Record mula sa primary source
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
ADC Therapeutics Inihayag ang Pagrestruktura ng Pananalapi at Mga Presentasyon ng Data sa ASH 2026 para sa ZYNLONTA