This is a Multi-Center Study of IBI3026 in Participants With Locally Advanced, Unresectable or Metastatic Solid Tumors

A Multi-Center, Open-Label, Phase 1 Study of IBI3026 in Participants With Locally Advanced, Unresectable or Metastatic Solid Tumors

This is a multicenter, open-label, phase I dose-escalation and expansion study of IBI3026 in participants with unresectable, locally advanced, or metastatic solid tumors. The study will be conducted in two phases: Phase 1 dose escalation and Phase 2 dose expansion. Safety will be monitored by the Safety Review Committee (SRC).

Study Overview

• Status: Recruiting
• Conditions: Solid Tumor
• Intervention / Treatment: Drug: IBI3026

• Study Type: Interventional
• Enrollment (Estimated): 300
• Phase: Early Phase 1

Contacts and Locations

• Study Contact: Name: Haiyun Zuo; Phone Number: 021-31852088; Email: Haiyun.zuo@innoventbio.com

Study Locations

• China
  • Sichuan
    • Chengdu, Sichuan, China, 610041
      • Recruiting
      • Sichuan Cancer Hospital
      • Principal Investigator: Tongyu Lin
      • Contact: Tongyu Lin; Phone Number: 028-85420509; Email: tongyulin@hotmail.com

Participation Criteria

Eligibility Criteria

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

Description

inclusion criteria:

1. Participants must have the ability to understand and sign a written informed consent form for participation in this study, including all assessments and procedures specified in the protocol;
2. Male or female participants aged ≥18 years;
3. At least one measurable lesion as defined by RECIST v1.1 within 28 days prior to the first dose of IBI3026;
4. ECOG performance status of 0-1;
5. Life expectancy of at least 12 weeks at the start of treatment;
6. The screening period confirms that bone marrow and organ functions are good.
7. Male or female participants who are either of non-reproductive potential or agree to use at least one highly effective method of contraception during the study period (starting from screening or 2 weeks prior to first dosing, whichever comes first, and continuing until 6 months after the last dose of study drug);
8. Not amenable to curative surgical resection or definitive chemoradiotherapy.

Exclusion criteria:

1. Prior treatment with IL-12 class cytokines or IL-12 inhibitors;
2. Participation in any interventional clinical study other than observational (non-interventional) studies, or currently in the follow-up period of an interventional study;
3. Adverse reactions from prior anti-tumor therapies that have not resolved to Grade 0 or 1, or baseline levels, according to NCI CTCAE v5.0, prior to the first dose of study drug (exceptions include alopecia, fatigue, hyperpigmentation, or other conditions deemed without safety risk by the investigator);
4. Prior immune checkpoint inhibitor therapy associated with severe adverse reactions sufficient to compromise participant safety;
5. Known hypersensitivity, allergic reaction, or intolerance to IBI3026 or its excipients (refer to Investigator's Brochure).
6. Received major surgery (e.g., craniotomy, thoracotomy, or laparotomy, or other surgeries as determined by the investigator) within 4 weeks prior to the first dose of study drug, excluding core biopsy; or anticipated to undergo major surgery during the study period; or presence of serious non-healing wounds, trauma, ulcers, etc.
7. Known symptomatic central nervous system (CNS) metastases. Participants with asymptomatic CNS metastases (i.e., no neurological syndrome and metastatic lesion diameter ≤1.5 cm) or those with stable disease post-treatment as judged by the investigator may be considered under the following conditions: absence of midbrain, pons, cerebellum, meninges, medulla oblongata, or spinal cord involvement; clinically stable for at least 4 weeks prior to the first dose of study drug (stable on ≤1.5 mg/day dexamethasone or equivalent corticosteroid and baseline anticonvulsant therapy), with no clinically confirmed new or enlarging CNS lesions.
8. Tumor invasion into surrounding critical structures (e.g., mediastinal vessels, superior vena cava, trachea, esophagus, etc.) or at risk of gastrointestinal/respiratory fistula formation.

Study Plan

How is the study designed?

Design Details

• Primary Purpose: Treatment
• Allocation: N/A
• Interventional Model: Single Group Assignment
• Masking: None (Open Label)

Number of Arms

1

Arms and Interventions

Participant Group / Arm	Intervention / Treatment
Experimental: IBI3026	Drug: IBI3026; Recombinant anti-programmed death receptor-1 (PD-1) antibody fused with interleukin-12 (IL-12) bispecific molecule injection

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Time Frame
Adverse Event	up to 2 years
Serious Adverse Event	up to 2 years
Maximum Tolerated Dose	up to 2 years
DLT(Dose-limiting Toxicity)	up to 2 years

Secondary Outcome Measures

Outcome Measure	Time Frame
PK concentration: IBI3026 serum concentration	up to 2 years
ORR (Objective Response Rate)	up to 2 years
DoR(Duration of Response)	up to 2 years
DCR(Disease Control Rate)	up to 2 years
TTR(Time to Response)	up to 2 years
PFS(Progression-free Survival)	up to 2 years
OS(Overall Survival)	up to 2 years
Incidence and number of patients with ADA	up to 2 years
Incidence and number of patients with NAb	up to 2 years

Collaborators and Investigators

• Sponsor: Innovent Biologics Technology Limited (Shanghai R&D Center)

Study record dates

Study Major Dates

• Study Start (Actual): January 29, 2026
• Primary Completion (Estimated): December 31, 2026
• Study Completion (Estimated): December 31, 2028

Study Registration Dates

• First Submitted: December 26, 2025
• First Submitted That Met QC Criteria: December 26, 2025
• First Posted (Actual): January 8, 2026

Study Record Updates

• Last Update Posted (Actual): February 4, 2026
• Last Update Submitted That Met QC Criteria: February 2, 2026
• Last Verified: February 1, 2026

More Information

Terms related to this study

• Other Study ID Numbers: CIBI3026A101

Drug and device information, study documents

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