Immix Biopharma, Inc.

Equities

IMMX

US45258H1068

Pharmaceuticals

Market Closed - Nasdaq 04:00:00 2024-04-26 pm EDT 5-day change 1st Jan Change
2.13 USD +1.43% Intraday chart for Immix Biopharma, Inc. -2.74% -69.22%

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Immix Biopharma on Track to Dose First Patients with AL Amyloidosis Therapy by Mid-Year MT
Immix Biopharma, Inc. Announces on Track to Dose NXC-201 Patients in United States CI
Immix Biopharma, Inc. Reports Earnings Results for the Full Year Ended December 31, 2023 CI
Immix Biopharma, Inc. Announces Major Comprehensive Cancer Center as Lead Site for NXC-201 Al Amyloidosis Clinical Trial CI
Immix Biopharma Prices $15 Million Stock Offering MT
Immix Biopharma Proposes Stock Offering; Shares Slump MT
Immix Biopharma, Inc. Announces New Clinical Data from Its Phase 1b/2a NEXICART-1 CI
Immix Biopharma, Inc. to Host KOL Event to Discuss Its BCMA-Targeted CAR-T Cell Therapy Candidate NXC-201 for Relapsed/Refractory AL Amyloidosis CI
Immix Biopharma Says FDA Clears Investigational New Drug Application for NXC-201; Shares Fall MT
Immix Biopharma, Inc. Reports Earnings Results for the Third Quarter and Nine Months Ended September 30, 2023 CI
Immix Biopharma Presents NXC-201 Data at 65th American Society of Hematology Annual Meeting in 9 Relapsed/Refractory AL Amyloidosis Patients CI
Immix Biopharma Completes 3rd NXC-201 Engineering Batch at its U.S. CAR-T Manufacturing Site CI
Immix Biopharma, Inc. Announces Complete Response in 9Th Relapsed/Refractory AL Amyloidosis Patient in NXC-201 Clinical Trial At IMS 20Th Annual Meeting CI
Top Midday Gainers MT
Immix Biopharma Inc. Announces 72-Patient NXC-201 Clinical Data at the IMS 20th Annual Meeting, 95% Overall Response Rate in Multiple Myeloma CI
Immix Biopharma Files Registration Statement on Behalf of Selling Stockholder MT
Immix Biopharma Gets FDA Orphan Drug Label For NXC-201 to Treat Amyloid Light Chain Amyloidosis MT
Sector Update: Health Care Stocks Rising Late Afternoon MT
Sector Update: Health Care MT
Immix Biopharma Says US FDA Grants Orphan Drug Designation for NXC-201 to Treat Multiple Myeloma MT
Immix Biopharma Shares Rise 11% Premarket on Key FDA Designation DJ
Immix Biopharma, Inc Announces U.S. Food and Drug Administration Approves Orphan Drug Designation for Immix Biopharma NXC-201 as a Treatment for Multiple Myeloma CI
Immix Biopharma, Inc. Appoints Yekaterina Chudnovsky as Member of the Board CI
Immix Biopharma, Inc. announced that it has received $9.999998 million in funding CI
Immix Biopharma, Inc. announced that it expects to receive $9.999998 million in funding CI
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Immix Biopharma, Inc. is a clinical-stage biopharmaceutical company. The Company is focused on the application of chimeric antigen receptor cell therapy (CAR- T) in light chain (AL) Amyloidosis and autoimmune disease. The Company's lead cell therapy asset is CAR-T NXC-201 for autoimmune disease, relapsed/refractory AL Amyloidosis, and relapsed/refractory multiple myeloma, which is being evaluated in its ongoing Phase Ib/IIa NEXICART-1 (NCT04720313) clinical trial. Its tissue specific therapeutic IMX-110 is in clinical trials as a monotherapy, and in combination with tislelizumab (BeiGene anti-PD-1 - IMMINENT-01 NCT05840835) for advanced solid tumors, such as relapsed/refractory colorectal cancer (CRC). IMX-110 in Phase Ib/IIa clinical trials, is a Tissue-Specific Therapeutic with TME Normalization, a technology that the Company is developing initially for mCRC and Soft Tissue Sarcoma (STS).
More about the company
Sell
Consensus
Buy
Mean consensus
OUTPERFORM
Number of Analysts
1
Last Close Price
2.13 USD
Average target price
14 USD
Spread / Average Target
+557.28%
Consensus
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