Nasdaq StockholmIFRS · SEK

Stayble Therapeutics

Stayble Therapeutics AB is a Swedish clinical-stage biopharmaceutical company based in Gothenburg. It develops STA363, an injectable treatment concept for pain caused by herniated disc, with the aim of addressing the underlying cause of symptoms rather than only providing temporary relief.

Operating profit (EBIT)-12.8m SEK
+46.6 %y/y
Net income-12.4m SEK
+47.7 %y/y

Fiscal year 2024 · change from previous year

Development 2023–2024

-25-20-15-10-50m SEK2023: EBIT -24 m SEK20232024: EBIT -13 m SEK2024-13
RevenueOperating profit (EBIT)

Business

Share of revenue
Drug candidate development100 %

Development of STA363 as a treatment for pain caused by herniated disc.

Clinical research and trials0 %

Clinical study work to test safety, efficacy, and dosing of the candidate.

Licensing and commercialization rights0 %

Potential future out-licensing or partnering of the treatment concept.

Customers

Stayble does not appear to sell a commercial product yet; its near-term counterparties are clinical trial participants, investigators, and development partners. In a future commercial model, the end users would be patients with persistent pain after disc herniation, while buyers would likely include healthcare providers, hospitals, and potentially licensed pharmaceutical partners.

Clinical trial participants

Patients enrolled to evaluate STA363 safety and efficacy in disc-related pain.

Clinical investigators and trial sites

Hospitals and research centers that administer the study protocol and collect data.

Potential licensing partners

Pharmaceutical or biotech companies that may acquire rights to develop or commercialize STA363.

Future treating physicians and clinics

Healthcare providers that would prescribe or administer the treatment if approved.

Strategy

Stayble’s strategy is centered on advancing STA363 through clinical development and building evidence that the treatment can address disc-related pain with a simple, one-time injection. The company also emphasizes using an existing active substance, which can shorten development timelines and support future partnering or licensing discussions.

Advance clinical development of STA363Short term

Clinical data is the main value driver for a pre-commercial biotech company.

Differentiate with a one-time injection conceptMedium term

A simple treatment profile can improve adoption and partnering appeal.

Prepare for partnering or commercializationMedium term

External partners may be needed to fund late-stage development and market access.

Geography

Stayble is headquartered in Gothenburg, Sweden, and its corporate and development activities are anchored there. The available reports do not disclose a commercial revenue geography, which is consistent with a development-stage company whose operations are centered on Sweden and external clinical development partners.

Risks

Stayble is exposed to the classic risks of a clinical-stage biotech company: funding needs, uncertain trial outcomes, and dependence on third-party development partners. Because it does not yet generate product sales, setbacks in clinical development or capital raising could materially affect its ability to continue operations.

Sorted by severity
LowMediumHighLowMediumHighImpact →Likelihood →Financing risk1Clinical trial risk2Regulatory approval risk3
Impact is the risk’s severity and likelihood how probable it is over the next few years, both assessed from the company’s reports. Numbers match the list.
  1. Financing riskImpact: CriticalLikelihood: Medium

    The company has no approved treatment generating sales and must fund ongoing development.

    Exposure: Clinical development and corporate overhead

  2. Clinical trial riskImpact: HighLikelihood: Medium

    Drug development depends on proving safety and efficacy in human studies.

    Exposure: STA363 development program

  3. Regulatory approval riskImpact: HighLikelihood: Medium

    Even promising clinical data may not translate into marketing authorization.

    Exposure: Future commercialization pathway

  4. Partner dependency riskImpact: High

    Development and future commercialization may rely on external collaborators.

    ExposureClinical operationsProductionLicensing

Accounting

Judgemental items
Research and development expense recognition

Clinical-stage biotech spending is usually expensed as incurred and drives reported losses.

Impact: Affects operating result and comparability across periods

Accruals for clinical trial and advisory costs

Trial services are often recognized before invoices are received.

Impact: Can shift expenses between quarters

Going concern and liquidity assumptions

A pre-revenue company must assess whether it can fund future operations.

Impact: Affects disclosure and valuation of the business

Impairment and capitalization judgments

Development-related assets or costs may require judgment on recoverability.

Impact: Can materially affect balance sheet and earnings

Publicly listed companies with a comparable business focus.

Last updated: 24/09/2026