Afatinib Plus Nimotuzumb for NSCLC

Phase 1

• Conditions: NSCLC
• Interventions: Drug: afatinib (30 or 40mg) + nimotuzumab (100 or 200mg)

• Registration Number: NCT01861223
• Lead Sponsor: Samsung Medical Center

Brief Summary

To find the optimal dose of afatinib and nimotuzumab in patients who acquired resistance to gefitinib or erlotinib.

Detailed Description

Not available

Basic Information
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Recruitment & Eligibility
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Study & Design
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Trial Locations

Study Timeline

• Study Start: 2013-05
• Study First Submitted: 2013-05-21
• Study First Submitted QC: 2013-05-22
• Study First Posted: 2013-05-23
• Status Verified: 2014-02
• Last Update Submitted: 2014-02-23
• Last Update Posted: 2014-02-25
• Primary Completion: 2015-05
• Study Completion: 2016-05

Recruitment & Eligibility

• Status: UNKNOWN
• Sex: All
• Target Recruitment: 50

Inclusion Criteria

• Histologically confirmed diagnosis of stage IIIB or IV NSCLC
• Presence of EGFR sensitizing mutations (L858R mutation in exon 21 or exon 19 deletion) or response by RECIST on prior gefitinib or erlotinib or stable disease on prior gefitinib or erlotinib for at least 6 months
• Disease progression on treatemtn with gefitinib or erlotinib within 30 days
• Biopsy on disease progression
• Age ≥20 years
• ECOG performance status of 0, 1, or 2
• Measurable disease by the criteria of RECIST 1.1
• Adequate organ function as evidenced by the following; Absolute neutrophil count > 1.5 x 109/L; platelets > 100 x 109/L; total bilirubin ≤1.5 UNL; AST and/or ALT < 5 UNL; creatinine clearance ≥ 45 mL/min

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Exclusion Criteria

• Known interstitial lung disease
• Prior treatment with EGFR targeting antibodies or BIBW 2992
• Prior three or more lines of chemotherapy for advanced NSCLC
• Significant bowel disease impairing drug absorption
• Uncontrolled systemic illness such as DM, CHF, unstable angina, hypertension or arrhythmia
• Have symptomatic, untreated, or uncontrolled central nervous system (CNS) metastases. Patients with treated CNS metastases are eligible provided their disease is radiographically stable, asymptomatic, and corticosteroid use has been discontinued for at least 2 weeks prior to the first dose of study drug. Screening of asymptomatic patients without history of CNS metastases is not required.

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Study & Design

• Study Type: INTERVENTIONAL
• Study Design: SINGLE_GROUP

Arm && Interventions

Group	Intervention	Description
afatinib + nimotuzumab	afatinib (30 or 40mg) + nimotuzumab (100 or 200mg)	-

Primary Outcome Measures

Name	Time	Method
Maximal tolerated dose	4 weeks	To establish maximum tolerated dose (MTD) and recommended Phase II dose (RP2D) for BIBW 2992 and nimotuzumab in patients with acquired resistance to erlotinib or gefitinib

Trial Locations

Locations (1)

Samsung Medical Center; 🇰🇷 Seoul, Korea, Republic of