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Last Updated: December 11, 2024

CLINICAL TRIALS PROFILE FOR HMPL-523


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Clinical Trials for HMPL-523

Trial ID Title Status Sponsor Phase Summary
NCT02105129 ↗ A Study of the Safety, Tolerability and Pharmacokinetics of HMPL-523 Completed Hutchison Medipharma Limited Phase 1 The primary objective of this study is to assess the safety and tolerability of a single dose of up to 800 mg in Part A (evaluated in planned steps of 5, 20, 50, 100, 200, 300 mg under fasted conditions, followed by 300, 400, 600 and 800 mg HMPL-523 under fed conditions of a standard meal, followed by multiple doses of 200, 300, 400 and 500 mg of HMPL-523 in Part B, in healthy male volunteers. The secondary objective is to determine the pharmacokinetic profile of single (Part A) and multiple (Part B) oral doses of HMPL-523 in healthy male volunteers and to determine the preliminary effect of food (Part C)
NCT02503033 ↗ A Study of HMPL-523 in Relapsed or Refractory Hematologic Malignancies Active, not recruiting Iqvia Pty Ltd Phase 1 The purpose of this study is to evaluate the safety and tolerability of HMPL-523 administered to patients with relapsed or refractory Hematologic Malignancies To determine the maximum tolerated dosage/recommended phase 2 dosage and characterize the dose limited toxicities associated with HMPL-523 when administered to patients with relapsed or refractory Hematologic Malignancies
NCT02503033 ↗ A Study of HMPL-523 in Relapsed or Refractory Hematologic Malignancies Active, not recruiting Hutchison Medipharma Limited Phase 1 The purpose of this study is to evaluate the safety and tolerability of HMPL-523 administered to patients with relapsed or refractory Hematologic Malignancies To determine the maximum tolerated dosage/recommended phase 2 dosage and characterize the dose limited toxicities associated with HMPL-523 when administered to patients with relapsed or refractory Hematologic Malignancies
NCT02857998 ↗ A Study of Hutchison MediPharma Limited(HMPL)-523 in Patients With Relapsed or Refractory Mature B-cell Neoplasms Unknown status Hutchison Medipharma Limited Phase 1 A Phase I, Open-label, Dose-escalation Study of the Safety and Pharmacokinetics of HMPL-523 in Patients With Relapsed or Refractory Mature B-cell Neoplasms
>Trial ID >Title >Status >Phase >Summary

Clinical Trial Conditions for HMPL-523

Condition Name

Condition Name
Intervention Trials
Relapsed or Refractory Lymphoma 2
Immune Thrombocytopenia (ITP) 2
Imumune Thrombocytopenia(ITP) Human Mass Balance 1
Mature B-cell Neoplasms 1
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Condition MeSH

Condition MeSH
Intervention Trials
Thrombocytopenia 3
Purpura, Thrombocytopenic, Idiopathic 2
Neoplasms 2
Lymphoma, Non-Hodgkin 1
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Clinical Trial Locations for HMPL-523

Trials by Country

Trials by Country
Location Trials
Australia 7
China 5
United States 4
Italy 1
Spain 1
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Trials by US State

Trials by US State
Location Trials
Texas 3
South Carolina 1
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Clinical Trial Progress for HMPL-523

Clinical Trial Phase

Clinical Trial Phase
Clinical Trial Phase Trials
Phase 3 1
Phase 2/Phase 3 1
Phase 1 9
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Clinical Trial Status

Clinical Trial Status
Clinical Trial Phase Trials
Not yet recruiting 3
Recruiting 3
Active, not recruiting 2
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Clinical Trial Sponsors for HMPL-523

Sponsor Name

Sponsor Name
Sponsor Trials
Hutchison Medipharma Limited 9
Hutchmed 3
Iqvia Pty Ltd 1
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Sponsor Type

Sponsor Type
Sponsor Trials
Industry 13
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