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A Phase 1/2a Open-Label, Dose-Escalation/Dose-Expansion Safety, Tolerability and Anti-tumor Activity Study of IMX-110 in Combination With Tislelizumab in Patients With Advanced Solid Tumors

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Trial Profile

A Phase 1/2a Open-Label, Dose-Escalation/Dose-Expansion Safety, Tolerability and Anti-tumor Activity Study of IMX-110 in Combination With Tislelizumab in Patients With Advanced Solid Tumors

Status: Recruiting
Phase of Trial: Phase I/II

Latest Information Update: 10 Aug 2023

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At a glance

  • Drugs IMX-110 (Primary) ; Tislelizumab (Primary)
  • Indications Colorectal cancer; Solid tumours
  • Focus Adverse reactions
  • Acronyms IMMINENT-01
  • Sponsors Immix Biopharma

    • Most Recent Events

    • 17 Jul 2023 Second interim results (As of 7 July 2023; n=3) presented in an Immix Biopharma Media Release.
    • 26 Jun 2023 According to an Immix Biopharma media release, lead TSTx asset IMX-110, is currently in Phase 1b/2a clinical trials as a monotherapy and IMMINENT-01 combination clinical trial with BeiGenes anti-PD-1 antibody tislelizumab, holds Orphan Drug Designation (ODD) and Rare Pediatric Disease Designation (RPDD) by the FDA.
    • 14 Jun 2023 According to an Immix Media Release, the company announced that it has completed its previously announced at-the market equity offering program. It has completed 5 million dollars common stock offering. It intends to use net proceeds from the ATM offering for its IMX-110 plus tislelizumab phase 1b combination clinical trial, its IMX-110 monotherapy clinical trial and general corporate purposes.

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