Study of Tarlatamab maintenance treatment after chemotherapy and radiation therapy in patients with limited stage small cell lung cancer who cannot receive both treatments together

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What is this study about?

This clinical trial focuses on patients with Small Cell Lung Cancer (SCLC) who have completed chemotherapy and radiation therapy but were unable to receive both treatments simultaneously. The study evaluates a medication called Tarlatamab (also known as AMG 757), which is given as a solution through intravenous administration.

The purpose of this research is to determine if using Tarlatamab as a maintenance treatment after completing standard chemotherapy and radiation therapy can help prevent cancer from progressing. The study compares two groups of patients – one group receives Tarlatamab while the other continues with standard care after their initial treatment.

During the study, participants receive Tarlatamab through an intravenous infusion at specified intervals. The maximum daily dose is 10 milligrams, and the treatment may continue for up to 24 months. The medication is a biological product, meaning it is derived from living organisms rather than chemical synthesis. Patients will be monitored regularly to assess how well the treatment works and to check for any side effects.

1 Initial assessment

Your medical condition must be confirmed as small cell lung cancer (SCLC) through tissue examination

Your doctor will check if you meet all health requirements, including adequate organ function and blood test results

Your heart function will be evaluated through an echocardiogram test

Your oxygen levels must be above 90% when breathing room air

2 Previous treatment completion

You must have completed either chemotherapy alone or chemotherapy followed by radiation therapy

Any side effects from previous treatments must be resolved to mild level or less

Your cancer must not show signs of progression after these treatments

3 Treatment assignment

You will be randomly assigned to one of two groups:

Group 1: Receiving Tarlatamab as maintenance treatment

Group 2: Standard follow-up care without Tarlatamab

4 Treatment period

If assigned to the Tarlatamab group, you will receive the medication through intravenous infusion

The medication comes as a powder that will be prepared as a solution for infusion

Regular assessments will track your cancer’s response to treatment

Your doctor will monitor for any side effects throughout the treatment period

5 Follow-up period

Your cancer will be regularly monitored using imaging scans

Blood tests will be performed to check your overall health and immune response

The treatment will continue until either your disease progresses or you experience unacceptable side effects

Your survival and cancer status will be tracked for up to 2 years

Who Can Join the Study?

  • Must be diagnosed with small cell lung cancer confirmed by tissue or cell examination
  • Must be at least 18 years old when signing consent form
  • Must have completed chemotherapy or combined chemotherapy and radiation therapy without disease progression
  • Must have at least one measurable tumor lesion
  • Must have a life expectancy of at least 3 months
  • Must be able to perform daily activities with minimal assistance (ECOG status of 0 to 2)
  • Must have normal heart function with:
    – No significant heart rhythm abnormalities
    – Heart pumping strength (ejection fraction) of 50% or higher
    – No significant fluid around the heart
  • Must have adequate lung function:
    – Oxygen level above 90% when breathing room air
    – No significant fluid in the lungs
  • Must have adequate blood test results showing:
    – Sufficient white blood cells (neutrophils)
    – Sufficient blood platelets
    – Adequate hemoglobin levels
    – Normal blood clotting function
    – Adequate kidney function
    – Acceptable liver function tests
  • Must have recovered from previous treatment side effects (except hair loss)
  • Must voluntarily agree to participate and sign an informed consent form

Who Cannot Join the Study?

  • Age under 18 years old
  • Active brain metastases (cancer that has spread to the brain) or brain disease that requires treatment
  • History of another type of cancer within the last 3 years, except for successfully treated skin cancer or early-stage cancer
  • Severe heart conditions including:
    • Uncontrolled high blood pressure
    • Recent heart attack (within 6 months)
    • Unstable heart rhythm problems
  • Active, uncontrolled infections requiring treatment
  • Known HIV infection, active hepatitis B, or active hepatitis C
  • Pregnancy or breastfeeding
  • Any condition that, in the opinion of the study doctor, would make participation unsafe
  • Current participation in other clinical trials or use of investigational drugs within 30 days before starting this study
  • Known allergies to the study medication or its components
  • Inability to swallow oral medications
  • Major surgery within 4 weeks before starting the study

Where you can join this trial?

Verified and Recommended Sites

No sites found in this category

Verified Sites

Site Name City Country Status
Hospital Universitario De Navarra Pamplona Spain
Hospital Clinico San Carlos Madrid Spain
Hospital Jerez de la Frontera Jerez De La Frontera Spain

Other Sites

Site Name City Country Status
Hospital Universitario Puerta De Hierro De Majadahonda Majadahonda Spain
Hospital Universitario Basurto Bilbao Spain
Althaia Xarxa Assistencial Universitaria De Manresa Fundacio Privada Manresa Spain
Hospital General Universitario De Albacete Albacete Spain
Hospital Clinic De Barcelona Barcelona Spain
Hospital Universitario Fundacion Jimenez Diaz Madrid Spain
Hospital General Universitario De Valencia Valencia Spain
Hospital Son Llatzer Palma Spain
Hospital Universitario Lucus Augusti Lugo Spain
Servei De Salut De Les Illes Balears Palma Spain
Hpyvlonk Dw Lo Stbyo Cmgb I Slrs Pcf Barcelona Spain
Hmijsovh Vnja ddckxivp Barcelona Spain

Want to learn more about this study or check if you can participate? Contact us.

Trial status

Country Status Recruitment Start
Spain Spain
Recruiting
02.09.2025

Trial locations

Investigated drugs:

Tarlatamab is a medication being studied as a maintenance treatment for small cell lung cancer (SCLC). It is given to patients after they complete a course of sequential chemotherapy and radiation therapy. This medication is designed to help maintain the benefits of initial treatment and potentially prevent or delay the cancer from returning. It is being tested in patients who are not eligible for concurrent chemotherapy and radiation therapy.

Chemotherapy and radiation therapy (also called chemo-radiotherapy) is a standard treatment approach that uses anti-cancer drugs along with radiation to kill cancer cells. In this trial, these treatments are given sequentially, meaning one after the other, rather than at the same time.

Small Cell Lung Cancer (SCLC) – A fast-growing type of lung cancer that typically starts in the bronchi, the airways in the center of the chest. The cancer cells are small and oval-shaped when examined under a microscope, which gives the disease its name. SCLC tends to grow and spread more rapidly than other types of lung cancer. The disease usually begins in the lung tissue but can quickly spread to other parts of the body. Early in the disease, cancer cells multiply quickly and form large masses in the lungs.

Trial ID:
2024-515201-26-00
Protocol code:
MERLIN (GECP 24/02)
Trial Phase:
Therapeutic exploratory (Phase II)

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