Immutep Limited
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About the company
Immutep Limited, a biotechnology company, engages in developing novel Lymphocyte Activation Gene-3 related immunotherapies for cancer and autoimmune diseases in Australia. Its lead product candidate is the eftilagimod alfa (efti or IMP321), a soluble LAG-3lg fusion based on LAG-3 immune control mechanism for the treatment of different types of cancers. The company’s product pipeline also includes TACTI-004, which is in phase III clinical trial for the treatment of first line non-small cell lung cancer (1L NSCLC); TACTI-003, which is in phase IIb clinical trial to treat first line head and neck squamous cell carcinoma (HNSCC); INSIGHT-005 which is in phase I for metastatic urothelial carcinoma; TACTI-002, which in phase II trial for the treatment NSCLC and HNSCC; AIPAC-003, which is in phase II/III clinical trial to treat metatastic breast cancer; and EFTISARC-NEO, which is in phase II clinical trial for the treatment of soft tissue sarcoma.
- CEO
- Marc Voigt
- IPO
- 1988
- Employees
- 57
- HQ
- Sydney, NSW, AU
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- Market Cap
- $78.11M
- P/E
- -0.92
- PEG
- 0.02
- P/S
- 13.07
- P/B
- 0.79
- EV/EBITDA
- -0.09
- Div Yield
- 0.00%
- Gross Margin
- -522.59%
- Op Margin
- -2052.18%
- Net Margin
- -1404.13%
- ROE
- -69.20%
- ROIC
- -122.10%
Latest fiscal year · YoY change
- Revenue
- $5.04M+31.3%
- Gross Profit
- $-56,366,759-49.5%
- Op Income
- $-126,421,795
- Net Income
- $-61,434,165-43.8%
- EPS
- $-0.04-18.5%
- OCF Growth
- -78.2%
- FCF Growth
- -73.7%
- 52W High
- $0.47
- 52W Low
- $0.03
- 50D MA
- $0.05
- 200D MA
- $0.19
- Beta
- 2.19
- RSI (14)
- 58
- Avg Volume
- 14.36M
Earnings call summaries
Pick a quarter — each call distilled into takeaways, results, and a bull vs bear read.
Prima’s call highlighted progress on CVac data, U.S. investor interest, and a pragmatic approach to trial execution and messaging.· August 5, 2013
- ICS results are expected to be a much larger, longitudinal dataset across all 63 patients, not just the small snapshot shared last year.
- Management said increased NASDAQ trading volume likely reflects more U.S. investor outreach and growing interest in biotech and immune therapy.
- The company says foreign exchange risk is buffered by euro and U.S. dollar holdings, with hedging contracts tied to projected operations.
- For the CANVAS trial, Prima is targeting up to 120 sites in the protocol, about 80 clinical centers, and roughly 50 targeted centers.
- Management said they will keep publicity measured, focusing on credible clinical data before leaning harder into broad media promotion.
No revenue, EPS, gross margin, or year-over-year financial figures were reported in this Q&A-only call. On guidance, management said the upcoming ICS assessment will evaluate all 63 patients from baseline through dosing and then look at durability of response, while CANVAS is targeting up to 120 sites in the protocol, about 80 clinical centers, and roughly 50 targeted centers. They also said recruitment can vary materially by center and country, with some sites expected to enroll from about half a patient to about one patient per clinical center per month.
Matthew Lehman framed the recent increase in U.S. trading activity as a sign that the company’s story is getting broader attention, especially as immune therapy has gained traction in both the scientific and financial communities. He emphasized that Prima is spending more time in the U.S. introducing itself to investors and sees growing interest on both the Australian and U.S. exchanges. On communications, he said the company wants to get its message out, but not overdo it; they prefer to release news through the proper channels and stay balanced.
Marc Voigt said the company holds significant euro and U.S. dollar balances, which provide a buffer against Australian dollar weakness. He added that Prima uses hedging contracts based on projected ongoing operations and believes that approach is reasonable given FX risk. He also noted that most clinical operations run in Europe and the United States, so the currency mix leaves the company in a comparatively good position.
The main clinical question was what the ICS test results might show versus last year’s limited snapshot. Sharron Gargosky answered that this time the company is focusing on baseline-to-dosing changes across all 63 patients, with durability of response as a secondary question. Another question asked why NASDAQ trading volume had increased; Lehman attributed it to more U.S. outreach, a stronger biotech backdrop, and rising attention on immune therapy. Investors also asked about media strategy and recruitment capacity, and management said it would stay conservative on publicity while targeting large, high-referral centers for the CANVAS trial.
The call suggested the company is moving from a small snapshot of data to a far more informative dataset, which could strengthen the CVac story if the broader ICS analysis is supportive. Management also sounded encouraged by rising U.S. investor interest and said the FX position is relatively protected by euro and U.S. dollar cash and hedging.
The biggest risk on this call is that the company still has not shown the larger ICS dataset, so investors are waiting on evidence rather than results. Recruitment also looks operationally challenging because enrollment depends heavily on center quality, patient timing after diagnosis, and country-by-country differences, which could slow execution.
AI summary of the company's earnings call · Paraphrased · Not investment advice
- Free Float
- 97.1%
- Shares Outstanding
- 1.47B
- Float Shares
- 1.43B
Held by 3 ETFs
Biggest fund positions in IMM.AX by dollar value.
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Generate IMM.AX report →Immutep Announces Abstract Accepted for Presentation at the European Society for Medical Oncology (ESMO) Congress 2026
globenewswire.com · Jul 24
Systemic immune activation with eftilagimod alfa associated with statistically significant increased overall survival in late-stage cancer patients
globenewswire.com · May 28
Immutep Receives Nasdaq Notice of Bid Price Deficiency
globenewswire.com · Apr 30
Immutep Quarterly Activities Report Q3 FY26
globenewswire.com · Apr 30
Immutep Reports Progress from Phase I Study of LAG-3 Agonist for Autoimmune Diseases
globenewswire.com · Mar 19
TACTI-004 Phase III Study in First Line NSCLC to be discontinued following Futility Analysis
globenewswire.com · Mar 13
Immutep Announces Strong Operational Progress in Global TACTI-004 (KEYNOTE-F91) Phase III and Enrolment Continues at Robust Pace
globenewswire.com · Dec 16
Immutep and Dr. Reddy’s enters into Strategic Collaboration for Commercialisation of an Innovative Oncology Drug, Eftilagimod Alfa
globenewswire.com · Dec 8
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