Tarlatamab is designed to help the body’s immune cells find, attach to, and attack cancer cells.

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Who is able to join this study?

Patients who are 18 years or older

Diagnosed with small cell lung cancer (SCLC) confirmed by tumor sample

Whose cancer has returned after first-line treatment

With tumor(s) that can be seen on imaging

Study participants must also meet additional eligibility criteria.

Click to download and print a description of the study to bring to your doctor.
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Where can I get more information?

To determine if you may be eligible for a clinical study for tarlatamab, talk to your doctor or contact an Amgen Medical Information Healthcare Professional.

AmgenMedInfo.com

866-572-6436

Monday - Friday 8am to 8pm (ET)

What will be asked of you if you take part in this study?

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Step 1: Screening

At your first study visit(s), you will:

  • Meet the study doctor and study team at your study site, which may be different from where you have received treatment in the past
  • Review and sign an informed consent with the study staff to join the DeLLphi-304 study
  • Complete a general health assessment, including a physical exam, medical history, blood tests, and imaging
  • Have your tumor sampled*

*This may not be needed in all cases. The study doctor will let you know if this is not needed.

If you meet the requirements and decide to join the study, you will move on to Step 2.

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Step 2: Treatment with tarlatamab (study drug) OR standard of care chemotherapy

Each participant will be randomly assigned to receive either tarlatamab (study drug) or standard of care chemotherapy.

The tarlatamab group (~350 participants) will:

  • Receive tarlatamab by infusion (in a vein) once a week for the first 3 weeks and then once every 2 weeks afterwards*
  • Attend study appointments and check-ups to record your progress

* As a precaution, you will need to stay in the hospital for at least 48 hours after your first two tarlatamab treatments to monitor your health status. For later treatments, you may need to stay in the hospital if you have side effects from the medication.

The standard of care chemotherapy group (~350 participants) will:

  • Receive either topotecan (Hycamtin®) by infusion or by mouth OR lurbinectedin (Zepzelca®) by infusion^
  • Attend study appointments and check-ups to record your progress

^These two drugs are approved for treatment of SCLC in the United States after first-line treatment with platinum-based chemotherapy. Treatment may vary in other countries.

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Step 3: End of treatment

You will continue to receive treatment in the study based on the results of your bloodwork and imaging. Your study treatment may stop if:

  1. Your cancer gets worse*
  2. You experience serious side-effects from treatment
  3. You decide to stop the study at any time

The study team will schedule a follow-up visit with you approximately 6 weeks after your last study treatment.

* You may stay on the study drug if you are eligible and if the study doctor agrees it is still helping you.

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Step 4: Long term follow-up (up to 3 years)

The study team may follow-up with you by phone or ask you to visit the clinic approximately once every 3 months.

Study Locations

If you are a physician or another healthcare professional interested in learning more about a tarlatamab clinical study or referring a patient, please contact an Amgen Medical Information Healthcare Professional.

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Where can I get more information?

To determine if you may be eligible for a clinical study for tarlatamab, talk to your doctor or contact an Amgen Medical Information Healthcare Professional.

AmgenMedInfo.com

866-572-6436

Monday - Friday 8am to 8pm (ET)