 
then moved to 2 to 8 °Cfor 12 weeks. 
Samples will be pulled for testing every 
2 weeks throughout protocol.8weeks On-going
EL1491
(Pfizer, Puurs)Stability, Emergency 
Supplya, Clinical, Process 
performance qualificationDecember 2020 Long Term -90 to -60 C 3 months On-going
Accelerated -20 5 C 3 months On-going
Accelerated 5 3 C 3 months On-going
EH9899
Pfizer, Kalamazoo)Stability, Emergency 
SupplyaNovember 2020 Long Term -90 to -60 C 3 months On-going
Accelerated -20 5 C 3 months On-going
Accelerated 5 3 C 3 months Complete
Thermal Stress 25 2 C/ 60 5 % RH 1 month Complete
EJ1688
(mibe/Pfizer, Puurs)Stability, Emergency 
SupplyaNovember 2020 Long Term -90 to -60 C 3 months On-going
Accelerated -20 5 C 3 months On-going
Accelerated 5 3 C 3 months Complete
Thermal Stress 25 2 C/ 60 5 % RH 1 month Complete
EK1768
(Polymun 
Scientific/Pfizer, PuursNovember 2020 Stability, 
Emergency 
Supplya, Clinical 
inventoryLong Term -90 to -60 C 3 months On-going
Accelerated -20 5 C 3 months On-going
Accelerated 5 3 C 3 months Complete
Thermal Stress 25 2 C/ 60 5 % RH 1 month Complete
Thermal Cycling Thermal Cycling: 2 weeks at -90 
to -60°C followed by 4 weeks at -20 ±
5 °C and then 8 weeks at 2 to 8 °C. 
Samples will be pulled for testing every 
2 weeks throughout protocol.14weeks Complete
EJ1686
(Polymun 
Scientific/Pfizer, Puurs)November/
December 2020Stability, 
Emergency 
Supplya, Clinical 
inventoryLong Term -90 to -60 C 3 months On-going
Accelerated -20 5 C 3 months On-going
Accelerated 5 3 C 3 months Complete
Thermal Stress 25 2 C/ 60 5 % RH 1 month Complete
Thermal Cycling Thermal Cycling: 2 weeks at -90 
to -60°Cfollowed by 4 weeks at -20 ±
5 °C and then 8 weeks at 2 to 8 °C. 
Samples will be pulled for testing every 
2 weeks throughout protocol.14weeks Complete
EJ1685 November 2020 Long Term -90 to -60 C 3 months On-going
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PFIZER CONFIDENTIAL
Page 8Table 2.3.P.8-1. Summary of On -going Stability Studies 
Lot Number Stability Study Start Drug Product 
Batch UseStudy Type Storage Condition Data 
Available Study 
Status
(Polymun 
Scientific/Pfizer, Puurs)Stability, 
Emergency 
Supplya, Clinical 
inventoryAccelerated -60 to -30 C 3 months On-going
Accelerated -20 5 C 3 months On-going
Accelerated 5 3 C 3 months Complete
Thermal Stress 25 2 C/ 60 5 % RH 1 month Complete
EJ0553
(Polymun 
Scientific/Pfizer, Puurs)November 2020 Stability, 
Emergency 
Supplya, Clinical 
inventoryLong Term -90 to -60 C 3 months On-going
Accelerated -60 to -30 C 3 months On-going
Accelerated -20 5 C 3 months On-going
Accelerated 5 3 C 3 months Complete
Thermal Stress 25 2 C/ 60 5 % RH 1 month Complete
EE8493
(Polymun 
Scientific/Pfizer, Puurs)September 2020 Stability, 
Emergency 
Supplya, Clinical 
inventoryLong Term -90 to -60 C 6months On-going
Accelerated -60 to -30 C 6month s On-going
Accelerated -20 5 C 6 months Complete
Accelerated 5 3 C 3 months Complete
Thermal Stress 25 2 C/ 60 5 % RH 1 month Complete
Thermal Stress 30 2 C/ 65 5 % RH 1 month Complete
EE8492
(Polymun
Scientific/Pfizer, Puurs)September 2020 Stability, 
Emergency 
SupplyaLong Term -90 to -60 C 6months On-going
Accelerated -20 5 C 6 months Complete
Accelerated 5 3 C 3 months Complete
EE3813c
(Polymun 
Scientific/Pfizer, Puurs)August 2020 Stability, Clinical Long Term -70 10 C 6months Complete
Accelerated 5 3 C 3 months Complete
ED3938d
(Polymun 
Scientific/Pfizer, Puurs)August 2020 Stability, Clinical 
inventoryLong Term -70 10 C 6months Complete
Accelerated 5 3 C 3 months Complete
BCV40720 -C
(Polymun Scientific)August 2020 Stability, Clinical Long Term -70 10 C 6months Complete
Accelerated 5 3 C 3 months Complete
BCV40720 -A August 2020 Stability, Clinical Long Term -70 10 C 6months Complete
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Page 9Table 2.3.P.8-1. Summary of On -going Stability Studies 
Lot Number Stability Study Start Drug Product 
Batch UseStudy Type Storage Condition Data 
Available Study 
Status
(Polymun Scientific) Accelerated 5 3 C 3 months Complete
BCV40620 -E
(Polymun Scientific)July 2020 Stability, 
NonclinicalLong Term -70 10 C 6months Complete
Accelerated 5 3 C 3 months Complete
BCV40620 -A
(Polymun Scientific)July 2020 Stability, Clinical Long Term -70 10 C 6months Complete
Accelerated 5 3 C 3 months Complete
BCV40420 -A
(Polymun Scientific)May 2020 Stability, Clinical Long Term -70 10 C 9 months On-going
Accelerated -40 5 C 9 months On-going
Accelerated 5 3 C 6 months Complete
Thermal Stress 25 2 C 4 months Complete
CoVVAC/270320
(Polymun Scientific)March 2020 Stability, 
non-clinical 
toxicologybLong Term -70 10 C 6 months Complete
Accelerated -40 5 C 3 months On-going
Accelerated 5 3 C 6 months Complete
a.   Emergency supply designation applies to US market.
b.   -40 °C study started in April 2020.
c.  This lot number is equivalent to BCV40820 -P
d.  This lot number is equivalent to BCV40720 -P.
RH = Relative Humidity
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Page 102.3.P.8.1.3. Protocol for Testing at the Long Term Condition (- 90 to -60 C)
Vials from drug product lots were stored at the recommended storage condition of -90 
to -60C. Testing is currently  being performed on thirteen PPQ lots and eight emergency  
supply  lots according to the protocol indicated in Table 2.3.P.8-2
Additionally , testing at -70 ± 10 C is being performed on seven clinical lots and one 
non-clinical lot according to the protocol indicated in Table 2.3.P.8-3.
Table 2.3.P.8 -2. Protocol for BNT162b2 DP at the Long Term Condition of 
-90to -60°C
Analytical Procedure Test Intervalabe
Appearance (Visible) 0, 1Wf, 2W, 1M, 2M, 3M, 6M, 9M , 12M, 18M, 
24M Appearance (Visible Particulates)
Dynamic Light Scattering (LNP Size)
Dynamic Light Scattering (LNP Polydispersity)
Fluorescence Assay (RNA Encapsulation)
Fluorescence Assay (RNA Content)
HPLC -CAD (ALC -0315 Content)
HPLC -CAD (ALC -0159 Content)
HPLC -CAD (DSPC Content)
HPLC -CAD (Cholesterol Content)
Cell-based Flow  Cytom etry  (In vitro expression)
Capillary Gel Electrophoresis (RNA Integrity)
Subvisible Particles 0, 3Md, 6M, 12M, 18M, 24M
Container Closure Integrity Test 0, 12M, 24Mc
Endotoxin 0, 12M, 24Mc
Sterility 0, 12M, 24M
a. Testing not performed at the 1W, 2W or 2M timepoint for lot EE8493, EJ0553, EL3249, EL3248, EL783, 
EK4242 and EL1491.
b. Testing not performed at the 2M time point fo r lots EH9899, EJ1688, EK1768, EJ1686 and EJ1685. 
c. Being performed at 3 and 6M time points for EE8493, EE8492 and EJ0553.
d. Being performed at 3 time points for EE8493, EE8492 and EJ0553.
e. Testing not performed at the 1W or 2W timepoint for lot EN1195
f.  1W testing performed on lots EH9899, EJ1688, EK1768, EJ1686 and EJ1685
W = Week,   M = Month,   LNP = Lipid Nanoparticle
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PFIZER CONFIDENTIAL
Page 11Table 2.3.P.8 -3. Protocol for BNT162b2 Early Clinical and Non -clinical and 
Stability DP at the Long Term Condition of -70 ± 10°C
Analytical Procedure Test Interval (m onths)abcd
Appearance (Visible & Visible Particles ) 0, 1, 3, 6, 9, 12, 18, 24
LNP Size
LNP Polydispersity
RNA Encapsulation
RNA Content
ALC -0315 Content
ALC -0159 Content
DSPC Content
Cholesterol Content
RNA Integrity
Subvisible Particles 0, 12, 24
pH
Sterilityd0, 24
a. For BNT162b2 lot BCV40420 -A, a 4 month time point was added and tested
b. For BNT162b2 lot CoVVAC/270320, a 2 week and 2 month time point were tested. Study ends at 6 month time point.
c. Sterility testing not performed on non -clinical lot CoVVAC/270320.
d. For BNT162b2 lots BCV40620 -A, BCV40620 -E, BCV40720 -A, BCV40720 -C, BCV40720 -P & BCV40820 -P, only 
testing on 0, 1, 3 and 6 mon ths is being performed. Sterility is being performed on 6M end point rather than 24M for this 
lot.
2.3.P.8.1.4. Protocol of Testing at the Accelerated Condition
To study  the effects of temporary  excursions above the recommended storage temperature, 
drug product is being stored under the accelerated conditions of -60 to -30 C, -40± 
5C, -20 5 C and 5  3 C. 
Testing at - 60 to -30 C is currentl y being perfor med on five process performance 
qualification and three emergency suppl y lots according to the protocol indicated in 
Table 2.3.P.8-4 .
Additionally , testing at -40  5 C is currently  being performed on one clinical lot and one 
non-clinical lot according to the protocol indicated in Table 2.3.P.8-5.
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Page 12Table 2.3.P.8 -4. Protocol for BNT162b2 DP at the Accelerated Condition of
-60to -30°C 
Analytical Procedure Test Interval ab
Appearance (Visible) 0, 1M, 3M, 6M, 12M , 18M, 24M
Appearance (Visible Particulates)
Dynamic Light Scattering (LNP Size)
Dynamic Light Scattering (LNP Polydispersity)
Fluorescence Assay (RNA Encapsulation)
Fluorescence Assay (RNA Content)
HPLC -CAD (ALC -0315 Content)
HPLC -CAD (ALC -0159 Content)
HPLC -CAD (DSPC Content)
HPLC -CAD (Cholesterol Content)
Cell-based Flow  Cytom etry  (In vitro expression)
Capillary Gel Electrophoresis (RNA Integrity)
Subvisible Particlesc6M, 12M, 18M, 24M
a. Testing not performed at the 12M, 18M and 24M timepoint for emergency supply lot EE8493, EJ0553 and EJ1685. 
b. 6M, 12M, 18M and 24M only time points being performed on PPQ lots EN6199, EL9267, EM4965, EM6950, and 
EL8723 
c. Testing being performed on P PQ lots only as well as 6M time point for emergency supply lot EE8493
W = Week,   M = Month,   LNP = Lipid Nanoparticle
Table 2.3.P.8 -5. Protocol for BNT162b2 DP at the Accelerated Cond ition of -40 
± 5°C
Analytical Procedure Test Interval (m onths)a
Appearance (Visible & Visible Particles ) 0, 1, 2, 3, 6, 9, 12, 18, 24
LNP Size
LNP Polydispersity
RNA Encapsulation
RNA Content
ALC -0315 Content
ALC -0159 Content
DSPC Content
Cholesterol Content
RNA Integrity
pH 0, 12, 24
Subvisible Particles
Sterilityb0, 24
a. For BNT162b2 lot BCV40420 -A, a 4 month time point was added and tested
b. For BNT162b2 lot CoVVAC/270320, bioburden is being tested at final time point
Testing at -20  5 C is currentl y being performed on thirteen process performance 
qualification lots and eight emergency  suppl y lots according to the protocol indicated in 
Table 2.3.P.8 -6.
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Page 13Table 2.3.P.8 -6. Protocol for BNT162b2 DP at the Accelerated Condition of -20 
± 5°C 
Analytical Procedure Test Interval abc
Appearance (Visible) 0, 1W, 2W, 1M, 2M, 3M, 6M
Appearance (Visible Particulates)
Dynamic Light Scattering (LNP Size)
Dynamic Light Scattering (LNP Polydispersity)
Fluorescence Assay (RNA Encapsulation)
Fluorescence Assay (RNA Content)
HPLC -CAD (ALC -0315 Content)
HPLC -CAD (ALC -0159 Content)
HPLC -CAD (DSPC Content)
HPLC -CAD (Cholesterol Content)
Cell-based Flow  Cytom etry (In vitro expression)
Capillary Gel Electrophoresis (RNA Integrity)
Subvisible Particlesd0, 6M
a. 1W testing performed on emergency supply lot EE8492 only.
b. Testing not performed at the 1W, 2W or 2M time point for emergency supply lot EE8493, EJ0553, EJ1685, EJ1686, 
and EK1768 or process performance qualification lots EL1491, EK4242, EL7834, EL3248, and EL3249. 
c. Testing not performed at the 1W or 2W time point for emergency supply lots EJ1688 an d EH9899 and process 
performance qualification lot EN1195.
d. Testing not performed on emergency supply lots EJ1685, EJ1686 and EK1768.
W = Week,   M = Month,   LNP = Lipid Nanoparticle
Testing at 5  3 C is currently  being performed on thirteen process performance 
qualification lots and eight emergency  suppl y lots according to the protocol indicated in 
Table 2.3.P.8 -7.
Additionally , testing at 5 3 C is currently being performed on seven clinical lots and one 
non-clinical lot according to the protocol indicated in Table 2.3.P.8-8
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Page 14Table 2.3.P.8 -7. Protocol BNT162b2 DP at the Accelerated Condition of 5 ± 3°C 
Analytical Procedure Test Interval abcd
Appearance (Visible) 0, 1W, 2W, 1M, 2M, 3M, 6M
Appearance (Visible Particulates)
Dynamic Light Scattering (LNP Size)
Dynamic Light Scattering (LNP Polydispersity)
Fluorescence Assay (RNA Encapsulation)
Fluorescence Assay (RNA Content)
HPLC -CAD (ALC -0315 Content)
HPLC -CAD (ALC -0159 Content)
HPLC -CAD (DSPC Content)
HPLC -CAD (Cholesterol Content)
Cell-based Flow  Cytom etry (In vitro expression)
Capillary Gel Electrophoresis (RNA Integrity)
Subvisible Particlese0, 6M
a. 1W testing performed on emergency supply lots EE8492, EJ1685, EJ1686, EK1768, EJ1688 and EH9899 
only.
b. 1M, 3M and 6M testing only performed on process performance qualification lots EL3249, EL3248, 
EL7834, EN1195, EK4242 and EL1491.
c. 2M and 6M testing not perfomed on emergency supply lots EH9899, EJ1688, EK1768, EJ1686, EJ1685. 
d. 1M and 3M testing on ly performed on emergency supply lots EJ0553 and EE8493. Emergency supply lot 
EE8492 ends at 3M time point.
e. Testing not performed on emergency supply lots EJ0553, EJ1685, EJ1686, EK1768, EJ1688 and EH9899. 
W = Week,   M = Month,   LNP = Lipid Nanoparti cle
Table 2.3.P.8-8. Protocol for BNT162b2 DP Manufactured by Polymun Scientific 
at theAccelerated Condition of 5 ± 3 °C
Analytical Procedure Test Interval (m onths)abd
Appearance (Visible & Visible Particles ) 0, 1, 2, 3, 6
LNP Size
LNP Polydispersity
RNA Encapsulation
RNA Content
ALC -0315 Content
ALC -0159 Content
DSPC Content
Cholesterol Content
RNA Integrity
pH 0, 6c
a. For BNT162b2 lot BCV40420 -A, a 4 month time point was added and tested
b. For BNT162b2 lot CoVVAC/270320, testing was also performed at the 2 week and 6 week time points
c. pH testing not performed on non -clinical lot CoVVAC/270320
d. Study ends at the 3M time point for BNT162b2 lots BCV40820 -P, BCV40720 -P, BCV40720 -C, BCV40720 -A, 
BCV40620 -E and BCV40620 -A. pH performed on the final 3M time point.
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Page 152.3.P.8.1.5. Protocol for Testing at the Thermal Stress Conditions
To study  the effects of temporary  excursions above the recommended storage temperature, 
drug product is being stored under thermal stress c onditions at 25  2 C/60 ± 5% RH and 
302 C/65% ± 5 RH and tested per the protocols indicated in Table 2.3.P.8 -9and
Table 2.3.P.8-10for emergency  suppl y lots (lot EE8493 only  placed on 30 2 C/65% ± 
5RH stability  and lots EE8493, EJ0553, EJ1685, EJ1 686,EK1768, EH9899 and EJ1688 
placed on 25 2C/60 ± 5% RH stability ). Process performance qualification lots EL 8723 
and EL3248 were also each placed on formal stability  according to the protocols indicated in 
Table 2.3.P.8 -9andTable 2.3.P.8-10.
Additionally , testing at 25 2 Cis currently being performed on one clinical lot according 
to the protocol indicated in Table 2.3.P.8 -11.
Table 2.3.P.8 -9. Protocol for BNT162b2 DP at the Thermal Stress Condition of
25 ± 2°C/60 ±5% RH
Analytical Procedure Test Intervalab
Appearance (Visible) 0, 1W, 2W, 1M
Appearance (Visible Particulates)
Dynamic Light Scattering (LNP Size)
Dynamic Light Scattering (LNP Polydispersity)
Fluorescence Assay (RNA Encapsulation)
Fluorescence Assay (RNA Content)
HPLC -CAD (ALC -0315 Content)
HPLC -CAD (ALC -0159 Content)
HPLC -CAD (DSPC Content)
HPLC -CAD (Cholesterol Content)
Cell-based Flow  Cytom etry(In vitro expression)
Capillary Gel Electrophoresis (RNA Integrity)
a. 1W timepoint not performed on lot EE8493.
b. 3W testing also performed on PPQ lot EL3248
W = Week,   M = Month, LNP = Lipid Nanoparticle
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Page 16Table 2.3.P.8-10. Protocol for BNT162b2 DP at the Thermal Stress Condition of
30 ± 2°C/65 ±5% RH
Analytical Procedure Test Intervalab
Appearance (Visible) 0, 1W, 2W, 1M
Appearance (Visible Particulates)
Dynamic Light Scattering (LNP Size)
Dynamic Light Scattering (LNP Polydispersity)
Fluorescence Assay (RNA Encapsulation)
Fluorescence Assay (RNA Content)
HPLC -CAD (ALC -0315 Content)
HPLC -CAD (ALC -0159 Content)
HPLC -CAD (DSPC Content)
HPLC -CAD (Cholesterol Content)
Cell-based Flow  Cytom etry(In vitro expression)
Capillary Gel Electrophoresis (RNA Integrity)
a. 1W timepoint not performed on lot EE8493. 
b. 3W testing also performed on PPQ lot EL3248
W = Week,   M = Month, LNP = Lipid Nanoparticle
Table 2.3.P.8 -11. Protocol for BNT162b2 DP at the Thermal Stress 
Condition of25 ± 2°C
Analytical Procedure Test Interval (months)
Appearance (Visible & Visible Particles ) 0, 0.5, 1, 2, 3
LNP Size
LNP Polydispersity
RNA Encapsulation
RNA Content
ALC -0315 Content
ALC -0159 Content
DSPC Content
Cholesterol Content
RNA Integrity
pH 0, 3
Thermal cy cling studies are in progress for emergency  suppl y lots EK1768 and EJ1686 
according to the protocols indicated in Table 2.3.P.8 -12. Thermal cy cling studies are also in 
progress for process performance qualification lots according to the protocols indicated in 
Table 2.3.P.8 -13through Table 2.3.P.8 -16.
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Page 17Table 2.3.P.8 -12. Protocol for BNT162b2 Emergency Supply DP Thermal Cycling 
Studies (Lots EK1768 and EJ1686)
Thermal Cycling Conditions:
-Day 0, all inventory placed at -90 to -60°C for 2 w eeks
-At T=2w eeks, samples pulled for testing and all other inventory transferred to -20 ± 5°C for 4 w eeks. 
Samples will be pulled and testing will occur at the 2 and 4 week time points while at the -20 ± 5°C condition 
(week 4 and 6 of study).
-At T=6 w eeks, all remaining inventory will be transferred to 2 to 8°C for 8 w eeks. Samples will be pulled 
and testing will occur at the 2, 4, 6 & 8 w eek time points while at the 2 to 8°C condition (week 8, 10, 12 & 
14 of study).
Analytical Procedure Test Interval (weeks) a 
Appearance (Visible) 0, 2, 4, 6, 8, 10, 12, 14
Appearance (Visible Particulates)
Dynamic Light Scattering (LNP Size)
Dynamic Light Scattering (LNP Polydispersity)
Fluorescence Assay (RNA Encapsulation)
Fluorescence Assay (RNA Content)
HPLC -CAD (ALC -0315 Content)
HPLC -CAD (ALC -0159 Content)
HPLC -CAD (DSPC Content)
HPLC -CAD (Cholesterol Content)
Cell-based Flow  Cytom etry (In vitro expression)
Capillary Gel Electrophoresis (RNA Integrity)
a. Thermal cycling being initiated for lots EK1768 and EJ1686
Table 2.3.P.8 -13. Protocol for BNT162b2 PPQ DP Thermal Cycling Studies (Lots 
EL8723, EN1195 and EL9266)
Thermal Cycling Conditions:
-Day 0, all inventory (previously frozen to ultra cold temperatures of -90 to -60°C after manufacture) placed 
at -20 ± 5°C for 4 w eeks
-At T=4 w eeks, samples pulled for testing and all other inventory transferred to 2 to 8°C for 12 w eeks. 
Analytical Procedure Test Interval (weeks)
Appearance (Visible) 0, 2, 4, 6, 8, 10, 12, 14, 16
Appearance (Visible Particulates)
Dynamic Light Scattering (LNP Size)
Dynamic Light Scattering (LNP Polydispersity)
Fluorescence Assay (RNA Encapsulation)
Fluorescence Assay (RNA Content)
HPLC -CAD (ALC -0315 Content)
HPLC -CAD (ALC -0159 Content)
HPLC -CAD (DSPC Content)
HPLC -CAD (Cholesterol Content)
Cell-based Flow  Cytom etry (In vitro expression)
Capillary Gel Electrophoresis (RNA Integrity)
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Page 18Table 2.3.P.8 -14. Protocol for BNT162b2 PPQ DP Thermal Cycling Studies 
(LotEL3249)
Thermal Cycling Conditions:
-Day 0, all inventory placed at -90 to -60°C for 1 w eek
-At T=1 w eek, inventory transferred to -20 ± 5°C for 2 w eeks. 
-At T=3 w eeks, samples pulled for testing and all remaining inventory transferred to 2 to 8°C for 4 w eeks. 
-At T=7 w eeks, samples pulled for testing and all remaining inventory transferred to 25 ± 2°C/60 ± 5%RH 
for 1 w eek
Analytical Procedure Test Interval (weeks) 
Appearance (Visible) 0, 3, 4, 5, 6, 7, 8
Appearance (Visible Particulates)
Dynamic Light Scattering (LNP Size)
Dynamic Light Scattering (LNP Polydispersity)
Fluorescence Assay (RNA Encapsulation)
Fluorescence Assay (RNA Content)
HPLC -CAD (ALC -0315 Content)
HPLC -CAD (ALC -0159 Content)
HPLC -CAD (DSPC Content)
HPLC -CAD (Cholesterol Content)
Cell-based Flow  Cytom etry (In vitro expression)
Capillary Gel Electrophoresis (RNA Integrity)
Table 2.3.P.8 -15. Protocol for BNT162b2 PPQ DP Thermal Cycling Studies 
(LotEK4242)
Thermal Cycling Conditions:
-Day 0, all inventory placed at -90 to -60°C for 1 w eek
-At T=1 w eek, all other inventory transferred to 2 to 8°C for 4 weeks, with testing occurring weekly while at 
2 to 8°C 
Analytical Procedure Test Interval (weeks) 
Appearance (Visible) 0, 2, 3, 4, 5
Appearance (Visible Particulates)
Dynamic Light Scattering (LNP Size)
Dynamic Light Scattering ( LNP Polydispersity)
Fluorescence Assay (RNA Encapsulation)
Fluorescence Assay (RNA Content)
HPLC -CAD (ALC -0315 Content)
HPLC -CAD (ALC -0159 Content)
HPLC -CAD (DSPC Content)
HPLC -CAD (Cholesterol Content)
Cell-based Flow  Cytom etry (In vitro expression)
Capillary Gel Electrophoresis (RNA Integrity)
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Page 19Table 2.3.P.8 -16. Protocol for BNT162b2 PPQ DP Thermal Cycling Studies 
(LotEL7834)
Thermal Cycling Conditions:
-Day 0, all inventory placed at -90 to -60°C for 1 w eek
-At T=1 w eek, inventory transferred to -20 ± 5°C for 4 w eeks. 
-At T=5 w eeks, samples pulled for testing and all remaining inventory transferred to 2 to 8°C for 4 w eeks. 
-At T=9 w eeks, samples pulled for testing and all remaining inventory transferred to 25 ± 2°C/60 ± 5%RH 
for 1 w eek
Analytical Procedure Test Interval (weeks)
Appearance (Visible) 0, 3, 5, 6, 7, 8, 9, 10
Appearance (Visible Particulates)
Dynamic Light Scattering (LNP Size)
Dynamic Light Scattering (LNP Polydispersity)
Fluorescence Assay (RNA Encapsulation)
Fluorescence Assay (RNA Content)
HPLC -CAD (ALC -0315 Content)
HPLC -CAD (ALC -0159 Content)
HPLC -CAD (DSPC Content)
HPLC -CAD (Cholesterol Content)
Cell-based Flow  Cytom etry (In vitro expression)
Capillary Gel Electrophoresis (RNA Integrity)
2.3.P.8.1.6. Summary of Stability Data
2.3.P.8.1.6.1. Summary of Stability Data at the Long Term Storage Condition (-90
to -60C)
Results from stability  studies on BNT162b2 DP stored at the long term condition of -70 ±
10C are currentl y available for seven clinical lots and one non -clinical lot of BNT162b2 
material . Results from stability  studies on BNT162b2 DP stored at the long term condition of 
-90 to -60 C are also currently  available for process performance qualification and 
emergency  use lots . All results are provided in Section 3.2.P.8.3 L ong-Term. 
Up to 9 months of data are currently  available for the lots manufactured by  Poly mun 
Scientific stored at the long term condition of - 70 ± 10C. All data remained within the 
clinical acceptance criteria in place at the time of testing through the nine month time point 
for clinical lots BCV40420-A, through the 6 month time point for clinical lots BCV40620- A, 
BCV40620 -E, BCV40720 -A, BCV40720 -C, BCV40720 -P and BCV40820- P and through 
the 6 month time point for non -clinical lot CoVVAC/270320 (study  has completed). Overall, 
the data indicate that there have been no significant changes in terms of quality , purity , or 
strength for the drug product.
Thirteen process perform ance qualification and eight emergency  lots of emergency  have 
been placed on formal stability  at the long term condition of -90 to -60 C, with up to 
6months of  data available at this time . Overall, the data generated to date indicate that there 
have been no significant changes in terms of quality , purit y, or strength for the drug product.
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Page 202.3.P.8.1.7. Summary of Stability Data at the Accelerated Storage Condition
Accelerated -40 ± 5C Stability
Results from stability  studies on BNT162b2 DP stored at the accelerat ed condition of - 40 ± 
5C are presented for one clinical lot and one non -clinical lot. Results are provided in 
Section 3.2.P.8.3 Accelerated.  All data remained within the clinical acceptance criteria in 
place at the time of testing through the nine month time point for clinical lot BCV40420 -A 
and through the 3 month time point for non-clinical lot CpVVAC/270320. The - 40 ± 5 C 
accelerated condition provides additional supportive data for the long -term storage under 
recommended condition and supports temporary  temperature excursions from the 
recommended storage condition.
Accelerated -60 to -30C Stability
Three lots of emergency  supply  drug product have been placed on formal stability  at the 
accelerated condition of -60 to -30 C, with up to six mont hs of stability  data currently  
available at this time for one lot and 3 months of available data for the other two . Five 
performance qualification lots have also been enrolled in formal stability  programs at the -60 
to -30 C condition with release data av ailable at this time. Results are provided in 
Section 3.2.P.8.3 Accelerated. All data generated to date remained within the acceptance 
criteria in place at the time of testing, as well as the proposed commercial specifications, 
through the 6 month time points and provide additional supportive data for the long -term 
storage under recommended condition.
Accelerated -20 ± 5C Stability
Results from stability  studies on BNT162b2 DP stored at the accelerated condition of -20 ± 
5C are presented for thirteen process performance qualification lots and eight emergency  
supply  lots. Results are provided in Section 3.2.P.8.3 Accelerated. Up to sixmonths of data 
are currentl y available for emergency suppl y lots EE8492 and EE8493, with t he others 
having up to 3 months of data currentl y available. Up to three month sof data are available 
for the process performance qualification lots. All data generated to date were also within the 
stated specifications at the accelerated condition of -20 ± 5°C through at least the 1 month 
time point. L ot EE8493 was out of specification at the 3 and 6 month time points and lot 
EK4242 was out of specification at the 3 month time point for  at the accelerated 
-20 ± 5°C condition. The -20 ± 5 C accel erated condition provides additional supportive 
data for the long- term storage under recommended condition, supports temporary  
temperature excursions from the recommended storage condition, and supports storage of the 
drug product for up to 1 month at -20 ± 5 C.
Accelerated 2 to 8 C Stability
Results from stability  studies on BNT162b2 DP stored at the accelerated condition of 
5 ± 3C are presented for seven clinical lots, one non- clinical lot, eight emergency  suppl y 
lots and thirteen process perform ance qualification lots. Results are presented in 
Section 3.2.P.8.3 Accelerated.
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Page 212.3.P.8.1.8. Summary of Stability Data at the Thermal Stress Storage Conditions
To support short term temperature excursions, drug product was exposed to the thermal stress 
condition of 25 ± 2°C. Results for one clinical lotispresented in Section 3.2.P.8.3 Thermal –
Stress and Cy cling. There is currentl y up to four months of available data. All data remained 
within the clinical acceptance criteria in place at the time of testing through the two weeks 
(half month) time point. At the onemonth time point and bey ond, drug product lot 
BCV40420 -A was out of specification for . Changes can be expected at 
stressed stability  conditions and does not impact the overall stability  strate gy for this 
material.
Process performance qualification and emergency  supply  lots have been exposed to the 
thermal stress conditions of 25 ± 2 °C/60 ± 5% RH and 30 ± 2 °C/65 ± 5% RH. There is up 
to one month of available data for process performance qualification and emergency  suppl y 
lots presented in Section 3.2.P.8.3 Thermal –Stress and Cy cling.
2.3.P.8.1.9. Summary of Stability Data at the Thermal Cycling Storage Conditions
Two emergency  suppl y drug product lots, EK1768 and EJ1686, have thermal cy cling studie s 
initiated, with up to 14weeks of data available at this time. These studies are being 
performed to provide further support to the in -use period for the drug product. Results 
available thr ough the 14week time points for emergency  suppl y lots are present ed in 
Section 3.2.P.8.3 Thermal – Stress and Cy cling. All data generated to date remained within 
the acceptance criteria in place at the time of testing through the 14week time points
(completion of the studies).
Additionally , process performance qualification lots have thermal studies initated at this time 
to provide further support to the in -use period for the drug product. Results available to date 
for the process performance qualification lot thermal cycling st udies are presented in 
Section 3.2.P.8.3 Thermal – Stress and Cy cling. Lots EN1195, EL 9266 and EL 8723 are 
enrolled in the same thermal cy cling study  design and have up to 8 weeks of data available. 
Thermal cy cling study  for lot EL 3249 and EL7834 have compl eted with 8 weeks of available 
data for EL3249 and 10 weeks for EL7834. Thermal cy cling study  for lot EK4242 has also 
completed, with up to 5 weeks of available stability  data. The  are 
 over time for lot EK4242, however al l data generated to date remained within 
the acceptance criteria in place at the time of testing through the completion of the study . All 
other thermal cy cling data also remained within the acceptance criteria in place at the time of 
testing through time p oints tested to date
2.3.P.8.1.10. Summary of Photostability Stability in Drug Product Vials
One process validation drug product lo t, EL8734, was subjected to the ICH photostability  
condition (option 2). D rug product vials were exposed to a light source that provides an
overall illumination of not less than 1.2 million lux hours and an integrated ultraviolet energy  
of not less than 200 watt hours/m2, per I CH Q1B. Dark control vials were wrapped in 
aluminum foil to prevent exposure to light. All samples were stored invert ed, at 2 to 8 °C for 
the duration of the stud y, as it is not feasible to maintain the samples at the intended storage 
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Page 22condition of - 90 to -60 °C for this study  and the 2 to 8 °C condition is considered a worse 
case exposure condition.
Results for both the dark control and the light exposed samples were within the specifications 
in place at the time of testing. There was a  
 generated on the samples exposed to light as compared to the dark 
control samples, however that is not unexpected and all results generated were within the 
proposed commercial specifications.
2.3.P.8.1.11. Shelf Life and Conclusions
The initial shelf life for the BNT162b2 DP is 6 months when stored at the recommended 
temperature of -90 to -60 C. Additionally , the stability  data generated to date on the 
emergency  use and process performance qualification lots also support an additional storage 
at -20 ± 5°C for up to 2 week s as well as short term storage at 5± 3°C for up to one month 
(within the 6 month shelf life).
The initial shelf life is based on:
Up to 6 months of current available stability  data on emergency  supply  lots and 
process performance qualification lots at both the - 90 to -60 °C intended storage 
condition, as well as the -20 ± 5°C storage condition, and up to 3 months at the 5± 
3°C storage condition.
Up to 9 months of current available stability  data on seven lots of clinical drug 
product
Up to 6 months of curr ent available stability  data on one lot of non- clinical drug 
product
Up to 9 months of current available stability  data on two clinical lots of BNT162b1 
drug product
Comprehensive comparability  assessments performed during development.
Additionally , the in itial in -use period for the thawed, undiluted vial is room temperature for 
not more than 2 hours, which is further discussed in Section 3.2.P.2.6 Compatibility .
These stability  studies are currently  on-going and data from these studies will be used to 
confirm the initial shelf life of the BNT162b2 DP, as well as extend the shelf life based on 
the acceptability  of the data. 
The shelf life will be extended bey ond the 6 months initial shelf life, as data allows, at the 
intended storage condition of - 90 to -60 °C and/or bey ond the 2 weeks at the storage at -20 
±5°C or 5± 3°C storage for up to one month using real time stability  data on a minimum of 
three batches of commercially  representative material.
090177e197037416\Approved\Approved On: 12-May-2021 07:52 (GMT)
(b) (4)
(b) (4)
FDA-CBER-2021-5683-1149007
BNT162b2
2.3.P.8 Stability
PFIZER CONFIDENTIAL
Page 232.3.P.8.2. Post Approval Stability Protocol and Stability Commitmen t
The commercial shelf life of the drug product will be established based on the I CH stability  
studies that are being carried out per protocols detailed in Section 3.2.P.8.1 Stability  
Summary  and Conclusions.
Post-approval, a minimum of one lot of BNT162 b2 drug product will be enrolled in the 
commercial stability  program at the long term storage condition of - 90 to -60 C each year 
that drug product is manufactured. The protocol is provided in Table 2.3.P.8-17 for the long 
term storage conditions of - 90 to -60C.
Table 2.3.P.8 -17. Post-Approval Commercial Stability Protocol for Drug Product 
Stored at -90 to -60 °C
Analytical Procedure/ Quality Attribute Test Intervals (Months)a
Appearance (Visible) 0, 6, 12, 18, 24
Appearance (Visible Particulates)
pH
Subvisible Particulate Matter
Dynamic Light Scattering (DLS) LNP Size
LNP Polydispersity
Fluorescense Assay RNA Encapsulation
RNA Content
HPLC -CAD ALC -0315 Content
ALC -0159 Content
DSPC Content
Cholesterol Content
Cell-based Flow  Cytom etry In Vitro Expression
Capillary Gel Electrophoresis RNA Integrity
Container Closure Integrity Test Annually through end of shelf life
Sterility 0, End of shelf life
Endotoxin
a.Additional test intervals may be included for the purpose of extending expiry.
Abbreviations: LNP = Lipid Nanoparticle
2.3.P.8.3. Stability Data 
Stability  data for long term conditions, accelerated condition, thermal stress and phostability  
studies are provided in Section 3.2. P.8.3.Stability  Data .
090177e197037416\Approved\Approved On: 12-May-2021 07:52 (GMT)
FDA-CBER-2021-5683-1149008