| Breakdown | TTM | Jun 2025 | Jun 2024 | Jun 2023 | Jun 2022 | Jun 2021 |
|---|---|---|---|---|---|---|
Income Statement | ||||||
| Total Revenue | 5.28M | 4.94M | 4.60M | 4.14M | 1.09M | 0.00 |
| Gross Profit | 1.40M | 1.71M | 1.10M | 1.40M | 543.55K | 0.00 |
| EBITDA | -8.69M | -7.26M | -7.06M | -7.78M | -13.28M | -12.17M |
| Net Income | -9.07M | -8.16M | -7.68M | -7.95M | -18.60M | -12.65M |
Balance Sheet | ||||||
| Total Assets | 15.36M | 21.23M | 16.17M | 18.69M | 16.46M | 12.10M |
| Cash, Cash Equivalents and Short-Term Investments | 9.60M | 15.09M | 8.99M | 11.81M | 8.01M | 9.16M |
| Total Debt | 730.14K | 1.01M | 1.32M | 518.92K | 1.02M | 333.64K |
| Total Liabilities | 2.20M | 2.92M | 3.58M | 2.67M | 4.78M | 2.97M |
| Stockholders Equity | 13.16M | 18.30M | 12.59M | 16.02M | 11.69M | 9.12M |
Cash Flow | ||||||
| Free Cash Flow | -8.91M | -7.77M | -7.00M | -7.45M | -15.62M | -9.79M |
| Operating Cash Flow | -8.91M | -7.77M | -6.99M | -7.28M | -15.58M | -9.79M |
| Investing Cash Flow | 0.00 | 0.00 | -9.29K | -661.80K | -673.00K | -1.73K |
| Financing Cash Flow | 10.90M | 12.27M | 4.65M | 10.68M | 15.07M | 10.85M |
Name | Overall Rating | Market Cap | P/E Ratio | ROE | Dividend Yield | Revenue Growth | EPS Growth |
|---|---|---|---|---|---|---|---|
51 Neutral | $7.86B | -0.30 | -43.30% | 2.27% | 22.53% | -2.21% | |
50 Neutral | $7.47M | -1.38 | -60.33% | ― | 13.30% | 22.70% | |
45 Neutral | $7.19M | -1.13 | -167.97% | ― | ― | 68.59% | |
43 Neutral | $2.39M | ― | -82.17% | ― | -3.27% | 51.83% | |
43 Neutral | $2.12M | -0.46 | -386.72% | ― | 1.51% | 77.64% |
On March 9, 2026, InMed outlined its 2026 pharmaceutical development outlook, highlighting significant 2025 preclinical progress for lead Alzheimer’s candidate INM-901, including reduced inflammatory and neurodegenerative biomarkers, evidence of neuroprotection and neurite outgrowth, behavioral improvements, and favorable oral bioavailability, alongside advances in formulation, manufacturing scale-up and regulatory preparation. The company plans a pre-IND meeting with the U.S. FDA for INM-901 in Q3 2026 and continued IND-enabling studies to support a targeted Phase 1 trial initiation in 2027, while its INM-089 dry age-related macular degeneration program has generated supportive preclinical and manufacturing data ahead of a planned Q4 2026 pre-IND meeting, underscoring InMed’s bid to strengthen its position in neuroinflammation-focused and ocular therapeutics and to create longer-term value for shareholders.
MainPoint1: InMed reported strong 2025 preclinical gains for INM-901, showing anti-neuroinflammatory effects, neuroprotection, behavioral benefits and oral bioavailability, while advancing formulation, manufacturing and regulatory groundwork.
MainPoint2: The company’s 2026 plan centers on FDA pre-IND meetings and IND-enabling work for INM-901 and INM-089, aiming to launch a Phase 1 Alzheimer’s trial in 2027 and reinforce its neuroscience and ocular disease pipeline.
The most recent analyst rating on (INM) stock is a Hold with a $0.84 price target. To see the full list of analyst forecasts on InMed Pharmaceuticals stock, see the INM Stock Forecast page.
InMed Pharmaceuticals said that on March 4, 2026, its board ratified BayMedica LLC’s decision to wind down and exit its commercial operations in rare, non-intoxicating cannabinoids before the end of the fiscal year ending June 30, 2026, in response to the expected impact of H.R. 5371, which would prohibit aspects of BayMedica’s business from November 12, 2026. During the wind-down period, BayMedica will continue limited sales and manufacturing, while InMed will incur about $550,000 in severance and $120,000 in other wind-down costs, then shift to focus exclusively on advancing its pharmaceutical pipeline, including drug candidates INM-901 for Alzheimer’s disease and INM-089 for dry age-related macular degeneration.
The company expects these wind-down expenditures to be partially offset by profits from product sales before operations cease, although it cautioned that actual costs, timing and additional charges could differ materially from current estimates. On March 6, 2026, InMed issued a press release detailing the decision and provided unaudited pro forma financial information to reflect BayMedica’s commercial operations as discontinued, underscoring a strategic pivot away from commercial cannabinoid ingredients toward clinical-stage drug development.
The most recent analyst rating on (INM) stock is a Hold with a $0.73 price target. To see the full list of analyst forecasts on InMed Pharmaceuticals stock, see the INM Stock Forecast page.
On February 11, 2026, InMed reported second-quarter fiscal 2026 results for the period ended December 31, 2025, highlighting progress in its neurology and ophthalmology programs while managing a tightening cash position. The company completed key pharmacokinetic studies for Alzheimer’s candidate INM-901, showing robust oral bioavailability with no adverse neurological effects in large animals, and advanced preclinical work on INM-089 for dry AMD, as it prepares for pre-IND meetings and GLP-enabling studies supporting future IND submissions.
Financially, BayMedica revenue fell 26% year over year to $0.8 million on weaker demand linked to pending U.S. legislative changes, while R&D expenses declined to $0.6 million and G&A held roughly flat at $1.6 million. Cash, cash equivalents and short-term investments dropped to $7.0 million from $11.1 million at June 30, 2025, with management expecting liquidity to last into the fourth quarter of calendar 2026, though potential implementation of H.R. 5371 could force BayMedica inventory write-offs, strategic divestiture or shutdown, posing a material risk to future operations and financial performance.
The most recent analyst rating on (INM) stock is a Sell with a $0.88 price target. To see the full list of analyst forecasts on InMed Pharmaceuticals stock, see the INM Stock Forecast page.
On December 17, 2025, InMed Pharmaceuticals held its 2025 Annual General and Special Meeting of Shareholders, where 35.43% of its 2.8 million outstanding common shares were represented in person or by proxy. Shareholders re-elected five directors to serve until the 2026 annual meeting, approved CBIZ CPAs P.C. as the company’s auditor for the coming year, and endorsed the potential issuance of 20% or more of the company’s outstanding common shares as of December 13, 2024 under a Standby Equity Purchase Agreement with YA II PN, Ltd., in line with Nasdaq listing rules, signaling continued shareholder support for the existing board, governance structure and flexible equity financing options. No other matters came to a vote at the meeting, and the company reported the voting results on SEDAR on December 17, 2025.
The most recent analyst rating on (INM) stock is a Sell with a $2.50 price target. To see the full list of analyst forecasts on InMed Pharmaceuticals stock, see the INM Stock Forecast page.
On December 12, 2025, InMed Pharmaceuticals announced that the recently signed H.R. 5371 Act in the United States could materially negatively impact its subsidiary, BayMedica Inc., by prohibiting certain aspects of its commercial business related to rare, non-intoxicating cannabinoids. Despite this, InMed’s core pharmaceutical programs, including treatments for Alzheimer’s and age-related macular degeneration, remain unaffected and continue to progress under FDA guidance.
The most recent analyst rating on (INM) stock is a Sell with a $2.50 price target. To see the full list of analyst forecasts on InMed Pharmaceuticals stock, see the INM Stock Forecast page.