Thinking of joining a study?

Register your interest

Become a volunteer?

NCT06859762 | NOT YET RECRUITING | Advanced Solid Tumor

A First-in-Human Study of YL217 in Patients with Advanced Solid Tumors
Sponsor:

MediLink Therapeutics (Suzhou) Co., Ltd.

Brief Summary:

A Phase 1 First-in-Human study of YL217 in Patients with Advanced Solid Tumors

Condition or disease

Advanced Solid Tumor

Intervention/treatment

YL217 every 3 weeks (Q3W) intravenous (IV) infusion

Phase

PHASE1

Detailed Description:

YL217 is an antibody-drug conjugate (ADC) that targets CDH17 (Cadherin-17) protein and is being developed for the treatment of cancer. YL217 is comprised of three components: 1) YL217-mAb, a CDH17-targeting recombinant humanized immunoglobulin G1 (IgG1) monoclonal antibody, 2) YL0010014, a topoisomerase I inhibitor, and 3) an enzymatically cleavable methylsulfonyl pyrimidine tripeptide drug linker. The in vivo anti-tumor efficacy of YL217 was evaluated in immune-deficient mice bearing human colorectal cancer, gastric cancer and patient derived colorectal cancer xenograft tumors. The results indicated that YL217 was well tolerated, and YL217 suppressed growth of established human tumors in a dose-dependent manner in cancer cells or patient derived xenograft models. Therefore, in order to meet the huge unmet medical needs in the field of gastrointestinal cancer treatment, it is planned to conduct the first human phase I clinical study of YL217 in patients with advanced solid tumors.

Study Type : INTERVENTIONAL
Estimated Enrollment : 220 participants
Masking : NONE
Primary Purpose : TREATMENT
Official Title : A Phase 1, Multicenter, Open-Label, First-in-Human Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy of YL217 in Patients with Advanced Solid Tumors
Actual Study Start Date : 2025-05
Estimated Primary Completion Date : 2027-07
Estimated Study Completion Date : 2027-07

Information not available for Arms and Intervention/treatment

Ages Eligible for Study: 18 Years
Sexes Eligible for Study: ALL
Accepts Healthy Volunteers:
Criteria
Inclusion Criteria
  • * Informed of the study before the start of the study and voluntarily sign their name and date in the informed consent form (ICF)
  • * Able and willing to comply with protocol visits and procedures
  • * Aged ≥ 18 years
  • * Eastern Cooperative Oncology Group performance status (ECOG PS) of 0 or 1
  • * Tumor types as below
    • For Part 1 and Part 2: Pathologically confirmed diagnosis of an advanced solid tumor, including adenocarcinoma and neuroendocrine neoplasm in gastrointestinal (GI), esophagus, gastroesophageal junction, pancreas or ampulla, and other solid tumors.
    • For Part 3 (Histologically or cytologically confirmed diagnosis+ locally advanced unresectable or metastatic disease):CohortA（colorectal adenocarcinoma）: Have clear documentation of rat sarcoma (RAS), vrafmurine sarcoma viral oncogene homolog B (BRAF), and microsatellite instability/mismatch repair status. Participants must have received at least one line of prior cytotoxic chemotherapeutic regimen. CohortB（ Human Epidermal Growth Factor Receptor 2 （HER2）-negative gastric, esophageal or gastroesophageal junction adenocarcinoma）: Participants must have received at least one line of prior cytotoxic chemotherapeutic regimen. CohortC(pancreatic adenocarcinoma): Participants must have received at least one line of prior cytotoxic chemotherapeutic regimen. CohortD(other advanced solid tumors)
    • * Adequate organ and bone marrow function.
    • * Have at least 1 extracranial measurable tumor lesion.
    • * Adequate archival formalin-fixed paraffin embedded （FFPE） tissue from prior biopsy.
    Exclusion Criteria
    • * Prior treatment with an agent targeting CDH17
    • * Prior discontinuation of a topoisomerase I inhibitor due to treatment-related toxicities.
    • * Have received a topoisomerase I inhibitor within 6 months before the first dose of study drug.
    • * Have received an ADC consisting of a topoisomerase I inhibitor.
    • * Concurrent enrollment in another clinical study, unless it is an observational clinical study.
    • * Inadequate washout period for prior anticancer treatment before the first dose of study drug
    • * Undergone major surgery within 4 weeks before the first dose of study drug or expect major surgery during the study.
    • * Received long term systemic steroids or other immunosuppressive therapy within 2 weeks before the first dose of study drug.
    • * Received any live vaccine within 4 weeks before the first dose of study drug or intend to receive a live vaccine during the study.
    • * Diagnosis or evidence of spinal cord compression or leptomeningeal carcinomatosis.
    • * Uncontrolled or clinically significant cardiovascular and cerebrovascular diseases.
    • * A history of non-infectious interstitial lung disease (ILD)/pneumonitis that requires steroids, current active ILD/pneumonitis.
    • * Have clinically severe pulmonary compromise resulting from intercurrent pulmonary illnesses.
    • * Uncontrolled third-space fluid that requires repeated drainage.
    • * Digestive system disease that may cause bleeding, perforation, jaundice, gastrointestinal obstruction.
    • * An active tuberculosis based on medical history.
    • * Known human immunodeficiency virus (HIV) infection.
    • * Active hepatitis C infection.
A First-in-Human Study of YL217 in Patients with Advanced Solid Tumors

Location Details

NCT06859762

Please Choose a site

How to Participate

Want to participate in this study, select a site at your convenience, send yourself email to get contact details and prescreening steps.

Locations

Not yet recruiting

United States, Texas

Next Oncology

San Antonio, Texas, United States, 78229