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US45258H1068

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Jul. 01	HC Wainwright Initiates Immix Biopharma at Buy With $7 Price Target	MT
May. 10	Immix Biopharma, Inc. Announces Positive NXC-201 Relapsed/Refractory AL Amyloidosis Clinical Data in ASGCT 2024 Latebreaking Oral Presentation	CI

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Immix Biopharma, Inc. Announces Positive NXC-201 Relapsed/Refractory AL Amyloidosis Clinical Data in ASGCT 2024 Latebreaking Oral Presentation	May. 10
Immix Biopharma, Inc. Reports Earnings Results for the First Quarter Ended March 31, 2024	May. 09
Immix Biopharma Gets Orphan Drug Label in Europe For Multiple Myeloma Treatment	Apr. 29
Immix Biopharma, Inc. Announces on Track to Dose NXC-201 Patients in United States	Apr. 18
Immix Biopharma, Inc. Reports Earnings Results for the Full Year Ended December 31, 2023	Mar. 29
Immix Biopharma, Inc. Announces Major Comprehensive Cancer Center as Lead Site for NXC-201 Al Amyloidosis Clinical Trial	Mar. 20
Immix Biopharma Proposes Stock Offering; Shares Slump	Feb. 05
Immix Biopharma, Inc. Announces New Clinical Data from Its Phase 1b/2a NEXICART-1	Dec. 11
Immix Biopharma, Inc. to Host KOL Event to Discuss Its BCMA-Targeted CAR-T Cell Therapy Candidate NXC-201 for Relapsed/Refractory AL Amyloidosis	Nov. 22
GNW-Adhoc: Immix Biopharma gibt die FDA-Genehmigung des IND-Antrags für CAR-T NXC-201 bekannt, der die Verabreichung an US-Patienten ermöglicht	Nov. 22
La FDA approuve le dossier d’essai clinique de Immix Biopharma CAR-T NXC-201, et en permet ainsi l’administration aux patients américains	Nov. 22
Immix Biopharma gibt die FDA-Genehmigung des IND-Antrags für CAR-T NXC-201 bekannt, der die Verabreichung an US-Patienten ermöglicht	Nov. 22
Immix Biopharma Says FDA Clears Investigational New Drug Application for NXC-201; Shares Fall	Nov. 21
Immix Biopharma, Inc. Reports Earnings Results for the Third Quarter and Nine Months Ended September 30, 2023	Nov. 13
Immix Biopharma Presents NXC-201 Data at 65th American Society of Hematology Annual Meeting in 9 Relapsed/Refractory AL Amyloidosis Patients	Nov. 06
Immix Biopharma Completes 3rd NXC-201 Engineering Batch at its U.S. CAR-T Manufacturing Site	23-10-16
Immix Biopharma, Inc. Announces Complete Response in 9Th Relapsed/Refractory AL Amyloidosis Patient in NXC-201 Clinical Trial At IMS 20Th Annual Meeting	23-10-03
Top Midday Gainers	23-10-02
Immix Biopharma Inc. Announces 72-Patient NXC-201 Clinical Data at the IMS 20th Annual Meeting, 95% Overall Response Rate in Multiple Myeloma	23-10-02
Immix Biopharma Files Registration Statement on Behalf of Selling Stockholder	23-09-26

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