Catalyst overview
Research summary
This catalyst tracks a Phase 1/2 data readout for Efarindodekin Alfa (XTX301) in Solid tumor/s. The expected timing is based on the latest available company guidance and may change.
3/28/24- Partnered w/GILD. 12/19/24- Reported preliminary data. 5/8/25- Maximum tolerated dose not yet established. 9/9/25- Ph2 trial initiated. 11/13/25:- SITC Ph1 monotherapy data showed promising anti-tumor activity and well-tolerated safety; RP2D selected, Ph2 dosing ongoing, and Ph1A/Ph1B enrollment completed with evaluation continuing. 01/08/26:- Deliver Ph1/2 option data package to Gilead for efarindodekin alfa in H1 2027. 03/23/26:- Expects to deliver Gilead option data package from ongoing Ph2 monotherapy trial in H1 2027. 05/12/26:- Reiterates plan to deliver Gilead option data package for efarindodekin alfa in H1 2027. 08/12/26:- Ongoing Ph2 monotherapy trial continues. Gilead option data package is expected in H1 2027.
Verification
Confirm timing and program details against the company announcement or filing.