ADCT: LOTIS-5 Fase 3 topline cumplió el objetivo de SLP para ZYNLONTA + rituximab
El ensayo de Fase 3 LOTIS-5 cumplió su objetivo primario de SLP con significación estadística (HR 0.73, p=0.008). ADC Therapeutics planea una reunión previa a la sBLA con la FDA en agosto de 2026 y una presentación de sBLA en el cuarto trimestre de 2026 para solicitar la aprobación completa de ZYNLONTA más rituximab en DLBCL r/r.
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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