Last updated 13 months ago
A PHASE II, RANDOMIZED STUDY TO ASSESS MAINTENANCE THERAPY WITH CEMIPLIMAB VERSUS BEST SUPPORTIVE CARE AFTER 1ST LINE PLATINUM-BASED CHEMOTHERAPY IN ADVANCED/RECURRENT PENILE CANCER
42 patients around the world
Available in Brazil
Hospital Israelita Albert Einstein
1Research sites
42Patients around the world
This study is for people with
Penile Cancer
Requirements for the patient
From 18 Years
Male
Medical requirements
- Male participants.At least 18 years old on the day of signing the informed consent.Histologically confirmed diagnosis of penile squamous cell carcinoma, clinical stages III-IV or relapsed disease, not amenable of curative intent therapy - as per AJCC 8th edition.Measurable disease (as per RECIST v1.1) prior to starting first-line chemotherapy.Lesions located in a previously irradiated area are deemed as measurable if progression has been shown in such lesions.Previous chemotherapy performed in localized disease setting, with curative intent and platinum-based is allowed, provided that the time off this treatment is longer than 6 months.Previous first-line chemotherapy should have been comprised of at least 4 cycles and no more than 6 platinum-based chemotherapy cycles.No evidence of progressive disease after completing first-line chemotherapy (e.g., ongoing complete response (CR), (partial response) PR or stable disease (SD) as per RECIST v1.1 guidelines).An Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1 or 2.
- History of allergy or hypersensitivity to the study drug components.Persisting NCI CTCAE v5.0 Grade > 1 toxicity related to previous therapy; however, Grade ≤ 2 sensory neuropathy and Grade ≤ 2 chronic kidney disease are acceptable.Previous immune therapy with IL-2, IFN-α, or anti-PD-1, anti-PD-L1, anti-PD-L2, anti-CD137, or anti-T cytotoxic lymphocyte related to antigen-4 (CTLA-4), or any other antibody or drug specifically targeted to T-cell co-stimulation or immune checkpoint pathways.Untreated or active primary brain tumor, metastases to central nervous system, leptomeningeal disease or spinal cord compression.History of allogenic organ transplant.Ongoing or recent evidence (within 5 years) of significant autoimmune disease requiring treatment with systemic immunosuppressants.History of other primary malignancy within the last 3 years, except locally curable cancers which have been apparently cured, such as skin basal- or squamous-cell cancer, superficial bladder cancer, breast carcinoma in situ or cervical carcinoma in situ.Uncontrolled infection by human immunodeficiency virus, hepatitis B or C infection; or immunodeficiency diagnosis.Have received a live vaccine within 4 weeks of the planned start of the study drug.Have received any previous systemic biological therapy within 5 half-lives of the first study therapy dose.Exception: participants previously treated with bevacizumab, cetuximab, rituximab or other non-immunomodulating antibodies with half-lives longer than 7 days are allowed after a discussion with the sponsor, if at least 28 days have elapsed since last treatment.
Sites
Hospital Israelita Albert Einstein
StudyBRAVA PENILE
SponsorHospital Israelita Albert Einstein
Study typeInterventional
Conditions
Penile Cancer
Requirements
From 18 YearsMale
Unique study IDclinicaltrials.gov
NCT07101822
