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Clinical Trials in China / NCT06598306
Recruiting Phase 1

Subcutaneous Tarlatamab in Participants With Extensive Stage Small Cell Lung Cancer (DeLLphi-308)

NCT06598306 · tracked via the Priya Life Science China tracker
Sponsor
Amgen
Phase
Phase 1
Started
2024-10-07
Last updated
2026-06-26

Condition(s) studied

Extensive Stage Small Cell Lung Cancer

Investigational drug(s) / intervention(s)

Tarlatamab

Tarlatamab: Administered by SC injection.

Study summary

The primary objective of this study is to evaluate the safety and tolerability of subcutaneous (SC) tarlatamab.

Eligibility

Sex
ALL
Min age
18 Years
Max age
Healthy volunteers
No
Inclusion Criteria: * Participants ≥ 18 years of age (or ≥ legal adult age within country if it is older than 18 years) at time of signing informed consent. * Participants with histologically or cytologically confirmed ES-SCLC that progressed or recurred following at least one line of platinum-based anti-cancer therapy for SCLC. Note: Participants with prior treatment for LS-SCLC should have also received another regimen for their recurrent, ES-SCLC disease. * Eastern Cooperative Oncology Group (ECOG) Performance Status (PS) of 0 or 1. * Participants must have adequate organ function (cardiac, pulmonary, kidney, and liver). * Participants must be able to have SC injections administered in the abdomen. * Participants without measurable disease or tumor tissue (fresh biopsy or archival) available may be permitted after discussion with and approval by Amgen Medical Monitor. Exclusion Criteria: * Participants that have received prior DLL3 targeted therapy. * Participants with untreated or symptomatic brain metastases or those requiring therapy with steroids. * Note: Participants with asymptomatic brain metastatic lesions are allowed following definitive treatment (Amgen Medical Monitor may approve untreated, asymptomatic brain metastasis if local therapy is not required per investigator judgment). * Participants with leptomeningeal disease. * Participants with baseline oxygen requirement.

Primary outcome measure(s)

Trial sites (31)

FacilityCityRegionStatus
University of Southern California, Norris Comprehensive Cancer Center Los Angeles California Recruiting
University of Illinois Chicago Chicago Illinois Recruiting
Trinity Health Saint Joseph Mercy Ann Arbor Ann Arbor Michigan Recruiting
Avera Cancer Institute Sioux Falls South Dakota Recruiting
University of Texas MD Anderson Cancer Center Houston Texas Recruiting
Swedish Cancer Institute Seattle Washington Recruiting
Chris OBrien Lifehouse Camperdown New South Wales Recruiting
Calvary Mater Newcastle Hospital Waratah New South Wales Recruiting
The Alfred Hospital Melbourne Victoria Recruiting
Universitair Ziekenhuis Gent Ghent Belgium Recruiting
Universitair Ziekenhuis Leuven - Campus Gasthuisberg Leuven Belgium Recruiting
Centre Hospitalier Universitaire de Liege - Sart Tilman Liège Belgium Recruiting
Jilin Cancer Hospital Changchun Jilin Recruiting
Shanghai Pulmonary Hospital Shanghai Shanghai Municipality Recruiting
Universitaetsklinikum Regensburg Regensburg Germany Recruiting
Universitaetsklinikum Wuerzburg Würzburg Germany Recruiting
Okayama University Hospital Okayama Okayama-ken Recruiting
Wakayama Medical University Hospital Wakayama Wakayama Recruiting
Uniwersyteckie Centrum Kliniczne Gdansk Poland Recruiting
Instytut Centrum Zdrowia Matki Polki Lodz Poland Recruiting
Wojewodzki Szpital im Sw Ojca Pio w Przemyslu Przemyśl Poland Recruiting
Hospital Regional Universitario de Malaga Málaga Andalusia Recruiting
Hospital Universitari Vall d Hebron Barcelona Catalonia Recruiting
Hospital Universitari i Politecnic La Fe Valencia Valencia Recruiting
Hospital Universitario 12 de Octubre Madrid Spain Recruiting
Kantonsspital Graubuenden Chur Switzerland Recruiting
Freiburg Spital Fribourg Switzerland Recruiting
Kantonsspital Winterthur Winterthur Switzerland Recruiting
Adana Sehir Egitim ve Arastirma Hastanesi Adana Turkey (Türkiye) Recruiting
Ankara Bilkent Sehir Hastanesi Ankara Turkey (Türkiye) Recruiting
Koc Universitesi Hastanesi Istanbul Turkey (Türkiye) Recruiting

More Amgen trials in China

Other trials for the same condition

Official registry record

This page summarises publicly available registry data for informational purposes — not medical advice. Eligibility is determined by each study team; patients should discuss participation with their clinician.

View NCT06598306 on ClinicalTrials.gov ↗ ← All trials in China