Recruitment

Recruitment Status
Terminated
Estimated Enrollment
30

Summary

Conditions
Malignant Melanoma
Type
Interventional
Phase
Phase 2
Design
Allocation: N/AIntervention Model: Single Group AssignmentMasking: None (Open Label)Primary Purpose: Treatment

Participation Requirements

Age
Between 18 years and 125 years
Gender
Both males and females

Description

Secondarily to studying the efficacy of the treatment; the investigators examine if treatment with IDO/Survivin peptide can induce a measurable cellular T-cell response when the vaccine is given in combination with temozolomide treatment for melanoma patients.

Secondarily to studying the efficacy of the treatment; the investigators examine if treatment with IDO/Survivin peptide can induce a measurable cellular T-cell response when the vaccine is given in combination with temozolomide treatment for melanoma patients.

Tracking Information

NCT #
NCT01543464
Collaborators
Copenhagen University Hospital at Herlev
Investigators
Principal Investigator: Trine Zeeberg Iversen, MD Center for Cancer ImmuneTherapy Study Director: Inge Marie Svane, MD, PhD, Prof. Center for Cancer ImmunoTherapy