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Phase 1/2 study of combination chemotherapy with Carboplatin, nab-Paclitaxel, and Bevacizumab for advanced non-squamous non-small cell lung cancer

Phase 1/2 study of combination chemotherapy with Carboplatin, nab-Paclitaxel, and Bevacizumab for advanced non-squamous non-small cell lung cancer - Phase 1/2 study of combination chemotherapy with Carboplatin, nab-Paclitaxel, and Bevacizumab for advanced non-squamous non-small cell lung cancer

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000016735
Enrollment
35
Registered
2015-03-08
Start date
2015-03-01
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-squamous Non-small-cell Lung Cancer

Interventions

Patients receive paclitaxelon days 1,8,15 and Carboplatin(AUC6) on day1 and Bevacizumab (15mg/kg) on day1, every four weeks, up to six cycles. Patients who still control disease without unacceptable

Sponsors

Hiroshima Asa City Hospital
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1) Histologically determined non small cell lung cancer 2) Unresectable or StageIIIB or IV without any indications for radiotherapy 3) Have measurable lesions by RECIST 4) No prior chemotherapy 5) Aged 20 to 74 years old 6) ECOG perfornmance status 0 or 1 7)8) adequate organ function 9)Patients are excepted to live at least 3 months 10) Written informed consent

Exclusion criteria

Exclusion criteria: 1) Squamous cell lung cancer 2) History of Severe drug allergies. 3) Double malignancies within 5 years 4) Uncontrolled ascites, pleural effusion or cardiac effusion 5) Current history of hemoptysis 6-7) High risk of bleeding or thrombus events 8) Evidence of bleeding diathesis or coagulopathy 9) Current or previous history of Pericardial effusion 10) Superior vena cava syndrome 11) Spinal cord compression 12) Current or previous (within the last 1 year) history of cerebrovascular disease 13) Traumatic fracture of unrecovery 14) History of active infection 15) Scheduled operation 16) Antithrombotic agent 17) Uncontrollable Gastrointestinal ulceration 18) Current or previous (within the last 1 year)history of GI perforation 19) Uncontrollable hypertension 20) Severe cardiac disease 21) Interstitial pneumonia or pulmonary fibrosis detectable on X ray 22) With grade2 or more neuropathy 23) Treatment history of bevacizumab 24) Pregnancy, breastfeeding or suspected of being pregnant 25) HBs positive patient 26) Others judged by attending physician

Design outcomes

Primary

MeasureTime frame
PhaseI Recommended Dose PhaseII Response Rate

Secondary

MeasureTime frame
DCR, PFS, OS, Safety

Countries

Japan

Contacts

Public ContactSouichi Kitaguchi

Hiroshima Asa City Hospital Medical oncology/Respiratory medicine

s-kitaguchi@asa-hosp.city.hiroshima.jp082-815-5211

Outcome results

None listed

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