For Healthcare Professionals

Trilaciclib, a CDK 4/6 Inhibitor, in Patients With Advanced/Metastatic Bladder Cancer Receiving Chemotherapy Then Avelumab

clipboard-pencil

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.
user-3

Who can take part

You may be eligible to participate in the study if you meet the following criteria:

INCLUSION CRITERIA

Inclusion Criteria:


  1. Age ≥18 years
  2. Histologically documented, locally advanced (T4b, any N; or any T, N 2-3) or metastatic urothelial carcinoma (M1, Stage IV)
  3. Measurable disease as defined by RECIST v1.1
  4. No prior systemic therapy in the inoperable, locally advanced, or metastatic setting including chemotherapy, immune checkpoint inhibitor therapy, targeted therapy, or investigational agents
  5. Archival tumor tissue must be available or a fresh biopsy must be obtained, unless approved by the Medical Monitor
  6. Eastern Cooperative Oncology Group (ECOG) performance status of 0-2
  7. Adequate organ function as demonstrated by normal laboratory values

EXCLUSION CRITERIA

Exclusion Criteria:


  1. 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
  2. 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)
  3. Presence of central nervous system (CNS) metastases/leptomeningeal disease requiring immediate treatment with radiation therapy or steroids.
  4. QTcF interval > 480 msec. For patients with ventricular pacemakers, QTcF > 500 msec
  5. Known hypersensitivity or allergy to avelumab, gemcitabine, cisplatin or carboplatin
  6. Known severe hypersensitivity reactions to monoclonal antibodies (Grade ≥3), any history of anaphylaxis, or uncontrolled asthma
  7. Prior hematopoietic stem cell or bone marrow transplantation, or solid organ transplantation
  8. Pregnant or lactating women
  9. Active autoimmune disease that might deteriorate when receiving an immunostimulatory agent

Current use of immunosuppressive medication, EXCEPT for the following:


  1. Intranasal, inhaled, topical steroids, or local steroid injection (e.g., intra-articular injection)
  2. Systemic corticosteroids at physiological doses ≤10 mg/day of prednisone or equivalent
  3. Steroids as premedication for hypersensitivity reactions (e.g., CT scan premedication)

pin location

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

Understanding Clinical Trials


Get answers to your questions about clinical trials.What is a clinical research?What does taking part in clinical trials involve?What should I ask the trial doctor?
Vector

Interested?

Sign up to save your favorites, 
receive newsletters, resources, and alerts 
about clinical trials related to your conditions of interest.