SKB103 for Injection in Advanced Solid Tumors

A Phase 1/2 Study to Evaluate the Safety, Tolerability, Pharmacokinetics, and Efficacy of SKB103 for Injection in Participants With Advanced Solid Tumors

This is a phase 1/2 clinical study to evaluate the safety and efficacy of SKB103 in participants with advanced solid tumors. The study includes a dose escalation stage, a dose expansion stage, and a indication expansion stage.

Study Overview

• Status: Recruiting
• Conditions: Advanced Solid Tumors
• Intervention / Treatment: Drug: SKB103 for injection monotherapy

Detailed Description

This is a multi-center, open-label, phase 1/2 clinical study to evaluate the safety, tolerability, pharmacokinetics (PK) characteristics, immunogenicity, and efficacy of SKB103 in participants with advanced solid tumors. The study includes a Phase 1 dose escalation stage, a Phase 1 dose expansion stage, and a Phase 2 indication expansion stage.

• Study Type: Interventional
• Enrollment (Estimated): 277
• Phase: Phase 2; Phase 1

Contacts and Locations

• Study Contact: Name: Yina Diao; Phone Number: 86-028-67252634; Email: diaoyina@kelun.com

Study Locations

• China
  • Heilongjiang
    • Harbin, Heilongjiang, China, 150001
      • Recruiting
      • Harbin Medical University Cancer Hospital
      • Contact: Qingwei Meng; Phone Number: 86-0451-86298104; Email: mqwei@126.com
  • Shanghai Municipality
    • Shanghai, Shanghai Municipality, China, 200123
      • Recruiting
      • Shanghai East Hospital, Tongj.University
      • Contact: Caicun Zhou; Phone Number: 86-021-38804515; Email: aicunzhoudr@163.com

Participation Criteria

Eligibility Criteria

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

Description

Inclusion Criteria:

1. Participants voluntarily joined this study and signed an informed consent form.
2. The age at the time of signing the informed consent form must be between 18 and 75 years.
3. Participants with histologically or cytologically confirmed advanced solid tumors who have failed standard therapy, have no standard therapy available, or are intolerant to standard therapy.
4. Participants should provide tumor tissue samples for biomarker testing as much as possible.
5. Researchers evaluated based on Response Evaluation Criteria in Solid Tumors(RECIST) Version 1.1 that there is at least one measurable lesion present.
6. Eastern Cooperative Oncology Group (ECOG) score is 0 or 1.
7. Expected survival period ≥ 12 weeks.
8. Participants have sufficient bone marrow, liver, kidney, and coagulation functions.
9. Male and female participants must agree to use highly effective contraceptive methods during the study period.

Exclusion Criteria:

1. Participants known to have meningeal metastasis, brainstem metastasis, spinal cord metastasis and/or compression, and active central nervous system (CNS) metastasis.
2. Patients with other malignant tumors within 3 years before the first administration.
3. There are serious heart or vascular diseases or high-risk factors present.
4. According to researchers' judgment, it is an uncontrollable systemic disease.
5. There are pleural effusion, pericardial effusion, or ascites with clinical symptoms or requiring repeated drainage (>1 time/week).
6. History of interstitial lung disease or non infectious pneumonia.
7. There are other lung diseases that may interfere with drug-related pulmonary toxicity.
8. Severe dry eye syndrome, severe meibomian gland disease and/or blepharitis, or a history of corneal diseases that hinder/delay corneal healing.
9. There is a risk of developing esophagotracheal fistula or esophageal pleural fistula, or tumor invasion or compression of surrounding important organs and blood vessels accompanied by related clinical symptoms.
10. Within 3 months prior to the first administration, there have been clinical symptoms of intestinal obstruction, gastrointestinal perforation or fistula, urethral fistula, and abdominal abscess.
11. The toxicity of previous anti-tumor treatments has not been relieved, defined as the toxicity has not recovered to Common Terminology Criteria for Adverse Events (CTCAE) Version 6.0 grade 0 or 1.
12. Serious infection occurred within 4 weeks before the first administration.
13. Active hepatitis B or C, or simultaneous infection with Hepatitis B virus(HBV) and Hepatitis C virus(HCV).
14. Human immunodeficiency virus (HIV) test is positive or there is a history of acquired immunodeficiency syndrome (AIDS); Known active syphilis infection.
15. Known active pulmonary tuberculosis.
16. Known history of allogeneic organ transplantation or hematopoietic stem cell transplantation.
17. History of allergies to any components of SKB103 injection or severe hypersensitivity reactions to other monoclonal antibodies.
18. Received chemotherapy, immunotherapy, biological therapy, or other large molecule anti-tumor drugs within 4 weeks before the first administration;
19. Within 6 months prior to the first administration, lung lesions received radiation therapy with a total dose greater than 30 Gray.
20. Have undergone major surgical procedures or suffered serious injuries within 4 weeks prior to the first administration of medication.
21. Those who have received treatment with other clinical investigational drugs within 4 weeks prior to their first administration.
22. Individuals who have previously received anti-tumor vaccines or have received any active vaccines within 4 weeks prior to their first treatment with the investigational drug.
23. Participants who received systemic corticosteroid therapy or other immunosuppressive drugs with>10 mg/day prednisone within 2 weeks prior to the first dose.
24. Within 14 days before the first administration or within 5 half lives of known drugs (whichever is longer), she received a strong inhibitor or strong inducer of cytochrome P450 or a breast cancer resistance protein (BCRP) inhibitor.
25. Pregnant or lactating women.
26. Participants with a known history of mental illness or substance abuse are unable to cooperate in completing the study.
27. Suffering from local or systemic diseases caused by non malignant tumors, or diseases or symptoms secondary to tumors, which may affect compliance.
28. Any condition that the researcher deems to interfere with the evaluation of the investigational drug, the safety of participants, or the interpretation of research results, or any other condition that the researcher deems unsuitable for participation in this study.

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: SKB103 monotherapy; Participants will be dosed with SKB103 for injection every 3 weeks(q3w)	Drug: SKB103 for injection monotherapy; IV infusion on Day 1 of each cycle, every 3 weeks (Q3W), until radiographic disease progression (PD), intolerable toxicity, participant request for discontinuation, lost to follow-up, or death (whichever occurs first).

What is the study measuring?

Primary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Number of subjects achieving Dose-limiting toxicity (DLT)	DLT is defined as an adverse event (AE) that meets protocol-defined DLT criteria during the first 21 days and is at least possibly related to the study drug.	From date of initial dose until up to 21 days for treatment
Objective response rate (ORR)	The sum of the number of cases with Complete Response (CR) and Partial Response (PR) in all treated tumor patients (CR + PR) divided by the total number of cases.	Up to approximately 3 years

Secondary Outcome Measures

Outcome Measure	Measure Description	Time Frame
Progression Free Survival (PFS)	Time from start of treatment to progression of disease (PD) or death, whichever occurs first, in patients with tumors.	Up to approximately 3 years
Duration of Response (DOR)	Time from the start of the first assessment of CR or PR in tumor patients to PD or death due to any reason.	Up to approximately 3 years
Overall Survival (OS)	Time from start of treatment to death due to any reason.	Up to approximately 3 years
Maximum observed plasma concentration (Cmax) of SKB103-ADC, SKB103-TAB, and free KL610348.	Pharmacokinetic (PK) parameters of SKB103-ADC, SKB103-TAB, and free KL610348.	Up to approximately 3 years

Collaborators and Investigators

• Sponsor: Sichuan Kelun-Biotech Biopharmaceutical Co., Ltd.

Study record dates

Study Major Dates

• Study Start (Actual): April 23, 2026
• Primary Completion (Estimated): December 31, 2029
• Study Completion (Estimated): December 31, 2030

Study Registration Dates

• First Submitted: March 4, 2026
• First Submitted That Met QC Criteria: March 4, 2026
• First Posted (Actual): March 10, 2026

Study Record Updates

• Last Update Posted (Actual): May 18, 2026
• Last Update Submitted That Met QC Criteria: May 14, 2026
• Last Verified: May 1, 2026

More Information

Terms related to this study

• Other Study ID Numbers: SKB103-I/II-01

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