H.C. Wainwright 28th Annual Global Investment Conference
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Actuate Therapeutics (ACTU) H.C. Wainwright 28th Annual Global Investment Conference summary

Event summary combining transcript, slides, and related documents.

Logotype for Actuate Therapeutics Inc

H.C. Wainwright 28th Annual Global Investment Conference summary

16 Sep, 2026

Drug development highlights

  • Oral elraglusib is advancing to clinical trials, aiming to improve upon IV results in difficult-to-treat cancers, especially metastatic pancreatic cancer, with significant efficacy and survival benefits demonstrated in over 500 patients.

  • The oral formulation is expected to enhance patient exposure and outcomes, with 95% bioavailability and daily dosing, overcoming limitations of IV administration and patient compliance.

  • Intellectual property protection extends to at least 2043, with the oral version potentially exceeding this due to ongoing registration review.

  • The development strategy focuses on expanding indications, establishing a standard-of-care backbone in multiple cancers, and targeting rare pediatric cancers with high unmet need.

Clinical and preclinical data

  • In first-line metastatic pancreatic cancer, combination therapy showed a 40% increase in median overall survival, doubling one-year survival, and a fivefold increase in two-year survival.

  • Synergy with RAS inhibitors was demonstrated in preclinical models, with all tested cell lines showing additive or synergistic effects.

  • Achieving a threshold plasma concentration of 210 ng/mL correlated with significantly better outcomes (hazard ratio 0.48), and the oral formulation is designed to help more patients reach this level.

  • Subgroup analyses and exposure-response relationships reinforce the benefit of higher, sustained drug exposure.

Regulatory and operational plans

  • IND clearance has been obtained for a phase I/II accelerated trial, with patient recruitment and site setup underway for a second-half-of-year start.

  • The phase I/II study will evaluate monotherapy in refractory melanoma, non-small cell lung cancer, colorectal, and pancreatic cancer, with PK and RP2D as endpoints.

  • EMA and FDA require full phase III trials for approval; the pivot to oral formulation aligns with the trend toward oral RAS inhibitors and combination regimens.

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