pembrolizumab for Non-small cell lung cancer|Unresectable stage III non-small cell lung cancer

Inclusion criteria

• {"criterion_text":"- Be willing and able to provide written informed consent/assent for the trial.\n- Be 18 years of age on day of signing informed consent.\n- Have measurable disease based on RECIST 1.1\n- Be willing to provide tissue from a newly obtained core, trucut biopsy or excisional biopsy of a tumor lesion. Newly-obtained is defined as a specimen obtained up to 6 weeks (42 days) prior to initiation of treatment on Day 1. Subjects for whom newlyobtained samples cannot be provided (e.g. inaccessible or subject safety concern) may submit an archived specimen only upon agreement from the PI\n- Have a performance status of 0 or 1 on the ECOG Performance Scale\n- Demonstrate adequate organ function as defined in Table 1, all screening labs should be performed within 10 days of treatment initiation\n- Female subject of childbearing potential should have a negative urine or serum pregnancy within 72 hours prior to receiving the first dose of study medication. If the urine test is positive or cannot be confirmed as negative, a serum pregnancy test will be required.\n- Female subjects of childbearing potential should be willing to use 2 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 (Section 8.14.2). Subjects of childbearing potential are those who have not been surgically sterilized or have not been free from menses for > 1 year.\n- Male subjects should agree to use an adequate method of contraception starting with the first dose of study therapy through 120 days after the last dose of study therapy."}

Exclusion criteria

• {"criterion_text":"- Is currently participating and receiving study therapy or has participated in a study of an investigational agent and received study therapy or used an investigational device within 4 weeks of the first dose of treatment\n- Has a history or current evidence of any condition, therapy, or laboratory abnormality that might confound the results of the trial, interfere with the subject’s participation for the full duration of the trial, or is not in the best interest of the subject to participate, in the opinion of the treating investigator.\n- Has known psychiatric or substance abuse disorders that would interfere with cooperation with the requirements of the trial\n- Is pregnant or breastfeeding, or expecting to conceive or father children within the projected duration of the trial, starting with the pre-screening or screening visit through 120 days after the last dose of trial treatment.\n- Has received prior therapy with an anti-PD-1, anti-PD-L1, or anti-PD-L2 agent.\n- Has a known history of Human Immunodeficiency Virus (HIV) (HIV 1/2 antibodies).\n- Has known active Hepatitis B (e.g., hepatitis B virus surface antigen [HBsAg] reactive) or Hepatitis C (e.g., HCV ribonucleic acid [RNA] qualitative is detected).\n- Has received a live vaccine within 30 days of planned start of study therapy\n- Has a diagnosis of immunodeficiency or is receiving systemic steroid therapy or any other form of immunosuppressive therapy within 7 days prior to the first dose of trial treatmen\n- Has a known history of active Bacillus Tuberculosis (TB)\n- Hypersensitivity to pembrolizumab or any of its excipients.\n- Has had a prior anti-cancer monoclonal antibody (mAb) within 4 weeks prior to study Day 1 or who has not recovered (i.e., ≤ Grade 1 or at baseline) from adverse events due to agents administered more than 4 weeks earlier\n- Has a known additional malignancy that is progressing or requires active treatment. Exceptions include basal cell carcinoma of the skin or squamous cell carcinoma of the skin that has undergone potentially curative therapy or in situ cervical cancer.\n- Has active autoimmune disease that has required systemic treatment in the past 2 years (i.e. with use of disease modifying agents, corticosteroids or immunosuppressive drugs). Replacement therapy (e.g., thyroxine, insulin, or physiologic corticosteroid replacement therapy for adrenal or pituitary insufficiency, etc.) is not considered a form of systemic treatment.\n- Has a history of (non-infectious) pneumonitis that required steroids or current pneumonitis, or has evidence of interstitial lung disease\n- Has an active infection requiring systemic therapy."}

Primary endpoints

• {"endpoint_text":"- Median overall survival (OS) time","definition_or_measurement_approach":""}

Secondary endpoints

• {"endpoint_text":"- Overall survival (OS) defined as the time from randomization to death or last follow-up","definition_or_measurement_approach":"OS defined as the time from randomization to death or last follow-up"}
• {"endpoint_text":"- Progression Free Survival (PFS) intended as the time from randomization to disease progression or death","definition_or_measurement_approach":"PFS intended as the time from randomization to disease progression or death"}
• {"endpoint_text":"- Overall Response Rate (ORR)","definition_or_measurement_approach":""}

Italy

Earliest CTIS Part Ii Submission Date

15-11-2024

Latest Decision Or Authorization Date

07-05-2025

Processing Time Days

173

Number Of Sites

13

Number Of Participants

126

Primary sponsor

Full Name

Universita' Degli Studi Di Torino

Organisation Type

Educational Institution

Country Of Registered Address

Italy

Third parties

• {"country":"Italy","full_name":"Depo-pack S.r.l.","duties_or_roles":"sponsorDuties code: 14","organisation_type":"Pharmaceutical company"}