View Future GrowthFirebrick Pharma 過去の業績過去 基準チェック /06Firebrick Pharmaは11.3%の年平均成長率で業績を伸ばしているが、Pharmaceuticals業界はgrowingで7.9%毎年増加している。売上は減少しており、年平均9%の割合である。主要情報11.29%収益成長率24.52%EPS成長率Pharmaceuticals 業界の成長31.22%収益成長率-9.02%株主資本利益率-126.43%ネット・マージン-596.85%前回の決算情報31 Dec 2025最近の業績更新Reported Earnings • Feb 25First half 2026 earnings released: AU$0.005 loss per share (vs AU$0.007 loss in 1H 2025)First half 2026 results: AU$0.005 loss per share (improved from AU$0.007 loss in 1H 2025). Net loss: AU$1.26m (loss narrowed 13% from 1H 2025). Over the last 3 years on average, earnings per share has increased by 57% per year but the company’s share price has fallen by 36% per year, which means it is significantly lagging earnings.Reported Earnings • Aug 31Full year 2025 earnings released: AU$0.012 loss per share (vs AU$0.007 loss in FY 2024)Full year 2025 results: AU$0.012 loss per share (further deteriorated from AU$0.007 loss in FY 2024). Revenue: AU$524.7k (down 81% from FY 2024). Net loss: AU$2.63m (loss widened 124% from FY 2024). Over the last 3 years on average, earnings per share has increased by 50% per year but the company’s share price has fallen by 39% per year, which means it is significantly lagging earnings.Reported Earnings • Feb 24First half 2025 earnings released: AU$0.007 loss per share (vs AU$0.005 loss in 1H 2024)First half 2025 results: AU$0.007 loss per share (further deteriorated from AU$0.005 loss in 1H 2024). Revenue: AU$197.1k (down 89% from 1H 2024). Net loss: AU$1.45m (loss widened 61% from 1H 2024). Over the last 3 years on average, earnings per share has increased by 34% per year but the company’s share price has fallen by 42% per year, which means it is significantly lagging earnings.Reported Earnings • Aug 31Full year 2024 earnings released: AU$0.007 loss per share (vs AU$0.04 loss in FY 2023)Full year 2024 results: AU$0.007 loss per share (improved from AU$0.04 loss in FY 2023). Net loss: AU$1.18m (loss narrowed 83% from FY 2023).Reported Earnings • Aug 30Full year 2023 earnings released: AU$0.04 loss per share (vs AU$0.033 loss in FY 2022)Full year 2023 results: AU$0.04 loss per share (further deteriorated from AU$0.033 loss in FY 2022). Net loss: AU$6.80m (loss widened 79% from FY 2022).すべての更新を表示Recent updatesNew Risk • Jun 26New major risk - Share price stabilityThe company's share price has been highly volatile over the past 3 months. It is more volatile than 90% of Australian stocks, typically moving 17% a week. This is considered a major risk. Share price volatility increases the risk of potential losses in the short-term as the stock tends to have larger drops in price more frequently than other stocks. It may also indicate the stock is highly sensitive to market conditions or economic conditions rather than being sensitive to its own business performance, which may also be inconsistent. Currently, the following risks have been identified for the company: Major Risks Share price has been highly volatile over the past 3 months (17% average weekly change). Revenue is less than US$1m (AU$411k revenue, or US$283k). Market cap is less than US$10m (AU$9.41m market cap, or US$6.48m). Minor Risk Shareholders have been diluted in the past year (27% increase in shares outstanding).New Risk • May 12New major risk - Market cap sizeThe company's market capitalization is less than US$10m. Market cap: AU$13.7m (US$9.88m) This is considered a major risk. Companies with a small market capitalization are most likely businesses that have not yet released a product to market or are simply a very small company without a wide reach. Either way, risk is elevated with these companies because there is a chance the product may not come to fruition or the company's addressable market or demand may not be as large as expected. In addition, if the company's size is the main factor, it is less likely to have many investors and analysts following it and scrutinizing its performance and outlook. Currently, the following risks have been identified for the company: Major Risks Revenue is less than US$1m (AU$411k revenue, or US$297k). Market cap is less than US$10m (AU$13.7m market cap, or US$9.88m). Minor Risks Share price has been volatile over the past 3 months (15% average weekly change). Shareholders have been diluted in the past year (27% increase in shares outstanding).New Risk • Apr 18New minor risk - Shareholder dilutionThe company's shareholders have been diluted in the past year. Increase in shares outstanding: 27% This is considered a minor risk. Shareholder dilution occurs when there is an increase in the number of shares on issue that is not proportionally distributed between all shareholders. Often due to the company raising equity capital or some options being converted into stock. All else being equal, if there are more shares outstanding then each existing share will be entitled to a lower proportion of the company's total earnings, thus reducing earnings per share (EPS). While dilution might not always result in lower EPS (like if the company is using the capital to fund an EPS accretive acquisition) in a lot cases it does, along with lower dividends per share and less voting power at shareholder meetings. Currently, the following risks have been identified for the company: Major Risk Revenue is less than US$1m (AU$411k revenue, or US$295k). Minor Risks Share price has been volatile over the past 3 months (14% average weekly change). Shareholders have been diluted in the past year (27% increase in shares outstanding). Market cap is less than US$100m (AU$19.4m market cap, or US$13.9m).お知らせ • Apr 17Firebrick Pharma Limited has completed a Follow-on Equity Offering in the amount of AUD 1.51692 million.Firebrick Pharma Limited has completed a Follow-on Equity Offering in the amount of AUD 1.51692 million. Security Name: Ordinary Shares Security Type: Common Stock Securities Offered: 21,636,603 Price\Range: AUD 0.047 Discount Per Security: AUD 0.00282 Security Features: Attached Options Security Name: Ordinary Shares Security Type: Common Stock Securities Offered: 10,638,298 Price\Range: AUD 0.047 Discount Per Security: AUD 0.00282 Security Features: Attached Options Transaction Features: Subsequent Direct ListingNew Risk • Apr 15New minor risk - Share price stabilityThe company's share price has been volatile over the past 3 months. It is more volatile than 75% of Australian stocks, typically moving 14% a week. This is considered a minor risk. Share price volatility indicates the stock is highly sensitive to market conditions or economic conditions rather than being sensitive to its own business performance, which may also be inconsistent. It also increases the risk of potential losses in the short term as the stock tends to have larger drops in price more frequently than other stocks. Currently, the following risks have been identified for the company: Major Risk Revenue is less than US$1m (AU$411k revenue, or US$293k). Minor Risks Share price has been volatile over the past 3 months (14% average weekly change). Market cap is less than US$100m (AU$16.9m market cap, or US$12.1m).お知らせ • Mar 31Firebrick Pharma Limited has filed a Follow-on Equity Offering in the amount of AUD 1.5 million.Firebrick Pharma Limited has filed a Follow-on Equity Offering in the amount of AUD 1.5 million. Security Name: Ordinary Shares Security Type: Common Stock Securities Offered: 31,914,893 Price\Range: AUD 0.047 Discount Per Security: AUD 0.00282 Security Features: Attached Options Transaction Features: Subsequent Direct ListingNew Risk • Feb 25New major risk - Financial positionThe company has less than a year of cash runway based on its current free cash flow trend. Free cash flow: -AU$2.3m This is considered a major risk. With less than a year's worth of cash, the company will need to raise capital or take on debt unless its cash flows improve. This would dilute existing shareholders or increase balance sheet risk. Currently, the following risks have been identified for the company: Major Risks Less than 1 year of cash runway based on free cash flow trend (-AU$2.3m free cash flow). Revenue is less than US$1m (AU$411k revenue, or US$292k). Market cap is less than US$10m (AU$13.4m market cap, or US$9.51m). Minor Risk Shareholders have been diluted in the past year (20% increase in shares outstanding).Reported Earnings • Feb 25First half 2026 earnings released: AU$0.005 loss per share (vs AU$0.007 loss in 1H 2025)First half 2026 results: AU$0.005 loss per share (improved from AU$0.007 loss in 1H 2025). Net loss: AU$1.26m (loss narrowed 13% from 1H 2025). Over the last 3 years on average, earnings per share has increased by 57% per year but the company’s share price has fallen by 36% per year, which means it is significantly lagging earnings.New Risk • Feb 20New major risk - Market cap sizeThe company's market capitalization is less than US$10m. Market cap: AU$13.4m (US$9.43m) This is considered a major risk. Companies with a small market capitalization are most likely businesses that have not yet released a product to market or are simply a very small company without a wide reach. Either way, risk is elevated with these companies because there is a chance the product may not come to fruition or the company's addressable market or demand may not be as large as expected. In addition, if the company's size is the main factor, it is less likely to have many investors and analysts following it and scrutinizing its performance and outlook. Currently, the following risks have been identified for the company: Major Risks Revenue is less than US$1m (AU$516k revenue, or US$363k). Market cap is less than US$10m (AU$13.4m market cap, or US$9.43m). Minor Risk Shareholders have been diluted in the past year (20% increase in shares outstanding).Board Change • Jan 05Less than half of directors are independentFollowing the recent departure of a director, there is only 1 independent director on the board. The company's board is composed of: 1 independent director. 2 non-independent directors. Independent Non-Executive Director Rick Legleiter was the last independent director to join the board, commencing their role in 2025. The company's minority of independent directors is a risk according to the Simply Wall St Risk Model.お知らせ • Oct 16Firebrick Pharma Limited has filed a Follow-on Equity Offering in the amount of AUD 0.102 million.Firebrick Pharma Limited has filed a Follow-on Equity Offering in the amount of AUD 0.102 million. Security Name: Ordinary Shares Security Type: Common Stock Securities Offered: 1,200,000 Price\Range: AUD 0.085 Transaction Features: Subsequent Direct Listingお知らせ • Sep 29Firebrick Pharma Limited, Annual General Meeting, Nov 26, 2025Firebrick Pharma Limited, Annual General Meeting, Nov 26, 2025.Reported Earnings • Aug 31Full year 2025 earnings released: AU$0.012 loss per share (vs AU$0.007 loss in FY 2024)Full year 2025 results: AU$0.012 loss per share (further deteriorated from AU$0.007 loss in FY 2024). Revenue: AU$524.7k (down 81% from FY 2024). Net loss: AU$2.63m (loss widened 124% from FY 2024). Over the last 3 years on average, earnings per share has increased by 50% per year but the company’s share price has fallen by 39% per year, which means it is significantly lagging earnings.お知らせ • Aug 30Firebrick Pharma Limited has completed a Follow-on Equity Offering in the amount of AUD 1.4 million.Firebrick Pharma Limited has completed a Follow-on Equity Offering in the amount of AUD 1.4 million. Security Name: Ordinary Shares Security Type: Common Stock Securities Offered: 22,222,222 Price\Range: AUD 0.063 Security Features: Attached Options Transaction Features: Subsequent Direct Listingお知らせ • Aug 26+ 1 more updateFirebrick Pharma Limited has filed a Follow-on Equity Offering in the amount of AUD 1.4 million.Firebrick Pharma Limited has filed a Follow-on Equity Offering in the amount of AUD 1.4 million. Security Name: Ordinary Shares Security Type: Common Stock Securities Offered: 22,222,222 Price\Range: AUD 0.063 Security Features: Attached Options Transaction Features: Subsequent Direct ListingNew Risk • Aug 06New minor risk - Shareholder dilutionThe company's shareholders have been diluted in the past year. Increase in shares outstanding: 16% This is considered a minor risk. Shareholder dilution occurs when there is an increase in the number of shares on issue that is not proportionally distributed between all shareholders. Often due to the company raising equity capital or some options being converted into stock. All else being equal, if there are more shares outstanding then each existing share will be entitled to a lower proportion of the company's total earnings, thus reducing earnings per share (EPS). While dilution might not always result in lower EPS (like if the company is using the capital to fund an EPS accretive acquisition) in a lot cases it does, along with lower dividends per share and less voting power at shareholder meetings. Currently, the following risks have been identified for the company: Major Risks Earnings have declined by 1.4% per year over the past 5 years. Revenue is less than US$1m (AU$1.1m revenue, or US$735k). Minor Risks Share price has been volatile over the past 3 months (15% average weekly change). Shareholders have been diluted in the past year (16% increase in shares outstanding). Market cap is less than US$100m (AU$17.7m market cap, or US$11.5m).New Risk • Jun 27New minor risk - Share price stabilityThe company's share price has been volatile over the past 3 months. It is more volatile than 75% of Australian stocks, typically moving 13% a week. This is considered a minor risk. Share price volatility indicates the stock is highly sensitive to market conditions or economic conditions rather than being sensitive to its own business performance, which may also be inconsistent. It also increases the risk of potential losses in the short term as the stock tends to have larger drops in price more frequently than other stocks. Currently, the following risks have been identified for the company: Major Risks Earnings have declined by 1.4% per year over the past 5 years. Revenue is less than US$1m (AU$1.1m revenue, or US$740k). Market cap is less than US$10m (AU$13.5m market cap, or US$8.82m). Minor Risk Share price has been volatile over the past 3 months (13% average weekly change).お知らせ • Jun 26Firebrick Pharma Limited has completed a Follow-on Equity Offering in the amount of AUD 0.195 million.Firebrick Pharma Limited has completed a Follow-on Equity Offering in the amount of AUD 0.195 million. Security Name: Ordinary Shares Security Type: Common Stock Securities Offered: 3,095,238 Price\Range: AUD 0.063 Security Features: Attached Options Transaction Features: Subsequent Direct ListingNew Risk • Apr 09New major risk - Market cap sizeThe company's market capitalization is less than US$10m. Market cap: AU$16.0m (US$9.65m) This is considered a major risk. Companies with a small market capitalization are most likely businesses that have not yet released a product to market or are simply a very small company without a wide reach. Either way, risk is elevated with these companies because there is a chance the product may not come to fruition or the company's addressable market or demand may not be as large as expected. In addition, if the company's size is the main factor, it is less likely to have many investors and analysts following it and scrutinizing its performance and outlook. Currently, the following risks have been identified for the company: Major Risks Earnings have declined by 1.4% per year over the past 5 years. Revenue is less than US$1m (AU$1.1m revenue, or US$684k). Market cap is less than US$10m (AU$16.0m market cap, or US$9.65m). Minor Risk Shareholders have been diluted in the past year (17% increase in shares outstanding).お知らせ • Mar 05Firebrick Pharma Limited announced that it expects to receive AUD 1.1 million in funding from Pharma Nutria N.a. (metro Manila Luzon), Inc.Firebrick Pharma Limited announce that it has secured an investment from Pharma Nutria N.A., Inc to issue 11,578,947 ordinary shares at a price of AUD 0.095 per share for gross proceeds of AUD 1,099,999.965 on March 4, 2025. The Shares are subject to a voluntary escrow of 12 months. The 11,578,947 Shares will represent 5.2% of all Firebrick shares outstanding and therefore PNAI will become a substantial shareholder in Firebrick.Reported Earnings • Feb 24First half 2025 earnings released: AU$0.007 loss per share (vs AU$0.005 loss in 1H 2024)First half 2025 results: AU$0.007 loss per share (further deteriorated from AU$0.005 loss in 1H 2024). Revenue: AU$197.1k (down 89% from 1H 2024). Net loss: AU$1.45m (loss widened 61% from 1H 2024). Over the last 3 years on average, earnings per share has increased by 34% per year but the company’s share price has fallen by 42% per year, which means it is significantly lagging earnings.New Risk • Feb 21New major risk - Financial positionThe company has less than a year of cash runway based on its current free cash flow trend. Free cash flow: -AU$2.0m This is considered a major risk. With less than a year's worth of cash, the company will need to raise capital or take on debt unless its cash flows improve. This would dilute existing shareholders or increase balance sheet risk. Currently, the following risks have been identified for the company: Major Risks Less than 1 year of cash runway based on free cash flow trend (-AU$2.0m free cash flow). Earnings have declined by 1.4% per year over the past 5 years. Revenue is less than US$1m (AU$1.1m revenue, or US$720k). Minor Risks Share price has been volatile over the past 3 months (11% average weekly change). Shareholders have been diluted in the past year (17% increase in shares outstanding). Market cap is less than US$100m (AU$17.6m market cap, or US$11.3m).New Risk • Feb 10New minor risk - Share price stabilityThe company's share price has been volatile over the past 3 months. It is more volatile than 75% of Australian stocks, typically moving 12% a week. This is considered a minor risk. Share price volatility indicates the stock is highly sensitive to market conditions or economic conditions rather than being sensitive to its own business performance, which may also be inconsistent. It also increases the risk of potential losses in the short term as the stock tends to have larger drops in price more frequently than other stocks. Currently, the following risks have been identified for the company: Major Risk Earnings have declined by 14% per year over the past 5 years. Minor Risks Share price has been volatile over the past 3 months (12% average weekly change). Shareholders have been diluted in the past year (17% increase in shares outstanding). Revenue is less than US$5m (AU$2.8m revenue, or US$1.7m). Market cap is less than US$100m (AU$17.9m market cap, or US$11.2m).お知らせ • Oct 29Firebrick Pharma Limited, Annual General Meeting, Nov 27, 2024Firebrick Pharma Limited, Annual General Meeting, Nov 27, 2024.お知らせ • Oct 17Firebrick Pharma Limited has completed a Follow-on Equity Offering in the amount of AUD 0.1587 million.Firebrick Pharma Limited has completed a Follow-on Equity Offering in the amount of AUD 0.1587 million. Security Name: Ordinary Shares Security Type: Common Stock Securities Offered: 2,885,454 Price\Range: AUD 0.055 Discount Per Security: AUD 0 Transaction Features: Subsequent Direct Listingお知らせ • Sep 12+ 1 more updateFirebrick Pharma Limited has filed a Follow-on Equity Offering in the amount of AUD 2 million.Firebrick Pharma Limited has filed a Follow-on Equity Offering in the amount of AUD 2 million. Security Name: Ordinary Shares Security Type: Common Stock Securities Offered: 36,363,636 Price\Range: AUD 0.055Reported Earnings • Aug 31Full year 2024 earnings released: AU$0.007 loss per share (vs AU$0.04 loss in FY 2023)Full year 2024 results: AU$0.007 loss per share (improved from AU$0.04 loss in FY 2023). Net loss: AU$1.18m (loss narrowed 83% from FY 2023).お知らせ • May 17Firebrick Pharma Limited has filed a Follow-on Equity Offering in the amount of AUD 0.8 million.Firebrick Pharma Limited has filed a Follow-on Equity Offering in the amount of AUD 0.8 million. Security Name: Ordinary Shares Security Type: Common Stock Securities Offered: 16,000,000 Price\Range: AUD 0.05 Transaction Features: Subsequent Direct ListingNew Risk • Apr 17New minor risk - Share price stabilityThe company's share price has been volatile over the past 3 months. It is more volatile than 75% of Australian stocks, typically moving 17% a week. This is considered a minor risk. Share price volatility indicates the stock is highly sensitive to market conditions or economic conditions rather than being sensitive to its own business performance, which may also be inconsistent. It also increases the risk of potential losses in the short term as the stock tends to have larger drops in price more frequently than other stocks. Currently, the following risks have been identified for the company: Major Risks Less than 1 year of cash runway based on free cash flow trend (-AU$4.6m free cash flow). Earnings have declined by 34% per year over the past 5 years. Market cap is less than US$10m (AU$9.13m market cap, or US$5.85m). Minor Risks Share price has been volatile over the past 3 months (17% average weekly change). Shareholders have been diluted in the past year (5.5% increase in shares outstanding). Revenue is less than US$5m (AU$1.8m revenue, or US$1.2m).お知らせ • Sep 15Firebrick Pharma Limited Announces That Trial Statisticians Have Completed Their Efficacy Analysis of the Headline Results in the Phase 3 Trial of Nasodine® Nasal Spray as A Treatment for the Common ColdFirebrick Pharma Limited announced that trial statisticians have completed their efficacy analysis of the headline results in the Phase 3 trial of Nasodine® Nasal Spray as a treatment for the common cold. The analysis has shown that the trial did not meet its primary endpoint, which was the impact of Nasodine on overall cold severity (GSS) in subjects with a confirmed viral infection (ITTi). Based on the reported results, the placebo (sterile water) performed better than Nasodine. In the QoL (`quality-of-life') measure (functional impairment caused by a cold), the results were also in favour of the placebo in the ITTi. Similar enigmatic results were seen in other population subsets. The results provided to the Company are shown in the table titled: Trial Headline Results Summary. These results are compared in summary form with the previous (2019) Phase 3 trial in the table titled: Phase 3 Trial Comparisons on Key Endpoints. The 2019 trial used the same protocol and treatment regimen as the current (2022-23) trialand both trials were robust Phase 3 trials. The 2019 trial took place in Australia, so a comparison of the results with the current trial for Australian sites only has been undertaken (not shown in summary tables). In the 2019 trial, the GSS benefit of Nasodine in the viral-infected subjects (N=52) was 22.9% (p=0.048), but in the current trial, for Australian sites, the benefit was reversed, with the water placebo outperforming Nasodine by 22.7% in the ITTi (N=181), the result being statistically significant (p=0.024). The reported results also appear to conflict with the Company's recently reported Phase 2 COVID-19 trial, where Nasodine treatment led to 100% clearance of the SARS-CoV-2 virus from the nasal passages. That result was significantly better than the placebo (p=0.028), which was the same water placebo as used in the 2022-23 Phase 3 trial. The Company is concerned that the results are so confounding, unexpected and at odds with previous data that there may be a systematic error or other issue in the data, and a detailed analysis is now underway to try to identify any causes of such an error. To that end, the Company is working with the Contract Research Organisation (CRO) responsible for trial governance and other service providers to thoroughly investigate the trial results. At this time, there is no evidence that the placebo and Nasodine treatments were switched during production, distribution or treatment.Reported Earnings • Aug 30Full year 2023 earnings released: AU$0.04 loss per share (vs AU$0.033 loss in FY 2022)Full year 2023 results: AU$0.04 loss per share (further deteriorated from AU$0.033 loss in FY 2022). Net loss: AU$6.80m (loss widened 79% from FY 2022).分析記事 • Aug 14Here's Why We're Watching Firebrick Pharma's (ASX:FRE) Cash Burn SituationJust because a business does not make any money, does not mean that the stock will go down. For example, although...お知らせ • Jul 22Firebrick Update on Administrative Appeals Tribunal ProcessFirebrick Pharma Limited announced that the scheduled conciliation meeting with the TGA (Therapeutic Goods Administration), which was moderated by the Administrative Appeals Tribunal (AAT) took place in Sydney on 19 July 2023. The meeting between the parties was cordial with a frank exchange on the issues relating to the approval of Nasodine Nasal Spray ("Nasodine"). Confidential discussions between the parties are ongoing and Firebrick is hopeful that an agreement on the approval of Nasodine can be reached. This announcement was authorized for release by Dr. Peter Molloy, Executive Chairman, Firebrick Pharma Limited.お知らせ • May 16Firebrick Pharma Limited, Annual General Meeting, Jun 20, 2023Firebrick Pharma Limited, Annual General Meeting, Jun 20, 2023, at 11:00 E. Australia Standard Time. Agenda: To consider the ratification of tranche 1 placement shares; to consider the issue of tranche 2 placement shares to related party Stephen Goodall; and to consider the issue of tranche 2 placement shares to related party Peter Molloy.分析記事 • May 02We Think Firebrick Pharma (ASX:FRE) Needs To Drive Business Growth CarefullyThere's no doubt that money can be made by owning shares of unprofitable businesses. For example, although Amazon.com...分析記事 • Dec 14We Think Firebrick Pharma (ASX:FRE) Needs To Drive Business Growth CarefullyThere's no doubt that money can be made by owning shares of unprofitable businesses. For example, although...Board Change • Nov 16No independent directorsFollowing the recent departure of a director, there are no independent directors on the board. The company's board is composed of: No independent directors. 4 non-independent directors. Non-Executive Director Richard Treagus was the last director to join the board, commencing their role in 2022. The company's lack of independent directors is a risk according to the Simply Wall St Risk Model.お知らせ • Nov 14Firebrick Pharma Limited Announces CFO ChangesFirebrick Pharma Limited advises that Ms Kyla Garic has resigned her position as Chief Financial Officer (CFO). and through her company, Onyx Corporate, the provision of accounting and bookkeeping services for Firebrick, with an effective date of 25 January 2023. The Company also advise that Mr. Kavi Bekarma will take over the CFO duties and through his company, TripleEight Corporate, the provision of accounting and bookkeeping services for the Company from 1 December 2022 to allow for a smooth handover before 25 January 2023. Kavi Bekarma is the Managing Director of TripleEight Corporate, a corporate accounting firm offering various services for listed and non-listed companies in the mining, oil and gas, technology and biotechnology sectors. Mr. Bekarma is a Chartered Accountant of Australia and New Zealand, holds a Masters of Professional Accounting and a Bachelor's Degree in Management with Information Systems.お知らせ • Nov 01Firebrick Pharma Limited Provides Update on its Phase 3 Clinical Trial of Nasodine Nasal Spray in Treatment of Common ColdFirebrick Pharma Limited provided an update on its Phase 3 clinical trial of Nasodine Nasal Spray in the treatment of the common cold. As at 31 October, the trial has so far successfully recruited 224 subjects with early-stage colds into the ITT (Intent-To-Treat population), with an estimated 100 qualifying for the primary endpoint population of those with confirmed viral infection (ITTi), based on PCR of a throat and nasal swab. This represents at least 51% of the trial's full recruitment target of 196 subjects in the ITTi. The primary endpoint for the trial is the benefit of Nasodine treatment on overall cold severity 2 in the ITT. In the previous Phase 3 trial, Nasodine produced a statistically significant benefit in the 52 subjects who had confirmed viral infection (see p. 20 of the Company's Prospectus). The current Phase 3 trial was designed to support international registration of Nasodine and if completed by mid-2023, the EU application for approval could be filed by the end of calendar 2023. The US application will require a further Phase 3 trial to be conducted in the US.お知らせ • Oct 27Rebrick Pharma Limited Announces Nasodine Patent Granted in SingaporeFirebrick Pharma Limited announced that its patent covering Nasodine® Nasal Spray ("Nasodine") as a treatment and preventative for the common cold has been granted in Singapore. The patent is still pending in Canada and Japan. The pending application in China has now been withdrawn, following a recent assessment of the likelihood and costs of gaining any commercially-useful protection in that market. Granted claims include treating and preventing colds, reducing the viral load of common cold viruses, prevention of secondary complications of colds, and reducing the risk of serious complications in at-risk populations.お知らせ • Sep 28Firebrick Pharma Limited, Annual General Meeting, Nov 23, 2022Firebrick Pharma Limited, Annual General Meeting, Nov 23, 2022, at 15:00 AUS Eastern Standard Time. Location: Level 18, 600 Bourke Street, Melbourne, Melbourne Victoria Australia分析記事 • Aug 30Companies Like Firebrick Pharma (ASX:FRE) Are In A Position To Invest In GrowthEven when a business is losing money, it's possible for shareholders to make money if they buy a good business at the...お知らせ • May 26Firebrick Appoints Richard Treagus as DirectorFirebrick Pharma Limited announced the appointment of Dr. Richard Treagus as a non-executive director on the Firebrick board of directors, with effect from 1 June 2022. Dr. Treagus was previously Commercial Director for Aspen Pharmacare in South Africa, responsible for sales and marketing of pharmacy and consumer products. More recently, from 2006 to 2012, he was CEO of Acrux Limited, which grew 10-fold in value during his tenure and from 2013 to 2020, he was Executive Chairman of Neuren Pharmaceuticals Limited, which grew 6-fold in value during his tenure.お知らせ • May 04Firebrick Pharma Limited Starts Phase 3 Common Cold TrialFirebrick Pharma Limited announced that the first patient has been recruited into its confirmatory Phase 3 trial for Nasodine® Nasal Spray ("Nasodine") as a treatment for the common cold. The randomized controlled Phase 3 trial expects to recruit up to 450 adult subjects with early cold symptoms to achieve a target treatment population of 196 subjects, who are confirmed by PCR, to have a viral cold. The primary endpoint of the trial will be the impact of Nasodine treatment (3 sprays per nostril, 4 times daily for 5 days) on overall cold severity in the viral-infected population. Overall cold severity will be measured using the Global Severity Score (GSS) from the WURSS-21 cold severity survey. The trial is a multi-centre international study, with recruitment planned at three sites in Australia and two sites in South Africa. The first site to recruit patients is in Adelaide, with Victorian and South African sites planned to come online over the next month. Trial recruitment at all sites is expected to be completed by October this year. Any subjects found by PCR testing to have SARS-CoV-2 infection (COVID-19) will be excluded from the population for assessment of the primary endpoint but retained in the overall study population for assessment of some secondary endpoints. The company has previously completed a Phase 3 trial for the common cold in 2019 at sites in Adelaide and Brisbane. Following the completion of the trial, Firebrick filed a registration dossier with the TGA to determine whether Nasodine could be approved as an OTC (over the counter) treatment for the common cold based on then current data. The TGA has since provided advice to the Company that it has no concerns with the quality or safety of Nasodine, but that clinical efficacy was not satisfactorily established. This second Phase 3 trial was originally intended to support international regulatory approvals, but if the Australian appeal is unsuccessful, it will also be used to support approval in Australia.Board Change • Apr 27No independent directorsFollowing the recent departure of a director, there are no independent directors on the board. The company's board is composed of: No independent directors. 4 non-independent directors. Non-Executive Director Phyllis Gardner was the last director to join the board, commencing their role in 2020. The company's lack of independent directors is a risk according to the Simply Wall St Risk Model.お知らせ • Apr 26Firebrick Pharma Limited Starts COVID-19 Trial of NasodineFirebrick Pharma Limited announced that the first patient had been recruited into its Phase 2 clinical trial in South Africa of Nasodine® Nasal Spray ("Nasodine") for the management of COVID-19. The trial is scheduled to recruit up to 210 adults who are COVID-positive by Rapid Antigen Test (RAT) to achieve a target treatment population of 144 subjects who will be confirmed by viral culture to be shedding SARS-CoV-2 virus. Depending on patient recruitment, the trial could be completed by August 2022. The study is a randomised, placebo-controlled Phase 2 trial, titled: `Reduction of nasal shedding of SARS-CoV-2 in COVID-19 positive patients by the use of Nasodine® (povidone- iodine 0.5%) Nasal Spray.' The short title for the trial is `Nasodine for Elimination of COVID- 19 Shedding study' or `NASO-ELOCS'. The primary aim of the trial will be to show that frequent Nasodine application (every 2 hours,up to eight-times-daily) over three days leads to a significant reduction in nasal shedding of SARS-CoV-2 virus, compared with a placebo nasal spray. Secondary aims will include whether Nasodine treatment (compared with placebo) reduces the number of days to a negative RAT and increases the percentage of subjects who have cleared the virus from the upper respiratory tract within 5 days, based on a combined throat and nasal swab. Prior to gaining regulatory approval for any role in the management of COVID-19, Nasodine would likely need to undergo a confirmatory Phase 3 trial in a specific aspect of COVID-19 that is clinically relevant to the management of the disease. Nasodine has already completed a Phase 3 clinical trial as a treatment for the common cold and Firebrick is preparing to start a second Phase 3 common cold trial this year, in order to support international regulatory approvals, and if the Australian appeal is unsuccessful it will also be used to support approval in Australia.お知らせ • Feb 11Firebrick Pharma Limited Announces the Results of in Vitro Studies of Nasodine® Nasal SprayFirebrick Pharma Limited announced that the results of in vitro studies of Nasodine® Nasal Spray (povidone-iodine 0.5%) against SARS-CoV-2, and a pilot human study in a small number of COVID-19 subjects, had been published in the Australian Journal of Otolaryngology (AJO). The in vitro experiments showed a 15-second exposure to Nasodine Nasal Spray (Nasodine) reduced infectivity of SARS-CoV-2 by 99.97%, while a 60-second exposure completely eliminated viral infectivity. The subsequent in vivo pilot study of six COVID-19 patients who were shedding the virus from the nose, showed that a single Nasodine dose (4 sprays per nostril) reduced viral shedding in 5 of the 6 subjects (83%) at 5 minutes after the dose, with an overall 79% reduction in viral shedding at one hour after the dose.お知らせ • Feb 01Firebrick Pharma Limited Announces That Its Planned Clinical Trial of Nasodine Nasal Spray (Povidone-Iodine 0.5%) in Covid-19 Patients in South Africa, Had Received Approval to Proceed from the South African Health Products Regulatory AuthorityFirebrick Pharma Limited announced that its planned clinical trial of Nasodine Nasal Spray (povidone-iodine 0.5%) in COVID-19 patients in South Africa, had received approval to proceed from the South African Health Products Regulatory Authority (SAHPRA). The trial is titled: "Reduction of nasal shedding of SARS-CoV-2 in COVID-19 positive patients by the use of Nasodine® (povidone-iodine 0.5%) Nasal Spray." It is intended to demonstrate that frequent, repeated application of Nasodine Nasal Spray ("Nasodine") in COVID-19 subjects who are RAT-positive, leads to reduction or elimination of nasal shedding of the Sars-CoV-2 virus. The SAHPRA approval specifically allows Firebrick Pharma to import Nasodine into South Africa for the trial and to administer the product to patients during the trial, according to the trial protocol submitted to SAHPRA. As noted in the Company's prospectus (section 2.4.4(b)), prior to commencing the trial the Company will also need approval from the local clinical Ethics Committee, which has been applied for but has yet to be received.Board Change • Jan 28No independent directorsFollowing the recent departure of a director, there are no independent directors on the board. The company's board is composed of: No independent directors. 3 non-independent directors. Non-Executive Director Phyllis Gardner was the last director to join the board, commencing their role in 2020. The company's lack of independent directors is a risk according to the Simply Wall St Risk Model.収支内訳Firebrick Pharma の稼ぎ方とお金の使い方。LTMベースの直近の報告された収益に基づく。収益と収入の歴史ASX:FRE 収益、費用、利益 ( )AUD Millions日付収益収益G+A経費研究開発費31 Dec 250-22130 Sep 250-32130 Jun 251-32131 Mar 251-22131 Dec 241-22130 Sep 242-12130 Jun 243-12231 Mar 242-32331 Dec 232-52430 Sep 231-62430 Jun 230-72431 Mar 231-62431 Dec 221-52430 Sep 221-52330 Jun 221-42231 Mar 221-32231 Dec 210-32130 Sep 210-32130 Jun 210-22130 Jun 201-10230 Jun 190-101質の高い収益: FREは現在利益が出ていません。利益率の向上: FREは現在利益が出ていません。フリー・キャッシュフローと収益の比較過去の収益成長分析収益動向: FREは利益を出していないが、過去 5 年間で年間11.3%の割合で損失を削減してきた。成長の加速: FREの過去 1 年間の収益成長を 5 年間の平均と比較することはできません。現在は利益が出ていないためです。収益対業界: FREは利益が出ていないため、過去 1 年間の収益成長をPharmaceuticals業界 ( 1.2% ) と比較することは困難です。株主資本利益率高いROE: FREは現在利益が出ていないため、自己資本利益率 ( -126.43% ) はマイナスです。総資産利益率使用総資本利益率過去の好業績企業の発掘7D1Y7D1Y7D1YPharmaceuticals-biotech 、過去の業績が好調な企業。View Financial Health企業分析と財務データの現状データ最終更新日（UTC時間）企業分析2026/08/21 18:39終値2026/08/20 00:00収益2025/12/31年間収益2025/06/30データソース企業分析に使用したデータはS&P Global Market Intelligence LLC のものです。本レポートを作成するための分析モデルでは、以下のデータを使用しています。データは正規化されているため、ソースが利用可能になるまでに時間がかかる場合があります。パッケージデータタイムフレーム米国ソース例会社財務10年損益計算書キャッシュ・フロー計算書貸借対照表SECフォーム10-KSECフォーム10-Qアナリストのコンセンサス予想+プラス3年予想財務アナリストの目標株価アナリストリサーチレポートBlue Matrix市場価格30年株価配当、分割、措置ICEマーケットデータSECフォームS-1所有権10年トップ株主インサイダー取引SECフォーム4SECフォーム13Dマネジメント10年リーダーシップ・チーム取締役会SECフォーム10-KSECフォームDEF 14A主な進展10年会社からのお知らせSECフォーム8-K* 米国証券を対象とした例であり、非米国証券については、同等の規制書式および情報源を使用。特に断りのない限り、すべての財務データは1年ごとの期間に基づいていますが、四半期ごとに更新されます。これは、TTM（Trailing Twelve Month）またはLTM（Last Twelve Month）データとして知られています。詳細はこちら。分析モデルとスノーフレークこのレポートを生成するために使用した分析モデルの詳細は、当社のGitHubページでご覧いただけます。また、レポートの活用方法に関するガイドやYouTubeのチュートリアルも用意しています。シンプリー・ウォールストリート分析モデルを設計・構築した世界トップクラスのチームについてご紹介します。業界およびセクターの指標私たちの業界とセクションの指標は、Simply Wall Stによって6時間ごとに計算されます。アナリスト筋Firebrick Pharma Limited 0 これらのアナリストのうち、弊社レポートのインプットとして使用した売上高または利益の予想を提出したのは、 。アナリストの投稿は一日中更新されます。0
Reported Earnings • Feb 25First half 2026 earnings released: AU$0.005 loss per share (vs AU$0.007 loss in 1H 2025)First half 2026 results: AU$0.005 loss per share (improved from AU$0.007 loss in 1H 2025). Net loss: AU$1.26m (loss narrowed 13% from 1H 2025). Over the last 3 years on average, earnings per share has increased by 57% per year but the company’s share price has fallen by 36% per year, which means it is significantly lagging earnings.
Reported Earnings • Aug 31Full year 2025 earnings released: AU$0.012 loss per share (vs AU$0.007 loss in FY 2024)Full year 2025 results: AU$0.012 loss per share (further deteriorated from AU$0.007 loss in FY 2024). Revenue: AU$524.7k (down 81% from FY 2024). Net loss: AU$2.63m (loss widened 124% from FY 2024). Over the last 3 years on average, earnings per share has increased by 50% per year but the company’s share price has fallen by 39% per year, which means it is significantly lagging earnings.
Reported Earnings • Feb 24First half 2025 earnings released: AU$0.007 loss per share (vs AU$0.005 loss in 1H 2024)First half 2025 results: AU$0.007 loss per share (further deteriorated from AU$0.005 loss in 1H 2024). Revenue: AU$197.1k (down 89% from 1H 2024). Net loss: AU$1.45m (loss widened 61% from 1H 2024). Over the last 3 years on average, earnings per share has increased by 34% per year but the company’s share price has fallen by 42% per year, which means it is significantly lagging earnings.
Reported Earnings • Aug 31Full year 2024 earnings released: AU$0.007 loss per share (vs AU$0.04 loss in FY 2023)Full year 2024 results: AU$0.007 loss per share (improved from AU$0.04 loss in FY 2023). Net loss: AU$1.18m (loss narrowed 83% from FY 2023).
Reported Earnings • Aug 30Full year 2023 earnings released: AU$0.04 loss per share (vs AU$0.033 loss in FY 2022)Full year 2023 results: AU$0.04 loss per share (further deteriorated from AU$0.033 loss in FY 2022). Net loss: AU$6.80m (loss widened 79% from FY 2022).
New Risk • Jun 26New major risk - Share price stabilityThe company's share price has been highly volatile over the past 3 months. It is more volatile than 90% of Australian stocks, typically moving 17% a week. This is considered a major risk. Share price volatility increases the risk of potential losses in the short-term as the stock tends to have larger drops in price more frequently than other stocks. It may also indicate the stock is highly sensitive to market conditions or economic conditions rather than being sensitive to its own business performance, which may also be inconsistent. Currently, the following risks have been identified for the company: Major Risks Share price has been highly volatile over the past 3 months (17% average weekly change). Revenue is less than US$1m (AU$411k revenue, or US$283k). Market cap is less than US$10m (AU$9.41m market cap, or US$6.48m). Minor Risk Shareholders have been diluted in the past year (27% increase in shares outstanding).
New Risk • May 12New major risk - Market cap sizeThe company's market capitalization is less than US$10m. Market cap: AU$13.7m (US$9.88m) This is considered a major risk. Companies with a small market capitalization are most likely businesses that have not yet released a product to market or are simply a very small company without a wide reach. Either way, risk is elevated with these companies because there is a chance the product may not come to fruition or the company's addressable market or demand may not be as large as expected. In addition, if the company's size is the main factor, it is less likely to have many investors and analysts following it and scrutinizing its performance and outlook. Currently, the following risks have been identified for the company: Major Risks Revenue is less than US$1m (AU$411k revenue, or US$297k). Market cap is less than US$10m (AU$13.7m market cap, or US$9.88m). Minor Risks Share price has been volatile over the past 3 months (15% average weekly change). Shareholders have been diluted in the past year (27% increase in shares outstanding).
New Risk • Apr 18New minor risk - Shareholder dilutionThe company's shareholders have been diluted in the past year. Increase in shares outstanding: 27% This is considered a minor risk. Shareholder dilution occurs when there is an increase in the number of shares on issue that is not proportionally distributed between all shareholders. Often due to the company raising equity capital or some options being converted into stock. All else being equal, if there are more shares outstanding then each existing share will be entitled to a lower proportion of the company's total earnings, thus reducing earnings per share (EPS). While dilution might not always result in lower EPS (like if the company is using the capital to fund an EPS accretive acquisition) in a lot cases it does, along with lower dividends per share and less voting power at shareholder meetings. Currently, the following risks have been identified for the company: Major Risk Revenue is less than US$1m (AU$411k revenue, or US$295k). Minor Risks Share price has been volatile over the past 3 months (14% average weekly change). Shareholders have been diluted in the past year (27% increase in shares outstanding). Market cap is less than US$100m (AU$19.4m market cap, or US$13.9m).
お知らせ • Apr 17Firebrick Pharma Limited has completed a Follow-on Equity Offering in the amount of AUD 1.51692 million.Firebrick Pharma Limited has completed a Follow-on Equity Offering in the amount of AUD 1.51692 million. Security Name: Ordinary Shares Security Type: Common Stock Securities Offered: 21,636,603 Price\Range: AUD 0.047 Discount Per Security: AUD 0.00282 Security Features: Attached Options Security Name: Ordinary Shares Security Type: Common Stock Securities Offered: 10,638,298 Price\Range: AUD 0.047 Discount Per Security: AUD 0.00282 Security Features: Attached Options Transaction Features: Subsequent Direct Listing
New Risk • Apr 15New minor risk - Share price stabilityThe company's share price has been volatile over the past 3 months. It is more volatile than 75% of Australian stocks, typically moving 14% a week. This is considered a minor risk. Share price volatility indicates the stock is highly sensitive to market conditions or economic conditions rather than being sensitive to its own business performance, which may also be inconsistent. It also increases the risk of potential losses in the short term as the stock tends to have larger drops in price more frequently than other stocks. Currently, the following risks have been identified for the company: Major Risk Revenue is less than US$1m (AU$411k revenue, or US$293k). Minor Risks Share price has been volatile over the past 3 months (14% average weekly change). Market cap is less than US$100m (AU$16.9m market cap, or US$12.1m).
お知らせ • Mar 31Firebrick Pharma Limited has filed a Follow-on Equity Offering in the amount of AUD 1.5 million.Firebrick Pharma Limited has filed a Follow-on Equity Offering in the amount of AUD 1.5 million. Security Name: Ordinary Shares Security Type: Common Stock Securities Offered: 31,914,893 Price\Range: AUD 0.047 Discount Per Security: AUD 0.00282 Security Features: Attached Options Transaction Features: Subsequent Direct Listing
New Risk • Feb 25New major risk - Financial positionThe company has less than a year of cash runway based on its current free cash flow trend. Free cash flow: -AU$2.3m This is considered a major risk. With less than a year's worth of cash, the company will need to raise capital or take on debt unless its cash flows improve. This would dilute existing shareholders or increase balance sheet risk. Currently, the following risks have been identified for the company: Major Risks Less than 1 year of cash runway based on free cash flow trend (-AU$2.3m free cash flow). Revenue is less than US$1m (AU$411k revenue, or US$292k). Market cap is less than US$10m (AU$13.4m market cap, or US$9.51m). Minor Risk Shareholders have been diluted in the past year (20% increase in shares outstanding).
Reported Earnings • Feb 25First half 2026 earnings released: AU$0.005 loss per share (vs AU$0.007 loss in 1H 2025)First half 2026 results: AU$0.005 loss per share (improved from AU$0.007 loss in 1H 2025). Net loss: AU$1.26m (loss narrowed 13% from 1H 2025). Over the last 3 years on average, earnings per share has increased by 57% per year but the company’s share price has fallen by 36% per year, which means it is significantly lagging earnings.
New Risk • Feb 20New major risk - Market cap sizeThe company's market capitalization is less than US$10m. Market cap: AU$13.4m (US$9.43m) This is considered a major risk. Companies with a small market capitalization are most likely businesses that have not yet released a product to market or are simply a very small company without a wide reach. Either way, risk is elevated with these companies because there is a chance the product may not come to fruition or the company's addressable market or demand may not be as large as expected. In addition, if the company's size is the main factor, it is less likely to have many investors and analysts following it and scrutinizing its performance and outlook. Currently, the following risks have been identified for the company: Major Risks Revenue is less than US$1m (AU$516k revenue, or US$363k). Market cap is less than US$10m (AU$13.4m market cap, or US$9.43m). Minor Risk Shareholders have been diluted in the past year (20% increase in shares outstanding).
Board Change • Jan 05Less than half of directors are independentFollowing the recent departure of a director, there is only 1 independent director on the board. The company's board is composed of: 1 independent director. 2 non-independent directors. Independent Non-Executive Director Rick Legleiter was the last independent director to join the board, commencing their role in 2025. The company's minority of independent directors is a risk according to the Simply Wall St Risk Model.
お知らせ • Oct 16Firebrick Pharma Limited has filed a Follow-on Equity Offering in the amount of AUD 0.102 million.Firebrick Pharma Limited has filed a Follow-on Equity Offering in the amount of AUD 0.102 million. Security Name: Ordinary Shares Security Type: Common Stock Securities Offered: 1,200,000 Price\Range: AUD 0.085 Transaction Features: Subsequent Direct Listing
お知らせ • Sep 29Firebrick Pharma Limited, Annual General Meeting, Nov 26, 2025Firebrick Pharma Limited, Annual General Meeting, Nov 26, 2025.
Reported Earnings • Aug 31Full year 2025 earnings released: AU$0.012 loss per share (vs AU$0.007 loss in FY 2024)Full year 2025 results: AU$0.012 loss per share (further deteriorated from AU$0.007 loss in FY 2024). Revenue: AU$524.7k (down 81% from FY 2024). Net loss: AU$2.63m (loss widened 124% from FY 2024). Over the last 3 years on average, earnings per share has increased by 50% per year but the company’s share price has fallen by 39% per year, which means it is significantly lagging earnings.
お知らせ • Aug 30Firebrick Pharma Limited has completed a Follow-on Equity Offering in the amount of AUD 1.4 million.Firebrick Pharma Limited has completed a Follow-on Equity Offering in the amount of AUD 1.4 million. Security Name: Ordinary Shares Security Type: Common Stock Securities Offered: 22,222,222 Price\Range: AUD 0.063 Security Features: Attached Options Transaction Features: Subsequent Direct Listing
お知らせ • Aug 26+ 1 more updateFirebrick Pharma Limited has filed a Follow-on Equity Offering in the amount of AUD 1.4 million.Firebrick Pharma Limited has filed a Follow-on Equity Offering in the amount of AUD 1.4 million. Security Name: Ordinary Shares Security Type: Common Stock Securities Offered: 22,222,222 Price\Range: AUD 0.063 Security Features: Attached Options Transaction Features: Subsequent Direct Listing
New Risk • Aug 06New minor risk - Shareholder dilutionThe company's shareholders have been diluted in the past year. Increase in shares outstanding: 16% This is considered a minor risk. Shareholder dilution occurs when there is an increase in the number of shares on issue that is not proportionally distributed between all shareholders. Often due to the company raising equity capital or some options being converted into stock. All else being equal, if there are more shares outstanding then each existing share will be entitled to a lower proportion of the company's total earnings, thus reducing earnings per share (EPS). While dilution might not always result in lower EPS (like if the company is using the capital to fund an EPS accretive acquisition) in a lot cases it does, along with lower dividends per share and less voting power at shareholder meetings. Currently, the following risks have been identified for the company: Major Risks Earnings have declined by 1.4% per year over the past 5 years. Revenue is less than US$1m (AU$1.1m revenue, or US$735k). Minor Risks Share price has been volatile over the past 3 months (15% average weekly change). Shareholders have been diluted in the past year (16% increase in shares outstanding). Market cap is less than US$100m (AU$17.7m market cap, or US$11.5m).
New Risk • Jun 27New minor risk - Share price stabilityThe company's share price has been volatile over the past 3 months. It is more volatile than 75% of Australian stocks, typically moving 13% a week. This is considered a minor risk. Share price volatility indicates the stock is highly sensitive to market conditions or economic conditions rather than being sensitive to its own business performance, which may also be inconsistent. It also increases the risk of potential losses in the short term as the stock tends to have larger drops in price more frequently than other stocks. Currently, the following risks have been identified for the company: Major Risks Earnings have declined by 1.4% per year over the past 5 years. Revenue is less than US$1m (AU$1.1m revenue, or US$740k). Market cap is less than US$10m (AU$13.5m market cap, or US$8.82m). Minor Risk Share price has been volatile over the past 3 months (13% average weekly change).
お知らせ • Jun 26Firebrick Pharma Limited has completed a Follow-on Equity Offering in the amount of AUD 0.195 million.Firebrick Pharma Limited has completed a Follow-on Equity Offering in the amount of AUD 0.195 million. Security Name: Ordinary Shares Security Type: Common Stock Securities Offered: 3,095,238 Price\Range: AUD 0.063 Security Features: Attached Options Transaction Features: Subsequent Direct Listing
New Risk • Apr 09New major risk - Market cap sizeThe company's market capitalization is less than US$10m. Market cap: AU$16.0m (US$9.65m) This is considered a major risk. Companies with a small market capitalization are most likely businesses that have not yet released a product to market or are simply a very small company without a wide reach. Either way, risk is elevated with these companies because there is a chance the product may not come to fruition or the company's addressable market or demand may not be as large as expected. In addition, if the company's size is the main factor, it is less likely to have many investors and analysts following it and scrutinizing its performance and outlook. Currently, the following risks have been identified for the company: Major Risks Earnings have declined by 1.4% per year over the past 5 years. Revenue is less than US$1m (AU$1.1m revenue, or US$684k). Market cap is less than US$10m (AU$16.0m market cap, or US$9.65m). Minor Risk Shareholders have been diluted in the past year (17% increase in shares outstanding).
お知らせ • Mar 05Firebrick Pharma Limited announced that it expects to receive AUD 1.1 million in funding from Pharma Nutria N.a. (metro Manila Luzon), Inc.Firebrick Pharma Limited announce that it has secured an investment from Pharma Nutria N.A., Inc to issue 11,578,947 ordinary shares at a price of AUD 0.095 per share for gross proceeds of AUD 1,099,999.965 on March 4, 2025. The Shares are subject to a voluntary escrow of 12 months. The 11,578,947 Shares will represent 5.2% of all Firebrick shares outstanding and therefore PNAI will become a substantial shareholder in Firebrick.
Reported Earnings • Feb 24First half 2025 earnings released: AU$0.007 loss per share (vs AU$0.005 loss in 1H 2024)First half 2025 results: AU$0.007 loss per share (further deteriorated from AU$0.005 loss in 1H 2024). Revenue: AU$197.1k (down 89% from 1H 2024). Net loss: AU$1.45m (loss widened 61% from 1H 2024). Over the last 3 years on average, earnings per share has increased by 34% per year but the company’s share price has fallen by 42% per year, which means it is significantly lagging earnings.
New Risk • Feb 21New major risk - Financial positionThe company has less than a year of cash runway based on its current free cash flow trend. Free cash flow: -AU$2.0m This is considered a major risk. With less than a year's worth of cash, the company will need to raise capital or take on debt unless its cash flows improve. This would dilute existing shareholders or increase balance sheet risk. Currently, the following risks have been identified for the company: Major Risks Less than 1 year of cash runway based on free cash flow trend (-AU$2.0m free cash flow). Earnings have declined by 1.4% per year over the past 5 years. Revenue is less than US$1m (AU$1.1m revenue, or US$720k). Minor Risks Share price has been volatile over the past 3 months (11% average weekly change). Shareholders have been diluted in the past year (17% increase in shares outstanding). Market cap is less than US$100m (AU$17.6m market cap, or US$11.3m).
New Risk • Feb 10New minor risk - Share price stabilityThe company's share price has been volatile over the past 3 months. It is more volatile than 75% of Australian stocks, typically moving 12% a week. This is considered a minor risk. Share price volatility indicates the stock is highly sensitive to market conditions or economic conditions rather than being sensitive to its own business performance, which may also be inconsistent. It also increases the risk of potential losses in the short term as the stock tends to have larger drops in price more frequently than other stocks. Currently, the following risks have been identified for the company: Major Risk Earnings have declined by 14% per year over the past 5 years. Minor Risks Share price has been volatile over the past 3 months (12% average weekly change). Shareholders have been diluted in the past year (17% increase in shares outstanding). Revenue is less than US$5m (AU$2.8m revenue, or US$1.7m). Market cap is less than US$100m (AU$17.9m market cap, or US$11.2m).
お知らせ • Oct 29Firebrick Pharma Limited, Annual General Meeting, Nov 27, 2024Firebrick Pharma Limited, Annual General Meeting, Nov 27, 2024.
お知らせ • Oct 17Firebrick Pharma Limited has completed a Follow-on Equity Offering in the amount of AUD 0.1587 million.Firebrick Pharma Limited has completed a Follow-on Equity Offering in the amount of AUD 0.1587 million. Security Name: Ordinary Shares Security Type: Common Stock Securities Offered: 2,885,454 Price\Range: AUD 0.055 Discount Per Security: AUD 0 Transaction Features: Subsequent Direct Listing
お知らせ • Sep 12+ 1 more updateFirebrick Pharma Limited has filed a Follow-on Equity Offering in the amount of AUD 2 million.Firebrick Pharma Limited has filed a Follow-on Equity Offering in the amount of AUD 2 million. Security Name: Ordinary Shares Security Type: Common Stock Securities Offered: 36,363,636 Price\Range: AUD 0.055
Reported Earnings • Aug 31Full year 2024 earnings released: AU$0.007 loss per share (vs AU$0.04 loss in FY 2023)Full year 2024 results: AU$0.007 loss per share (improved from AU$0.04 loss in FY 2023). Net loss: AU$1.18m (loss narrowed 83% from FY 2023).
お知らせ • May 17Firebrick Pharma Limited has filed a Follow-on Equity Offering in the amount of AUD 0.8 million.Firebrick Pharma Limited has filed a Follow-on Equity Offering in the amount of AUD 0.8 million. Security Name: Ordinary Shares Security Type: Common Stock Securities Offered: 16,000,000 Price\Range: AUD 0.05 Transaction Features: Subsequent Direct Listing
New Risk • Apr 17New minor risk - Share price stabilityThe company's share price has been volatile over the past 3 months. It is more volatile than 75% of Australian stocks, typically moving 17% a week. This is considered a minor risk. Share price volatility indicates the stock is highly sensitive to market conditions or economic conditions rather than being sensitive to its own business performance, which may also be inconsistent. It also increases the risk of potential losses in the short term as the stock tends to have larger drops in price more frequently than other stocks. Currently, the following risks have been identified for the company: Major Risks Less than 1 year of cash runway based on free cash flow trend (-AU$4.6m free cash flow). Earnings have declined by 34% per year over the past 5 years. Market cap is less than US$10m (AU$9.13m market cap, or US$5.85m). Minor Risks Share price has been volatile over the past 3 months (17% average weekly change). Shareholders have been diluted in the past year (5.5% increase in shares outstanding). Revenue is less than US$5m (AU$1.8m revenue, or US$1.2m).
お知らせ • Sep 15Firebrick Pharma Limited Announces That Trial Statisticians Have Completed Their Efficacy Analysis of the Headline Results in the Phase 3 Trial of Nasodine® Nasal Spray as A Treatment for the Common ColdFirebrick Pharma Limited announced that trial statisticians have completed their efficacy analysis of the headline results in the Phase 3 trial of Nasodine® Nasal Spray as a treatment for the common cold. The analysis has shown that the trial did not meet its primary endpoint, which was the impact of Nasodine on overall cold severity (GSS) in subjects with a confirmed viral infection (ITTi). Based on the reported results, the placebo (sterile water) performed better than Nasodine. In the QoL (`quality-of-life') measure (functional impairment caused by a cold), the results were also in favour of the placebo in the ITTi. Similar enigmatic results were seen in other population subsets. The results provided to the Company are shown in the table titled: Trial Headline Results Summary. These results are compared in summary form with the previous (2019) Phase 3 trial in the table titled: Phase 3 Trial Comparisons on Key Endpoints. The 2019 trial used the same protocol and treatment regimen as the current (2022-23) trialand both trials were robust Phase 3 trials. The 2019 trial took place in Australia, so a comparison of the results with the current trial for Australian sites only has been undertaken (not shown in summary tables). In the 2019 trial, the GSS benefit of Nasodine in the viral-infected subjects (N=52) was 22.9% (p=0.048), but in the current trial, for Australian sites, the benefit was reversed, with the water placebo outperforming Nasodine by 22.7% in the ITTi (N=181), the result being statistically significant (p=0.024). The reported results also appear to conflict with the Company's recently reported Phase 2 COVID-19 trial, where Nasodine treatment led to 100% clearance of the SARS-CoV-2 virus from the nasal passages. That result was significantly better than the placebo (p=0.028), which was the same water placebo as used in the 2022-23 Phase 3 trial. The Company is concerned that the results are so confounding, unexpected and at odds with previous data that there may be a systematic error or other issue in the data, and a detailed analysis is now underway to try to identify any causes of such an error. To that end, the Company is working with the Contract Research Organisation (CRO) responsible for trial governance and other service providers to thoroughly investigate the trial results. At this time, there is no evidence that the placebo and Nasodine treatments were switched during production, distribution or treatment.
Reported Earnings • Aug 30Full year 2023 earnings released: AU$0.04 loss per share (vs AU$0.033 loss in FY 2022)Full year 2023 results: AU$0.04 loss per share (further deteriorated from AU$0.033 loss in FY 2022). Net loss: AU$6.80m (loss widened 79% from FY 2022).
分析記事 • Aug 14Here's Why We're Watching Firebrick Pharma's (ASX:FRE) Cash Burn SituationJust because a business does not make any money, does not mean that the stock will go down. For example, although...
お知らせ • Jul 22Firebrick Update on Administrative Appeals Tribunal ProcessFirebrick Pharma Limited announced that the scheduled conciliation meeting with the TGA (Therapeutic Goods Administration), which was moderated by the Administrative Appeals Tribunal (AAT) took place in Sydney on 19 July 2023. The meeting between the parties was cordial with a frank exchange on the issues relating to the approval of Nasodine Nasal Spray ("Nasodine"). Confidential discussions between the parties are ongoing and Firebrick is hopeful that an agreement on the approval of Nasodine can be reached. This announcement was authorized for release by Dr. Peter Molloy, Executive Chairman, Firebrick Pharma Limited.
お知らせ • May 16Firebrick Pharma Limited, Annual General Meeting, Jun 20, 2023Firebrick Pharma Limited, Annual General Meeting, Jun 20, 2023, at 11:00 E. Australia Standard Time. Agenda: To consider the ratification of tranche 1 placement shares; to consider the issue of tranche 2 placement shares to related party Stephen Goodall; and to consider the issue of tranche 2 placement shares to related party Peter Molloy.
分析記事 • May 02We Think Firebrick Pharma (ASX:FRE) Needs To Drive Business Growth CarefullyThere's no doubt that money can be made by owning shares of unprofitable businesses. For example, although Amazon.com...
分析記事 • Dec 14We Think Firebrick Pharma (ASX:FRE) Needs To Drive Business Growth CarefullyThere's no doubt that money can be made by owning shares of unprofitable businesses. For example, although...
Board Change • Nov 16No independent directorsFollowing the recent departure of a director, there are no independent directors on the board. The company's board is composed of: No independent directors. 4 non-independent directors. Non-Executive Director Richard Treagus was the last director to join the board, commencing their role in 2022. The company's lack of independent directors is a risk according to the Simply Wall St Risk Model.
お知らせ • Nov 14Firebrick Pharma Limited Announces CFO ChangesFirebrick Pharma Limited advises that Ms Kyla Garic has resigned her position as Chief Financial Officer (CFO). and through her company, Onyx Corporate, the provision of accounting and bookkeeping services for Firebrick, with an effective date of 25 January 2023. The Company also advise that Mr. Kavi Bekarma will take over the CFO duties and through his company, TripleEight Corporate, the provision of accounting and bookkeeping services for the Company from 1 December 2022 to allow for a smooth handover before 25 January 2023. Kavi Bekarma is the Managing Director of TripleEight Corporate, a corporate accounting firm offering various services for listed and non-listed companies in the mining, oil and gas, technology and biotechnology sectors. Mr. Bekarma is a Chartered Accountant of Australia and New Zealand, holds a Masters of Professional Accounting and a Bachelor's Degree in Management with Information Systems.
お知らせ • Nov 01Firebrick Pharma Limited Provides Update on its Phase 3 Clinical Trial of Nasodine Nasal Spray in Treatment of Common ColdFirebrick Pharma Limited provided an update on its Phase 3 clinical trial of Nasodine Nasal Spray in the treatment of the common cold. As at 31 October, the trial has so far successfully recruited 224 subjects with early-stage colds into the ITT (Intent-To-Treat population), with an estimated 100 qualifying for the primary endpoint population of those with confirmed viral infection (ITTi), based on PCR of a throat and nasal swab. This represents at least 51% of the trial's full recruitment target of 196 subjects in the ITTi. The primary endpoint for the trial is the benefit of Nasodine treatment on overall cold severity 2 in the ITT. In the previous Phase 3 trial, Nasodine produced a statistically significant benefit in the 52 subjects who had confirmed viral infection (see p. 20 of the Company's Prospectus). The current Phase 3 trial was designed to support international registration of Nasodine and if completed by mid-2023, the EU application for approval could be filed by the end of calendar 2023. The US application will require a further Phase 3 trial to be conducted in the US.
お知らせ • Oct 27Rebrick Pharma Limited Announces Nasodine Patent Granted in SingaporeFirebrick Pharma Limited announced that its patent covering Nasodine® Nasal Spray ("Nasodine") as a treatment and preventative for the common cold has been granted in Singapore. The patent is still pending in Canada and Japan. The pending application in China has now been withdrawn, following a recent assessment of the likelihood and costs of gaining any commercially-useful protection in that market. Granted claims include treating and preventing colds, reducing the viral load of common cold viruses, prevention of secondary complications of colds, and reducing the risk of serious complications in at-risk populations.
お知らせ • Sep 28Firebrick Pharma Limited, Annual General Meeting, Nov 23, 2022Firebrick Pharma Limited, Annual General Meeting, Nov 23, 2022, at 15:00 AUS Eastern Standard Time. Location: Level 18, 600 Bourke Street, Melbourne, Melbourne Victoria Australia
分析記事 • Aug 30Companies Like Firebrick Pharma (ASX:FRE) Are In A Position To Invest In GrowthEven when a business is losing money, it's possible for shareholders to make money if they buy a good business at the...
お知らせ • May 26Firebrick Appoints Richard Treagus as DirectorFirebrick Pharma Limited announced the appointment of Dr. Richard Treagus as a non-executive director on the Firebrick board of directors, with effect from 1 June 2022. Dr. Treagus was previously Commercial Director for Aspen Pharmacare in South Africa, responsible for sales and marketing of pharmacy and consumer products. More recently, from 2006 to 2012, he was CEO of Acrux Limited, which grew 10-fold in value during his tenure and from 2013 to 2020, he was Executive Chairman of Neuren Pharmaceuticals Limited, which grew 6-fold in value during his tenure.
お知らせ • May 04Firebrick Pharma Limited Starts Phase 3 Common Cold TrialFirebrick Pharma Limited announced that the first patient has been recruited into its confirmatory Phase 3 trial for Nasodine® Nasal Spray ("Nasodine") as a treatment for the common cold. The randomized controlled Phase 3 trial expects to recruit up to 450 adult subjects with early cold symptoms to achieve a target treatment population of 196 subjects, who are confirmed by PCR, to have a viral cold. The primary endpoint of the trial will be the impact of Nasodine treatment (3 sprays per nostril, 4 times daily for 5 days) on overall cold severity in the viral-infected population. Overall cold severity will be measured using the Global Severity Score (GSS) from the WURSS-21 cold severity survey. The trial is a multi-centre international study, with recruitment planned at three sites in Australia and two sites in South Africa. The first site to recruit patients is in Adelaide, with Victorian and South African sites planned to come online over the next month. Trial recruitment at all sites is expected to be completed by October this year. Any subjects found by PCR testing to have SARS-CoV-2 infection (COVID-19) will be excluded from the population for assessment of the primary endpoint but retained in the overall study population for assessment of some secondary endpoints. The company has previously completed a Phase 3 trial for the common cold in 2019 at sites in Adelaide and Brisbane. Following the completion of the trial, Firebrick filed a registration dossier with the TGA to determine whether Nasodine could be approved as an OTC (over the counter) treatment for the common cold based on then current data. The TGA has since provided advice to the Company that it has no concerns with the quality or safety of Nasodine, but that clinical efficacy was not satisfactorily established. This second Phase 3 trial was originally intended to support international regulatory approvals, but if the Australian appeal is unsuccessful, it will also be used to support approval in Australia.
Board Change • Apr 27No independent directorsFollowing the recent departure of a director, there are no independent directors on the board. The company's board is composed of: No independent directors. 4 non-independent directors. Non-Executive Director Phyllis Gardner was the last director to join the board, commencing their role in 2020. The company's lack of independent directors is a risk according to the Simply Wall St Risk Model.
お知らせ • Apr 26Firebrick Pharma Limited Starts COVID-19 Trial of NasodineFirebrick Pharma Limited announced that the first patient had been recruited into its Phase 2 clinical trial in South Africa of Nasodine® Nasal Spray ("Nasodine") for the management of COVID-19. The trial is scheduled to recruit up to 210 adults who are COVID-positive by Rapid Antigen Test (RAT) to achieve a target treatment population of 144 subjects who will be confirmed by viral culture to be shedding SARS-CoV-2 virus. Depending on patient recruitment, the trial could be completed by August 2022. The study is a randomised, placebo-controlled Phase 2 trial, titled: `Reduction of nasal shedding of SARS-CoV-2 in COVID-19 positive patients by the use of Nasodine® (povidone- iodine 0.5%) Nasal Spray.' The short title for the trial is `Nasodine for Elimination of COVID- 19 Shedding study' or `NASO-ELOCS'. The primary aim of the trial will be to show that frequent Nasodine application (every 2 hours,up to eight-times-daily) over three days leads to a significant reduction in nasal shedding of SARS-CoV-2 virus, compared with a placebo nasal spray. Secondary aims will include whether Nasodine treatment (compared with placebo) reduces the number of days to a negative RAT and increases the percentage of subjects who have cleared the virus from the upper respiratory tract within 5 days, based on a combined throat and nasal swab. Prior to gaining regulatory approval for any role in the management of COVID-19, Nasodine would likely need to undergo a confirmatory Phase 3 trial in a specific aspect of COVID-19 that is clinically relevant to the management of the disease. Nasodine has already completed a Phase 3 clinical trial as a treatment for the common cold and Firebrick is preparing to start a second Phase 3 common cold trial this year, in order to support international regulatory approvals, and if the Australian appeal is unsuccessful it will also be used to support approval in Australia.
お知らせ • Feb 11Firebrick Pharma Limited Announces the Results of in Vitro Studies of Nasodine® Nasal SprayFirebrick Pharma Limited announced that the results of in vitro studies of Nasodine® Nasal Spray (povidone-iodine 0.5%) against SARS-CoV-2, and a pilot human study in a small number of COVID-19 subjects, had been published in the Australian Journal of Otolaryngology (AJO). The in vitro experiments showed a 15-second exposure to Nasodine Nasal Spray (Nasodine) reduced infectivity of SARS-CoV-2 by 99.97%, while a 60-second exposure completely eliminated viral infectivity. The subsequent in vivo pilot study of six COVID-19 patients who were shedding the virus from the nose, showed that a single Nasodine dose (4 sprays per nostril) reduced viral shedding in 5 of the 6 subjects (83%) at 5 minutes after the dose, with an overall 79% reduction in viral shedding at one hour after the dose.
お知らせ • Feb 01Firebrick Pharma Limited Announces That Its Planned Clinical Trial of Nasodine Nasal Spray (Povidone-Iodine 0.5%) in Covid-19 Patients in South Africa, Had Received Approval to Proceed from the South African Health Products Regulatory AuthorityFirebrick Pharma Limited announced that its planned clinical trial of Nasodine Nasal Spray (povidone-iodine 0.5%) in COVID-19 patients in South Africa, had received approval to proceed from the South African Health Products Regulatory Authority (SAHPRA). The trial is titled: "Reduction of nasal shedding of SARS-CoV-2 in COVID-19 positive patients by the use of Nasodine® (povidone-iodine 0.5%) Nasal Spray." It is intended to demonstrate that frequent, repeated application of Nasodine Nasal Spray ("Nasodine") in COVID-19 subjects who are RAT-positive, leads to reduction or elimination of nasal shedding of the Sars-CoV-2 virus. The SAHPRA approval specifically allows Firebrick Pharma to import Nasodine into South Africa for the trial and to administer the product to patients during the trial, according to the trial protocol submitted to SAHPRA. As noted in the Company's prospectus (section 2.4.4(b)), prior to commencing the trial the Company will also need approval from the local clinical Ethics Committee, which has been applied for but has yet to be received.
Board Change • Jan 28No independent directorsFollowing the recent departure of a director, there are no independent directors on the board. The company's board is composed of: No independent directors. 3 non-independent directors. Non-Executive Director Phyllis Gardner was the last director to join the board, commencing their role in 2020. The company's lack of independent directors is a risk according to the Simply Wall St Risk Model.