A Phase 1, First-in-Human, Open Label, Dose Escalation, Dose Optimization, and Cohort Expansion Study of MGC030 in Participants With Advanced Solid Tumors

MacroGenics0 个研究点目标入组 314 人开始时间: 2026年9月1日最近更新: 2026年9月16日

适应症

干预措施

试验速览

阶段: 1 期
状态: 尚未招募
发起方: MacroGenics
入组人数: 314
主要终点: Number of participants with adverse events (AEs), serious AEs (SAEs), AEs leading to dose interruption, AEs leading to dose reduction or treatment discontinuation, does limiting toxicities and AEs of special interest.

研究概览研究设计入排标准研究组 & 干预措施结局指标研究者记录与标识符相似试验

研究概览

简要总结

The study is designed to characterize safety, tolerability, pharmacokinetics (PK), immunogenicity, and preliminary anti-tumor activity of MGC030. Participants with relapsed or refractory, unresectable, locally advanced or metastatic solid tumors of select types.

The main question the study aims to answer is:

What types of side effects will participants experience when receiving MGC030?
Can MGC030 cause cancer to shrink, remain stable, or able to control disease progression of participants with advanced solid tumors? Participants will
Undergo screening procedures to determine eligibility
Receive study treatments initially every 3 weeks.
Have blood samples taken for routine and research tests
Have other examinations to check heart and lung function, and general health status
Be asked about any side effects that may be happening or other medications you are taking. The study doctor will provide treatment for side effects, if necessary.
Have the study doctor assess your tumor status at regular intervals to determine how you are responding to treatment.

研究设计

研究类型: Interventional
分配方式: Non Randomized
干预模型: Sequential
主要目的: Treatment
盲法: None

入排标准

年龄范围: 18 Years 至 —（Adult, Older Adult）
性别: All
接受健康志愿者: 否

入选标准

•Participants in dose escalation cohorts must have histologically proven unresectable, locally advanced or metastatic solid tumor limited to one of the following types: urothelial cancer, colorectal cancer (CRC), gastric or gastroesophageal junction (GEJ) cancer, esophageal cancer, or pancreatic carcinoma that is refractory to standard therapy, or for which standard therapy does not exist, has proven to be intolerable, or has been refused by the participant.
•Participants in expansion cohorts must have histologically proven, unresectable, locally advanced or metastatic solid tumors
•Urothelial cancer with progression following platinum-containing chemotherapy for metastatic or locally advanced/unresectable cancer, or within 12 months from completion of neo-adjuvant or adjuvant platinum-containing chemotherapy for localized muscle-invasive cancer.
•Gastric/GEJ carcinoma with progression during or following at least 1 systemic therapy.
•Esophageal cancer with progression during or following at least 1 systemic therapy.
•CRC with progression during or following treatment with at least 2 prior lines of systemic therapy (containing a fluoropyrimidine plus a platinum analogue and/or irinotecan) for metastatic disease.
•CRC harboring an activating EGFR mutation must have progressed during or following at least one EGFR targeted therapy, if available.
•Participants should have received no more than 4 prior lines of systemic therapy for advanced or metastatic disease.
•Pancreatic cancer with progression during or following at least 1 systemic therapy. Participants should have received no more than 2 prior lines of cytotoxic chemotherapy for advanced or metastatic disease.
•Participants must have at least one lesion that meets the definition of measurable disease by RECIST v1.
•Participants must have an available archival or formalin-fixed paraffin-embedded tumor tissue or be willing to undergo a biopsy procedure to obtain a fresh tumor sample.
•Participants have acceptable physical condition and laboratory values.
•Participants of childbearing potential must agree to use highly effective methods of birth control.
•Participants must not be pregnant, planning to be pregnant, or breastfeeding.

排除标准

•Any underlying medical or psychiatric condition impairing participant's ability to receive, tolerate, or comply with the planned treatment or study procedures.
•Active brain metastases or leptomeningeal metastases.
•Prior stem cell, tissue, or solid organ transplant.
•Another malignancy that required treatment within the past 2 years, with the exception of those with a negligible risk of metastasis or death such as adequately treated non-melanomatous skin cancer, localized prostate cancer (Gleason Score < 6), or carcinoma in situ.
•History of primary immunodeficiency.
•Active viral, bacterial, or fungal infection
•Prior treatment with Topoisomerase 1-based ADCs for cancer.
•Prior treatment with major surgery, mediastinal or lung radiation, vaccination with live virus vaccines, systemic cancer treatment, chimeric antigen receptor (CAR)-T cell therapy, or experimental treatment within 4 weeks of the start of study treatment.

研究组 & 干预措施

Dose escalation Cohort 1

Experimental

MGC030 Dose Level 1

干预措施: MGC030 (Biological)

Dose escalation Cohort 2

Experimental

MGC030 Dose Level 2

干预措施: MGC030 (Biological)

Dose escalation Cohort 3

Experimental

MGC030 Dose Level 3

干预措施: MGC030 (Biological)

Dose escalation Cohort 4

Experimental

MGC030 Dose Level 4

干预措施: MGC030 (Biological)

Dose escalation Cohort 5

Experimental

MGC030 Dose Level 5

干预措施: MGC030 (Biological)

Dose escalation Cohort 6

Experimental

MGC030 Dose Level 6

干预措施: MGC030 (Biological)

Dose Optimization Cohort 1

Experimental

Dose Optimization Dose Level 1

干预措施: MGC030 (Biological)

Dose Optimization Cohort 2

Experimental

Dose Optimization Dose Level 2

干预措施: MGC030 (Biological)