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Clinical Trial Details — Status: Completed

Administrative data

NCT number NCT01734564
Other study ID # CD-2010-01
Secondary ID
Status Completed
Phase Phase 2
First received November 21, 2012
Last updated April 10, 2017
Start date November 2012
Est. completion date December 2016

Study information

Verified date May 2016
Source Clinica Universidad de Navarra, Universidad de Navarra
Contact n/a
Is FDA regulated No
Health authority
Study type Interventional

Clinical Trial Summary

In this phase II study, patients with solid tumors will receive treatment with hiltonol and autologous dendritic cells.


Description:

In this phase II study, patients with solid tumors will receive treatment with intratumoral hiltonol and two cycles of autologous dendritic cells loaded with autologous tumor and administered subcutaneously. A new cohort will explore the role of radiation therapy, looking for an abscopal effect.


Recruitment information / eligibility

Status Completed
Enrollment 15
Est. completion date December 2016
Est. primary completion date December 2016
Accepts healthy volunteers No
Gender All
Age group 18 Years and older
Eligibility Inclusion Criteria:

- Confirmed diagnosis of advanced solid tumors

- Measurable disease

- Performance status 0, 1 or 2.

- Adequate renal, hepatic and bone marrow function

- Availability of tumor tissue, for maturing dendritic cells

Exclusion Criteria:

- Clinically relevant diseases or infections.

- concurrent participation in other clinical trial or administration or other antitumoral treatment

- Concurrent cancer, with the exceptions allowed by the PI.

- Pregnant or breast feeding women

- immunosuppressant treatment

- known uncontrolled central nervous system metastasis

Study Design


Related Conditions & MeSH terms


Intervention

Biological:
Hiltonol and autologous dendritic cells
Hiltonol and autologous dendritic cells
Radiation:
Hiltonol, dendritic cells and radiation
Hiltonol, autologous dendritic cells and radiation therapy. Radiation therapy will pursue an abscopal effect.

Locations

Country Name City State
Spain Clinica Universidad de Navarra Pamplona Navarra

Sponsors (1)

Lead Sponsor Collaborator
Clinica Universidad de Navarra, Universidad de Navarra

Country where clinical trial is conducted

Spain, 

Outcome

Type Measure Description Time frame Safety issue
Primary Response rate 8-10 weeks
Secondary Safety (Common Toxicity Criteria 4.0) 8-10 weeks
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