Primärquellen-Eintrag
Xilio Therapeutics hat einen erwarteten Zeitplan für erste Phase-1-Daten seines XTX501-Programms, einer bispezifischen PD-1 / maskierten IL-2-Therapie, bereitgestellt. Das Unternehmen erwartet, diese Daten in der zweiten Hälfte von 2027 zu berichten, abhängig von der Freigabe der Investigational New Drug (IND)-Anmeldung durch die FDA, die für Mitte 2026 angestrebt wird.
EX-99.1 2 xlo-ex99_1.htm EX-99.1 Unlocking the Potential of Immuno-Oncology Therapies March 9, 2026 © 2026 Xilio Therapeutics, Inc. ® This presentation contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995, as amended, including, without limitation, statements regarding plans, timing and expectations related to: development timelines and anticipated milestones for Xilio’s programs; the ultimate safety, efficacy, and potential benefits of any of Xilio’s current or future product candidates in any indication; any potential indications or commercial opportunities of our product candidates; the timing and receipt of future payments under Xilio’s collaboration or partnership agreements with AbbVie and Gilead; Xilio’s preliminary, unaudi