Study of Dato-DXd Plus Pembrolizumab vs Pembrolizumab Alone in the First-line Treatment of Subjects With Advanced or Metastatic NSCLC Without Actionable Genomic Alterations

Inclusion Criteria:

Participants eligible for inclusion in the study must meet all inclusion criteria within 28 days of randomization into the study.

• Sign and date the Tissue Screening and Main Informed Consent Forms, prior to thestart of any study-specific qualification procedures.

• Adults ≥18 years or the minimum legal adult age (whichever is greater) at the timeof informed consent.

• Histologically documented non-squamous NSCLC that meets all of the followingcriteria (Note: Subjects with squamous histology were eligible prior to ProtocolVersion 5.0. After Protocol Version 5.0, subjects with squamous histology are noteligible. Subjects with mixed histology, including those with a squamous component,remain eligible the study even after Protocol Version 5.0):

1. Stage IIIB or IIIC disease and not candidates for surgical resection ordefinitive chemoradiation, or Stage IV NSCLC disease at the time ofrandomization (based on the American Joint Committee on Cancer, EighthEdition). Participants with early-stage NSCLC who have relapsed should berestaged during screening to ensure their eligibility for the study.

2. Documented negative test results for epidermal growth factor receptor (EGFR),lymphoma kinase (ALK), and proto-oncogene1 (ROS1) actionable genomicalterations (AGAs) based on analysis of tumor tissue. If test results for EGFR,ALK, and ROS1 are not available, subjects are required to undergo testingperformed locally for these genomic alterations.

3. No known AGAs in neurotrophic tyrosine receptor kinase (NTRK), proto-oncogeneB-raf (BRAF), rearranged during transfection (RET), mesenchymal-epithelialtransition factor (MET), or other actionable driver kinases with locallyapproved therapies. (Testing for genomic alterations besides EGFR, ALK, andROS1 is not required prior to randomization). Subjects whose tumors harbor KRASmutations are eligible for the study.

• Has provided a formalin-fixed tumor tissue sample for the measurement of trophoblastcell surface protein 2 (TROP2) protein expression and for the assessment of otherexploratory biomarkers.

• Tumor has high programmed death receptor-1 (PD-L1) expression (TPS ≥50%) asdetermined by PD-L1 immunohistochemistry (IHC) 22C3 pharmDx assay by central testing (minimum of 6 slides).

• Has an adequate treatment washout period before Cycle 1 Day 1.

• Measurable disease based on local imaging assessment using RECIST Version 1.1.

• Has left ventricular ejection fraction (LVEF) ≥50% by either an echocardiogram (ECHO) or multigated acquisition scan (MUGA) within 28 days before randomization.

• Eastern Cooperative Oncology Group (ECOG) performance status (PS) of 0 or 1 atscreening.

• Has a life expectancy of at least 3 months.

• Adequate bone marrow function within 7 days before randomization.

Exclusion Criteria:

• Has received prior systemic treatment for advanced or metastatic NSCLC.

• Has received prior treatment for NSCLC with any of the following, including in theadjuvant/neoadjuvant setting:

1. Any agent, including an antibody-drug conjugate, containing a chemotherapeuticagent targeting topoisomerase I.

2. TROP2-targeted therapy.

3. Any anti-programmed death receptor-1 (PD-1), anti-PD-L1, or anti-PD-ligand 2 (L2) agent or with an agent directed to another stimulatory or co-inhibitoryT-cell receptor (eg, CTLA-4, OX40, CD137).

4. Any other immune checkpoint inhibitors. Participants who received adjuvant orneoadjuvant therapy OTHER than those listed above, are eligible if theadjuvant/neoadjuvant therapy was completed at least 6 months prior to thediagnosis of advanced/metastatic disease.

• Has spinal cord compression or active and untreated central nervous system (CNS)metastases and/or carcinomatous meningitis. Participants with previously treatedbrain metastases and who are asymptomatic may participate provided they areradiologically stable.

• Has received prior radiotherapy < 4 weeks of start of study intervention or morethan 30 Gy (unit of ionizing radiation dose in the International System of Units) tothe lung within 6 months of Cycle 1 Day 1.

• History of another primary malignancy (beyond NSCLC) except for:

1. Malignancy treated with curative intent and with no known active disease ≥3years before the first dose of study treatment and of low potential risk forrecurrence.

2. Adequately treated non-melanoma skin cancer or lentigo maligna without evidenceof disease.

3. Adequately treated carcinoma in situ without evidence of disease.

4. Participants with a history of prostate cancer (tumor/node/metastasis stage) ofStage ≤T2cN0M0 without biochemical recurrence or progression and who in theopinion of the Investigator are not deemed to require active intervention.

• Has a history of (non-infectious) interstitial lung disease (ILD)/pneumonitisincluding radiation pneumonitis that required steroids, has current ILD/pneumonitis,or where suspected ILD/pneumonitis cannot be ruled out by imaging at screening.

• Clinically severe pulmonary compromise, as judged by the investigator, resultingfrom intercurrent pulmonary illnesses including, but not limited to, any underlyingpulmonary disorder, or any autoimmune, connective tissue or inflammatory disorderswith pulmonary involvement or prior complete pneumonectomy.

• Uncontrolled or significant cardiovascular disease, including:

1. Mean QT interval corrected for heart rate using Fridericia's formula (QTcF)interval >470 ms regardless of sex (based on the average of the 12-leadelectrocardiogram determination at screening).

2. Myocardial infarction within 6 months prior to randomization.

3. Uncontrolled angina pectoris within 6 months prior to randomization.

4. LVEF <50% by ECHO or MUGA scan within 28 days before randomization.

5. New York Heart Association Class 2 to 4 congestive heart failure (CHF) atscreening.

6. Uncontrolled hypertension (resting systolic blood pressure >180 mmHg ordiastolic blood pressure >110 mmHg) within 28 days before randomization.

Participants with a history of Class 2 to 4 CHF prior to screening, must have returned to Class 1 CHF and have LVEF ≥50% (by either an ECHO or MUGA scan within 28 days before randomization) in order to be eligible.

• Clinically significant corneal disease.

• Has received a live vaccine or live-attenuated vaccine (messenger ribonucleic acidand replication-incompetent adenoviral vaccines are not considered attenuated livevaccines) within 30 days prior to the first dose of study drug. For any participantreceiving an approved severe acute respiratory syndrome coronavirus 2 (SARS-CoV2)vaccine, please follow the vaccine label and/or local guidance.

• Active, known, or suspected autoimmune disease (has an active autoimmune diseasethat has required systemic treatment in the past 2 years).

• Has a diagnosis of immunodeficiency or is receiving chronic systemic steroid therapy (in dosage >10 mg daily of prednisone equivalent) or any other form ofimmunosuppressive therapy ≤7 days prior to the first dose of study drug.

• Has known human immunodeficiency virus (HIV) infection that is not well controlled.

• Has an active hepatitis or uncontrolled hepatitis B or active hepatitis C infection.

• Has an uncontrolled infection requiring IV antibiotics, antivirals, or antifungals.

• Had an allogeneic tissue/solid organ transplant.

• Has a history of severe hypersensitivity reactions to either the drug or inactiveingredients (including but not limited to polysorbate 80) of Dato-DXd orpembrolizumab.