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NCT06453902RecruitingPhase 2

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

A Single-arm, Open-label, Multi-center Phase II Study Evaluating Efficacy and Safety of TGRX-678 in CML-AP Patients Relapsed or Refractory From 3rd-generation TKI Treatment

Source: ClinicalTrials.gov · Last updated 21 Feb 2025 · Not updated for over 12 months - ask the site whether it is still open

Brief summary (registry, in English)

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

Status (registry)
Recruiting
Phase (registry)
Phase 2
Study type
Interventional
Enrollment
40 (estimated)
First submitted
28 May 2024
Start date
15 Jul 2024
Primary completion date
30 Jun 2026
Lead sponsor
Shenzhen TargetRx Co., Ltd.
NCT number
NCT06453902

What you commit to

  • Study type: Interventional · Phase 2
  • Planned participants: 40
  • From 15 Jul 2024 to the primary completion date, 30 Jun 2026
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Usage of drugs associated with Torsades de Pointes within 1 months before screening
  • Presence of other medical conditions that require using treatment that may have drug-drug interaction with the investigational drug
  • History of any heart or cardiovascular conditions (except for patients with hypertension which is controlled by anti-hypertensive drugs, and blood pressure is controlled at no higher than 160/100 mmHg for 1 months before screening)
  • Usage of any Traditional Chinese Medicine indicated for anti-tumor purpose 2 weeks before first dose
  • Reception of major surgery 14 days before first dose

Other illness

  • History of hemapoietic stem cell transplant
  • Presence of active central nervous system conditions
  • Presence or having uncontrolled condition for cardiovascular diseases
  • Severe hemorrhagic disease unrelated to CML
  • History of severe cardiovascular condition during past TKI treatment for CML
  • History of pancreatic inflammation or alcohol abuse within 3 years before first dose
  • Presence of malabsorption or other conditions that may affect drug absorption
  • Diagnosis of other primary malignant tumor within 5 years
  • Presence of continuous or active infection (including HIV, hepatitis B, hepatitis C)
  • Presence of other conditions that the investigators or medical monitor deem unfit for the study

Other

  • Reception of TKI treatment or presence of unrecovered TKI treatment related non-hematological adverse events within 7 days of first dose
  • Reception of other anti-tumor treatments
  • In need for immune suppressive treatment
  • CML-AP patients who already reached major hematological response
  • CML-AP patients who used to progress to Blast Phase (BP)
  • Uncontrolled Hypertriglyceridemia

Who the study is looking for

  • Willing to consent
  • 18 years of age or above at time of screening; both sexes eligible
  • Relapsed or refactory from 3rd-generation Tyrosine kinase inhibitor (TKI) treatment
  • For patients without T315I mutation, the patients must received 1st, 2nd and 3rd generation TKI
  • For patients with T315I mutation, the patients much received Olverembatinib or Ponatinib treatment
  • Diagnosis of CML-AP by bone marrow morphological test, molecular biology test or cytogenetic tests
  • ECOG score \</=2
  • Minimum life expectancy of at least 3 months
  • Adequate hematological indicators
  • Adequate kidney function
  • Adequate liver function
  • Adequate coagulation function
  • Adequate pancreatic function
  • Adequate QTc interval as confirmed by electrocardiogram (ECG) test
  • Negative pregnancy result at screening for female patients of child-bearing potential
  • Willing to take contraceptive measure during the study (For male and female patients of child-bearing potential)

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Pick your city on the disease page to sort them by distance.

SiteCityCountrySite status
Peking University People's Hospital
Coordinator of this site? Confirm its status
BeijingChinaRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.