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Dendritic cell therapy based on nepantigen-gene analysis

Dendritic cell therapy based on nepantigen-gene analysis - Neoantigen-loaded DC therapy

Status
Recruiting
Phases
Phase 2
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCTc030210026
Enrollment
30
Registered
2021-04-09
Start date
2021-04-01
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

Malignant tumor (except leukemia)

Interventions

Sponsors

Tanigawa Keishi
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Patients must: - have ECOG Performance Status for 0, 1 or 2. - maintain adequate function of key organs when the eligibility is confirmed, in particular: 1. haemoglobin 8.0 g/dl or more 2. platelet 50.000 /mm3 or more 3. total bilirubin 3 x ULN or more 4. AST/ALT 3 x ULN or less 5. creatinine 3 x ULN or less - provide written consent for treatment of neoantigens-loaded DC vaccination. - have a proper mental condition and an ability to recognize the object and contents of the study when informed consent is obtained.

Exclusion criteria

Exclusion criteria: Patients must not: - be impossible to obtain blood sample by Leukapeheresis. - be positive in HIV antibody test. - have active auto-immune disorder. - have serious underlying disease. - be pregnant (including pregnancy seeker) - be judged ineligibles by clinician in this trial.

Design outcomes

Primary

MeasureTime frame
Safety

Secondary

MeasureTime frame
Delayed type hypersensitivity reaction at the injection site of neoantigen peptides-loaded dendritic cell vaccine

Countries

Japan

Contacts

Public ContactYasunobu Kobayashi

BioThera Clinic

ykobayashi@bio-c.jp+81-3-5919-1762

Outcome results

None listed

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