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    Could imx-110 improve the patient experience in oncology in the future?We believe that IMX-110 could become a potentially attractive option to improve the patient experience in oncology in the future.” The U.S. Food and Drug Administration (“FDA”) has approved orphan drug designation (“ODD”) for IMX-110 for the treatment of soft tissue sarcoma.
    Is imx-110 safe?IMX-110 is currently being evaluated in a phase 1b /2a open-label, dose-escalation/dose-expansion safety, tolerability and pharmacokinetic study in patients with advanced solid tumors in the United States and Australia.
    What does imx-110 stand for?IMX-110 holds orphan drug designation (ODD) by the FDA for soft tissue sarcoma, and has received Rare Pediatric Disease Designation (RPDD) by the FDA the treatment of rhabdomyosarcoma, a life-threatening form of cancer in children.
    How does imx-110 work?IMX-110 then simultaneously attacks all 3 components of the TME (cancer associated fibroblasts, or CAFs; tumor-associated macrophages/immune cells, or TAMs, and cancer itself), severing the critical lifelines between the tumor and its metabolic and structural support.
  3. Immix Biopharma Announces 16th Patient Dosing in Ongoing …

  4. Immix Biopharma Announces Early Positive IMX-110 Interim …

  5. ImmixBio Announces Positive IMX-110 Phase 1b/2a …

    WEBJan 19, 2022 · IMX-110 is in clinical development as a monotherapy for soft tissue sarcoma (STS), a $3 billion market expected to grow to $6.5 billion by 2030. A chart accompanying this announcement is...

  6. ImmixBio Approves 4 Additional Clinical Trial Sites for IMX-110 ...

  7. Immix Biopharma Announces 16th Patient Dosing in Ongoing …

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  9. Immix Biopharma Announces Patient Dosing in Ongoing Phase …

  10. Immix Biopharma Announces Patient Dosing in Ongoing Phase

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  12. Immix Biopharma Doses Additional Patients in Ongoing Phase

  13. ImmixBio Announces Positive IMX-110 Phase 1b/2a Interim

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