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A Phase 1, Open-label Study to Evaluate Safety, Tolerability, and Pharmacokinetics of an Anti-LILRB2 / PD-L1 Bispecific Antibody SPX- 303 in Patients With Solid Tumors

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Trial Profile

A Phase 1, Open-label Study to Evaluate Safety, Tolerability, and Pharmacokinetics of an Anti-LILRB2 / PD-L1 Bispecific Antibody SPX- 303 in Patients With Solid Tumors

Status: Recruiting
Phase of Trial: Phase I

Latest Information Update: 26 Sep 2024

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At a glance

  • Drugs SPX 303 (Primary)
  • Indications Solid tumours
  • Focus Adverse reactions; First in man
  • Sponsors Sparx Therapeutics

    • Most Recent Events

    • 11 Apr 2024 According to a SparX Biopharmaceutical media release, the first patient has been dosed in this trial.With the successful dosing of SPX-303, SparX Group is initiating three additional study sites for the ongoing Phase 1 clinical study.
    • 20 Mar 2024 Status changed from not yet recruiting to recruiting.
    • 03 Nov 2023 New trial record

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