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Search / Trial NCT04485013

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

Hla G Ttx 080 Advanced Solid Tumor Cancer Ovarian Cancer Endometrial Cancer Cervical Cancer Kidney Cancer Head And Neck Squamous Cell Carcinoma Squamous Cell Lung Cancer Prostate Cancer Colorectal Cancer Gastric Cancer Breast Cancer Bladder Cancer Lung Adenocarcinoma Melanoma Metastatic Solid Tumor Renal Cell Carcinoma Acral Melanoma Triple Negative Breast Cancer Pembrolizumab Cetuximab Antineoplastic Agents, Immunological Antineoplastic Agents Head And Neck Cancer Lung Cancer

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.

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

YP

1 patients applied

Timeline

First submit

Trial launched

Trial updated

Estimated completion

Not reported

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