Eligibility Module
The Eligibility Module contains detailed information about who can participate in the clinical trial. This includes eligibility criteria, age restrictions, gender requirements, healthy volunteer status, and study population descriptions, helping researchers understand who is eligible to participate in the study.
Eligibility Module path is as follows:
Study -> Protocol Section -> Eligibility Module
Eligibility Module
Ignite Creation Date:
2025-12-25 @ 3:56 AM
Ignite Modification Date:
2025-12-25 @ 3:56 AM
NCT ID:
NCT02478502
Eligibility Criteria:
Inclusion Criteria:
* Male patients ≥ 18 years old
* Histologically verified metastatic germ cell cancer (GCC) of the testicle or extragonadal GCC originating from retroperitoneum or mediastinum
* Disease progression during cisplatin-based chemotherapy or Disease progression or relapse after high-dose chemotherapy or Disease progression or relapse after at least 2 different cisplatin-based regimens
* Eastern Cooperative Oncology Group (ECOG) Performance Status (PS): 0-2
* Life expectancy ≥ 3 months
* At baseline adequate function of liver, kidneys and bone marrow:
·Neutrophils ≥ 1.5 x 109/L·
* Hemoglobin ≥ 9.0 g/dL
* Platelets ≥ 100 x 109/L
* Creatinine ≤ 1.5 x upper limit of normal (ULN)
* Total Bilirubin ≤ 1.0 x ULN
* Serum glutamate oxaloacetate transaminase (SGOT/AST) ≤ 1.5 x ULN
* Serum glutamate pyruvate transaminase (SGPT/ALT) \< 1.5 x ULN
Exclusion Criteria:
* Systemic antitumor treatment within 21 days before study entry
* Simultaneous radiotherapy to the only target lesion
* Patients unwilling or unable to comply with the protocol
* Patients with unstable angina pectoris, myocardial infarction ≤ 6 months prior to first study treatment, congestive heart failure New York Heart Association (NYHA) III-IV or serious uncontrolled cardiac arrhythmias
* Patients with an active or uncontrolled infection
* Patients who have a history of another primary malignancy and are off treatment for ≤ 3 years, with the exception of non-melanoma skin cancer
* Patients who have undergone major surgery within 4 weeks prior to starting study drug (e.g. intra-thoracic, intra-abdominal, or intra-pelvic) or significant traumatic injury, or who have not recovered from the side effects of any of the above within 6 weeks
* Patients who have participated in another interventional clinical trial within 30 days before study entry
* Other serious medical conditions that could impair the ability of the patient to participate in the study
* Active infection requiring systemic antibiotic-, anti-viral-, or anti-fungal medication
* Neuropathy ≥Grade 2 Common Terminology Criteria for Adverse Events (CTCAE)
* Patient with reproductive potential not implementing accepted and effective method of contraception during the whole study period and up to 6 months after the last dose of cabazitaxel
* One or more of the following cabazitaxel-specific requirements:
* History of severe hypersensitivity reaction (≥ Grade 3) to docetaxel
* History of severe hypersensitivity reaction (≥ Grade 3) to polysorbate 80 containing drugs
* Concurrent or planned treatment with strong inhibitors or strong inducers of cytochrome P450 3A4 (CYP3A4) (a one week wash-out period is necessary for patients who are already on these treatments) (see Appendix A and B)
* Concurrent or planned treatment with Organic anion transporting polypeptide1B1 (OATP1B1) substrates e.g. statins, valsartan, repaglinide which have to be taken within 12 hours before cabazitaxel application and 3 hours after the end of infusion, refer table 9
Healthy Volunteers:
False
Sex:
MALE
Minimum Age:
18 Years
Study:
NCT02478502
Study Brief:
Protocol Section:
NCT02478502