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NCT07878988RecruitingPhase 1

This is a Phase 1/1b Study to Evaluate the Safety and Preliminary Antitumor Activity of LTZ-232 in Participants With Advanced/Metastatic Colorectal Cancer and Other Solid Tumors

A Phase 1/1b, Muticenter Study to Evaluate the Safety and Preliminary Antitumor Activity of LTZ-232 in Participants With Advanced/Metastatic Colorectal Cancer and Other Solid Tumors

Source: ClinicalTrials.gov · Last updated 3 Nov 2026

Brief summary (registry, in English)

This is a first-in-human, Phase 1, multi-center, open-label study to characterize the safety, pharmacokinetics, pharmacodynamics, and preliminary anti tumor activity of LTZ-232 as monotherapy in adult participants with unresectable or metastatic colorectal cancer and other solid tumors failing standard therapies.

Status (registry)
Recruiting
Phase (registry)
Phase 1
Study type
Interventional
Enrollment
152 (estimated)
First submitted
11 Oct 2026
Start date
28 Oct 2026
Primary completion date
Dec 2031
Lead sponsor
LTZ Therapeutics, Inc.
NCT number
NCT07878988

What you commit to

  • Study type: Interventional · Phase 1
  • Planned participants: 152
  • From 28 Oct 2026 to the primary completion date, Dec 2031
  • 1 site in 1 country
  • Visits and tests: ask the trial team, the registry does not list them

Built from the registry fields of ClinicalTrials.gov. It describes the study, not your situation.

Who cannot take part

Copied verbatim from ClinicalTrials.gov and grouped by topic. Only the trial team decides who can take part.

Prior treatment

  • Previous treatment with EpCAM targeting agent

Other illness

  • Active infection with hepatitis B or C
  • Active autoimmune disease
  • Clinically significant cardiovascular disease not adequately controlled with medication or impaired function
  • Non-colorectal active malignancy within 3 years that could interfere with study interpretation

Other

  • Uncontrolled CNS metastases
  • Pregnant or breast feeding

Who the study is looking for

  • Advanced /metastatic colorectal tumors that have failed standard treatments
  • Measurable disease per Response Evaluation Criteria in Solid Tumors (RECIST v1.1)
  • Eastern Cooperative Oncology Group performance status (ECOG PS) ≤ 1
  • Adequate organ function based on laboratory testing

Age in the registry: 18 years to - · Sex: All · Does not accept healthy volunteers

Full criteria on ClinicalTrials.gov

Sites (1)

Sites in registry order. Save your city in your profile to sort them by distance.

SiteCityCountrySite status
HonorHealth Research Institute
Coordinator of this site? Confirm its status
ScottsdaleUnited StatesRecruiting

This page is information, not medical advice. Discuss any trial with your doctor.