Last update 22 Oct 2025

SON-DP

Overview

Basic Info

Drug Type
Protein drugs
Synonyms
SON DP
Target-
Action-
Mechanism-
Therapeutic Areas
NeoplasmsDigestive System DisordersEndocrinology and Metabolic Disease+ [2]
Active Indication
Advanced gastric carcinomaAdvanced Malignant Solid NeoplasmGastroesophageal junction adenocarcinoma+ [5]
Inactive Indication-
Originator Organization
Qurgen, Inc.
Active Organization
Qurgen, Inc.
Suzhou Fuente Pharmaceutical Co., Ltd.
Inactive Organization-
License Organization-
Drug Highest PhasePhase 1
First Approval Date-
Regulation-
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Related

2
Clinical Trials associated with SON-DP
NCT06873659
/ RecruitingPhase 1
A Phase I Dose Escalation and Expansion Study to Evaluate the Safety, Tolerability, Efficacy, Pharmacokinetics, and Pharmacodynamics of SON-DP in Subjects With Advanced Solid Tumors
NCT05989724
/ RecruitingPhase 1
A First-in-Human (FIH), Open-Label, Phase Ia/Ib Dose Escalation and Expansion Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Pharmacodynamics of SON-DP in Participants With Relapsed/Metastatic Solid Tumors
100 Clinical Results associated with SON-DP
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100 Translational Medicine associated with SON-DP
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100 Patents (Medical) associated with SON-DP
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100 Deals associated with SON-DP
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R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
Advanced gastric carcinomaPhase 1
China
Qurgen, Inc.
26 Feb 2025
Advanced Malignant Solid NeoplasmPhase 1
China
Qurgen, Inc.
26 Feb 2025
Gastroesophageal junction adenocarcinomaPhase 1
China
Qurgen, Inc.
26 Feb 2025
Primary Malignant Liver NeoplasmPhase 1
China
Qurgen, Inc.
26 Feb 2025
Breast CancerPhase 1
United States
Qurgen, Inc.
19 Sep 2023
Colorectal CancerPhase 1
United States
Qurgen, Inc.
19 Sep 2023
Ovarian CancerPhase 1
United States
Qurgen, Inc.
19 Sep 2023
Pancreatic CancerPhase 1
United States
Qurgen, Inc.
19 Sep 2023
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Clinical Result

Indication
Phase
Evaluation
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Study
Phase
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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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