Actively Recruiting

Phase 1
Age: 18Years - 90Years
All Genders
NCT07037758

A Study of Tarlatamab in Combination With AB248 in Participants With Extensive Stage Small Cell Lung Cancer (DeLLphi-311)

Led by Amgen · Updated on 2026-03-27

380

Participants Needed

19

Research Sites

278 weeks

Total Duration

On this page

Sponsors

A

Amgen

Lead Sponsor

A

Asher Biotherapeutics, Inc.

Collaborating Sponsor

AI-Summary

What this Trial Is About

The primary objective for dose exploration and dose expansion is to evaluate the safety and tolerability of tarlatamab in combination with AB248. The primary objective for dose exploration only is to determine the recommended dose for expansion and/or maximum tolerated combination dose (MTCD) of AB248 in combination with tarlatamab.

CONDITIONS

Official Title

A Study of Tarlatamab in Combination With AB248 in Participants With Extensive Stage Small Cell Lung Cancer (DeLLphi-311)

Who Can Participate

Age: 18Years - 90Years
All Genders

Eligibility Criteria

Eligible

You may qualify if you...

  • Participant has provided informed consent before starting any study procedures
  • Age 18 years or older (or legal age in country if older) at consent
  • Histologically or cytologically confirmed extensive stage small cell lung cancer that progressed or recurred after at least one prior anti-cancer therapy
  • At least one measurable lesion per RECIST 1.1 within 21 days before screening, not previously irradiated
  • Adequate organ function including hematological, coagulation, cardiac, pulmonary, kidney, and liver function
  • Able to provide a fresh tumor biopsy at screening or archival tissue collected after last anticancer therapy if fresh biopsy is unsafe or not feasible
Not Eligible

You will not qualify if you...

  • Symptomatic central nervous system metastases
  • Prior treatment with any DLL3-directed therapy including tarlatamab
  • Previous interleukin (IL)-2, IL-7, or IL-15 targeted therapy
  • Baseline need for supplemental oxygen at rest

AI-Screening

AI-Powered Screening

Complete this quick 3-step screening to check your eligibility

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Trial Site Locations

Total: 19 locations

1

Banner MD Anderson Cancer Center

Gilbert, Arizona, United States, 85234

Actively Recruiting

2

University of Southern California, Norris Comprehensive Cancer Center

Los Angeles, California, United States, 90033

Actively Recruiting

3

Moffitt Cancer Center

Tampa, Florida, United States, 33612

Actively Recruiting

4

Emory University

Atlanta, Georgia, United States, 30322

Actively Recruiting

5

Norton Cancer Institute - Downtown

Louisville, Kentucky, United States, 40202-1703

Actively Recruiting

6

Dana-Farber Cancer Institute

Boston, Massachusetts, United States, 02215

Actively Recruiting

7

Memorial Sloan Kettering Cancer Center

Boston, Massachusetts, United States, 02215

Actively Recruiting

8

Siteman Cancer Center

St Louis, Missouri, United States, 63110

Actively Recruiting

9

Sidney Kimmel Cancer Center

Philadelphia, Pennsylvania, United States, 19107

Actively Recruiting

10

Allegheny General Hospital

Pittsburgh, Pennsylvania, United States, 15212

Actively Recruiting

11

Avera Cancer Institute

Sioux Falls, South Dakota, United States, 57105

Actively Recruiting

12

Baptist Cancer Center

Memphis, Tennessee, United States, 38120

Actively Recruiting

13

Swedish Cancer Institute Medical Oncology

Seattle, Washington, United States, 98109

Actively Recruiting

14

Chungbuk National University Hospital

Cheongju Chungbuk, South Korea, 28644

Actively Recruiting

15

Seoul National University Bundang Hospital

Seongnam-si, Gyeonggi-do, South Korea, 13620

Actively Recruiting

16

Severance Hospital Yonsei University Health System

Seoul, South Korea, 03722

Actively Recruiting

17

Adana Sehir Egitim ve Arastirma Hastanesi

Adana, Turkey (Türkiye), 01370

Actively Recruiting

18

Hacettepe Universitesi Tip Fakultesi Hastanesi

Ankara, Turkey (Türkiye), 06230

Actively Recruiting

19

Ankara Bilkent Sehir Hastanesi

Ankara, Turkey (Türkiye), 06800

Actively Recruiting

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Research Team

A

Amgen Call Center

CONTACT

How is the study designed?

Study Type

INTERVENTIONAL

Masking

NONE

Allocation

NON_RANDOMIZED

Model

SEQUENTIAL

Primary Purpose

TREATMENT

Number of Arms

2

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