A Safety and Efficacy Study of EIK1001 in Combination With Pembrolizumab and Chemotherapy in Participants With Stage 4 Non-Small Cell Lung Cancer.

Prior treatment

• is currently actively enrolled in or has recently participated in a study of an investigational agent and received investigational therapy within 4 weeks or 5 half-lives (whichever is longer) of administration of EIK1001 or placebo.
• has had major surgery (\< 3 weeks prior to the first dose of study intervention administration).
• has received a live-virus vaccination within 30 days of the start of study intervention initiation.
• has received radiation therapy within 7 days of the first dose of study intervention administration.
• has completed palliative radiotherapy within 7 days of the first dose of study intervention administration.

Other

• has small cell elements present histologically and/or the tumors are not predominantly non-squamous or squamous NSCLC.

• Participant must be ≥ 18 years old at the time of signing the informed consent.
• Participant has a life expectancy of at least 3 months.
• Participant has histologically or cytologically confirmed Stage 4 NSCLC predominately squamous or non-squamous) and is considered a candidate for standard therapy with pembrolizumab and chemotherapy. Participants with NSCLC-NOS (not otherwise specified) will be considered as non-squamous NSCLC.
• Participant must have documented evidence that mutation-directed therapy is not indicated, based on the absence of tumor-activating mutations or fusions (e.g., but not limited to EGFR, ALK, RET, ROS1, BRAF) for which approved first-line targeted therapies are available to the participant in their respective country.
• Participant has at least 1 lesion with measurable disease at Baseline according to RECIST 1.1 as determined locally. Lesions situated in a previously irradiated area are considered measurable if progression has been shown in such lesions.
• Participant has not received prior systemic therapy for advanced/metastatic NSCLC.
  • Note: Participants who received adjuvant or neoadjuvant treatment (after surgery and/or radiation therapy) and developed recurrent or metastatic disease more than 1 year after completing therapy are eligible.
• Participant has an ECOG Performance Status of 0 to 1 assessed no more than 10 days before start of the treatment.
• Participant has tumor tissue available for PD-L1 testing from a site that was not radiated prior to biopsy, and was obtained, ideally, after diagnosis of metastatic disease. Biopsies obtained prior to receipt of adjuvant/neoadjuvant chemotherapy will be permitted if recent biopsy is not feasible (provided the specimen is \< 3yrs old).