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临床试验/EUCTR2017-001265-24-PL
EUCTR2017-001265-24-PL进行中（未招募）1 期

A Phase 1/2, Open-Label, Safety, Pharmacokinetic and Efficacy Study of Ascending Doses of Oral CK-101 in Patients with Advanced Solid Tumors

Checkpoint Therapeutics, Inc.0 个研究点目标入组 122 人开始时间: 2017年6月22日最近更新:
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试验速览

阶段
1 期
状态
进行中（未招募）
入组人数
122
研究概览入排标准研究者记录与标识符相似试验

研究概览

简要总结

暂无简介。

研究设计

研究类型
Interventional clinical trial of medicinal product

入排标准

性别
All

入选标准

  • •All patients enrolling into either Phase 1 or Phase 2 must meet all of the following inclusion criteria:
  • •Written consent on an IRB-approved Informed Consent Form (ICF) prior to any study-specific evaluation.
  • •At least one lesion, not previously irradiated and not chosen for biopsy during the study screening period, that can be accurately measured at baseline as = 10mm in the longest diameter (except lymph nodes which must have short axis = 15mm) with computed tomography (CT) or magnetic resonance imaging (MRI) which is suitable for accurate repeated measurements. Phase 2 patients: if only one measurable lesion exists, it is acceptable to be used as long as it has not been previously irradiated and baseline tumor assessment scans are done at least 14 days after the screening biopsy is performed.
  • •Life expectancy of at least 3 months
  • •Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1
  • •Age =18 years
  • •Adequate hematological and biological function, confirmed by the following laboratory values:
  • •Bone Marrow Function
  • •- Absolute neutrophil count (ANC) =1.5 x 109/L
  • •- Platelets =100.0 × 109/L
  • •- Hemoglobin =9 g/dL (or 5.6 mmol/L)
  • •Hepatic Function
  • •- Aspartate aminotransferase (AST) and alanine aminotransferase (ALT) =3 × upper limit of normal (ULN); or =5 × ULN if liver metastases
  • •- Bilirubin =1.5 × ULN; or =3 × ULN in the presence of documented Gilbert’s Syndrome (unconjugated hyperbilirubinaemia) or liver metastases
  • •Renal Function
  • •- Serum creatinine =1.5 × ULN
  • •Patients enrolling into Phase 1 also meet the following inclusion criteria:
  • •Histologically or cytologically confirmed diagnosis of any one of the following:
  • •Metastatic or unresectable locally advanced, recurrent NSCLC:
  • •- with documented evidence that the tumor harbors an EGFR mutation known to be associated with EGFR TKI sensitivity (including G719X, exon 19 deletion, L858R, L861Q, T790M); or
  • •- whose disease has not progressed after four cycles of platinum-based first-line chemotherapy (maintenance); or
  • •- after failure of at least one prior chemotherapy regimen and immunotherapy; or
  • •- EGFR WT patients and patients with non-sensitizing EGFR mutations as a later line of treatment.
  • •Any refractory solid tumor setting where targeting EGFR may be reasonable, for example:
  • •- Treatment of patients with locally advanced, unresectable or metastatic pancreatic cancer; or
  • •- KRAS wild-type adenocarcinoma of the colon or rectum that is metastatic and/or unresectable; or
  • •- Squamous cell carcinoma of the head and neck.
  • •For Phase 1 EGFR mutation-positive NSCLC expansion cohorts ONLY, patients enrolling must also meet the following inclusion criteria:
  • •Histologically or cytologically confirmed diagnosis of one of the following:
  • •- Metastatic or unresectable locally advanced NSCLC:
  • •? with documented evidence that the tumor harbors one of the two common EGFR mutations known to be associated with EGFR tyrosine kinase inhibitor (TKI) sensitivity (exon 19 deletion, L858R), either alone or in combination with other EGFR mutations, determined by PCR-based testing of the tumor tissue or plasma sample; and
  • •? treatment naïve for locally advanced or metastatic NSCLC. Prior adjuvant and neo-adjuvant therapy is permitted (chemotherapy, radiotherapy, investigational agents), however, prior exposure to an EGFR TKI is not permitted.
  • •- Metastatic or unresectable locally advanced NSCLC:
  • •? with documented evidence that the tumor harbors an EGFR mutation known to be associated with EGFR tyros

排除标准

  • •Any of the following criteria will exclude patients from study participation:
  • •Active second malignancy or other prior malignancy treated with chemotherapy = 6 months prior to treatment with CK-101.
  • •History of interstitial lung disease or evidence of clinically active interstitial lung disease.
  • •Brain metastases unless asymptomatic, stable and not requiring steroids for = 2 weeks.
  • •Treatment with any of the following:
  • •- An EGFR TKI (erlotinib, gefitinib, neratinib, afatinib, dacomitinib, osimertinib) within 3 days of the first dose of CK-101.
  • •- Any cytotoxic chemotherapy, investigational agent or other anti-cancer drugs from a previous treatment regimen or clinical study within 14 days of the first dose of CK-101.
  • •- Radiotherapy treatment to more than 30% of the bone marrow or with a wide field of radiation within 4 weeks of the first dose of CK-101 (palliative radiation treatment with a limited field of radiation is allowed up to 7 days prior to first dose of CK-101).
  • •- Patients currently receiving (or unable to stop use at least 1 week prior to receiving the first dose of CK-101) medications known to be potent inhibitors of CYP2C8 and potent inhibitors of CYP3A4 (see Appendix E).
  • •Any toxicity related to prior treatment must have resolved to Grade 1 or less, with the exception of alopecia and Grade 2, prior platinum-therapy related neuropathy.
  • •Any of the following cardiac criteria:
  • •- Mean resting corrected QT interval (QTc) > 470 msec obtained from 3 electrocardiograms (ECGs).
  • •- Any clinically important abnormalities in rhythm, conduction or morphology of resting ECG e.g., complete left bundle branch block, third degree heart block, second degree heart block, PR interval > 250 msec.
  • •- Any factors that increase the risk of QTc prolongation or risk of arrhythmic events such as heart failure, hypokalaemia, congenital long QT syndrome, family history of long QT syndrome or unexplained sudden death under 40 years of age in first degree relatives or any concomitant medication known to prolong the QT interval (see Appendix D).
  • •Surgical procedures =14 days prior to administration of CK-101. In all cases, the patient must be sufficiently recovered and stable before treatment administration.
  • •Females who are pregnant or breastfeeding.
  • •Refusal to use adequate contraception for fertile patients (females and males) for 6 months after the last dose of CK-101 (see Appendix C).
  • •Presence of any serious or unstable concomitant systemic disorder incompatible with the clinical study (e.g., substance abuse, uncontrolled psychiatric condition, uncontrolled intercurrent illness including active infection, arterial thrombosis, and symptomatic pulmonary embolism).
  • •Refractory nausea and vomiting, chronic gastrointestinal diseases, inability to swallow the formulated product or previous significant bowel resection that would preclude adequate absorption of CK-101.
  • •For patients enrolling into Phase 1 expansion cohorts and Phase 2, the following criteria will also exclude patients from study participation:
  • •Prior treatment with CK-101 or other third generation TKIs that target EGFR T790M mutation-positive NSCLC (e.g., rociletinib or osimertinib).
  • •Evidence that the tumor harbors an exon 20 insertion mutation.

研究者

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