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Clinical Trial Summary

Patients with unresectable locally advanced or metastatic squamous cell penile carcinoma (SPC) who are in response or with stable disease after first line platinum containing polychemotherapy who meet the inclusion/exclusion criteria will be offered to take part in the study. The patients may be pre-screened at the time of the 1st line chemotherapy. In order for patients to be enrolled, the investigator must have carried out a radiological assessment of the disease during first line systemic treatment (a maximum of between 3 and 6 cycles): the cancer must be controlled. Patients with disease progression cannot be included in the PULSE study as this is a maintenance study. After inclusion, Avelumab will be administered at a dose of 10 mg/kg, at a frequency of once every 2 weeks with appropriate supportive care.


Clinical Trial Description

n/a


Study Design


Related Conditions & MeSH terms


NCT number NCT03774901
Study type Interventional
Source Centre Hospitalier Universitaire de Besancon
Contact Elise Robert
Phone 0033381219086
Email e1robert@chu-besancon.fr
Status Recruiting
Phase Phase 2
Start date March 12, 2019
Completion date September 22, 2024

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