First in Human Study of SIM0610 in Solid Tumors (SIM0610-101)

An Open-Label, Multicenter, First-in-Human Phase 1 Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Preliminary Antitumor Activity of SIM0610 in Adult Subjects With Locally Advanced/Metastatic Solid Tumors

This is a multicenter, open-label, first-in-human (FIH) study to evaluate the safety, tolerability, pharmacokinetic/pharmacodynamic profile, and preliminary antitumor activity of SIM0610 in subjects with locally advanced/metastatic solid tumors. Accelerated titration (ATD) and Bayesian optimal interval design (BOIN) will be used to guide dose escalation in part1, the preliminary anti-tumor effect of SIM0610 will to be further evaluated in part 2.

Study Overview

• Status: Recruiting
• Conditions: Hepatocellular Carcinoma; Colorectal Cancer; Non-Small Cell Lung Cancer; Head and Neck Squamous Cell Carcinoma; Advanced Solid Tumours
• Intervention / Treatment: Drug: SIM0610 for Injection

• Study Type: Interventional
• Enrollment (Estimated): 260
• Phase: Phase 1

Contacts and Locations

• Study Contact: Name: Jiawei Yao; Phone Number: +8618868816194; Email: yaojiawei@zaiming.com

Study Locations

• China
  • Chongqing Municipality
    • Chongqing, Chongqing Municipality, China, 400000
      • Not yet recruiting
      • Chongqing Cancer Hospital
      • Contact: Yongsheng Li
  • Heilongjiang
    • Harbin, Heilongjiang, China, 150000
      • Not yet recruiting
      • Harbin medical university cancer hospital
      • Contact: Tongsen Zheng
  • Liaoning
    • Shenyang, Liaoning, China, 110000
      • Not yet recruiting
      • The First Hospital of China Medical University
      • Contact: Xiujuan Qu
  • Shandong
    • Jinan, Shandong, China, 250117
      • Recruiting
      • The Affiliated Cancer Hospital of Shandong First Medical University& Shan Dong Cancer Hospital
      • Contact: Jinming Yu
  • Shanghai Municipality
    • Shanghai, Shanghai Municipality, China, 200000
      • Not yet recruiting
      • Shanghai Pulmonary Hospital
      • Contact: Shengxiang Ren
    • Shanghai, Shanghai Municipality, China, 200000
      • Not yet recruiting
      • Shanghai East Hospital
      • Contact: Ye Guo
    • Shanghai, Shanghai Municipality, China, 200000
      • Not yet recruiting
      • Zhongshan Hospital, Fudan University
      • Contact: Tianshu Liu

Participation Criteria

Eligibility Criteria

• Ages Eligible for Study: Adult; Older Adult
• Accepts Healthy Volunteers: No

Description

Inclusion Criteria:

• Voluntarily participate and sign the informed consent form
• At least 18 years old, male or female
• Subjects with locally advanced/metastatic solid tumors confirmed by histology and/or cytology;
• Subjects in Part 1 should have at least one tumor lesion evaluable by RECIST v1.1 criteria, and subjects in Part 2 should have at least one measurable tumor lesion by RECIST v1.1 (lesions that have received radiotherapy or other local treatments cannot be used as target lesions unless there is clear progression of the lesion)
• Subjects with locally advanced/metastatic solid tumors who have failed standard treatment: Part 1: Subjects with solid tumors who have experienced disease progression during/after at least one previous standard systemic anti-tumor regimen and are not suitable for standard treatment. Part 2: Non-small cell lung cancer, liver cancer, head and neck squamous cell carcinoma, colorectal cancer that have experienced disease progression during/after at least one previous standard systemic anti-tumor regimen and are not suitable for standard treatment
• Eastern Cooperative Oncology Group (ECOG) performance status of 0 or 1
• Expected survival period ≥ 12 weeks
• Adequate organ and bone marrow function
• Archived formalin-fixed, paraffin-embedded (FFPE) tumor tissue or fresh biopsy tissue within 5 years must be provided before the first administration

Exclusion Criteria:

• A history of active second primary malignancy within the past 2 years, except for localized tumors that are considered cured and have a low risk of recurrence as assessed by the investigator.
• Symptomatic central nervous system (CNS) metastases occurring within 2 weeks prior to the first dose of study treatment; or requirement for local therapy (e.g., radiotherapy or surgery) for CNS metastases; or requirement for corticosteroid therapy for CNS metastases.
• A history of non-infectious interstitial lung disease (ILD)/pulmonary inflammation requiring corticosteroid treatment; current ILD/pulmonary inflammation; or suspected ILD/pulmonary inflammation that cannot be ruled out by screening imaging.
• Uncontrolled pleural effusion, pericardial effusion, or ascites, or occurrence of such effusions requiring drainage or medical intervention within 4 weeks prior to the first dose of study treatment.
• Failure to recover from adverse events (AEs) induced by prior anti-tumor therapy (i.e., recovery to Grade 1 or baseline level).
• Current participation in a study involving investigational drugs or medical devices, or participation in such a study within 4 weeks prior to the first dose of study treatment.

• Receipt of the following therapies prior to the first dose of study treatment:

  1. Cytotoxic therapy within 3 weeks; or anti-tumor targeted small-molecule drugs (e.g., tyrosine kinase inhibitors) within 2 weeks.
  2. Anti-tumor antibody-based immune checkpoint inhibitors, antibody-drug conjugates (ADCs), or other anti-tumor biologics within the shorter of 5 half-lives or 4 weeks.
  3. Traditional Chinese medicines (TCMs)/herbal preparations with anti-tumor indications within 2 weeks.
  4. Radiotherapy within 4 weeks.
• Received antibody-drug conjugate (ADC) with topoisomerase I inhibitor (TOP1i) or other ADC targeting EGFR/cMET.
• Received any live vaccine within 4 weeks prior to the first dose of study treatment.

• Received the following medications ≤ 14 days prior to the first dose of study treatment:

  1. Strong or moderate CYP3A4 induction/inhibitor;
  2. Drugs known to be at risk for torsade de pointes (TdP);
  3. Drugs associated with QTcF interval prolongation (TdP risk equivocal).
• Known human immunodeficiency virus (HIV) infection or known acquired immunodeficiency syndrome (AIDS).
• A history of clinically significant cardiovascular diseases within 6 months prior to the first dose of study treatment, including but not limited to myocardial infarction, severe/unstable angina pectoris, primary cardiomyopathy, cerebrovascular accident (including transient ischemic attack, cerebral hemorrhage, cerebral infarction) or congestive heart failure (New York Heart Association [NYHA] Functional Classification > Class II); symptomatic coronary artery disease requiring pharmacotherapy.
• A history of allogeneic organ transplantation or graft-versus-host disease (GVHD).
• A history of hypersensitivity to the active ingredients, inactive excipients of SIM0610, or drugs with similar chemical structures or classifications to SIM0610.

• Pregnant or lactating women. For women of childbearing potential (WOCBP), they are also excluded unless:

  1. The result of serum pregnancy test within 72 hours prior to the first dose of study treatment is negative;
  2. They use highly effective contraceptive methods from the time of signing the informed consent form (ICF) until 180 days after the last dose of study treatment.
• Male subjects with female partners of childbearing potential are excluded unless they use highly effective contraceptive methods from the time of signing the ICF until 180 days after the last dose of study treatment.
• Any other conditions that may increase subject-related risks or interfere with the interpretation of study results, and that, in the investigator's judgment, render the subject unsuitable for study enrollment.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: Non-Randomized
• Interventional Model: Sequential Assignment
• Masking: None (Open Label)

Number of Arms

2

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: Dose escalation; SIM0610 administered intravenously at selected dose levels according to protocol	Drug: SIM0610 for Injection; intravenous infusion
Experimental: Cohort expansion; SIM0610 administered intravenously at Recommended dosage(RDs) according to protocol	Drug: SIM0610 for Injection; intravenous infusion

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Dose Limiting Toxicity (DLT)		From time of first dose of SIM0610 to end of DLT period (approximately 21 days)
Safety and Tolerability		From time of Informed Consent to 28 days post last dose of SIM0610
Objective response rate (ORR)	Objective response rate (ORR) assessed by the investigator per Response Evaluation Criteria in Solid Tumors (RECIST) version 1.1	From date of first dose of SIM0610 up until progression, or the last evaluable assessment in the absence of progression (approximately 2 years)

Collaborators and Investigators

• Sponsor: Jiangsu Simcere Pharmaceutical Co., Ltd.
• Collaborators: Shanghai Xianwei Medical Technology Co., Ltd.

Study record dates

Study Major Dates

• Study Start (Actual): January 19, 2026
• Primary Completion (Estimated): December 1, 2027
• Study Completion (Estimated): July 1, 2029

Study Registration Dates

• First Submitted: December 24, 2025
• First Submitted That Met QC Criteria: January 9, 2026
• First Posted (Actual): January 16, 2026

Study Record Updates

• Last Update Posted (Actual): January 23, 2026
• Last Update Submitted That Met QC Criteria: January 21, 2026
• Last Verified: January 1, 2026

More Information

Terms related to this study

• Keywords: Locally Advanced/Metastatic Solid Tumors
• Additional Relevant MeSH Terms: Neoplasms by Site; Neoplasms; Intestinal Diseases; Respiratory Tract Diseases; Neoplasms by Histologic Type; Gastrointestinal Neoplasms; Digestive System Neoplasms; Digestive System Diseases; Gastrointestinal Diseases; Intestinal Neoplasms; Rectal Diseases; Lung Diseases; Head and Neck Neoplasms; Liver Diseases; Neoplasms, Glandular and Epithelial; Adenocarcinoma; Liver Neoplasms; Respiratory Tract Neoplasms; Thoracic Neoplasms; Colonic Diseases; Lung Neoplasms; Carcinoma; Carcinoma, Bronchogenic; Bronchial Neoplasms; Carcinoma, Squamous Cell; Squamous Cell Carcinoma of Head and Neck; Carcinoma, Hepatocellular; Colorectal Neoplasms; Carcinoma, Non-Small-Cell Lung; Therapeutics; Drug Administration Routes; Drug Therapy; Injections
• Other Study ID Numbers: SIM0610-101

Plan for Individual participant data (IPD)

• Plan to Share Individual Participant Data (IPD)?: NO

Drug and device information, study documents

• Studies a U.S. FDA-regulated drug product: No
• Studies a U.S. FDA-regulated device product: No