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Phase 2 trial of weekly Nab paclitaxel for advanced gastric cancer patients with prior chemotherapy

Phase 2 trial of weekly Nab paclitaxel for advanced gastric cancer patients with prior chemotherapy - Phase 2 trial of weekly Nab paclitaxel for advanced gastric cancer patients with prior chemotherapy

Status
Active, not recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000011882
Enrollment
21
Registered
2013-09-30
Start date
2013-08-20
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

Advanced Gastric Cancer

Interventions

Nab paclitaxel(80mg/m2 day1,8,15) every 4 weeks

Sponsors

Teikyo University School of Medicine
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: 1.Patients who provided written informed consent. 2.Patients with gastric cancer by histological or cytological examination. 3.Patients with prior on chemothrapy. (including recurrence within 6 months after last adjuvant chemotherapy) 4.More than 2 weeks last chemotherapy 5.ECOG performance status<=2 6.Patients with adequately maintained organ functions and fulfilling the following conditions within 7 days before registration WBC count more than 3,000/mm3 Neutrophils count more than 1,200/mm3 Hemoglobin more than 8.0 g/dl Platelet count more than 75,000/mm3 Serum bilirubin level less than 2.0mg/dl AST and ALT less than 100 IU/l 20 years old or more Patients expected to survive for 90 more than days

Exclusion criteria

Exclusion criteria: 1.History of serious drug hypersensitivity 2.Any other serious illness or medical conditions including interstitial pneumonia or pulmonary fibrosis, renal failure, liver failure,cerebrovascular disordar or Uncontrolled diabates 3.Active infection or fever suspicious of infection. 4.Surgical procedure within 4 weeks before registration 5.Uncontrolled unstable angina, congestive heart failure, myocardial infarction or ventricular arrhythmia 6.History of mental disorder, central nerve disorder. 7.Pregnant women, nursing mothers 8.Patients who were considered by the primary care physician to be inappropriate for this trial

Design outcomes

Primary

MeasureTime frame
Progression-free survival

Secondary

MeasureTime frame
Incidence and grade of Adverse Event, Response Rate,Over all Survival

Countries

Japan

Contacts

Public ContactRyoji Fukushima

Teikyo University School of Medicine Surgery

ryojif@med.teikyo-u.ac.jp03-3964-1231

Outcome results

None listed

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