Validation of in Vitro Method for Anti-MCPyV Immunotherapy on Patients With Cutaneous Merkel Cell Carcinoma

Trial statusRecruiting
Trial phaseNot listed
Trial typeObservational
Biological sexAll
Age18+
SponsorAssistance Publique - Hôpitaux de Paris

About this trial

The aim of the study is to test and validate in vitro a cell therapy approach for MCPyV+ Merkel Cell Carcinoma patients.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Patients >= 18 years old;

Diagnosed with Merkel cell carcinoma of skin, ongoing for local treatment, systemic treatment, complementary treatment or an active follow-up;

Informed for the study and no-opposed for participation;

Affiliated with a social security scheme or in an equivalent situation.

Disqualifiers

Patients ongoing another interventional clinical trial;

Patients under guardianship or trusteeship;

Pregnancy or breastfeed;

Patients refusal.

Trial population

Adult patients of Merkel cell carcinoma of skin, ongoing for local treatment, systemic treatment, complementary treatment or with an active follow-up beside dermatologist.

Trial design

Design model

Cohort

Time perspective

Prospective

Treatments tested in this trial

Not listed

Trial groups

No trial groups listed

Trial outcomes

Primary outcomes

1

Anti-MCPyV functionality

Anti-MCPyV functionality, including cytotoxicity, of T cells obtained after in vitro culture.

Time frame
Day 0 and Day 4

Secondary outcomes

Other outcomes

Sponsors and contacts

Click on the lead sponsor to view all of their trials.

Assistance Publique - Hôpitaux de Paris

Lead sponsor

Institut National de la Santé Et de la Recherche Médicale, France

Collaborator