Convidecia is under clinical development by CanSino Biologics and currently in Phase III for Coronavirus Disease 2019 (COVID-19). According to GlobalData, Phase III drugs for Coronavirus Disease 2019 (COVID-19) have a 13% phase transition success rate (PTSR) indication benchmark for progressing into Pre-Registration. GlobalData’s report assesses how Convidecia’s drug-specific PTSR and Likelihood of Approval (LoA) scores compare to the indication benchmarks. Buy the report here.
GlobalData tracks drug-specific phase transition and likelihood of approval scores, in addition to indication benchmarks based off 18 years of historical drug development data. Attributes of the drug, company and its clinical trials play a fundamental role in drug-specific PTSR and likelihood of approval.
Convidecia overview
COVID-19 [adenovirus type 5] vaccine (Convidecia) is an recombinant adenovirus type 5 vector vaccine. It is formulated as suspension and solution for intramuscular route and solution for inhalational route of administration. Convidecia is indicated for the prevention of coronavirus disease 2019 (COVID-19).
Vaccine candidate is under development for the prevention of coronavirus disease 2019 (COVID-19) virus infection and omicron variant BA.1, BA.2.75, BA.4/5 and XBB.1. The vaccine is a recombinant vector vaccine developed based on non-replicating viral vector platform and uses adenovirus type 5 vector. It is administered through intramuscular. It acts by targeting coronavirus spike protein S.
CanSino Biologics overview
CanSino Biologics. (CanSinoBIO) is a biopharmaceutical company that researches, develops, manufactures, and commercializes vaccine products for human use. The company offers pipeline products such as ConvideciaAir (Recombinant COVID-19 vaccine (adenovirus type 5 Vector) for Inhalation), Convidecia (recombinant novel coronavirus vaccine (adenovirus type 5 vector), Menphecia (group A and group C meningococcal conjugate vaccine (CRM197 vector), Menhycia (group ACYW135 meningococcal conjugate vaccine (CRM197 vector), and Ad5-EBOV. CanSinoBIO’s technology platform includes adenovirus-based viral vector technology, synthetic biotechnology, protein structure design and VLP assembly, mRNA and LNP technology, and formulation and drug delivery technology. The company operates manufacturing offices in Mexico, China, Pakistan, and Malaysia. CanSino Biologics is headquartered in Tianjin, China.
For a complete picture of Convidecia’s drug-specific PTSR and LoA scores, buy the report here.
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GlobalData, the leading provider of industry intelligence, provided the underlying data, research, and analysis used to produce this article.
GlobalData’s Likelihood of Approval analytics tool dynamically assesses and predicts how likely a drug will move to the next stage in clinical development (PTSR), as well as how likely the drug will be approved (LoA). This is based on a combination of machine learning and a proprietary algorithm to process data points from various databases found on GlobalData’s Pharmaceutical Intelligence Center.
