A Phase II Clinical Study of HRS-7058 in Combination With Antitumor Drugs in Patients With Advanced Malignant Tumour

NCT06915142 · Status: RECRUITING · Phase: PHASE2 · Type: INTERVENTIONAL · Enrollment: 300

Last updated 2026-01-26

No results posted yet for this study

Summary

This study is a multicentre, open phase II clinical study of dose escalation, dose extension and efficacy extension of HRS-7058 in combination with antitumor drugs in subjects with advanced malignant tumour. To evaluate the safety, tolerability and efficacy of HRS-7058 in combination with antitumor drugs.

Conditions

  • Advanced Malignant Tumour

Interventions

DRUG

HRS-7058 + SHR-1316 + Platinum-containing doublet chemotherapy

HRS-7058 + SHR-1316 + Platinum-containing doublet chemotherapy

DRUG

HRS-7058 + Cetuximab

HRS-7058 + Cetuximab

DRUG

HRS-7058 + SHR-1826

HRS-7058 + SHR-1826

DRUG

HRS-7058 + SHR-1826 + SHR-1316

HRS-7058 + SHR-1826 + SHR-1316

DRUG

HRS-7058 + SHR-A1202

HRS-7058 + SHR-A1202

DRUG

HRS-7058 + BP102

HRS-7058 + BP102

DRUG

HRS-7058 + SHR-9839

HRS-7058 + SHR-9839

DRUG

HRS-7058 +SHR-A2102 +SHR-1316

HRS-7058 +SHR-A2102 +SHR-1316

DRUG

HRS-7058 +SHR-9839(sc)+SHR-1316

HRS-7058 +SHR-9839(sc)+SHR-1316

DRUG

HRS-7058 +SHR-1316 +BP102

HRS-7058 +SHR-1316 +BP102

DRUG

HRS-7058 +SHR-A2102 +BP102

HRS-7058 +SHR-A2102 +BP102

DRUG

HRS-7058 +SHR-A2102 +SHR-1316 +BP102

HRS-7058 +SHR-A2102 +SHR-1316 +BP102

DRUG

HRS-7058 + SHR-1316

HRS-7058 + SHR-1316

Sponsors & Collaborators

  • Shandong Suncadia Medicine Co., Ltd.

    lead INDUSTRY

Study Design

Allocation
NON_RANDOMIZED
Purpose
TREATMENT
Masking
NONE
Model
SINGLE_GROUP

Eligibility

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

Timeline & Regulatory

Start
2025-04-28
Primary Completion
2026-12-31
Completion
2027-10-31

Countries

  • China

Study Locations

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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 NCT06915142 on ClinicalTrials.gov