Last update 01 Nov 2025

LvID(Guangxi University)

Overview

Basic Info

Drug Type
Toxin
Synonyms
α4/7-conotoxin (CTx) LvID
Target
CHRNA7
Action
antagonists
Mechanism
α7 receptor antagonists(Neuronal acetylcholine receptor protein alpha-7 subunit antagonists)
Therapeutic Areas
NeoplasmsImmune System DiseasesNervous System Diseases+ [3]
Active Indication
Alzheimer DiseaseAtherosclerosisLung Cancer+ [1]
Inactive Indication-
Originator Organization
Hainan UniversityHainan UniversityZhejiang UniversityZhejiang UniversityGuangxi UniversityGuangxi University
Active Organization
Zhejiang UniversityZhejiang UniversityGuangxi UniversityGuangxi UniversityHainan UniversityHainan University
Inactive Organization-
License Organization-
Drug Highest PhasePreclinical
First Approval Date-
Regulation-

Related

100 Clinical Results associated with LvID(Guangxi University)
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100 Translational Medicine associated with LvID(Guangxi University)
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100 Patents (Medical) associated with LvID(Guangxi University)
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100 Deals associated with LvID(Guangxi University)
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R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
Alzheimer DiseasePreclinical
China
Zhejiang UniversityZhejiang University
10 Apr 2025
Alzheimer DiseasePreclinical
China
Hainan UniversityHainan University
10 Apr 2025
Alzheimer DiseasePreclinical
China
Guangxi UniversityGuangxi University
10 Apr 2025
AtherosclerosisPreclinical
China
Hainan UniversityHainan University
10 Apr 2025
AtherosclerosisPreclinical
China
Zhejiang UniversityZhejiang University
10 Apr 2025
AtherosclerosisPreclinical
China
Guangxi UniversityGuangxi University
10 Apr 2025
Lung CancerPreclinical
China
Guangxi UniversityGuangxi University
10 Apr 2025
Lung CancerPreclinical
China
Zhejiang UniversityZhejiang University
10 Apr 2025
Lung CancerPreclinical
China
Hainan UniversityHainan University
10 Apr 2025
Myasthenia GravisPreclinical
China
Hainan UniversityHainan University
10 Apr 2025
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date

No Data

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Deal

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Clinical Trial

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Approval

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Biosimilar

Competitive landscape of biosimilars in different countries/locations. Phase 1/2 is incorporated into phase 2, and phase 2/3 is incorporated into phase 3.
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Competitive landscape of biosimilars in different countries/locations. Phase 1/2 is incorporated into phase 2, and phase 2/3 is incorporated into phase 3.

Regulation

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