Last update 25 Oct 2025

RBD SARS-CoV-2 HBsAg VLP vaccine (Serum Institute of India/SpyBiotech)

Overview

Basic Info

Drug Type
Virus-like particle vaccine, Prophylactic vaccine
Synonyms
Receptor Binding Domain (RBD) COVID19 Vaccine Serum Institute of India/SpyBiotech, Viruslike particle (VLP) vaccine Serum Institute of India/SpyBiotech
Target
SARS-CoV-2 S protein
Action
inhibitors
Mechanism
SARS-CoV-2 S protein inhibitors(SARS-CoV-2 S protein inhibitors)
Therapeutic Areas
Infectious DiseasesRespiratory Diseases
Active Indication-
Inactive Indication
COVID-19
Originator Organization
Spybiotech Ltd.Spybiotech Ltd.
Active Organization-
Inactive Organization
Spybiotech Ltd.Spybiotech Ltd.
Serum Institute of India Pvt Ltd.Serum Institute of India Pvt Ltd.
License Organization-
Drug Highest PhasePendingPhase 1/2
First Approval Date-
Regulation-
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Related

2
Clinical Trials associated with RBD SARS-CoV-2 HBsAg VLP vaccine (Serum Institute of India/SpyBiotech)
PACTR202112597608463
/ SuspendedPhase 1
A Phase I/II Study to Evaluate the Safety, Reactogenicity and Immunogenicity of RBD SARS-CoV-2 HBsAg VLP Vaccine in Healthy Adults.
ACTRN12620000817943
/ RecruitingPhase 1/2
A randomized, observer-blind, placebo-controlled, Phase I/II study to evaluate the safety, reactogenicity and immunogenicity of Receptor Binding Domain (RBD) SARS-CoV-2 (COVID-19) Hepatitis B surface antigen (HBsAg) virus like particle (VLP) Vaccine in Healthy Adults
100 Clinical Results associated with RBD SARS-CoV-2 HBsAg VLP vaccine (Serum Institute of India/SpyBiotech)
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100 Translational Medicine associated with RBD SARS-CoV-2 HBsAg VLP vaccine (Serum Institute of India/SpyBiotech)
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100 Patents (Medical) associated with RBD SARS-CoV-2 HBsAg VLP vaccine (Serum Institute of India/SpyBiotech)
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100 Deals associated with RBD SARS-CoV-2 HBsAg VLP vaccine (Serum Institute of India/SpyBiotech)
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R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
COVID-19Phase 2
Australia
Spybiotech Ltd.Spybiotech Ltd.
31 Jul 2020
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date

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Deal

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Core Patent

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Clinical Trial

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Approval

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Regulation

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