Eikon announces first patient dosed in TeLuRide-008 trial
The Phase 2/3 registrational study evaluates EIK1001 combined with pembrolizumab and chemotherapy as first-line therapy for stage 4 NSCLC.
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Late-stage clinical biopharmaceutical company
eikontx.comLast updated
In short: Eikon Therapeutics reached key clinical and financial milestones, including a $381 million IPO and the start of a Phase 2/3 cancer trial.
The Phase 2/3 registrational study evaluates EIK1001 combined with pembrolizumab and chemotherapy as first-line therapy for stage 4 NSCLC.
Francisco, former P&G CEO, brings leadership experience to the biopharma company's board, effective June 15, 2026.
The TeLuRide-008 trial will be presented as a poster at ASCO 2026.
The study evaluates EIK1005 as monotherapy and with pembrolizumab in advanced solid tumors, including MSI-H/dMMR.
The late-stage biopharmaceutical company said the first patient has been dosed in the phase 2/3 TeLuRide-008 registrational study evaluating EIK1001 in combination with pembrolizumab and...
Addition reflects Eikon's progress as a publicly traded company and increasing visibility within the investment ...
Discover high-conviction stock picks and new investing opportunities with the TipRanks Smart Investor Newsletter Eikon Therapeutics, Inc. ( (EIKN)) has shared an update. On May...
TeLuRide-005, a Phase 2 trial of EIK1001 in first-line patients with stage 4 NSCLC completed enrollment of both non-squamous and squamous cohorts and reports updated...
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