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A Phase 1 Study Evaluating CPI-0610 in Patients With Progressive Lymphoma
Bu çalışma, önceki tedaviye rağmen ilerleyen Non-Hodgkin veya Hodgkin lenfoma hastalarında CPI-0610 adlı ilacı inceliyor. Standart etkili tedavisi kalmamış, doğrulanmış lenfoması olan 18 yaş üstü hastalar dahil edilmiştir. Faz 1 aşamasında yürütülmüş ve tamamlanmıştır.
Yukarıdaki özet, resmî kaydın sade dile aktarılmış halidir. Orijinal İngilizce başlık referans için gösterilir.
Kriterler ClinicalTrials.gov kaydından orijinal İngilizce haliyle alınmıştır. Uygunluk kararını yalnızca deneyi yürüten ekip verebilir.
Inclusion Criteria: * Adults (aged ≥ 18 years) * Histologically confirmed diagnosis of a non-Hodgkin or Hodgkin lymphoma that has progressed in spite of prior treatment, and for which additional effective standard therapy is not available * Patients may have either measurable or non-measurable disease, but in all cases eligible patients must have disease that can be clinically evaluated for improvement or progression * Eastern Cooperative Oncology Group (ECOG) performance status ≤2 * Adequate hematological, renal, hepatic, and coagulation laboratory assessments * Written informed consent to participate in this study before the performance of any study-related procedure Exclusion Criteria: * A primary lymphoma of the central nervous system (CNS) or known lymphomatous involvement of the CNS. CNS imaging and cerebrospinal fluid sampling are not mandatory in the absence of a clinical suspicion of lymphomatous involvement of the CNS. * Current infection with HIV, Hepatitis B or Hepatitis C. Patients will have serologic testing performed during screening for HIV and Hepatitis B and C. Any serologic results suggestive of an ongoing viral infection will be further investigated as necessary to clarify the patient's status. * Impairment of gastrointestinal (GI) function or GI disease that may significantly alter the absorption of CPI-0610, including any unresolved nausea, vomiting, or diarrhea that is CTCAE grade \>1. * Impaired cardiac function or clinically significant cardiac diseases, including any of the following: * Acute myocardial infarction or angina pectoris ≤ 6 months prior to starting study drug * Serum cardiac troponin (cTn) level ≥ 99% percentile of the upper reference limit * QTcF \> 470 msec on the screening ECG * Left ventricular ejection fraction (LVEF) \< 40% * Uncontrolled cardiac arrhythmia (patients with rate-controlled atrial fibrillation are not excluded.) * Any other concurrent severe and/or uncontrolled concomitant medical condition that could compromise participation in the study (e.g., clinically significant pulmonary disease, clinically significant neurological disorder, active or uncontrolled infection) * Systemic anti-cancer treatment or radiotherapy less than 2 weeks before the first dose of CPI-0610 * Radioimmunotherapy (e.g., 131I-tositumomab, 90Y-ibritumomab tiuxetan) less than 6 weeks before the first dose of CPI-0610 * Treatment with an investigational small molecule less than 2 weeks before the first dose of CPI-0610. In addition, the first dose of CPI-0610 should not occur before a period equal to or greater than 5 half-lives of the small molecule investigational agent has elapsed. * Treatment with a therapeutic antibody less than 4 weeks before the first dose of CPI-0610. A minimum 2-week period between the last treatment with a therapeutic antibody and the first dose of CPI-0610 may be permitted in patients with rapidly progressive or aggressive subtypes of lymphoma following discussion with the medical monitor. * Treatment with medications that are known to be strong inhibitors or inducers of CYP450 enzymes. * Treatment with medications that are known to carry a risk of Torsades de Pointes. * Immunosuppressive treatment that cannot be discontinued both prior to study entry and for the duration of the study. Oral prednisone at a dose of 10 mg or less per day is allowed, as are other oral corticosteroids given at glucocorticoid-equivalent doses. Topical, nasal and inhaled corticosteroids are also allowed. * Pregnant or lactating women * Women of child-bearing potential and men with reproductive potential, if they are unwilling to use adequate contraception while on study therapy and for 3 months thereafter * Patients unwilling or unable to comply with this study protocol