T-VEC in Non-melanoma Skin Cancer

  • STATUS
    Recruiting
  • End date
    Feb 26, 2022
  • participants needed
    20
  • sponsor
    University of Zurich
Updated on 26 March 2021
cancer
lymphoma
carcinoma
melanoma skin
skin cancer
squamous cell carcinoma
non-melanoma skin cancer
carcinoma of skin
merkel cell carcinoma
advanced squamous cell carcinoma

Summary

Evaluation of the mechanism of Action of talimogene laherparepvec (T-VEC) in patients with locally advanced non-melanoma skin cancer.

Description

This study evaluates the administration of T-VEC in non-melanoma skin cancer. The aim is to evaluate the effectiveness, safety and tolerability of T-VEC in patients with non-melanoma skin cancer through determination of local immune effects after repeated T-VEC injections.

Details
Condition Basal cell carcinoma, Neuroendocrine carcinoma, Carcinoma, Squamous cell carcinoma, Merkel cell carcinoma, Vulvar Dysplasia and Carcinoma, Advanced Malignancies, Cutaneous Lymphoma, Non-melanoma Skin Cancer, Non-melanoma Skin Cancer, basal cell carcinomas, basal cell carcinoma of skin, epidermoid carcinoma, squamous cell cancer, Non-melanoma Skin Cancer, Non-melanoma Skin Cancer
Treatment Talimogene Laherparepvec (T-VEC)
Clinical Study IdentifierNCT03458117
SponsorUniversity of Zurich
Last Modified on26 March 2021

Eligibility

Yes No Not Sure

Inclusion Criteria

Subjects Age 18 years
histologically confirmed diagnosis of locally advanced squamous cell carcinoma, basal cell, carcinoma, Merkel cell carcinoma or cutaneous T cell lymphoma
at least 1 injectable cutaneous lesion 20 mm in longest Diameter or multiple injectable lesions that in Aggregate have a longest Diameter of 50 mm
Eastern Cooperative Oncology Group-Status (ECOG Status) 0 or 1
Adequate organ functions

Exclusion Criteria

Hypersensitivity to T-VEC or any of ist components
Presence of organ and lymph node metastases
history or evidence of active autoimmune disease that requires systemic Treatment
Evidence of clinically significant immunosuppression
active herpetic skin lesions or prior complications hereof
pregnancy, breast feeding
requires intermittent or chronic systemic Treatment with an antiherpetic drug
acute or chronic active Hepatitis B or C infection or HIV infection
Clear my responses

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If you are confirmed eligible after full screening, you will be required to understand and sign the informed consent if you decide to enroll in the study. Once enrolled you may be asked to make scheduled visits over a period of time.

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Complete your scheduled study participation activities and then you are done. You may receive summary of study results if provided by the sponsor.

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