<HashMap><database>biostudies-literature</database><scores/><additional><omics_type>Unknown</omics_type><volume>12(3)</volume><submitter>Bartolomeo R</submitter><pubmed_abstract>Quality control testing of vaccines, including potency assessment, is critical to ensure equivalence of clinical lots. We developed a potency assay to support the clinical advancement of Nous-209, a cancer vaccine based on heterologous prime/boost administration of two multivalent viral vector products: GAd-209 and MVA-209. These consist of a mix of four Adeno (Great Ape Adenovirus; GAd) and four Modified Vaccinia Ankara (MVA) vectors respectively, each containing a different transgene encoding a synthetic polypeptide composed of antigenic peptide fragments joined one after the other. The potency assay employs quantitative Reverse Transcription PCR (RT-Q-PCR) to quantitatively measure the transcripts from the four transgenes encoded by each product in in vitro infected cells, enabling simu</pubmed_abstract><journal>Vaccines</journal><pagination>325</pagination><full_dataset_link>https://www.ebi.ac.uk/biostudies/studies/S-EPMC10975996</full_dataset_link><repository>biostudies-literature</repository><pubmed_title>Development of a Potency Assay for Nous-209, a Multivalent Neoantigens-Based Genetic Cancer Vaccine.</pubmed_title><pmcid>PMC10975996</pmcid><pubmed_authors>Troise F</pubmed_authors><pubmed_authors>Ruzza V</pubmed_authors><pubmed_authors>Garzia I</pubmed_authors><pubmed_authors>Vitale R</pubmed_authors><pubmed_authors>Cotugno G</pubmed_authors><pubmed_authors>Romano G</pubmed_authors><pubmed_authors>Sdruscia G</pubmed_authors><pubmed_authors>Bignone V</pubmed_authors><pubmed_authors>Allocca S</pubmed_authors><pubmed_authors>Siani L</pubmed_authors><pubmed_authors>Lanzaro F</pubmed_authors><pubmed_authors>Scarselli E</pubmed_authors><pubmed_authors>Petrone AM</pubmed_authors><pubmed_authors>D'Alise AM</pubmed_authors><pubmed_authors>Merone R</pubmed_authors><pubmed_authors>Colloca S</pubmed_authors><pubmed_authors>Leoni G</pubmed_authors><pubmed_authors>Bartolomeo R</pubmed_authors></additional><is_claimable>false</is_claimable><name>Development of a Potency Assay for Nous-209, a Multivalent Neoantigens-Based Genetic Cancer Vaccine.</name><description>Quality control testing of vaccines, including potency assessment, is critical to ensure equivalence of clinical lots. We developed a potency assay to support the clinical advancement of Nous-209, a cancer vaccine based on heterologous prime/boost administration of two multivalent viral vector products: GAd-209 and MVA-209. These consist of a mix of four Adeno (Great Ape Adenovirus; GAd) and four Modified Vaccinia Ankara (MVA) vectors respectively, each containing a different transgene encoding a synthetic polypeptide composed of antigenic peptide fragments joined one after the other. The potency assay employs quantitative Reverse Transcription PCR (RT-Q-PCR) to quantitatively measure the transcripts from the four transgenes encoded by each product in in vitro infected cells, enabling simu</description><dates><release>2024-01-01T00:00:00Z</release><publication>2024 Mar</publication><modification>2026-07-09T10:54:53.169Z</modification><creation>2025-04-04T19:11:13.994Z</creation></dates><accession>S-EPMC10975996</accession><cross_references><pubmed>38543959</pubmed><doi>10.3390/vaccines12030325</doi></cross_references></HashMap>