Last update 23 Oct 2025

ZT-003

Overview

Basic Info

Drug Type
Fusion protein
Synonyms
ZT 003, ZT003
Target
FGF21R x GLP-1R
Action
agonists
Mechanism
FGF21R agonists, GLP-1R agonists(Glucagon-like peptide 1 receptor agonists)
Therapeutic Areas
Digestive System DisordersEndocrinology and Metabolic Disease
Active Indication
ObesityNonalcoholic SteatohepatitisDiabetes Mellitus
Inactive Indication-
Originator Organization
Beijing Zhitai Biomedical Technology Co., Ltd.Beijing Zhitai Biomedical Technology Co., Ltd.
Active Organization
Beijing Zhitai Biomedical Technology Co., Ltd.Beijing Zhitai Biomedical Technology Co., Ltd.
Inactive Organization-
License Organization-
Drug Highest PhasePhase 1
First Approval Date-
Regulation-
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Related

1
Clinical Trials associated with ZT-003
NCT07184502
/ Not yet recruitingPhase 1
A Phase 1, Randomized, Double-blind, Placebo-controlled, Single and Multiple Ascending Dose Trial to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of ZT003 Injection in Healthy Volunteers and Overweight or Obese Volunteers
100 Clinical Results associated with ZT-003
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100 Translational Medicine associated with ZT-003
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100 Patents (Medical) associated with ZT-003
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100 Deals associated with ZT-003
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R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
ObesityPhase 1
Australia
Beijing Zhitai Biomedical Technology Co., Ltd.Beijing Zhitai Biomedical Technology Co., Ltd.
09 Oct 2025
Nonalcoholic SteatohepatitisIND Approval
United States
Beijing Zhitai Biomedical Technology Co., Ltd.Beijing Zhitai Biomedical Technology Co., Ltd.
30 Jun 2025
Diabetes MellitusPreclinical
China
Beijing Zhitai Biomedical Technology Co., Ltd.Beijing Zhitai Biomedical Technology Co., Ltd.
14 Jun 2024
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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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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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