Phase I/II Trial to Evaluate Safety, Tolerability and Pharmacokinetic Profile of HM61713 in NSCLC Patients

NCT ID: NCT01588145

Last Updated: 2018-04-24

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE1/PHASE2
• Total Enrollment: 273 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2012-03-31
• Study Completion Date: 2017-08-31

Brief Summary

The main objective of this study is to evaluate the safety and tolerability of HM61713.

Detailed Description

Besides the main objective, there are 3 other objectives as follows:

• To evaluate the anti-cancer effect of HM61713 in NSCLC patients with EGFR mutation
• To investigate the pharmacokinetic profile of HM61713 and its metabolites after oral administration
• To investigate biomarkers related to the safety and efficacy of HM61713

Conditions

Non Small Cell Lung Cancer

Study Design

• Allocation Method: NA
• Intervention Model: SINGLE_GROUP
• Primary Study Purpose: TREATMENT
• Blinding Strategy: NONE

Study Groups

HM61713

Group Type: EXPERIMENTAL

HM61713

Intervention Type: DRUG

BID or QD, PO X 21 day cycle Number of cycles: until progression or unacceptable toxicity develops

Interventions

HM61713

BID or QD, PO X 21 day cycle Number of cycles: until progression or unacceptable toxicity develops

Intervention Type: DRUG

Other Intervention Names

Olmutinib

Eligibility Criteria

Inclusion Criteria

• Patients with histologically or cytologically confirmed diagnosis of advanced NSCLC
• Patients with EGFR mutation-positive tumor
• Patients must have an Eastern Cooperative Oncology Group (ECOG) performance status of 2 or less
• Estimated life expectancy of at least 12 weeks
• Subjects with adequate bone marrow (WBC ≥4,000/mm3, Platelet ≥100,000/mm3, Hemoglobin≥9.0g/dL, ANC≥1,500/mm3), renal (Creatinine≤1.5 mg/dl) and hepatic [aspartate aminotransferase (AST)/ alanine aminotransferase (ALT)/ alkaline phosphatase (ALP)≤3 x ULN, Total bilirubin ≤2.0 mg/dL] function. No significant heart and lung disease.

※ For subjects with a liver metastases, AST/ALT/ALP≤ 5 x ULN is allowed; and for subjects with bone marrow metastases, ALP≤ 5 x ULN is allowed

• Patients with amylase level ≤ 1.5 x ULN
• Subjects who have provided voluntary consent to participate in the study, and signed the written consent document

<Dose escalation part>

• Malignancy that has progressed after at least two prior chemotherapy regimens, including EGFR-TKI

<Expansion part 1>

• Patients with disease progression despite anticancer therapy with EGFR-TKI (e.g., erlotinib, gefitinib, neratinib, afatinib, dacomitinib)
• Patients who have provided voluntary consent for collection of tumor tissue taken and archived after the last anticancer therapy or collection of new tissue specimen and signed the written consent document

<Expansion part 2> & <Phase 2>

• Patients with disease progression despite anticancer therapy with EGFR TKI (e.g., erlotinib, gefitinib, neratinib, afatinib, dacomitinib) (Except treatment with EGFR mutation selective inhibitor, the same class of drug as investigational drug in this study)
• T790M mutation-positive confirmed in tissue collected after PD is confirmed during or after the last anticancer therapy
• At least one measurable target lesion allowing repeated measurement according to RECIST ver1.1 as of screening

<Phase 1 Expansion part 3>

• Patients with disease progression despite anticancer therapy with EGFR TKI (e.g., erlotinib, gefitinib, neratinib, afatinib, dacomitinib) (Except treatment with EGFR mutation selective inhibitor, the same class of drug as investigational drug in this study)
• T790M mutation-negative confirmed in tissue collected after progressive disease (PD) is confirmed during or after the last anticancer therapy
• At least one measurable target lesion allowing repeated measurement according to RECIST ver1.1 as of screening

Exclusion Criteria

• Hematologic malignancies
• Symptomatic or uncontrolled central nervous system metastases
• Interstitial lung disease, including pulmonary fibrosis
• LVEF < 40% or NYHA Class III or IV heart failure
• History of pancreatitis
• History or current evidence, of any psychiatric or congenital disorder, including dementia or epilepsy
• Compromised organ function, infection or allergy
• Pregnant or breast-feeding women, or women of child-bearing potential who do not use an appropriate method of contraception (male patients should also use an appropriate method of contraception during the study period)
• Patients who had received other investigational product within 30 days prior to screening

• Minimum Eligible Age: 20 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: No

Sponsors

Hanmi Pharmaceutical Company Limited

INDUSTRY

Sponsor Role: lead

Responsible Party

Responsibility Role: SPONSOR

Principal Investigators

Dong-Wan Kim, MD PhD

Role: PRINCIPAL_INVESTIGATOR

Seoul National University Hospital

Locations

Seoul, , South Korea

Countries

South Korea

Other Identifiers

HM-EMSI-101

Identifier Type: -

Identifier Source: org_study_id