A Clinical Trial of HRS-7058 Combined Anti-tumor Drugs in Subjects With Solid Tumors

StatusRecruiting
PhasePhase 2
Started

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Record History

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  1. Notable Primary completion date: Jun 2026 to Jun 2027v4 Show 5 more changesShow less
    • Primary endpoints: 2 to 3
    • Secondary endpoints: 5 to 8
    • Site contact updated
    • Study title shortened, about 8 words
    • Eligibility criteria expanded, about 5 words
  2. Re-verified, no change to tracked fieldsv3
  3. Notable Trial status: Not Yet Recruiting to Recruiting
    • Start date changed from estimate of Jun 2025 to Jul 9, 2025
    • Site details revised
    v2
  4. Study First Submitted
  • Notable: the trial’s plan changed such as a big move in its timeline or size, a new primary endpoint, sponsor or phase, or recruiting opened or resumed.
This study aims to evaluate the safety and tolerability of HRS-7058 combined with antitumor drugs in subjects with solid tumors, and to determine the recommended dosage for Phase II. Evaluate the objective response rate of HRS-7058 in combination with anti-tumor drugs in subjects with solid tumors.
Trial Details
NCT Number NCT07032077
Lead Sponsor Shandong Suncadia Medicine Co., Ltd.
Conditions
(from sponsor)
Solid Tumors
Enrollment 100 participants
Start Date
Primary Completion (estimated)
Study Completion (estimated)
Updated on ClinicalTrials.gov