Last update 21 Nov 2024

TGRX-814

Overview

Basic Info

Drug Type
Small molecule drug
Synonyms
Target
Bcl-2 x Bcl-xl
Mechanism
Bcl-2 inhibitors(Apoptosis regulator Bcl-2 inhibitors), Bcl-xl inhibitors(Apoptosis regulator Bcl-X inhibitors)
Therapeutic Areas
NeoplasmsHemic and Lymphatic DiseasesImmune System Diseases
Active Indication
Acute Myeloid LeukemiaAdult Acute Lymphocytic LeukemiaMyelodysplastic Syndromes+ [1]
Inactive Indication-
Originator Organization
Shenzhen TargetRx, Inc.Shenzhen TargetRx, Inc.Startup
Active Organization
Shenzhen TargetRx, Inc.Shenzhen TargetRx, Inc.Startup
Inactive Organization-
Drug Highest PhasePhase 1/2
First Approval Date-
Regulation-
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Related

2
Clinical Trials associated with TGRX-814
CTR20240015 / RecruitingPhase 1/2
一项评价 TGRX-814 单药及联合疗法治疗血液系统恶性肿瘤 患者的安全性、耐受性、药代动力学和初步疗效的单臂、开放、 剂量递增及扩展的 I/II 期临床试验
[Translation] A single-arm, open-label, dose-escalation and expansion Phase I/II clinical trial to evaluate the safety, tolerability, pharmacokinetics and preliminary efficacy of TGRX-814 monotherapy and combination therapy in patients with hematological malignancies
NCT06206174 / RecruitingPhase 1/2
A Single-arm, Open-label, Dose Escalation and Expansion Phase I/II Study Evaluating Safety, Tolerability, Pharmacokinetics and Preliminary Efficacy of TGRX-814 Monotherapy and Combination Therapy in Patients With Hematological Malignancies
100 Clinical Results associated with TGRX-814
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100 Translational Medicine associated with TGRX-814
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100 Patents (Medical) associated with TGRX-814
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100 Deals associated with TGRX-814
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R&D Status

10 top R&D records.
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IndicationHighest PhaseCountry/LocationOrganizationDate
Acute Myeloid LeukemiaPhase 2
CN
Shenzhen TargetRx, Inc.Shenzhen TargetRx, Inc.Startup
06 Mar 2024
Adult Acute Lymphocytic LeukemiaPhase 2
CN
Shenzhen TargetRx, Inc.Shenzhen TargetRx, Inc.Startup
06 Mar 2024
Myelodysplastic SyndromesPhase 2
CN
Shenzhen TargetRx, Inc.Shenzhen TargetRx, Inc.Startup
06 Mar 2024
Non-Hodgkin LymphomaPhase 2
CN
Shenzhen TargetRx, Inc.Shenzhen TargetRx, Inc.Startup
06 Mar 2024
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Clinical Result

Indication
Phase
Evaluation
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Phase
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Approval

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Regulation

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