A Phase I Study of WTX212A Monotherapy or in Combination With Radiotherapy in Patients With Advanced Solid Tumors

NCT07269899 · Status: RECRUITING · Phase: PHASE1 · Type: INTERVENTIONAL · Enrollment: 12

Last updated 2025-12-08

No results posted yet for this study

Summary

This is a single-arm, open-label, investigator-initiated clinical study (IIT) designed to evaluate the preliminary efficacy, safety, tolerability, immunogenicity, and pharmacokinetic (PK) characteristics of WTX212A Injection in patients with advanced solid tumors.

Conditions

Interventions

DRUG

WTX212A injection

Erythrocyte-αPD-1 Antibody Conjugates

RADIATION

radiotherapy

Radiotherapy will be administered sequentially, with WTX212A treatment starting within one week after the completion of radiotherapy

Sponsors & Collaborators

  • Westlake Therapeutics

    collaborator INDUSTRY
  • Sun Yat-sen University

    lead OTHER

Principal Investigators

  • RuiHua Xu, PhD · Cancer Center of SUN YAT-senU

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
PARALLEL

Eligibility

Min Age
18 Years
Max Age
75 Years
Sex
ALL
Healthy Volunteers
No

Timeline & Regulatory

Start
2025-11-25
Primary Completion
2027-02-28
Completion
2027-08-30

Countries

  • China

Study Locations

More Related Trials

Entities

Diseases

Read the full study record

This page highlights key information. For complete eligibility criteria, study locations, investigator contacts, and the full protocol, visit the original record on ClinicalTrials.gov.

View NCT07269899 on ClinicalTrials.gov