Last update 01 Nov 2024

VIS-954

Overview

Basic Info

Drug Type
Monoclonal antibody
Synonyms
VIS 954, VIS954
Target
C5AR1
Mechanism
C5AR1 antagonists(C5a anaphylatoxin chemotactic receptor antagonists)
Therapeutic Areas
Immune System DiseasesCongenital DisordersOther Diseases
Active Indication
Disorder of ComplementHereditary Complement Deficiency Diseases
Inactive Indication-
Originator Organization
Visterra, Inc.Visterra, Inc.
Active Organization
Visterra, Inc.Visterra, Inc.
Inactive Organization-
Drug Highest PhasePhase 1
First Approval Date-
Regulation-
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Related

1
Clinical Trials associated with VIS-954
NCT06212804 / CompletedPhase 1
A Phase 1, Randomized, Placebo-controlled, Double Blind, Single Ascending Dose, First-in-human Study to Assess the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of VIS954 in Healthy Male and Female Participants
100 Clinical Results associated with VIS-954
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100 Translational Medicine associated with VIS-954
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100 Patents (Medical) associated with VIS-954
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100 Deals associated with VIS-954
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R&D Status

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IndicationHighest PhaseCountry/LocationOrganizationDate
Disorder of ComplementPhase 1
US
Visterra, Inc.Visterra, Inc.
-
Hereditary Complement Deficiency DiseasesPreclinical
US
Visterra, Inc.Visterra, Inc.
-
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date

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Clinical Trial

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Approval

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Regulation

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