Brief: Immix Biopharma Subsidiary Nexcella Enters Into U.S. Gmp Manufacturing Agreement To Expand Ongoing Nxc-201 Phase 1B/2 Clinical Trial To The U.S.
Feb 15 (Reuters) - Immix Biopharma Inc IMMX.O :
* IMMIX BIOPHARMA SUBSIDIARY NEXCELLA ENTERS INTO U.S. GMP
MANUFACTURING AGREEMENT TO EXPAND ONGOING NXC-201 PHASE 1B/2
CLINICAL TRIAL TO THE U.S.
* NEXCELLA - INITIATES PROCESS OF BRINGING NXC-201 TO UNITED
STATES BY ENTERING INTO AN AGREEMENT WITH A WELL-KNOWN GMP CELL
THERAPY MANUFACTURER
* NEXCELLA - U.S. MANUFACTURING SITE EXPECTED TO SUPPLY
NXC-201
MATERIAL FOR PHASE 1B/2 TRIAL IN U.S. AFTER IND SUBMISSION TO
FDA AND APPROVAL
* NEXCELLA - PLANS TO INITIATE A PRE-IND MEETING WITH FDA,
SUBMIT
IND APPLICATION, OBTAIN APPROVAL FOR A PHASE 1B/2 OF NXC-201
STUDY
Source text for Eikon: ID:nGNX2R5Kjv
Further company coverage: IMMX.O
((Reuters.Briefs@thomsonreuters.com;))
Recent news on Immix Biopharma
See all newsBrief: Immix Biopharma Announces Closing Of $125 Million Underwritten Offering Of Common Stock
US RESEARCH ROUNDUP-Alnylam Pharmaceuticals, Carvana, MongoDB
Brief: Immix Biopharma Announces Pricing Of $125 Million Underwritten Offering Of Common Stock
Brief: Immix Biopharma Announces 89% Complete Response Rate At Interim Update Across All Nexicart-2 Patients, With Mrd-Negativity Indicating Potential To Reach Up To 98% Complete Response Rate
Immix Biopharma, Inc. reports results for the quarter ended June 30 - Earnings Summary