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Enabling Lyophilized Pneumococcal Conjugate Vaccines Through Formulation Design and Excipient Selection Suitable for
Christopher Mensch1, Ramesh Chintala2, Denise Nawrocki3
1Biologics and Vaccines Analytical, MMD, Merck & Co., Inc., West Point, PA, USA.
Insights
Researchers developed a novel lyophilized pneumococcal conjugate vaccine (PCV) formulation with 15 serotypes. This innovation offers improved thermostability and broader coverage, addressing gaps in global vaccine access.
Area of Science:
- Vaccinology
- Pharmaceutical Formulation
- Microbiology
Background:
- Existing pneumococcal conjugate vaccines (PCVs) show consistent benefits but global coverage remains limited.
- A lack of lyophilized PCV formulations hinders wider accessibility and thermostability.
- Current vaccines do not cover all relevant Streptococcus pneumoniae serotypes.
Purpose of the Study:
- To evaluate the feasibility of a new formulation for a lyophilized adjuvanted PCV.
- To develop a vaccine containing 15 different pneumococcal serotypes.
- To enhance vaccine stability and global accessibility.
Main Methods:
- Formulation development for a lyophilized adjuvanted PCV.
- Evaluation of physical stability, antigen adsorption, and in-vitro potency.
- Assessment of lyophilized cake appearance and reconstitution times.
Main Results:
- Demonstrated a viable formulation design space for enhanced physical stability.
- Controlled vaccine agglomeration and preserved in-vitro potency.
- Achieved acceptable reconstitution times and maintained antigen adsorption.
Conclusions:
- Successful development of a stable lyophilized adjuvanted PCV formulation with 15 serotypes.
- Identified beneficial excipients for multivalent adjuvant-containing vaccines.
- This formulation offers potential for improved global vaccine access through enhanced stability.
Abstract:
Despite a consistent benefit of existing pneumococcal conjugate vaccine (PCV) on invasive pneumococcal disease and pneumonia across different epidemiological settings a tremendous gap exists towards global PCV coverage. Currently, no lyophilized dosage form exists in the PCV global vaccine marketplace and currently licensed vaccines target some, but not all relevant serotypes of Streptococcus pneumoniae. The development of lyophilized presentations of an adjuvanted multivalent vaccine formulation that aligns with the evolving epidemiological assessment of the pneumococcal disease offers broader coverage with distinct cold chain and thermostability advantages. To make progress towards this goal, we evaluated the feasibility of developing new formulation to enable a lyophilized adjuvanted PCV vaccine containing 15 different serotypes. Our findings successfully demonstrate a formulation design space that enables enhanced physical stability which controls vaccine agglomeration, preserves in-vitro vaccine potency, maintains PCV antigen adsorption, and yields elegant lyophilized cakes with acceptable clinically relevant reconstitution times. This research also demonstrates the benefit of utilizing specific vaccine formulation excipients and the effectiveness of excipient combinations that may be beneficial for other multivalent adjuvant containing vaccines to enable novel lyophilized formulations necessary for improved global vaccine access.
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