Logotype for EXACT Therapeutics AS

EXACT Therapeutics (EXTX) Status update summary

Event summary combining transcript, slides, and related documents.

Logotype for EXACT Therapeutics AS

Status update summary

4 Jun, 2026

Company status and clinical update

  • Focused on developing ultrasound-based targeted oncology therapies, with PS101 targeting locally advanced pancreatic cancer (LAPC).

  • ENACT Phase II trial in LAPC is ongoing, with promising early results showing significant tumor shrinkage, biomarker reduction, and some patients moving to curative treatment.

  • All clinical sites in the US and UK are open for enrollment, with dose escalation and safety reviews progressing as planned.

  • Interim readout for the phase II study is expected end of 2024 or mid-2026, with final analysis in the first half of 2027.

  • Recent advances in KRAS/RAS-targeted therapies validate the approach and increase enthusiasm in the field.

Rationale and process for delisting

  • Euronext Growth listing has low liquidity, with 50% of trading days seeing no trades and only 4.2% of shares traded year-to-date.

  • Shareholder structure is concentrated, with the top 10-20 holders owning 75-87% of shares, limiting liquidity.

  • Delisting is proposed to attract international VC funding, reduce costs, and support late-stage clinical development.

  • Board and management unanimously support delisting to build future value and enable capital access.

  • Feedback from venture capital and advisors indicates a private setting is needed for successful future financing.

Delisting process and shareholder impact

  • General assembly vote on June 12 will authorize the board to apply for delisting; requires two-thirds majority.

  • If approved, Oslo Stock Exchange will process the application, with last trading day likely in October and shares tradable until then.

  • Shareholder rights and protections remain unchanged, but trading will move to alternative channels post-delisting.

  • No exit offer is currently planned for minority shareholders; OSE will assess potential detriment before approval.

  • Regular updates on clinical and financial status will continue via company channels.

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