Evidence map›Paper›PMID 40692104›Full record

ArticleJournal of pharmaceutical sciences2025

Scale-up and cGMP manufacturing of next-generation vaccine adjuvant saponin/MPLA nanoParticles (SMNP).

Sammaiah Pallerla, Ivan S Pires, Mariane B Melo, DongSoo Yun, Andreas Wagner, Magdolna Budai, Daniel Kumar, Dietmar Katinger, Eddy Sayeed, Angela Lombardo and 1 more

Abstract read
In one paragraph

Article in Journal of pharmaceutical sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

8 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Sammaiah PallerlaIAVI, 125 Broad Street, 9th Floor, NY, NY 10004, USA. Electronic address: spallerla@iavi.org.
Ivan S PiresDept. of Chemical Engineering, Massachusetts Institute of Technology, 500 Main St., Cambridge, MA 02139, USA; Koch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, 500 Main St., Cambridge, MA 02139, USA.
Mariane B MeloDept. of Immunology & Microbiology, The Scripps Research Institute, 10550 North Torrey Pines Road, IMM-312, La Jolla, CA 92037, USA.
DongSoo YunKoch Institute for Integrative Cancer Research, Massachusetts Institute of Technology, 500 Main St., Cambridge, MA 02139, USA.
Andreas WagnerPolymun ScientificImmunbiologische Forschung GmbH, Donaustr. 99, 3400 Klosterneuburg, Austria.
Magdolna BudaiPolymun ScientificImmunbiologische Forschung GmbH, Donaustr. 99, 3400 Klosterneuburg, Austria.
Daniel KumarPolymun ScientificImmunbiologische Forschung GmbH, Donaustr. 99, 3400 Klosterneuburg, Austria.
Dietmar KatingerPolymun ScientificImmunbiologische Forschung GmbH, Donaustr. 99, 3400 Klosterneuburg, Austria.
Eddy SayeedIAVI, 125 Broad Street, 9th Floor, NY, NY 10004, USA.
Angela LombardoIAVI, 125 Broad Street, 9th Floor, NY, NY 10004, USA.
Darrell J IrvineDept. of Immunology & Microbiology, The Scripps Research Institute, 10550 North Torrey Pines Road, IMM-312, La Jolla, CA 92037, USA; Howard Hughes Medical Institute, 4000 Jones Bridge Rd., Chevy Chase, MD 20815, USA.

Funding

Identification of neutralizing epitopes on SARS-CoV-2 spike for design of vaccines and small-molecule antiviralsUM1AI144462 · NIAID · SCRIPPS RESEARCH INSTITUTE, THE · PI BURTON, DENNIS R. · 2019 to 2025
$201.6M
VIRUS PRODUCTION COREP30CA014051 · NCI · MASSACHUSETTS INSTITUTE OF TECHNOLOGY · PI Jacqueline A. Lees · 1985 to 2026
$93.9M
Howard Hughes Medical InstituteNCI NIH HHS P30 CA014051NIAID NIH HHS UM1 AI144462
6 · The paper itself

Abstract

Saponin/MPLA Nanoparticles (SMNP) is a novel vaccine adjuvant that exhibited excellent safety and potency in a range of preclinical models. Successful scale-up manufacturing under current Good Manufacturing Practices (cGMP) is vital for advancing the clinical development of this promising new adjuvant. Here we report studies transitioning from small-scale formulation to the production of clinical trial material (CTM) in accordance with cGMP. By optimizing the process, a 100-fold scale increase was achieved through closed-system dilution and diafiltration, ensuring both sterility and process efficiency. Analytical characterization confirmed that the SMNP produced under cGMP conditions maintained consistent particle size, morphology, and polydispersity compared to preclinical batches. Hemolysis testing validated safety by assessing QS-21-related activity. Stability studies, conducted in accordance with ICH (International Council for Harmonisation) guidelines, demonstrated both chemical and colloidal integrity during prolonged refrigeration, while also identifying potential degradation risks at frozen or elevated temperatures. This research emphasizes critical factors for ensuring reproducibility, managing raw material variability, and developing scalable, aseptic processes. These results provide a foundation for advancing SMNP-based adjuvants into early-phase clinical trials and subsequent commercial production.

Indexed as

Adjuvants, ImmunologicAdjuvants, VaccineNanoparticlesSaponinsAnimalsDrug StabilityHemolysisHumansParticle SizeAdjuvants, ImmunologicAdjuvants, VaccineSaponinsAdjuvantscGMPMonophosphoryl lipid ASaponinScale-upSMNPTangential flow filtration (TFF)

Identifiers

PMID40692104
PMCPMC12352820

What Socratic holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.