A Phase I/II Dose Escalation Trial of HDAC Inhibitor Tefinostat for Cancer Associated Inflamation in Hepatocellular Carcinoma
试验速览
- 阶段
- 1 期
- 入组人数
- 69
- 试验地点
- 4
- 主要终点
- Determine Maximum Tolerated Dose
研究概览
简要总结
This study is being carried out to assess the best dose of a new drug, called tefinostat, in treating liver cancer.
Tefinostat is a new drug that blocks enzymes called histone deacetylases (pronounced dee-as-et-isle-azes). Cells need these enzymes to grow and divide. Blocking them may stop cancer growing. Drugs that block these enzymes are called histone deacetylase inhibitors or 'HDAC inhibitors'.
Tefinostat has never been given to patients with liver cancer before so it isn't known which dose is best at treating liver cancer. To find this out the study will be testing one dose and if that is safe, then test a higher dose and so on.
The aim of this study is to find the best dose of tefinostat without causing side effects. The study will be looking closely at any side effects patients might experience from this treatment.
详细描述
This is an open label, dose escalating, phase I/II study of Tefinostat administered orally, once or twice daily in 28 day cycles of treatment in patients with advanced hepatocellular carcinoma.
The starting dose of the Phase I dose escalation stage of the study has been based on the results of a previous Phase I trial of Tefinostat in patients with haematological malignancies. The starting dose of Tefinostat will be 360mg OD. As Tefinostat has a median plasma half-life of 0.47h (range 0.19 to 1.18) and CHR-2847 a median half-life of 1.4 h (range 0.98 to 3.79) twice daily dosing will also be investigated, starting at 240mg BID.
Phase I Up to 5 cohorts of 3-6 patients will be treated for 28 days once or twice daily (360, 480mg once daily, then 240, 360, 480mg twice daily) to determine safety and tolerability of Tefinostat and to identify the recommended dose for Phase II (RP2D). Patients with stable disease or with a tumour response will be allowed to continue treatment until PD or unacceptable toxicity, at the discretion of the Investigator.
Patients with advanced HCC who have not received prior systemic therapy will be eligible for the study if they are Child-Pugh classification A and are not candidates for surgical treatment, with adequate bone marrow, hepatic and renal function. Patients should not have a history of organ allograft or any serious concurrent illness.
Doses will be increased in a stepwise fashion and the decision to do so will be made by the participating Investigators on the basis of DLT, PK and PD. The starting dose will be 360mg od. Should this dose not be safe the dose level may be reduced to 240mg od. Dosing will initially take place once a day, for 28 days, while later cohorts will investigate twice daily dosing. More than one DLT in a once daily dose cohort will not preclude investigation of twice daily dosing at a lower dose.
研究设计
- 研究类型
- Interventional
- 分配方式
- Na
- 干预模型
- Single Group
- 主要目的
- Treatment
- 盲法
- None
盲法说明
Open label
入排标准
- 年龄范围
- 18 Years 至 —（Adult, Older Adult）
- 性别
- All
- 接受健康志愿者
- 否
入选标准
- •Signed, informed consent.
- •Histologically or cytologically confirmed malignant HCC refractory to standard therapy or for which no standard therapy exists.
- •a. Patients with alcoholic cirrhosis may be included dependent on clinical judgement as to their ability to conform to the protocol.
- •Patient is not a transplant candidate.
- •Hepatitis is controlled by antiviral therapy (PEG-IFN, ribavirin, telaprevir, etc). Prophylactic Lamivudine for HBV carriers.
- •Child-Pugh classification A or B
- •Adequate bone marrow, hepatic and renal function including the following:
- •Hb ≥ 9.0g/dL, absolute neutrophil count ≥ 1.5 x 109/L, platelets ≥75 x 109/L.
- •Total bilirubin ≤ 1.5 x upper normal limit, excluding cases where elevated bilirubin can be attributed to Gilberts Syndrome.
- •AST (SGOT), ALT (SGPT) ≤ baseline + 4 x upper normal limit .
- •Creatinine ≤ 1.5 x upper normal limit.
- •Serum albumin > 28g/L.
- •INR < 1.5 or a Pt/PTT within normal limits.
- •Age ≥ 18 years.
- •Performance status (PS) 0-2 (ECOG scale).
- •Estimated life expectancy greater than 3 months.
- •Female patients with reproductive potential must have a negative serum pregnancy test within 7 days prior to start of trial. Both women and men must agree to use a medically acceptable method of contraception throughout the treatment period and for 3 months after discontinuation of treatment. Acceptable methods of contraception include IUD, oral contraceptive, subdermal implant and double barrier (condom with a contraceptive sponge or contraceptive pessary).
排除标准
- •Anti-cancer therapy including chemotherapy, radiotherapy, TACE, endocrine therapy, immunotherapy or use of other investigational agents within the 4 weeks prior to trial.
- •Use of medicines known to prolong QTc within 14 days prior to the first dose of study drug (see Appendix III).
- •Candidate for surgical resection, orthotopic liver transplantation, or loco-regional therapy such as radio-frequency ablation or chemoembolization.
- •History of organ allograft.
- •Co-existing active infection or serious concurrent illness.
- •Significant cardiovascular disease as defined by:
- •History of congestive heart failure requiring therapy.
- •History of unstable angina pectoris or myocardial infarction up to 6 months prior to trial entry.
- •Presence of severe valvular heart disease.
- •Presence of a ventricular arrhythmia requiring treatment.
- •LVEF < 50% (or less than institutional norm- some places have 45%).
- •QTc interval ≥ 450ms for men and ≥ 470ms for women (using Bazett's formula).
- •Any co-existing medical condition that in the Investigator's judgement will substantially increase the risk associated with the patient's participation in the study.
- •Psychiatric disorders or altered mental status precluding understanding of the informed consent process and/or completion of the necessary studies.
- •Gastrointestinal disorders that may interfere with absorption of the study drug.
- •Patients requiring palliative radiotherapy within the last 4 weeks of study entry.
- •Uncontrolled hypercalcaemia (>CTCAE v4.03 grade I).
- •Pregnant or breast-feeding women.
- •Patients who have received an investigational drug within the last 4 weeks.
研究组 & 干预措施
Tefinostat
This is an open label, dose escalating, phase I/II study of Tefinostat administered orally, once or twice daily in 28 day cycles of treatment in patients with advanced hepatocellular carcinoma.
Up to 5 cohorts of 3-6 patients (number is dependent on DLT occurrence) will be treated for 28 days once or twice daily (360, 480mg once daily, then 240, 360, 480mg twice daily) to determine safety and tolerability of Tefinostat and to identify the recommended dose for Phase II.
干预措施: Tefinostat (Drug)
结局指标
主要结局
Determine Maximum Tolerated Dose
时间窗: For 28 days following commencing IMP treatment. (Phase I)
Determining the maximal dose at either once or twice daily dosing at which no more than one patient (out of 3) at that dose level experiences a DLT.
次要结局
- Response Assessment(From registration to disease progression.)
- Phase I & II: To determine pharmacokinetic parameters for tefinostat and CHR-2847 when administered orally at different dose levels and dose schedules.(Phase I: End of 28 day treatment period; Phase II: End of 84 days period)