Immix Biopharma Inc IMMX announced preclinical data of its lead program, IMX-110.
- The data showed that IMX-110 produced a 50% response rate in first-line-therapy-resistant cancer - soft tissue sarcoma (STS) mouse study, surpassing the STS standard of care doxorubicin’s 0% response rate in the same mouse study.
- The responses were assessed by RECIST 1.1 criteria applied to mice, with progression assessed after one treatment cycle.
- The FDA has approved orphan drug designation for IMX-110 for soft tissue sarcoma. The FDA has already approved rare pediatric disease designation to IMX-110 for pediatric cancer, rhabdomyosarcoma.
- ImmixBio recently shared IMX-110 clinical data across multiple STS subtypes in several heavily pretreated patients demonstrating median progression-free survival (PFS) of 4 months.
- Zero drug-related severe adverse events and dose interruptions due to toxicity were observed.
- Price Action: IMMX shares are up 31.7% at $7.15 during the premarket session on the last check Wednesday.
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