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Clinical study of administration of alpha-GalactosylCeramide-pulsed DCs by bronchoscopy in patients with either advanced or recurrent non-small cell lung cancer (NSCLC)

Clinical study of administration of alpha-GalactosylCeramide-pulsed DCs by bronchoscopy in patients with either advanced or recurrent non-small cell lung cancer (NSCLC) - Clinical study of administration of alpha-GalactosylCeramide-pulsed DCs by the bronchoscopy

Status
Active, not recruiting
Phases
Phase 1
Study type
Interventional
Source
JPRN
Registry ID
JPRN-UMIN000005208
Enrollment
18
Registered
2011-03-08
Start date
2009-08-01
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

lung cancer

Interventions

Intratumoral or intranodal administrations of alpha-GalactocylCeramide pulsed DCs by bronchoscopy are performed on day 7 and 14 after the entry.

Sponsors

Department of General Thoracic Surgery, Graduate School of Medicine, Chiba University
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients with either advanced or recurrent non-small cell lung cancer, who have received chemotherapy or radiotherapy. Patients who have measurable disease in the lung and have lymph node over 5mm diameter. Patients whose life-expectancy is more than 6 months; Performance status 0-2; Normal bone marrow, liver and renal functions; NKT cells are detected at least 10 cells in 1 ml of peripheral blood.

Exclusion criteria

Exclusion criteria: Patients who have: uncontrolled diabetes mellitus, pulmonary fibrosis, and/or infection; synchronous multiple cancer; a history of hepatitis; a positive response for hepatitis B surface antigen, hepatitis C virus, or human immunodeficiency virus (HIV), or human T-lymphotrophic virus antibodies; serious cardiac diseases; pregnancy or lactation; autoimmune diseases; been judged to be inappropriate to practice in this study by principle investigator

Design outcomes

Primary

MeasureTime frame
Safety

Secondary

MeasureTime frame
The clinical effects and immunological responses

Countries

Japan

Contacts

Public ContactShinichiro Motohashi

raduate School of Medicine, Chiba University Department of immunology

043-222-7171

Outcome results

None listed

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