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A phase II study of Bevacizumab and Docetaxel for elderly patients advanced Non-Small Cell Lung Cancer

A phase II study of Bevacizumab and Docetaxel for elderly patients advanced Non-Small Cell Lung Cancer - A phase II study of Bevacizumab and Docetaxel for elderly patients with NSCLC

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000006322
Enrollment
30
Registered
2011-09-12
Start date
2011-08-01
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

DTX+BEV

Sponsors

University hospital, Hirosaki University School of Medicine Cardiology,respiratory medicine and nephrology
Lead Sponsor
Hirosaki Central Hospital Natonal Hospital Orgnization Hirosaki Hospital
Collaborator

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1)Histologically or cytrologically confirmed diagnosis of NSCLC (Non squamous cell carcinima) 2)No prior systemic treatment advanced NSCLC 3)Tumors must have measurable disease 4)ECOG performance status 0 or 1 5)Patients aged 70- years 6)Written informed consent from the patients 7)No problem adequate organ function

Exclusion criteria

Exclusion criteria: 1)Subjects with interstitial pneumonia or pulmonary fibrosis. 2)Uncontrolled systematic disease 3)Uncontrolled active infection 4)No other active malignancies 5)Concurrent use of steroid therapy 6)Subjects with brain metastases 7)Uncontrolled pleural effusion and ascites 8)have had or require continuous oral administration of hemostat/have had or require injectable administration of hemostat 9)Pregnant patients 10)Have a bleeding diathesis 11)Tumor invasion to major vessels 12)Cavity in tumor 13)History of uncontrolled gastroduodenal ulcer 14)Uncontrolled hypertension 15)Symptomatic heart failure,unstable angina, uncontrolled arrhythmia, myocardial infarction within 1 year 16)Symptomatic cerebrovasucular disease 17)Any other reason that,in the opinion of the investugator precludes the subject from participating in the study.

Design outcomes

Primary

MeasureTime frame
RR: response rate

Secondary

MeasureTime frame
PFS: progression free survival OS: overall survival safety

Countries

Japan

Contacts

Public ContactHisashi Tanaka

University hospital, Hirosaki University School of Medicine Cardiology,respiratory medicine and nephrology

Outcome results

None listed

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