Safety, Tolerability and Pharmacokinetics of Oral Tablet of Irinotecan in Adult Patients With Solid Tumors

Metastatic Colorectal Cancer Clinical Trial

Official title:

Irinotecan Gastro-resistant Tablet. An Open Label Phase I, Dose Escalating Study Evaluating Safety, Tolerability and Pharmacokinetics of Oral Administration of Irinotecan in Adult Patients With Solid Tumors

Clinical Trial Details — Status: Completed

Administrative data

• NCT number: NCT03295084
• Other study ID #: AA1446
• Status: Completed
• Phase: Phase 1
• Start date: July 15, 2015
• Est. completion date: October 30, 2018

Study information

• Verified date: October 2020
• Source: Herlev Hospital
• Contact: n/a
• Is FDA regulated: No
• Study type: Interventional

Clinical Trial Summary

This study evaluates the safety, tolerability and pharmacokinetics of oral administration of irinotecan in adult patients. Oral irinotecan will be administered as monotherapy in a dose escalation trial to establish the Maximal Tolerated Dose. Totally 25 patients will be treated with irinotecan tablets as mono-therapy. As an extension trial 12 patients will be treated with oral irinotecan in combination with oral capecitabine

Description:

The study is a phase I, open-label, dose escalation single center study in patients with solid tumors. The study will investigate safety, tolerability and Maximal Tolerated Dose as primary end-points of an irinotecan tablet given as single agent or in combination with oral capecitabine. Secondary end-points are pharmacokinetics and preliminary anti-tumor response.

Cohorts of 3 patients will be treated on selected dose level with oral irinotecan in order to identify Dose Limiting Toxicity (DLT) and Maximal Tolerated Dose (MTD). Totally 12 subjects will be treated at the MTD level. Patients will receive irinotecan tablets once daily in the morning for 14 consecutive days within 3 week treatment cycles. As an extension trial totally 12 subjects will be treated with oral irinotecan in combination with oral capecitabine. Patients treated in combination therapy will receive irinotecan tablets once daily in the morning for 14 consecutive days in combination with capecitabine dosed twice daily for 14 consecutive days within 3 week treatment cycles.

Recruitment information / eligibility

• Status: Completed
• Enrollment: 39
• Est. completion date: October 30, 2018
• Est. primary completion date: July 3, 2018
• Accepts healthy volunteers: No
• Gender: All
• Age group: 18 Years and older

Eligibility

Inclusion Criteria:

• Signed written Informed Consent

• 18 years of age or older

• Capable of understanding the protocol requirements and risk associated with the study

• Patients must have histological confirmed malignancy (solid tumor) that is metastatic or unresectable and for which standard curative or palliative measures do not exist or are no longer effective

• Patients with either measurable disease according to RECIST 1.1 or non-measurable disease

• Performance status 0-1 (ECOG)

• Life expectancy = 3 months

• Coagulation INR < 1.3 and APTT within normal limits

• WBC = 3000/mm3

• Absolute neutrophil count = 1500/mm3

• Hemoglobin = 6.0 mmol/L

• Platelet count = 100.000/mm3

• Bilirubin = 1.5 times upper limit of normal (ULN)

• AST and ALT = 2.5 times ULN AST and ALT = 2.5 times ULN. For patients with liver metastasis adequate hepatic function is defined by aspartate aminotransferase (AST) = 5 x ULN and alanine aminotransferase ALT = 5 x ULN

• No severe or uncontrolled renal condition (creatinine = than 1.5 ULN)

• No significant cardiovascular disease (New York Heart Association Class III and IV)

• No other severe cardiac condition not defined above

• No significant cardiovascular disease (incl. myocardial infarction, unstable angina, symptomatic congestive heart failure, serious uncontrolled cardiac arrhythmia) = 1 year prior for patients to be enrolled and treated in combination with oral capecitabine

• No severe or uncontrolled pulmonary condition

• No known prior hypersensitivity reaction to irinotecan

• No known prior hypersensitivity to capecitabine or 5-fluorouracil for patients to be enrolled and treated in combination with oral capecitabine

• No chronic enteropathy (e.g. active inflammatory bowel disease, extensive intestinal resection or chronic diarrhea)

• No bowel obstruction or sub-obstruction

• No prior history of intestinal malabsorption

• Patients have to be able to swallow normally and have to be willing to comply with the intake of tablets

• No psychiatric condition that would preclude study participation

• No co-existing active infection requiring antibiotics or any co-existing medical conditions likely to interfere with study procedures

• No other condition that will preclude study participation

• A negative pregnancy test for women of childbearing potential. For men and women of child-producing potential, the use of effective contraceptives methods during the study and at least 3 months after discontinuations of the study drug is required.

• Not pregnant or nursing

• Peripheral neuropathy NCI CTCAE grade less than 2 for patients to be enrolled and treated in combination with oral capecitabine

• The patient is willing and able to comply with hospitalization for treatment and scheduled follow-up visits and examinations

Exclusion Criteria:

• Simultaneous participation in any other study involving investigational drugs or having participated in a study within 4 weeks prior to start of study treatment

• Symptomatic brain metastases

• Intake of any prohibited concomitant medication

• Known Dihydropyrimidine dehydrogenase (DPD) deficiency for patients to be enrolled and treated in combination with oral capecitabine.

Related Conditions & MeSH terms

• Colorectal Neoplasms
• Metastatic Colorectal Cancer

Intervention

Drug:
• Irinotecan
Dose Escalation
• Capecitabine
Dose Escalation

Locations

Country	Name	City	State
Denmark	Herlev Hospital	Herlev

Sponsors (1)

Lead Sponsor	Collaborator
Dorte Nielsen

Country where clinical trial is conducted

Denmark, 

Outcome

Type	Measure	Description	Time frame	Safety issue
Primary	Maximal Tolerated Dose (MTD) and Dose Limiting Toxicity (DLT) of oral Irinotecan based on incidence of Treatment-Emergent Adverse Events	Number of patients with Treatment Related Adverse Events as assessed according to the NCI Common Terminology Criteria for Adverse events CTCAE version 4.0	2 treatment cycles of 3 weeks
Secondary	Maximum Tolerated Dose (MTD) and the Dose Limiting Toxicity (DLT) of oral Irinotecan in combination with oral Capecitabine based on incidence of Treatment-Emergent Adverse Events	Number of patients with Treatment Related Adverse Events as assessed according to the NCI Common Terminology Criteria for Adverse events CTCAE version 4.0	2 treatment cycles of 3 weeks
Secondary	Area under the Concentration-Time-Curve (AUC) for Irinotecan and its metabolites SN-38 and SN-38 glucoronide	PK samples will be collected at predetermined time intervals and pharmacokinetic parameter calculated and reported based on the plasma concentration profile	Day 1 and Day 14 of first 3 weeks treatment cycle
Secondary	Maximum Serum Concentration (Cmax) for irinotecan and its metabolites SN-38 and SN-38 glucoronide	PK samples will be collected at predetermined time intervals and pharmacokinetic parameter calculated and reported based on the plasma concentration profile	Day 1 and Day 14 of first 3 weeks treatment cycle
Secondary	Time to Maximum Serum Concentration (Tmax) for irinotecan and its metabolites SN-38 and SN-38 glucoronide	PK samples will be collected at predetermined time intervals and pharmacokinetic parameter calculated and reported based on the plasma concentration profile	Day 1 and Day 14 of first 3 weeks treatment cycle
Secondary	Half-life (t½) for irinotecan and its metabolites SN-38 and SN-38 glucoronide	PK samples will be collected at predetermined time intervals and pharmacokinetic parameter calculated and reported based on the plasma concentration profile	Day 1 and Day 14 of first 3 weeks treatment cycle
Secondary	Serum concentration 24 hours after dosing and prior to administration of the next dose (C24) for Irinotecan and its metabolites SN-38 and SN-38 glucoronide	PK samples will be collected at predetermined time intervals and pharmacokinetic parameter calculated and reported based on the plasma concentration profile	Day 1 and Day 14 of first 3 weeks treatment cycle
Secondary	Objective tumor response to treatment based on RECIST 1.1 criteria	CT scans with tumor response as assessed using RECIST 1.1. criteria	2 treatment cycles of 3 weeks