TTX-080 HLA-G Antagonist in Subjects With Advanced Cancers
Launched by TIZONA THERAPEUTICS, INC · Jul 21, 2020
Trial Information
Current as of August 19, 2025
Recruiting
Keywords
ClinConnect Summary
This clinical trial, called TTX-080-001, is looking at a new treatment for patients with advanced cancers that have not responded well to other therapies. The main goal is to test the safety and effectiveness of a drug called TTX-080, which works by blocking a protein called HLA-G that may help cancer cells survive. Participants in the trial may receive TTX-080 alone or in combination with other cancer treatments, like pembrolizumab or cetuximab. The study is currently recruiting patients who are 18 years or older and have a confirmed diagnosis of advanced or metastatic cancer, meaning the cancer has spread beyond its original location.
To join the trial, patients should have measurable disease and a good overall health status, indicated by a specific performance score. However, certain individuals may be excluded, such as those with severe allergies to similar medications or those currently using other investigational drugs. Participants can expect to have regular check-ups and monitoring throughout the study to assess how well they are responding to the treatment and to ensure their safety. This trial could be an important step in finding new options for people battling difficult cancers.
Gender
ALL
Eligibility criteria
- Abbreviated Inclusion Criteria:
- • 1. Subject with histological diagnosis of advanced/metastatic cancer
- • 2. Age 18 years or older, is willing and able to provide informed consent
- • 3. Evidence of measurable disease
- • 4. Eastern Cooperative Oncology Group (ECOG) performance status of 0 to 1 AND life expectancy of at least 12 weeks
- Abbreviated Exclusion Criteria:
- • 1. History of allergy or hypersensitivity to study treatment components. Subjects with a history of severe hypersensitivity reaction to any monoclonal antibody
- • 2. Use of an investigational agent within 28 days prior to the first dose of study treatment and throughout the study
- • 3. Receiving high-dose systemic steroid therapy or any other form of immunosuppressive therapy
- • 4. History of severe autoimmune disease
- • 5. Uncontrolled intercurrent illness or other active malignancy requiring ongoing treatment
About Tizona Therapeutics, Inc
Tizona Therapeutics, Inc. is an innovative biotechnology company dedicated to advancing the field of immunotherapy through the development of novel therapeutic agents for cancer treatment. Focused on harnessing the immune system's potential to combat tumors, Tizona employs cutting-edge research and technology to design and implement clinical trials that aim to improve patient outcomes. With a commitment to scientific excellence and collaboration, the company strives to translate its discoveries into effective therapies that address unmet medical needs in oncology.
Contacts
Jennifer Cobb
Immunology at National Institute of Allergy and Infectious Diseases (NIAID)
Locations
Los Angeles, California, United States
Los Angeles, California, United States
Charleston, South Carolina, United States
Ocala, Florida, United States
Pittsburgh, Pennsylvania, United States
Saint Paul, Minnesota, United States
Nashville, Tennessee, United States
Boston, Massachusetts, United States
Cincinnati, Ohio, United States
Indianapolis, Indiana, United States
Chicago, Illinois, United States
New Brunswick, New Jersey, United States
Denver, Colorado, United States
Oklahoma City, Oklahoma, United States
New York, New York, United States
Tacoma, Washington, United States
Vancouver, Washington, United States
Houston, Texas, United States
Pittsburgh, Pennsylvania, United States
Newport Beach, California, United States
Arlington Heights, Illinois, United States
Stony Brook, New York, United States
Saint Louis, Missouri, United States
Nashville, Tennessee, United States
Paris, Texas, United States
Louisville, Kentucky, United States
New Haven, Connecticut, United States
Columbus, Ohio, United States
Daytona Beach, Florida, United States
Silver Spring, Maryland, United States
San Antonio, Texas, United States
Tucson, Arizona, United States
Grand Rapids, Michigan, United States
Toledo, Ohio, United States
Omaha, Nebraska, United States
Fleming Island, Florida, United States
Newark, Delaware, United States
Washington, District Of Columbia, United States
Orlando, Florida, United States
Fairfax, Virginia, United States
Dallas, Texas, United States
Patients applied
Timeline
First submit
Trial launched
Trial updated
Estimated completion
Not reported
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