Last update 08 May 2025

68Ga-JH12

Overview

Basic Info

Drug Type
Peptide Conjugate Radionuclide, Diagnostic radiopharmaceuticals
Synonyms-
Target
CXCR4
Action
antagonists, enhancers
Mechanism
CXCR4 antagonists(C-X-C motif chemokine receptor 4 antagonists), PET imaging(Positron-emission tomography enhancers)
Therapeutic Areas
NeoplasmsHemic and Lymphatic Diseases
Active Indication
Hematologic NeoplasmsSolid tumorNeoplasms
Inactive Indication-
Originator Organization
First Affiliated Hospital Of Fujian Medical University
Active Organization
First Affiliated Hospital Of Fujian Medical UniversityBivision Biomedical Technology (Nanjing) Co., Ltd.Bivision Biomedical Technology (Nanjing) Co., Ltd.
Inactive Organization-
License Organization-
Drug Highest PhaseEarly Phase 1
First Approval Date-
Regulation-
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Structure/Sequence

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Related

1
Clinical Trials associated with 68Ga-JH12
NCT06688188
/ RecruitingEarly Phase 1IIT
68Ga-JH12 PET/CT: Dosimetry and Biodistribution Study in Patients With Various Cancers
100 Clinical Results associated with 68Ga-JH12
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100 Translational Medicine associated with 68Ga-JH12
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100 Patents (Medical) associated with 68Ga-JH12
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100 Deals associated with 68Ga-JH12
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R&D Status

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IndicationHighest PhaseCountry/LocationOrganizationDate
Hematologic NeoplasmsPhase 1
China
First Affiliated Hospital Of Fujian Medical University
01 Nov 2024
Solid tumorPhase 1
China
First Affiliated Hospital Of Fujian Medical University
01 Nov 2024
NeoplasmsPreclinical
China
Bivision Biomedical Technology (Nanjing) Co., Ltd.Bivision Biomedical Technology (Nanjing) Co., Ltd.
29 Apr 2025
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
PopulationAnalyzed EnrollmentGroupResultsEvaluationPublication Date

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Translational Medicine

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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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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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