Status:
UNKNOWN
Safety, Tolerability, Pharmacokinetics and Anti-tumour Activity of AC0010 in Advanced Non Small Cell Lung Cancer
Lead Sponsor:
Sun Yat-sen University
Collaborating Sponsors:
Acea Bio (Hangzhou) Co., Ltd.
Hangzhou ACEA Pharmaceutical Research Co., Ltd.
Conditions:
Non-Small Cell Lung Cancer
Eligibility:
All Genders
18-70 years
Phase:
PHASE1
PHASE2
Brief Summary
AC0010 Maleate Capsules is a new, irreversible, Epidermal Growth Factor Receptor (EGFR) mutation selective Tyrosine Kinase Inhibitor.Aim at local advanced or metastatic non-small cell lung cancer pati...
Detailed Description
This study will treat patients with advanced NSCLC who have already received at least one course of specific anti-cancer treatment but the tumor has started to re-grow following that treatment. This i...
Eligibility Criteria
Inclusion
- Patients of either gender, aged from 18 years older to 70.
- Histologically or cytologically confirmed metastatic, or unresectable locally advanced, recurrent NSCLC.
- At least one measurable disease by CT or MRI, according to RECIST Version 1.1.
- Documented evidence of any activating EGFR mutation in the tumor tissue.
- Have undergone or are able to undergo a biopsy of either primary or metastatic tumor tissue within 28 days of dosing of Avitinib, and have tissue available to send to central lab for further genetic profiling especially the status of T790M.
- Life expectancy of at least 3 months.
- ECOG performance status of 0 to 1.
- Adequate hematological and physiological functions of heart, lung, liver, and kidney according to definitions given in Appendix D.
- Disease progression under at least one treatment with current marketed EGFR TKI therapy for at least 30 days (e.g. Erlotinib, or Gefitinib, or Afatinib) with intervening treatment after most recent EGFR TKI therapy. The washout period for an EGFR TKI (Erlotinib, or Gefitinib) is at a minimum of 7 days. The washout period for an irreversible EGFR inhibitor (Afatinib) and chemotherapy is at a minimum of 14 days.
- Any toxicity related to prior EGFR inhibitor treatment must have resolved to Grade 1 or less.
- NSCLC patients with asymptomatic brain metastasis or drug-controllable brain metastasis.
- Signed consent on an Independent Ethics Committee-approved Informed Consent Form prior to any study-specific evaluation.
Exclusion
- No pathology confirmation
- History of interstitial lung disease related to prior EGFR inhibitor therapy.
- Symptomatic brain metastases or uncontrollable or unstable brain metastasis.
- Positive to HCV or HIV antibody.
- Treatment with prohibited medications (e.g., concurrent anticancer therapy including other chemotherapy, radiation, hormonal, or immunotherapy) ≤14 days prior to treatment with Avitinb.
- Clinically significant abnormal 12-lead ECG, QT interval corrected using Fridericia's method (QTcF) \>450 msec (males) or \>470 msec (females).
- Family history of long QT syndrome.
- Treatment with any Category 1 and 2 drugs (See:https://www.crediblemeds.org/ or www.qtdrug.org).
- 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).
- Any other reasons for the investigator to consider the patient should not participate in the study.
Key Trial Info
Start Date :
September 1 2014
Trial Type :
INTERVENTIONAL
Allocation :
ESTIMATED
End Date :
December 1 2017
Estimated Enrollment :
100 Patients enrolled
Trial Details
Trial ID
NCT02274337
Start Date
September 1 2014
End Date
December 1 2017
Last Update
November 23 2016
Active Locations (1)
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1
Sun Yat-Sen University Cancer Center
Guangzhou, Guangdong, China, 510060