Amur Minerals Corporation
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About the company
Amur Minerals Corporation (AMMCF), together with its subsidiary entities, specializes in the entire lifecycle of mineral resource development – from identifying promising sites to their assessment, acquisition, exploration, and eventual development – exclusively within Russia's Far Eastern region. The company primarily targets deposits of various valuable metals, including nickel, copper, cobalt, platinum, palladium, gold, and silver. Key to its portfolio is the Kun-Manie nickel-copper sulfide project, a significant asset encompassing 36 square kilometers located in the Amur Oblast.
- CEO
- Robin Jay Young
- IPO
- 2012
- Employees
- 4
- HQ
- Road Town, VG
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- Market Cap
- $1.38M
- P/E
- -0.62
- PEG
- -0.01
- P/S
- 0.00
- P/B
- 0.46
- EV/EBITDA
- 2.37
- Div Yield
- 1446.97%
- Gross Margin
- 0.00%
- Op Margin
- 0.00%
- Net Margin
- 0.00%
- ROE
- -18.86%
- ROIC
- -63.17%
Latest fiscal year · YoY change
- Revenue
- $31.28K+0.0%
- Gross Profit
- $26.27K+100.3%
- Op Income
- $-728,157
- Net Income
- $-759,435+64.6%
- EPS
- $-0.00+64.0%
- OCF Growth
- +46.7%
- FCF Growth
- +45.2%
- 52W High
- $6.77
- 52W Low
- $0.04
- 50D MA
- $6.77
- 200D MA
- $6.77
- Beta
- 0.27
- RSI (14)
- 100
- Avg Volume
- 3.37K
Earnings call summaries
Pick a quarter — each call distilled into takeaways, results, and a bull vs bear read.
CRISM said it cleared a key regulatory step for its ChemoSeed glioblastoma program and is now focused on starting clinical trials in early 2026, while also expanding into prostate cancer and managing cash runway.· September 16, 2025
- MHRA approval was received at the end of August, removing the main regulatory hurdle for the glioblastoma trial.
- Management said first patient treatment is targeted for early 2026, with trial setup now the main focus.
- The company raised GBP 874,000 in June/July and said net cash at end-September was just over GBP 900,000.
- ChemoSeed is being positioned as a broader platform for solid tumors, with a prostate cancer program already initiated and pancreatic cancer on the roadmap.
- Management framed the opportunity as potentially significant because glioblastoma has seen little progress for about 20 years and local delivery may overcome blood-brain barrier issues.
The company did not report revenue or EPS on this presentation. It said it raised GBP 874,000 in June/July and that net cash at the end of September was just over GBP 900,000. For the glioblastoma trial, management said setup costs are about GBP 250,000, roughly GBP 700,000 is needed to reach a reportable data point, and total Part 1 costs are expected to be around GBP 1 million. No forward revenue or earnings guidance was given; instead, the company guided to clinical trial setup, with first patient treatment hoped for early in 2026, and said Part 1 will initially enroll 12 patients, with around 60 patients planned in the broader initial phase.
Andrew Webb emphasized that ChemoSeed is the company’s core asset and said the MHRA approval was a major tipping point because it allows CRISM to move from regulation into trial execution. He highlighted the platform potential beyond brain tumors, pointing to an earlier-started prostate program and the possibility of broader solid-tumor use. His tone was upbeat but practical, repeatedly stressing cash discipline, trial setup, and the need to create value through data.
No formal CFO was present, but Andrew Webb covered financing and capital allocation comments. He said the company raised GBP 874,000 in the June/July fundraise and ended September with just over GBP 900,000 in net cash, while also noting service-contract revenue helps mitigate cash burn. He estimated about GBP 250,000 for trial setup, about GBP 700,000 to reach a reportable data point, and roughly GBP 1 million for total Part 1 costs, while saying the company is likely to partner eventually and must manage runway carefully.
In questions, management was asked how ChemoSeed could develop beyond glioblastoma, and Webb said it could be suitable for most solid tumors, with prostate using docetaxel and pancreatic viewed as more complex because of the 4-drug standard-of-care combination. They were also asked about the cost of treating the first 12 trial patients and how the cash would be raised; management gave the GBP 250,000 setup and about GBP 1 million total Part 1 estimate, saying recruitment speed and multiple clinical sites would matter. On whether the trial could materially improve outcomes, Cruickshank said he could not guarantee it but believed early, local treatment had a good chance of showing benefit, while acknowledging it would be a tall order to move 5-year survival from 5% to 25%.
The bullish case is that CRISM has cleared MHRA approval, has a clinical batch underway, and is moving toward first patient dosing with a differentiated local-delivery approach. Management believes the mechanism may work broadly in glioblastoma, not just in narrow biomarker-defined subsets, and the prostate program shows the platform could expand beyond the initial indication.
The main risks are execution and funding: the trial still needs to be set up, recruited, and financed, with total Part 1 costs around GBP 1 million and only just over GBP 900,000 in net cash at end-September. The company is targeting a disease with historically poor outcomes, high complexity, and no guarantee that the early promise in mice and prior small studies will translate into meaningful human benefit.
AI summary of the company's earnings call · Paraphrased · Not investment advice
- Free Float
- 99.5%
- Shares Outstanding
- 32.68M
- Float Shares
- 32.50M
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