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Phase I

A Phase 1 Study Evaluating the Safety, Tolerability and Pharmacokinetics of Tarlatamab in Subjects With Small Cell Lung Cancer (DeLLphi-300)

  • Study HIC#:2000024422
  • Last Updated:08/29/2023

A study to assess the safety, tolerability, and PK of tarlatamab in participants with SCLC

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    For more information about this study, including how to volunteer, contact:

    Kira Fitzsimons Pavlik

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    Trial Purpose and Description

    This is an open-label, ascending, multiple doses, phase 1 study evaluating tarlatamab monotherapy, in combination with anti-PD1 therapy and with additional cytokine release syndrome (CRS) mitigation strategies. Tarlatamab will be administered as a short term intravenous (IV) infusion in participants with SCLC. Tarlatamab is a Half-Life Extended (HLE) Bispecific T cell engager (BiTEĀ®) targeting delta-like protein 3 (DLL3)

    Eligibility Criteria

    Inclusion Criteria:

    • Participant has provided informed consent prior to initiation of any study-specific activities/procedures
    • Age greater than or equal to 18 years old at the time of signing the informed consent
    • Histologically or cytologically confirmed SCLC. For parts A, C, D, E, F, and G: relapsed/refractory small cell lung cancer (R/R SCLC) who progressed or recurred following platinum-based regimen
    • Eastern Cooperative Oncology Group (ECOG) performance status of 0-2
    • Participants with treated brain metastases are eligible provided they meet defined criteria
    • Adequate organ function as defined in protocol

    Exclusion Criteria:

    • History of other malignancy within the past 2 years prior to first dose of tarlatamab with exceptions
    • Major surgery within 28 days of first dose tarlatamab
    • Untreated (includes new lesions or progression in previously treated lesions) or symptomatic brain metastases and leptomeningeal disease
    • Prior anti-cancer therapy: at least 28 days must have elapsed between any prior anti-cancer therapy and first dose of tarlatamab with the following exceptions: participants who received conventional chemotherapy are eligible if at least 14 days have elapsed and if all treatment-related toxicity has been resolved to Grade less than or equal to 1; and prior palliative radiotherapy must have been completed at least 7 days before the first dose of tarlatamab
    • Participants who experienced severe, life-threatening or recurrent (Grade 2 or higher) immune-mediated AEs or infusion-related reactions including those that lead to permanent discontinuation while on treatment with immune-oncology agents
    • Has evidence of interstitial lung disease or active, non-infectious pneumonitis
    • 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 tarlatamab
    • Part C only: history of solid organ transplantation or active autoimmune disease that has required systemic treatment within the past 2 years
    • Participant with symptoms and/or clinical signs and/or radiographic signs that indicate an acute and/or uncontrolled active systemic infection within 7 days prior to the first dose of investigational product administration


    For more information about this study, including how to volunteer, contact: