PPBTNasdaqPharmaceutical PreparationsUS GAAP · USD

Purple Biotech Ltd

Purple Biotech Ltd. is an Israel-based clinical-stage biopharmaceutical company focused on developing oncology immunotherapy candidates. Its work centers on a tri-specific antibody platform designed to activate both T cells and NK cells against solid tumors, with development programs carried out from its Rehovot, Israel base and funded through public-market capital.

Business

Share of revenue
Lead clinical development program70 %

CAPTN-3 and its lead candidate IM1240, which are being advanced as oncology immunotherapy assets.

Preclinical pipeline20 %

Earlier-stage candidates such as IM1305 that broaden the platform beyond the lead program.

Platform discovery and optimization10 %

Tri-specific antibody engineering and proprietary capping technology used to design tumor-selective molecules.

Customers

Purple Biotech does not sell commercial medicines; its direct counterparties are research partners, clinical collaborators, and capital providers that support drug development. The eventual end customers for approved products would be oncology physicians, hospitals, and cancer patients, but today the business is primarily oriented toward advancing drug candidates through development milestones. Its collaborations also indicate engagement with external technology partners to accelerate antibody design.

Capital market investors

Buy equity exposure to the clinical-stage pipeline and platform value.

Research and technology partners

Collaborate on design, optimization, and acceleration of antibody candidates.

Clinical trial ecosystem

Hospitals, investigators, and CROs support development of oncology candidates.

Future oncology providers

Would use approved therapies for solid-tumor treatment if programs succeed.

Strategy

Purple Biotech’s strategy is to advance a differentiated oncology platform built around conditionally activated tri-specific antibodies and to extend that platform into multiple drug candidates. It is also using external collaborations, including AI-enabled design partnerships, to improve discovery speed and molecule quality while broadening the pipeline.

Advance lead oncology candidateShort term

Clinical progress is the main driver of platform validation and future value creation.

Develop a multi-asset platformMedium term

A broader pipeline reduces dependence on a single program and increases partnering optionality.

Use external technology collaborationShort term

AI-enabled design can shorten discovery cycles and improve candidate quality.

Geography

Purple Biotech is headquartered in Rehovot, Israel and is publicly listed on Nasdaq and the Tel Aviv Stock Exchange. Its development work is centered in Israel, while its capital access and investor base are international through U.S. and Israeli public markets. The company’s clinical and partnership footprint can extend beyond Israel as candidates progress into broader oncology development.

Risks

Purple Biotech faces the typical risks of a clinical-stage biotechnology company: programs may fail in preclinical or clinical development, timelines can be long and uncertain, and future value depends on successful validation of a narrow pipeline. As a public Israeli company with U.S. listing exposure, it also depends on capital markets access and continued Nasdaq compliance, while research partnerships and scientific execution remain critical to its strategy.

Sorted by severity
LowMediumHighLowMediumHighImpact →Likelihood →Clinical development failure1Capital market dependence2Scientific development risk3Listing and liquidity risk4
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. Clinical development failureImpact: CriticalLikelihood: High

    The pipeline is preclinical/clinical-stage, so efficacy or safety issues could halt programs.

    ExposureIM1240IM1305CAPTN-3 platform
  2. Capital market dependenceImpact: HighLikelihood: High

    Biotech development requires ongoing funding before any product revenue exists.

    Exposure: General corporate funding and R&D spend

  3. Scientific development riskImpact: HighLikelihood: High

    Tri-specific antibodies and tumor-selective activation are technically complex to design and validate.

    Exposure: Platform engineering and translational biology

  4. Listing and liquidity riskImpact: MediumLikelihood: Medium

    Maintaining exchange compliance is important for trading access and financing flexibility.

    Exposure: Nasdaq Capital Market listing

Accounting

Judgemental items
Fair value of warrants

Warrants are marked to market and can create non-cash volatility in reported profit or loss.

Impact: Can materially affect periodic earnings and equity

Share-based payment accounting

Employee and director equity awards are expensed over vesting periods, affecting operating costs.

Impact: Influences R&D and G&A expense

R&D expensing

Clinical and preclinical spending is typically expensed as incurred, not capitalized like a product asset.

Impact: Makes current-period losses reflect development intensity

Lease liabilities

Office and facility leases create right-of-use assets and liabilities under IFRS 16.

Impact: Affects leverage and finance expense

Post-employment benefit estimates

Actuarial assumptions influence pension or severance-related liabilities.

Impact: Can move equity and operating costs

Publicly listed companies with a comparable business focus.

Last updated: 28/09/2026