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WEBMay 3, 2023 · The novel approach combining TSTx IMX-110 with anti-PD-1 antibody tislelizumab is designed to expand the population of cancer patients experiencing …
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 …
WEBMay 20, 2022 · One cycle of IMX-110 produced 75% survival vs. 0% survival for Trabectedin (sold as YONDELIS ® by Janssen, a Johnson & Johnson Company, a U.S. FDA approved drug) In a connective tissue …
WEBLOS ANGELES, Jan. 19, 2022 (GLOBE NEWSWIRE) -- Immix Biopharma, Inc. (Nasdaq: IMMX) (“ImmixBio”, “Company”, “We” or “Us”), a biopharmaceutical company pioneering …
IMX-110 + anti-PD-1 Combination Produced Extended Median …
WEBIMX-110 + anti-PD-1 produced 63-day median survival in a genetic (KPC) pancreatic cancer mouse model in which mice develop their own pancreatic cancer and have an intact …
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IMX-110 Plus Tislelizumab Shows Early Activity in Advanced
WEBMay 3, 2023 · Immex Biopharma announces dosing of first 2 patients in its IMX-110 + BeiGene/Novartis anti-PD-1 tislelizumab phase 1b/2a combination clinical trial in patients …
Immix Biopharma Announces 16th Patient Dosing in Ongoing …
WEBDec 20, 2022 · Patients undergo CT scans every 8 weeks after dosing to assess tumor response to IMX-110; clinical data expected to be released on a rolling basis beginning …
ImmixBio Announces Positive IMX-110 Phase 1b/2a …
WEBJan 19, 2022 · Immix Biopharma, Inc. (NASDAQ:IMMX) 100% of patients treated with IMX-110 completed planned treatment cycles without drug-related interruptions in its ongoing Phase 1b/2a clinical trial.
FDA Grants Rare Pediatric Disease Designation for IMX-110 for …
WEBJan 4, 2022 · The FDA has granted a rare pediatric disease designation (RPDD) to IMX-110 for the treatment of rhabdomyosarcoma, according to an announcement from Immix …
IMX-110/Tislelizumab Yields Notable Tumor …
WEBMay 5, 2023 · Investigational agent IMX-110 plus tislelizumab resulted in tumor shrinkage at 2 months in patients with advanced metastatic colorectal cancer (CRC), according to a press release on interim data from the …
IMX-110 Granted Rare Pediatric Disease Designation by FDA for ...
WEBJan 5, 2022 · IMX-110 is a tissue-specific therapeutic that simultaneously attacks all 3 components of the tumor micro-environment, severing the critical lifelines between the …
Immix Biopharma Announces Early Positive IMX-110 Interim …
WEBMay 3, 2023 · The novel approach combining TSTx IMX-110 with anti-PD-1 antibody tislelizumab is designed to expand the population of cancer patients experiencing …
IMX-110 in Patients With Advanced Solid Tumors - Full Text View ...
WEBDec 22, 2017 · Maximum tolerated dose (MTD) of IMX-110 in patients with advanced solid tumors for evaluation in Phase 2a. [ Time Frame: 28 days ] The MTD is defined as the …
ImmixBio IMX-110 Produced 50% Positive Response Rate in
WEBJan 12, 2022 · IMX-110 response rate surpassed standard of care doxorubicin’s response rate of 0% after 1 cycle of treatment in the same study. IMX-110 is in clinical …
FDA Approves Rare Pediatric Disease Designation for IMX-110 …
WEBJan 19, 2022 · IMX-110, a tissue-specific therapeutic designed to accumulate at intended therapeutic sites at 3 to 5 times the rate of conventional therapeutics, has already …
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Immix Biopharma Doses Additional Patients in Ongoing Phase
WEBJan 13, 2023 · IMX-110 clinical trial data is expected to be released on a rolling basis beginning in Q1 2023; once dosing begins, patients undergo CT scans every 8 weeks to …
ImmixBio Initiates IMX-110 GMP Manufacturing Scale-Up,
WEBJan 31, 2022 · The U.S. Food and Drug Administration (“FDA”) has approved orphan drug designation (“ODD”) for IMX-110 for the treatment of soft tissue sarcoma. Additionally, …
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IMX-110 + anti-PD-1 Combination Produced Extended Median
WEBJan 25, 2022 · IMX-110 + anti-PD-1 produced 63-day median survival in a genetic (KPC) pancreatic cancer mouse model in which mice develop their own pancreatic cancer and …
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