Immutep Banks $857K R&D Tax Rebate to Extend Cash Runway Into 2028

Immutep's A$856,669 Immutep R&D Tax Incentive funding receipt — non-dilutive and government-backed — extends the biotech's cash runway into H1 CY2028 as efti and IMP761 advance through clinical development.
By Josua Ferreira -
  • Immutep received an A$856,669 cash rebate under Australia's R&D Tax Incentive program for FY2025 eligible expenditure, with AusIndustry's Advance overseas finding allowing certain overseas R&D activities to qualify.
  • The funding is non-dilutive, meaning existing shareholders face no ownership dilution from this cash inflow.
  • Immutep's expected cash reach now extends to H1 CY2028, reducing near-term pressure to raise capital from equity markets.
  • The company draws on R&D tax incentive programs across three jurisdictions — Australia, France, and Germany — creating a multi-layered non-dilutive funding base to support its clinical programmes.
  • IMP761 Phase I results presented at EULAR 2026 confirmed a favourable safety profile and statistically significant immunosuppressive activity, with the LAG-3 agonist described as the only candidate of its class currently in clinical development.
Summarise with AI:

Immutep banks ~A$856,669 R&D tax rebate, extending cash runway into 2028

Immutep Limited (ASX: IMM; NASDAQ: IMMP) has received an A$856,669 cash rebate under the Australian Federal Government’s R&D Tax Incentive program, relating to eligible R&D expenditure incurred in the 2025 fiscal year. The receipt followed AusIndustry’s approval of an Advance overseas finding, which allowed certain of Immutep’s overseas R&D activities to qualify for the incentive alongside its eligible Australian activities.

The non-dilutive funding will be directed towards advancing the company’s two product candidates, efti and IMP761. Immutep’s expected cash reach extends into H1 CY2028.

Capital Flow and Runway Extension Diagram

Understanding R&D tax incentives — why non-dilutive funding matters for biotech investors

Australia’s R&D Tax Incentive program provides eligible companies with a refundable cash offset based on qualifying R&D expenditure. In practice, a clinical-stage biotech that spends on research activities receives a portion of that spend back as a cash rebate from the government.

The term “non-dilutive” simply means the funding is received without issuing new shares. For existing shareholders, this is a meaningful distinction: the company replenishes its cash position without reducing the ownership percentage of current investors.

For a company like Immutep, which is developing its product candidates, non-dilutive inflows of this kind help extend the operational runway and reduce pressure to raise capital from markets in the near term.

A multi-jurisdictional R&D funding base

Immutep draws on R&D tax incentive programs across three jurisdictions, reflecting the geographic spread of its operations:

  • Australia: Federal R&D Tax Incentive — current receipt of A$856,669 for FY2025 eligible expenditure, supported by an Advance overseas finding
  • France: French CIR (Crédit d’Impôt Recherche) — received through subsidiary Immutep S.A.S. for eligible R&D expenditure conducted in the European Union
  • Germany: Forschungszulage — available through subsidiary Immutep GmbH for qualifying internal R&D personnel costs; first payment received in Q4 FY26; any future payments remain subject to the statutory application, assessment and review process, with amount and timing uncertain
Jurisdiction Program Name Status
Australia Federal R&D Tax Incentive Received — A$856,669 for FY2025
France Crédit d’Impôt Recherche (CIR) Active — via Immutep S.A.S.
Germany Forschungszulage First payment received Q4 FY26; future payments uncertain

What this means for Immutep’s investment case

The rebate feeds directly into Immutep’s ongoing R&D programmes for efti and IMP761, supporting continued clinical activity without drawing on equity markets. The headline investor takeaway is the cash reach: the company’s expected cash reach extends to H1 CY2028, which reduces near-term capital raise pressure.

IMP761 Phase I results presented at EULAR 2026 confirmed a favourable safety and tolerability profile and statistically significant immunosuppressive activity, establishing the LAG-3 agonist as the only candidate of its class currently in clinical development.

Recurring access to non-dilutive government incentives across Australia, France, and Germany provides a supplementary funding layer that complements Immutep’s broader financing strategy, though these inflows are modest relative to clinical-stage operating costs and should be viewed accordingly.

Alongside non-dilutive government incentives, the FDA Orphan Drug Designation for efti in soft tissue sarcoma provides a parallel form of capital efficiency, covering tax credits on clinical trial costs and exempting Immutep from FDA application fees on that indication.

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Frequently Asked Questions

What is the Australian R&D Tax Incentive and how does it benefit Immutep?

Australia's R&D Tax Incentive program provides eligible companies with a refundable cash offset based on qualifying R&D expenditure, meaning Immutep receives a portion of its research spend back as a government cash rebate without issuing new shares — the A$856,669 received for FY2025 is a direct result of this program.

What does non-dilutive funding mean for Immutep shareholders?

Non-dilutive funding means Immutep receives cash without issuing new shares, so existing shareholders' ownership percentages are not reduced — unlike a capital raise or placement, which would dilute the share count.

How long is Immutep's cash runway after the R&D tax rebate?

Following receipt of the A$856,669 R&D Tax Incentive rebate, Immutep's expected cash reach extends to H1 CY2028, reducing near-term pressure to raise capital from equity markets.

What R&D tax programs does Immutep access across its global operations?

Immutep draws on three government R&D incentive programs: Australia's Federal R&D Tax Incentive, France's Crédit d'Impôt Recherche via subsidiary Immutep S.A.S., and Germany's Forschungszulage via subsidiary Immutep GmbH, with the first German payment received in Q4 FY26.

What is IMP761 and what stage of development is it at?

IMP761 is a LAG-3 agonist described as the only candidate of its class currently in clinical development; Phase I results presented at EULAR 2026 confirmed a favourable safety and tolerability profile and statistically significant immunosuppressive activity.

Josua Ferreira
By Josua Ferreira
Partnership Director
Josua Ferreira holds a Bachelor of Commerce in Marketing and Advertising and brings a background in publication, business development, and ASX market storytelling. He has worked with listed companies across the resource sector and broader market, combining sharp commercial instincts with a genuine commitment to keeping investors informed.
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