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NCT06400472 · ClinicalTrials.gov registry record · Phase 1

A Study of LY4170156 in Participants With Selected Advanced Solid Tumors

A Phase 1 study of Carcinoma, Non-Small Cell Lung and Colorectal Neoplasms, sponsored by Eli Lilly and Company.

Recruiting
Registry status
Phase 1
Development phase
495
Enrollment target
20
Study locations

NCT06400472: Recruiting Phase 1 study of Carcinoma, Non-Small Cell Lung and Colorectal Neoplasms, sponsored by Eli Lilly and Company.

NCT06400472 is a Phase 1 study of Carcinoma, Non-Small Cell Lung and Colorectal Neoplasms that is actively recruiting participants, run by Eli Lilly and Company. The registered enrollment target is 495 participants, above the 320-participant average among 130 other Carcinoma, Non-Small Cell Lung trials with a reported enrollment target (55% higher). The trial reports 20 study locations across 8 states. According to ClinicalTrials.gov, the official US trial registry.

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The verdict

NCT06400472, a Phase 1 study of Carcinoma, Non-Small Cell Lung and Colorectal Neoplasms, is actively recruiting participants, sponsored by Eli Lilly and Company.

RECRUITING
Registry status
Phase 1
Development phase
495 participants
Enrollment target
20
Study locations

Study Summary

The purpose of this study is to find out whether the study drug, LY4170156, is safe, tolerable and effective in participants with advanced solid tumors. The study is conducted in two parts - phase Ia (dose-escalation, dose-optimization) and phase Ib (dose-expansion). The study will last up to approximately 4 years.

Primary Outcome

Number of participants with dose-limiting toxicities (DLTs)

Interventions

  • DRUG pembrolizumab
  • DRUG Itraconazole
  • DRUG carboplatin
  • DRUG bevacizumab
  • DRUG LY4170156

Study Locations (20)

Other

  • Cancer Research SA - Adelaide
  • Icon Cancer Centre South Brisbane - QLD
  • Centre Leon Berard - Lyon
  • Institut de Cancerologie de l'Ouest - site St-Herblain - Saint-Herblain
  • Oncopole Claudius Regaud - Toulouse
  • Istituto Europeo di Oncologia - Milan
  • Istituto Clinico Humanitas - Rozzano
  • Shizuoka Cancer Center - Shizuoka
  • National Cancer Center Hospital - Tokyo
  • Cancer Institute Hospital of JFCR - Tokyo
  • National Cancer Center - Goyang-si Gyeonggi-do

New York

  • NYU Langone Health - Long Island - Mineola
  • New York University (NYU) Clinical Cancer Center - New York
  • David H. Koch Center for Cancer Care at Memorial Sloan Kettering Cancer Center - New York

Arizona

  • HonorHealth - Scottsdale

California

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

Michigan

  • South Texas Accelerated Research Therapeutics (START) Midwest - Grand Rapids

Ohio

  • The Ohio State University (OSU) Wexner Medical Center - Columbus

Texas

  • The University of Texas - MD Anderson Cancer Center - Houston

Utah

  • START Mountain Region - West Valley City

Trial Details

FieldValue
Enrollment Target 495 participants
Start Date 2024-05-20
Est. Completion 2027-04
Phase Phase 1
Eli Lilly and Company

1,341 total trials

What NCT06400472 shows while recruiting

NCT06400472 is an interventional study that assigns participants to a tested intervention. The registered 495 participants enrollment target is mid-sized for trials with a published cap, above the 320-participant average among 130 other Carcinoma, Non-Small Cell Lung trials with a reported enrollment target (55% higher).

The record links to 7 conditions, with Carcinoma, Non-Small Cell Lung appearing as the primary indexed condition, and to 5 interventions - of which pembrolizumab is the first listed.

NCT06400472 names 20 study sites across 8 states, led by Other, New York, Arizona.

Frequently Asked Questions

What is clinical trial NCT06400472 about?

NCT06400472 is a clinical study titled "A Study of LY4170156 in Participants With Selected Advanced Solid Tumors". The purpose of this study is to find out whether the study drug, LY4170156, is safe, tolerable and effective in participants with advanced solid tumors. The study is conducted in two parts - phase Ia (dose-escalation, dose-optimization) and phase Ib (dose-expansion). The study will last up to approx...

What is the current status of trial NCT06400472?

This trial is currently recruiting. It is a Phase 1 study. The enrollment target is 495 participants. The study started on 2024-05-20. Estimated completion is 2027-04.

What conditions does trial NCT06400472 study?

This clinical trial studies the following conditions: Carcinoma, Non-Small Cell Lung, Colorectal Neoplasms, Ovarian Neoplasms, Endometrial Neoplasms, Pancreatic Neoplasm.

What interventions are being tested in trial NCT06400472?

The interventions under investigation include: pembrolizumab (DRUG), Itraconazole (DRUG), carboplatin (DRUG), bevacizumab (DRUG), LY4170156 (DRUG).

Who is sponsoring clinical trial NCT06400472?

This trial is sponsored by Eli Lilly and Company, which has 1,341 total clinical trials registered on ClinicalTrials.gov.

Where is trial NCT06400472 being conducted?

This trial has 20 study locations across Arizona, California, Michigan, New York, Ohio. Contact the study sites directly through ClinicalTrials.gov for enrollment availability.

Similar trials for Carcinoma, Non-Small Cell Lung

Matched on the same primary condition, ranked to surface studies in the same phase first, then by recruiting status, no relevance scoring or editorial curation.

Where NCT06400472's enrollment target sits among peer trials

495 30th of 130 higher than 101 of 130 other Carcinoma, Non-Small Cell Lung trials

participants (enrollment target), bucketed by value

Each bar is a band; taller bars hold more other Carcinoma, Non-Small Cell Lung trials. The dashed line + filled bar mark this entry. Hover or tap any bar for its full count and share, and where it sits relative to this entry.

Source ClinicalTrials.gov registry export · 2026-08-08

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Source: ClinicalTrials.gov NCT06400472, the US trial registry maintained by the National Library of Medicine. NCT06400472 (mid enrollment · wide site footprint · recruiting) retrieved and formatted by PlainTrial, see methodology.