Safety and Efficacy of NK510 to Treat Gastric Cancer and Colorectal Cancer

NCT07166263 | Not Yet Recruiting Early Phase 1

• 1 other identifier: NK510-13
• Study Type: interventional
• Target: 15
• Locations: 1 country
• Sites: 1

Brief Summary

This study will evaluate the safety and efficacy of NK510 in the treatment of relapsed and refractory advanced gastric cancer and colorectal cancer.NK510 will be administered by intravenous infusion for systemic therapy and intraperitoneal perfusion therapy. The safety and efficacy of this treatment will be evaluated.

Conditions

Gastric Cancer (GC); Colorectal Cancer

Outcome Measures

Primary Outcomes (3)

• Dose-Limiting Toxicity

  To evaluate the DLT during N510 treatment

  6 weeks

• Overall response rate (ORR)

  Effectiveness Metrics

  6 weeks

• Puncture-free survival (PuFS)

  Effectiveness Metrics

  6 weeks

Secondary Outcomes (1)

• Progression-free survival (PFS)

  2 years

Study Arms (2)

Systemic therapy with NK510 via intravenous infusion

EXPERIMENTAL

Systemic therapy with NK510 via intravenous infusion combined with PD-L1 or other regimens selected by the investigator

Drug: NK510

Intraperitoneal perfusion therapy with NK510

EXPERIMENTAL

Intraperitoneal perfusion therapy with NK510 plus IL-2, PD-L1 or other regimens selected by the investigator for systemic therapy

Drug: NK510

Interventions

NK510 DRUG

NK510 will be administered through intravenous infusion, once a week for a total of six times.

Systemic therapy with NK510 via intravenous infusion

Eligibility Criteria

• Age: 18 Years+
• Sex: all
• Healthy Volunteers: No
• Age Groups: Adult (18-64), Older Adult (65+)

You may qualify if:

• Aged ≥ 18 years, regardless of gender.
• Gastric cancer and colorectal cancer that are inoperable and unresectable with radiotherapy: For gastric cancer, molecular diagnosis confirms that it is not AFP-producing gastric cancer.
• Progressive disease or recurrence after receiving ≥ 2 lines of treatment.
• Patients are divided into two groups (Group A and Group B) based on the presence or absence of peritoneal metastasis. The criteria for determining peritoneal metastasis are as follows:
• Drained ascites ≥ 500ml, or B-ultrasound/CT in the supine position shows ascites depth ≥ 3cm.
• Peritoneal metastasis confirmed by any of the following criteria:
• i. Positive for exfoliated cancer cells in ascites. ii. Diagnosed as peritoneal metastatic carcinoma by imaging and symptoms. iii. Peritoneal metastasis confirmed by abdominal exploration. iv. Ascites confirmed as exudate by routine ascites examination and ascites biochemistry.
• At least one measurable lesion on CT or MRI according to RECIST v1.1 (Response Evaluation Criteria in Solid Tumors).
• ECOG performance status of 0-2.
• Expected survival period ≥ 3 months.
• Able to comply with the study protocol and follow-up procedures, and voluntarily sign the informed consent form for participation in this study.

You may not qualify if:

• Pregnant or lactating women.
• Subjects with central nervous system (CNS) metastases and/or carcinomatous meningitis with obvious symptoms.
• A history of other malignant tumors within the past 3 years.
• Subjects with active, known or suspected autoimmune diseases \[excluding type 1 diabetes, hypothyroidism requiring only hormone replacement therapy, skin diseases that do not require systemic treatment (e.g., vitiligo, psoriasis, or alopecia), or diseases that are not expected to relapse without external triggers\].
• Subjects with a history of immunodeficiency, including positive HIV test results, other acquired or congenital immunodeficiency diseases, or a history of organ transplantation.
• A history of severe cardiovascular and cerebrovascular diseases, including but not limited to: severe cardiac rhythm or conduction abnormalities such as ventricular arrhythmias requiring clinical intervention, third-degree atrioventricular block, etc.; QTc interval \> 480 ms on 12-lead electrocardiogram at rest; acute coronary syndrome, congestive heart failure, aortic dissection, stroke, or other grade 3 or higher cardiovascular and cerebrovascular events within 6 months before enrollment; New York Heart Association (NYHA) cardiac function classification ≥ class II or left ventricular ejection fraction (LVEF) \< 50%; clinically uncontrolled hypertension.

Sponsors & Collaborators

• Base Therapeutics (Shanghai) Co., Ltd.: lead

Study Sites (1)

Nanjing Drum Tower Hospital, Affiliated to the Medical School of Nanjing University

Nanjing, Jiangsu, China

Location

MeSH Terms

Conditions

Stomach Neoplasms; Colorectal Neoplasms

Condition Hierarchy (Ancestors)

Gastrointestinal Neoplasms; Digestive System Neoplasms; Neoplasms by Site; Neoplasms; Digestive System Diseases; Gastrointestinal Diseases; Stomach Diseases; Intestinal Neoplasms; Colonic Diseases; Intestinal Diseases; Rectal Diseases

Study Design

• Study Type: interventional
• Phase: early phase 1
• Allocation: NON RANDOMIZED
• Masking: NONE
• Purpose: TREATMENT
• Intervention Model: SINGLE GROUP
• Sponsor Type: INDUSTRY
• Responsible Party: SPONSOR

Study Record Dates

• First Submitted: September 3, 2025
• First Posted: September 10, 2025
• Study Start: November 1, 2025
• Primary Completion (Estimated): June 1, 2027
• Study Completion (Estimated): December 1, 2027
• Last Updated: September 10, 2025

Record last verified: 2025-09

Locations

CN (1)