Iniulat ng Allogene ang positibong interim futility data ng ALPHA3 para sa cema-cel
Inilalantad ng 8-K ang unang interim futility analysis mula sa pivotal Phase 2 ALPHA3 trial ng cema-cel sa 1L LBCL consolidation. Naabot ang MRD negativity sa 58.3% ng mga pasyenteng ginamot ng cema-cel kumpara sa 16.7% sa observation arm, kasama ang mabilis na ctDNA clearance at walang naiulat na CRS, ICANS, o GvHD. Nagpapatuloy ang trial nang nakatago para sa EFS, PFS, at OS endpoints, na may inaasahang buong enrollment sa katapusan ng 2027 at isang interim EFS analysis na binalak para sa kalagitnaan ng 2027.
8-K
false 0001737287 0001737287 2026-04-13 2026-04-13
UNITED STATES
SECURITIES AND EXCHANGE COMMISSION
WASHINGTON, D.C. 20549
FORM 8-K
CURRENT REPORT
Pursuant to Section 13 or 15(d)
of the Securities Exchange Act of 1934
Date of Report (Date of earliest event reported): April 13, 2026
Allogene Therapeutics, Inc.
(Exact name of Registrant as Specified in Its Charter)
Delaware
001-38693
82-3562771
(State or Other Jurisdiction
of Incorporation)
(Commission
File Number)
(IRS Employer
Identification No.)
210 East Grand Avenue
South San Francisco , CA
94080
(Address of Principal Executive Offices)
(Zip Code)
Registrant’s Telephone Number, Including Area Code: (650) 457-2700
N/A
(Former Name or Former Address, if Changed Since Last Report)
Check the appropriate box below if the Fo