A Study of Sofe-M in Participants With Selected Advanced Solid Tumors

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This is not medical advice. AI-assisted translation — inaccuracies may occur. Always verify the original and consult your oncologist before taking any steps.

About the trial

The purpose of this study is to find out whether the study drug, Sofetabart Mipitecan (LY4170156), is safe, tolerable and effective in participants with advanced solid tumors. The study is conducted in three parts - phase Ia (dose-escalation, dose-optimization), phase Ib (dose-expansion), and phase 2 (dose expansion). The study will last up to approximately 5 years.

Original English text from ClinicalTrials.gov

Who can (and can't) join

✓ Qualifies

  • •Diagnoza jednego z wymienionych typów nowotworu: rak jajnika, rak endometrium, rak szyjki macicy, rak płuca, rak piersi trojanegacyjny, rak trzustki lub rak jelita grubego
  • •Nowotwór musi być w zaawansowanym stadium

✗ Disqualifies

  • •Przerzuty do mózgu, które nie są kontrolowane
  • •Historia zapalenia opon mózgowych spowodowanego rakiem
  • •Aktywne, niekontrolowane infekcje bakteryjne, wirusowe, grzybiczne lub pasożytnicze
  • •Problemy z rogówką oka lub przeszczep rogówki w przeszłości
  • •Ciężkie działania niepożądane z poprzedniego leczenia
  • •Poważne choroby serca
  • •Ciąża, karmienie piersią lub planowanie karmienia podczas badania
  • •Historia zapalenia płuc lub chorób śródmiąższowych płuc

Simplified criteria — AI translation

Trial details

Minimum age
18 Years
Last updated (source)
October 7, 2026
Sex
No restrictions

Therapies / drugs in trial

Locations (25)

HonorHealth

Scottsdale, United States

University of California, San Diego (UCSD) - Moores Cancer Center

La Jolla, United States

Emory University

Atlanta, United States

South Texas Accelerated Research Therapeutics (START) Midwest

Grand Rapids, United States

NYU Langone Health - Long Island

Mineola, United States

New York University (NYU) Clinical Cancer Center

New York, United States

David H. Koch Center for Cancer Care at Memorial Sloan Kettering Cancer Center

New York, United States

The Ohio State University (OSU) Wexner Medical Center

Columbus, United States

The University of Texas - MD Anderson Cancer Center

Houston, United States

START Mountain Region

West Valley City, United States

Inova Schar Cancer Institute

Falls Church, United States

Cancer Research SA

Adelaide, Australia

Icon Cancer Centre South Brisbane

QLD, Australia

Centre Leon Berard

Lyon, France

Institut de Cancerologie de l'Ouest - site St-Herblain

Saint-Herblain, France

Oncopole Claudius Regaud

Toulouse, France

Humanitas San Pio X

Milan, Italy

Istituto Europeo di Oncologia

Milan, Italy

Shizuoka Cancer Center

Shizuoka, Japan

National Cancer Center Hospital

Tokyo, Japan

Cancer Institute Hospital of JFCR

Tokyo, Japan

National Cancer Center

Goyang-si Gyeonggi-do, South Korea

Hospital Universitario Vall d'Hebron

Barcelona, Spain

Hospital Universitario 12 de Octubre

Madrid, Spain

Hospital Clinico Universitario de Valencia

Valencia, Spain

Trial contact

Trial questions or participation questions: 1-877-CTLILLY (1-877-285-4559) or

Physicians interested in becoming principal investigators please contact

Contact information from ClinicalTrials.gov. Contact in English.

Share this trial

Data from ClinicalTrials.gov. AI-assisted translation, last sync: 9/5/2026.

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