Trilaciclib, a CDK 4/6 Inhibitor, in Patients With Advanced/Metastatic Bladder Cancer Receiving Chemotherapy Then Avelumab
About the study
This is a Phase 2, multicenter, randomized, open-label study evaluating the safety and efficacy of trilaciclib administered with platinum-based chemotherapy followed by trilaciclib administered with avelumab maintenance therapy compared with platinum-based chemotherapy followed by avelumab maintenance therapy in patients receiving first-line treatment for advanced/metastatic bladder cancer.
Who can take part
You may be eligible to participate in the study if you meet the following criteria:
INCLUSION CRITERIA
Inclusion Criteria:
- Age ≥18 years
- Histologically documented, locally advanced (T4b, any N; or any T, N 2-3) or metastatic urothelial carcinoma (M1, Stage IV)
- Measurable disease as defined by RECIST v1.1
- No prior systemic therapy in the inoperable, locally advanced, or metastatic setting including chemotherapy, immune checkpoint inhibitor therapy, targeted therapy, or investigational agents
- Archival tumor tissue must be available or a fresh biopsy must be obtained, unless approved by the Medical Monitor
- Eastern Cooperative Oncology Group (ECOG) performance status of 0-2
- Adequate organ function as demonstrated by normal laboratory values
EXCLUSION CRITERIA
Exclusion Criteria:
- Prior treatment with IL-2, IFN-α, or an anti-PD-1, anti-PD-L1, anti-PD-L2, anti-CD137 or CD137 agonists, or cytotoxic T-lymphocyte associated protein 4 (CTLA-4) antibody (including ipilimumab), or any other therapeutic antibody or drug specifically targeting T cell co-stimulation or immune checkpoint pathways in any setting
- Malignancies other than urothelial carcinoma within 3 years prior to randomization, except for adequately treated basal cell or squamous cell skin cancer, or carcinoma in situ of the breast or of the cervix, or low-grade (Gleason ≤6) prostate cancer on surveillance without any plans for treatment intervention (e.g., surgery, radiation, or castration)
- Presence of central nervous system (CNS) metastases/leptomeningeal disease requiring immediate treatment with radiation therapy or steroids.
- QTcF interval > 480 msec. For patients with ventricular pacemakers, QTcF > 500 msec
- Known hypersensitivity or allergy to avelumab, gemcitabine, cisplatin or carboplatin
- Known severe hypersensitivity reactions to monoclonal antibodies (Grade ≥3), any history of anaphylaxis, or uncontrolled asthma
- Prior hematopoietic stem cell or bone marrow transplantation, or solid organ transplantation
- Pregnant or lactating women
- Active autoimmune disease that might deteriorate when receiving an immunostimulatory agent
Current use of immunosuppressive medication, EXCEPT for the following:
- Intranasal, inhaled, topical steroids, or local steroid injection (e.g., intra-articular injection)
- Systemic corticosteroids at physiological doses ≤10 mg/day of prednisone or equivalent
- Steroids as premedication for hypersensitivity reactions (e.g., CT scan premedication)
Study Locations
Enter your ZIP code/Postal code/PIN code to locate study sites near you:
How to Apply
Contact the study center to learn if this study is a good match for you.
Study’s details
Contition
Urothelial Carcinoma,Bladder Cancer,Myelosuppression Adult,Chemotherapy-induced Neutropenia,Metastatic Bladder Cancer
Age (in years)
18+
Phase
Phase 2
Participants needed
92
Est. Completion Date
May 31, 2024
Treatment type
Interventional
Sponsor
G1 Therapeutics, Inc.
ClinicalTrials.gov identifier
NCT04887831
Study number
G1T28-209
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