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ACTUNasdaq

ACTUATE THERAPEUTICS, INC.

Pharmaceutical preparations·Phase 2·Fort Worth, TX, United States·CEO: Mr. Daniel M. Schmitt
OncologyNephrology

ACTU evidence brief

What we can confirm

No verified snapshot fields are available yet.

What it means

The company data is ready for cross-source review; unsupported conclusions remain unknown.

What to watch

Watch the next source-backed data update.
BioSniper AIPage evidence connected

Prepared research question

What matters most for ACTU—catalysts, financial risk and supporting evidence?

Run cited research

Traceable citations · Unknowns marked

BioSniper AI · ACTU

Actuate Therapeutics is a clinical-stage biopharmaceutical company developing elraglusib, a GSK-3β inhibitor, for advanced cancers; it has no approved products, no revenue, and a cash position of $4.4M as of June 30, 2026 [sec_mda].

Key risk: Cash runway insufficient

4.4/10

BioSniper Score

Based on 5 of 6 signals

Market Cap

$39.7M

Cash Runway

3.1 mo

Financial data as of Jun 30, 2026.

Tracking 3 pipeline candidates · 2 clinical trials · 1 catalyst for ACTUATE THERAPEUTICS, INC..

AI OverviewAI overview is shown in English only.

Actuate Therapeutics is a clinical-stage biopharmaceutical company developing elraglusib, a GSK-3β inhibitor, for advanced cancers; it has no approved products, no revenue, and a cash position of $4.4M as of June 30, 2026 [sec_mda].

  • Lead candidate elraglusib (GSK-3β inhibitor) is being developed for refractory, metastatic melanoma and colorectal cancer [sec_mda · as of 2025-03-13].
  • Cash and cash equivalents were $4.4M as of June 30, 2026, with working capital of $0.9M [sec_mda · as of 2026-08-14].
  • Net loss was $4.9M for the quarter ended June 30, 2026 [latest reported financials].
  • Accumulated deficit was approximately $125.9M as of September 30, 2024 [sec_mda · as of 2024-11-13].
  • Company has no products approved for sale and has not generated any revenue from product sales since inception [sec_mda · as of 2025-03-13].

What works

  • Elraglusib has advanced to a Phase 1/2 open-label, dose escalation study (Actuate-2401) for the oral tablet formulation, targeting multiple advanced refractory cancers [sec_mda · as of 2025-08-14].
  • The company has developed several oral dosage forms of elraglusib, which management believes could expand the number of targetable cancer indications and offer more convenient dosing [sec_mda · as of 2025-08-14].
  • Actuate has access to a Committed Equity Facility with 364,407 shares of common stock remaining capacity as of June 30, 2026, providing a potential source of future funding [sec_mda · as of 2026-08-14].

What to weigh

  • Cash and cash equivalents of $4.4M as of June 30, 2026 are insufficient to fund operations for twelve months from the issuance date of the financial statements [sec_mda · as of 2026-08-14].
  • The company has an accumulated deficit of approximately $125.9M (as of September 30, 2024) and expects losses to increase substantially as development and regulatory activities continue [sec_mda · as of 2024-11-13].
  • No products are approved for sale, and the company has never generated revenue from product sales; profitability is uncertain and may never be achieved [sec_mda · as of 2025-03-13].
  • There is no assurance that sufficient proceeds can be raised under the Committed Equity Facility or through other financings on acceptable terms [sec_mda · as of 2025-08-14].

From the filings

Quoted directly from source documents.

  • Cash position as of June 30, 2026

    As of June 30, 2026, we had cash and cash equivalents of $4,425,841 and working capital of $942,745.

    SEC MD&A · August 14, 2026

  • Accumulated deficit as of September 30, 2024

    As of September 30, 2024, we had an accumulated deficit of approximately $125.9 million.

    SEC MD&A · November 13, 2024

  • No approved products or revenue from product sales

    We do not have any products approved for sale and have not generated any revenue from product sales since inception.

    SEC MD&A · March 13, 2025

  • Phase 1/2 study for elraglusib oral tablet

    A clinical candidate tablet, the Elraglusib Oral Tablet, has been selected for further development and we are planning a Phase 1 study (Actuate-2401) to identify the maximum tolerated dose ("MTD") and recommended Phase 2 dose ("RP2D") for Elraglusib Oral Tablet in patients with advanced, refractory adult cancers, subject to future funding.

    SEC MD&A · August 14, 2025

Catalyst timeline

  • 2026-10-01 · Phase 2 Start — Phase 1/2 Open-Label, Dose Escalation Study to Evaluate the Safety, Tolerability, PharmacokineticsInitiation of the Phase 1/2 study for elraglusib oral tablet in advanced refractory cancers; enrollment and early safety data will be key to watch.
Risks & what to watch (4)

Key risks

  • Cash runway insufficientExisting cash of $4.4M as of June 30, 2026 will not fund operations for twelve months [sec_mda · as of 2026-08-14].
  • No revenue or approved productsCompany has never generated product revenue and may never become profitable [sec_mda · as of 2025-03-13].
  • Dependence on future financingNo assurance that Committed Equity Facility or other financings will provide sufficient funds [sec_mda · as of 2025-08-14].
  • Clinical development riskElraglusib is in early-stage trials; failure could halt all operations [sec_mda · as of 2025-08-14].

What to watch

  • Initiation and enrollment of the Phase 1/2 Actuate-2401 study for elraglusib oral tablet [sec_mda · as of 2025-08-14].
  • Ability to raise additional capital through the Committed Equity Facility or other financings [sec_mda · as of 2026-08-14].
  • Any clinical data readouts from ongoing or planned studies of elraglusib [sec_mda · as of 2025-08-14].
  • Cash burn rate and whether the company can extend runway beyond current estimates [sec_mda · as of 2026-08-14].

Sources: SEC filings · SEC MD&A · Generated August 30, 2026 · How we verify sources →

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Evidence & data

Score breakdownBased on 5 of 6 signals · derived from public data

Cash Runway0.9

3.1 months

Financial Health5.0

D/E 4.26 · 0% dilution

Pipeline Maturity6.0

Lead: Phase 1/Phase 2

Pipeline Breadth5.9

3 candidates

Catalyst Momentum4.0

1 upcoming, next in ~32d

Insider SignalN/A

No insider transactions in the last 180 days

Runway

Catalysts

Pipeline

Regulatory

Financials

Institutional Holdings

Source: SEC Form 13F · as of Mar 2026

Institutional holders

60

Total value held

$34.4M

Showing top 10 of 60 institutional holders of ACTUATE THERAPEUTICS, INC.. Open the full 13F history after sign-in.

Short Interest

as of May 20, 2026
% of float
9.2%
Days to cover
4.6
Shares short
947,782
Daily short volume
-

Short percent of float and days-to-cover reflect reported short positioning. Daily short volume is the exchange-reported short share of a single day's trading volume and is noisier. See the most-shorted biotech ranking →

ACTU short interest

Governance

Frequently asked questions

What is the AI investment thesis for ACTUATE THERAPEUTICS, INC.?

Actuate Therapeutics is a clinical-stage biopharmaceutical company developing elraglusib, a GSK-3β inhibitor, for advanced cancers; it has no approved products, no revenue, and a cash position of $4.4M as of June 30, 2026 [sec_mda].

What is ACTUATE THERAPEUTICS, INC.'s lead drug candidate?

ACTUATE THERAPEUTICS, INC.'s most advanced tracked candidate is elraglusib (Phase 1/Phase 2) for Advanced Malignant Solid Tumor.

What is ACTUATE THERAPEUTICS, INC.'s next catalyst?

ACTUATE THERAPEUTICS, INC.'s next tracked catalyst is a Phase2_Start event — "Phase 2 Start: Phase 1/2 Open-Label, Dose Escalation Study to Evaluate the Safety, Tolerability, Pharmacokinetics, " — expected October 1, 2026.

Who is the CEO of ACTUATE THERAPEUTICS, INC.?

Mr. Daniel M. Schmitt is the chief executive officer of ACTUATE THERAPEUTICS, INC. (ACTU).

Where is ACTUATE THERAPEUTICS, INC. headquartered?

ACTUATE THERAPEUTICS, INC. (ACTU) is headquartered in Fort Worth, TX, United States.

925 companies232,681 SEC filings21,419 clinical trials100% citation-verification pass rate (7d)How we verify →

The AI overview and BioSniper Score are neutral, data-derived signals built from public SEC filings, ClinicalTrials.gov and FDA records — not investment advice.