Lung Cancer Clinical Trial
A Trial of AN0025 With Chemoradiation Therapy in Stage III NSCLC Participants
Evaluate safety and toxicity of AN0025 in both the consolidative setting (after chemoradiation) and in the concurrent setting (during chemoradiation)
Evaluate efficacy by progression-free survival (PFS), objective response rate (ORR), and time to death or distant metastasis (TTMD), Duration of response (DOR), Overall survival (OS) with the addition of AN0025 in both the consolidative and concurrent settings Exploratory
Evaluate pharmacokinetics of AN0025 in conjunction with chemoradiation, and then with durvalumab
The purpose of the research is to evaluate the safety and preliminary efficacy of AN0025 in combination with chemoradiation + consolidation durvalumab in advanced (Stage III) Non-Small Cell Lung Cancer. Participant will receive the experimental combination of drugs (AN0025, chemoradiation and durvalumab) and undergo laboratory tests and study procedures on specified days during the study period. Complete end of study evaluations and tests, and participate in post-study follow up every three months for two years. The time in the study will take approximately four to six hours during pre-study, study and end of study visits.
Possible benefits of taking part may be improvement in your condition and slowing or stopping the growth of your cancer.
Be willing and able to provide written informed consent for the trial
Age 18 years or greater
Be fully active, able to carry on all pre-disease performance without restriction or restricted in physically strenuous activity but able to carry out work of a light or sedentary nature (e.g., light house work, office work)
Be diagnosed with confirmed locally advanced and nonresectable, or metastatic Stage III Non-Small Cell Lung Cancer
Have provided archival tumor tissue sample or newly obtained core or excisional biopsy of a tumor lesion not previously irradiated
Adequate staging of your disease
Adequate lung function
Adequate other organ functions
No active second cancers
Be willing and able to comply with all aspects of the protocol
Female patients of childbearing potential should have a negative pregnancy test within 72 hours prior to receiving the first dose of study medication
Female participants of childbearing potential should be willing to use two methods of birth control or be surgically sterile, or abstain from heterosexual activity for the course of the study through 120 days after the last dose of study medication
Male participants should agree to abstinence or use of an adequate method of contraception starting with the first dose of study therapy through 120 days after the last dose of study therapy
Age less than 18 years
Weight less than 30 Kg (~66 lbs)
Pregnant or breastfeeding women
Have been discontinued in a prior treatment study with immunotherapy drugs due to a severe toxicity (Grade 3 or higher)
Received a live vaccine within 30 days prior to the first dose of study drug. Examples of live vaccines include, but are not limited to, the following: measles, mumps, rubella, varicella/zoster (chicken pox), yellow fever, rabies, Bacillus Calmette-Guérin (BCG), and typhoid vaccine. Seasonal influenza vaccines for injection are generally killed virus vaccines and are allowed; however, intranasal influenza vaccines (e.g., FluMist®) are live attenuated vaccines and are not allowed.
Had an allogenic tissue/solid organ transplant
A diagnosis of immunodeficiency or is receiving chronic systemic steroid therapy or any other form of immunosuppressive therapy within seven days prior to the first dose of study drug
Known active cancer spread to central nervous system
Known severe hypersensitivity to study treatment components
An active autoimmune disease that has required systemic treatment in the past two years
Have inflammatory bowel disease
Have a history of (non-infectious) pneumonitis that required steroids or have current pneumonitis
Have a history of interstitial lung disease
Have an active infection requiring systemic therapy
Have human immunodeficiency virus (HIV) and/or history of Hepatitis B or C infections,
Have abnormal electrocardiogram (Prolongation of QT interval)
Significant cardiovascular impairment: history of congestive heart failure, uncontrolled arterial hypertension, unstable angina, myocardial infarction, or stroke within 6 months of the first dose of study drug; or cardiac arrhythmia
Major surgery within four weeks before the first dose of study drug
Inability to take oral medication, or malabsorption syndrome or any other uncontrolled gastrointestinal condition (eg, nausea, diarrhea, or vomiting)
Have a known psychiatric or substance abuse problems
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