About this trial
The DEPECA-1 trial is the first systematic Phase II trial to evaluate response and survival to a combination of antibody-drug conjugate enfortumab vedotin plus the PD-L1 inhibitor avelumab in patients with locally advanced and metastatic penile squamous cell carcinoma (PeCa) in the 1st line setting.
Eligibility criteria
Qualifiers
Patient has ability to understand and the willingness to sign a written informed consent.
Patient is ≥ 18 years of age at time of signing the written informed consent.
Male patients with histologically confirmed diagnosis of penile squamous cell carcinoma.
Stage 3 (cT3) disease with a single lymph node involved (N1).
Disqualifiers
Previous systemic therapy for metastatic or locally advanced PeCa in the palliative setting.
Previous treatment with investigational drugs or devices within 30 days prior to the first dose of trial treatment.
Known active central nervous system (CNS) metastases and/or carcinomatous meningitis.
Active, known, or suspected autoimmune disease requiring systemic treatment within the past 2 years. Patients with controlled autoimmune d disease not requiring systemic immunosuppressive treatment including diabetes type I, vitiligo, psoriasis, or hypo- or hyperthyroid diseases are eligible.
Trial design
Treatments tested in this trial
- Avelumab
- enfortumab vedotin
Treatment groups
Sponsors and collaborators
Institut für Klinische Krebsforschung IKF GmbH at Krankenhaus Nordwest
Lead sponsor
Merck KGaA, Darmstadt, Germany
Collaborator
Astellas Pharma GmbH
Collaborator
University Hospital Tübingen
Collaborator