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  3. IMX-110/Tislelizumab Yields Notable Tumor …

    WebMay 5, 2023. Russ Conroy. Article. Combination treatment with IMX-110 and tislelizumab yields no dose-limiting toxicities thus far in the first cohort of patients with advanced/metastatic colorectal cancer in the phase 1b/2a …

  4. Pipeline | Immix Biopharm

    WebOur tissue specific therapeutic IMX-110 is currently in clinical trials as a monotherapy, and in combination with tislelizumab (BeiGene anti-PD-1 – IMMINENT-01 NCT05840835) for advanced solid tumors which has …

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

  6. People also ask
    Can imx-110 be used in both clinical trials?Manufactured IMX-110 to be utilized in both clinical trials: 2022 planned monotherapy IMX-110 Clinical Trial in soft tissue sarcoma (“STS”) 2022 planned combination IMX-110 + BeiGene anti-PD-1 tislelizumab Clinical Trial in advanced solid tumors
    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.
    Is imx-110 an orphan drug?LOS ANGELES, Sept. 30, 2021 /PRNewswire/ -- Immix Biopharma, Inc. ("ImmixBio"), a biotechnology company pioneering Tissue Specific Therapeutics (TSTx) TM for oncology and inflammation, today announced that the U.S. Food and Drug Administration (FDA) has granted orphan drug designation (ODD) to IMX-110 for the treatment of soft tissue sarcoma.
  7. IMX-110 in Patients With Advanced Solid Tumors - Full Text View ...

  8. 2023-05-03 | NDAQ:IMMX | Press Release | Immix Biopharma …

  9. ImmixBio Announces Clinical Trial and Supply Agreement with

  10. ImmixBio Initiates IMX-110 GMP Manufacturing Scale-Up, …

  11. Immix Biopharma Announces Dosing of First 2 Patients in its

  12. Immix Cleared to Expand Phase 1/2a Trial of IMX-110 to US Sites

  13. IMX-110 Granted Rare Pediatric Disease Designation by FDA for ...

  14. IMX-110 Plus Tislelizumab Shows Early Activity in Advanced

  15. FDA Grants Rare Pediatric Disease Designation for IMX-110 for …

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  18. Île-de-France - Wikipedia

  19. U.S. Food and Drug Administration Approves Immix Biopharma

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  21. ImmixBio Initiates IMX-110 GMP Manufacturing Scale-Up,

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