ADCT: Nakamit ng LOTIS-5 Phase 3 topline ang endpoint ng PFS para sa ZYNLONTA + rituximab
Natugunan ng Phase 3 LOTIS-5 trial ang pangunahing endpoint ng PFS nito na may istatistikang kahalagahan (HR 0.73, p=0.008). Plano ng ADC Therapeutics ang isang pre-sBLA meeting sa FDA sa Agosto 2026 at isang pagsusumite ng sBLA sa Q4 2026 upang humingi ng buong pag-apruba para sa ZYNLONTA kasama ang rituximab sa r/r DLBCL.
false
0001771910
0001771910
2026-06-03
2026-06-03
iso4217:USD
xbrli:shares
iso4217:USD
xbrli:shares
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): June 3, 2026
ADC Therapeutics SA
(Exact Name of Registrant as Specified in Its Charter)
Switzerland
(State or Other Jurisdiction of Incorporation)
001-39071
(Commission File Number)
N/A
(IRS Employer Identification Number)
Biopôle
Route de la Corniche 3B
1066 Epalinges
Switzerland
(Address of Principal Executive Offices) (Zip Code)
+ 41 21 653 02 00
(Registrant’s Telephone Number)
N/A
(Former Name or Former Address, if Changed Since
Last Report)
Ch