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A phaseI/II study of Erlotinib/Carboplatin/Pemetrexed/Bevacizumab in chemotherapy-naive patients with EGFR mutation positive advanced non-squamous non-small-cell lung cancer

A phaseI/II study of Erlotinib/Carboplatin/Pemetrexed/Bevacizumab in chemotherapy-naive patients with EGFR mutation positive advanced non-squamous non-small-cell lung cancer - A phaseI/II study of Erlotinib/Carboplatin/Pemetrexed/Bevacizumab in chemotherapy-naive patients with EGFR mutation positive advanced non-squamous non-small-cell lung cancer

Status
Recruiting
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000013202
Enrollment
35
Registered
2014-02-19
Start date
2014-02-19
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Non-Small-Cell Lung Cancer

Interventions

level0:Erlotinib 50mg(daily) level1:Erlotinib 100mg(daily) level2:Erlotinib 150mg(daily) level0-2:Carboplatin AUC=6,Day1/Pemetrexed 500mg/m2,Day1/Bevacizumab 15mg/kg,Day1

Sponsors

Kansai Medical University Hirakata Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Histologically or cytologically proven non-squamous non-small cell lung cancer 2) Non-small cell lung cancer with stage IIIB,stage IV (UICC-7) 3) EGFR mutation positive 4) chemo naïve 5) Age: 20- years old 6) ECOG PS 0-1 7) Adequate organ function

Exclusion criteria

Exclusion criteria: 1)Interstitial pneumonia or pulmonary fibrosis detectable on chest Xp 2)History of radiation therapy for chest 3)With hemosputum 4)With active bleeding 5)Symptomatic brain metastasis 6)With active infectious disease 7)History of serious disease condition 8)With massive pleural effusion or ascitis 9)History of active double cancer 10)need to operation 11) History of pregnancy or lactation 12)History of active psychological disease 13) History of drug allergy

Design outcomes

Primary

MeasureTime frame
progression free survival

Secondary

MeasureTime frame
Safety, Response Rate, Disease Control Rate, Overall Survival

Countries

Japan

Contacts

Public ContactTakashi Yokoi

Kansai Medical University Hirakata Hospital Thoracic oncology

yokoit@hirakata.kmu.ac.jp072-804-0101

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026