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New treatment option for Carcinoma, Hepatocellular
Official title A Study of PTX-9908 Injection for Non-resectable HCC with TACE
ClinicalTrials.gov ID: NCT03812874
What this study is testing
What is PTX-9908 Injection?
PTX-9908 Injection is an investigational medicine, given as an once-weekly infusion into a vein, being studied as a potential treatment for carcinoma, hepatocellular.
Plain-language explanation of the investigational treatment - it is being studied and is not an approved or proven therapy. The study team can confirm the details.
- What it's testing
- This is a multicenter, Phase I/II study in patients with non-resectable hepatocellular carcinoma following TACE treatment. Phase I (Open-label dose escalation) This study will be an open-label study with an Accelerated Phase and a Standard Phase.
- Phase 2: a mid-size study of how well it works
- You might receive a placebo (an inactive treatment) instead of the study drug, decided by chance.
A plain-language read of the study's public ClinicalTrials.gov listing. The study team confirms the details.
Who can take part
Ages 20 and older
You may be able to join if
- Unresectable hepatocellular carcinoma and at intermediate-stage HCC (BCLC stage B or Child-Pugh class A/B with large or multifocal HCC, no vascular...
- Recovered from TACE treatment and procedure related toxicities including ALT/AST and bilirubin within normal limit or reference numeric value...
- ECOG (Eastern Cooperative Oncology Group) performance status \< 2.
- Have adequate organ and marrow function as defined below:
- Absolute neutrophil count \> 1,200/µL
You likely can't join if
- 1\. Patient with Child-Pugh B8-9.
- Patient who has had anti-cancer therapy including surgery, radiotherapy, immunotherapy, or chemotherapy (except in TACE regimen) within 4 weeks prior...
- Patient who has received any other investigational agents within 4 weeks prior to the screening visit.
- Patient who has not recovered from the side effects of the earlier investigational agent or had anti-cancer therapy including surgery, radiotherapy...
- Patient with known brain metastases, leptomeningeal or epidural metastases (unless treated and well controlled for \>= 3 months).
- Patient with prior history of co-malignancies, except for adequately treated carcinoma in situ of the cervix, ductal carcinoma in situ (DCIS) of the...
See the full eligibility criteria
- Unresectable hepatocellular carcinoma and at intermediate-stage HCC (BCLC stage B or Child-Pugh class A/B with large or multifocal HCC, no vascular invasion, or extrahepatic spread) with completed TACE procedure in 4...
- Recovered from TACE treatment and procedure related toxicities including ALT/AST and bilirubin within normal limit or reference numeric value (reference value is defined as the test value before TACE procedure).
- ECOG (Eastern Cooperative Oncology Group) performance status \< 2.
- Have adequate organ and marrow function as defined below:
- Absolute neutrophil count \> 1,200/µL
- Hemoglobin \> 9 g/dL
- Platelets \> 100,000/µL
- Total bilirubin \< 2 X ULN
- Have adequate kidney function as estimated glomerular filtration rate (eGFR) \> 60 mL/min/1.73m2
- A negative pregnancy test at screening. This applies to any female patient with childbearing potential.
- Agree to use adequate contraception after signing informed consent form, during the duration of study participation and for at least 4-weeks after completion or withdrawal from the study. This applies to any female...
- Established use of oral, injected or implanted hormonal methods of contraception
- Placement of an intrauterine device (IUD) or intrauterine system (IUS)
- Barrier methods of contraception: condom or occlusive cap (diaphragm or cervical/vault caps) \>=20 years of age. (Note: In Taiwan, age of majority recognized in law is 20 years of age)
- \>=20 years of age. (Note: In Taiwan, age of majority recognized in law is 20 years of age)
- Anticipated life expectancy of \>= 6 months at assessment during screening.
- Ability to understand and have signed a written informed consent document.
- 1\. Patient with Child-Pugh B8-9.
- Patient who has had anti-cancer therapy including surgery, radiotherapy, immunotherapy, or chemotherapy (except in TACE regimen) within 4 weeks prior to the screening visit.
- Patient who has received any other investigational agents within 4 weeks prior to the screening visit.
- Patient who has not recovered from the side effects of the earlier investigational agent or had anti-cancer therapy including surgery, radiotherapy, immunotherapy, or chemotherapy.
- Patient with known brain metastases, leptomeningeal or epidural metastases (unless treated and well controlled for \>= 3 months).
- Patient with prior history of co-malignancies, except for adequately treated carcinoma in situ of the cervix, ductal carcinoma in situ (DCIS) of the breast, and basal cell/squamous cell skin cancer.
- Patient with history of myocardial infarction or uncontrolled cardiac dysfunction, or unstable arrhythmia or symptomatic peripheral arterial vascular disease.
- Patient with history of positive serology for human immunodeficiency virus (HIV).
- Patient with active, uncontrolled bacterial, viral, or fungal infections, which require systemic therapy.
- Patient with poor liver function as indicated by serum bilirubin \> 2 mg/dL, Child-Pugh Class C, severe coagulopathy (INR \> 2) not correctable with vitamin K, or active hepatic encephalopathy.
- Patient with known allergic reactions to biological agent or polypeptides similar to PTX-9908 Injection.
- Woman who is pregnant or nursing.
- Patient with concomitant disease or condition that could interfere with the conduct of the study, or that would, in the opinion of the investigator, pose an unacceptable risk to the patient in this study.
- Patient with unwillingness or inability to comply with the study protocol for any reason.
- A marked baseline prolongation of QT/QTc interval (e.g., repeated demonstration of a QTc interval \>480 milliseconds (ms) (CTCAE grade 1) using Frederica's QT correction formula
- A history of additional risk factors for torsades de pointes (e.g., heart failure, hypokalemia, family history of Long QT Syndrome)
- The use of concomitant medications that prolong the QT/QTc interval
The study team makes the final eligibility decision.
Where it's taking place
- New Taipei City, Taiwan, Taiwan
Questions & answers
Do participants get paid in this trial?
This listing doesn't specify compensation. Many trials still reimburse travel or offer a stipend, so it's worth asking the study team when you connect.
Is it free to join, and do I need insurance?
Searching and applying through BridgeMD is free. In clinical trials the study-related treatment and visits are generally provided at no cost to you. You usually don't need insurance to take part - confirm specifics with the study team.
How long does this study last?
The listing doesn't state an exact length. The study team walks you through the schedule and number of visits before you decide to enroll.
Who can join this trial?
This study is enrolling all sexes, 20 years and older. The study team makes the final eligibility decision.
Where is this trial taking place?
Study sites include New Taipei City, Taiwan, Taiwan. Enter your location above to see the nearest site and check your eligibility.
Explore other conditions
BridgeMD is an information and trial-matching tool - not medical advice, and not the study sponsor. Details come from ClinicalTrials.gov; the study team decides eligibility.