Clinical trials

5

Search and review clinical trials. Use filters to narrow results by trial status, phase, treatment, biological sex and sponsor.

Condition / disease
Location
Status: Not yet recruiting

TGRX-678 Chinese Phase III in Chronic Myelogenous Leukemia (CML) Patients

A Phase III study evaluating the safety and efficacy of TGRX-678 in CML-CP patients resistant from or intolerant to at least 3 TKIs

Participants needed: 180
Trial details
Phase: Phase 3Age: 18+Biological sex: AllType: InterventionalSponsor: Shenzhen TargetRx Co., Ltd.Updated: Mar 24, 2026
Eligibility criteria

Willing to consent and to follow study procedures [+8]

Reception of TKI treatment or other anti-tumor treatments prior to first dose [+11]

Status: Recruiting

TGRX-1942 Chinese Phase I for Advanced Solid Tumor And/or Relapsed/Refractory Hematologic Malignancies

A phase I study to evaluate the safety, tolerability, pharmacokinetics and preliminary efficacy of TGRX-1942 in patients with advanced solid tumor and/or relapsed or refractory hematological malignancies

Participants needed: 90
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Shenzhen TargetRx Co., Ltd.Updated: Feb 24, 2025Locations: 1
Eligibility criteria

For dose escalation phase, patient is diagnosed with advanced/metastatic solid t... [+7]

Allergic to any of the ingredient of the investigational drug [+13]

Status: Recruiting

TGRX-678 Chinese Phase II in Chronic Myelogenous Leukemia (CML) Patients

A Phase II study evaluating the safety and efficacy of TGRX-678 in Chronic Myelogenous Leukemia (CML) patients in Accelerated phase (AP) and are relapsed or refractory from third-generation Tyrosine Kinase Inhibitor (TKI) treatment

Participants needed: 40
Trial details
Phase: Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Shenzhen TargetRx Co., Ltd.Updated: Feb 21, 2025Locations: 1
Eligibility criteria

Willing to consent [+15]

Reception of TKI treatment or presence of unrecovered TKI treatment related non-... [+20]

Status: Recruiting

TGRX-678 US Phase I for Subjects with Refractory or Advanced Chronic Myelogenous Leukemia

The purpose of this single-arm, open-label, dose escalation + cohort expansion study is to evaluate the safety, tolerability, pharmacokinetic and preliminary efficacy of TGRX-678 in Chronic Myelogenous Leukemia patients who had failure with or are intolerant to TKI treatments.

Participants needed: 90
Trial details
Phase: Phase 1Age: 18+Biological sex: AllType: InterventionalSponsor: Shenzhen TargetRx Co., Ltd.Updated: Feb 21, 2025Locations: 2
Eligibility criteria

Willing to participate in the study with informed consent; [+10]

Exposure to other antineoplastic therapies prior to study enrollment; [+28]

Status: Recruiting

TGRX-814 Chinese Phase I/II in Patients With Hematological Malignancies

The purpose of this single- arm, open-label, dose escalation and dose expansion phase I/II study is to evaluate the safety, tolerability, pharmacokinetic and preliminary efficacy of TGRX-814 in patients with hematological malignancies including non-Hodgkin lymphoma, acute myeloid leukemia, aute lymphoblastic leukemia and myelodysplastic syndromes.

Participants needed: 30
Trial details
Phase: Phase 1, Phase 2Age: 18+Biological sex: AllType: InterventionalSponsor: Shenzhen TargetRx Co., Ltd.Updated: Apr 10, 2024Locations: 1
Eligibility criteria

male or female ≥ 18 years of age [+9]

received BCL-2 inhibitor therapy prior to the first dose of study drug, unless d... [+16]