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Friday's Pharma Radar Sends (Nasdaq: INM) To The Top Of Our Watchlist (5 Potential Catalysts)

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Friday's Pharma Radar Sends (Nasdaq: INM) To The Top Of Our Watchlist (5 Potential Catalysts)


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March 20th

Greetings, Friend!


In a field facing immense urgency and cost, one organization is advancing a novel approach to address the complex impact of neurodegenerative conditions.


In 2025, total payments for healthcare, long-term care, and hospice services for individuals aged 65 and older with dementia reached an estimated $384Bn—a figure that underscores both the scale of the challenge and the opportunity for change.


This company is exploring unique pathways, offering a fresh direction for addressing cognitive decline and improving patient outcomes.


Their progress may be worth watching closely.


And with a low float under 3Mn shares and a key pharmaceutical development programs update, this Nasdaq profile has quickly risen to my watchlist's top spot:


InMed Pharmaceuticals Inc. (Nasdaq: INM)


InMed Pharmaceuticals is a pharmaceutical drug development company focused on developing a pipeline of proprietary small molecule drug candidates targeting the CB1/CB2 receptors.


Alzheimer’s Disease – A Major Medical & Societal Burden


Current treatment options do not reverse effects...


Alzheimer's is a subset of dementia that impacts the part of the brain that controls thought, memory and language and leads to increased morbidity and mortality.


The two most recognized hallmarks of Alzheimer’s disease are the build-up of amyloid-beta plaques and neurofibrillary tangles caused by tau proteins.


Emerging research indicates that the associated neuroinflammation is also a factor. Studies presented at AAIC 2025 further highlight neuroinflammation as a key contributor to disease progression and a promising therapeutic target.


Lifestyle and genetics are likely contributors to disease development.

InMed Pharmaceuticals Overview & Highlights


InMed has two key pharmaceutical programs – including preclinical programs in Alzheimer’s disease and age-related macular degeneration.


InMed’s small molecule compounds are demonstrating promising effects with potentially multiple mechanisms.


INM-901 Demonstrates Positive Impacts on AD Pathologies

INM-901 significantly reduces neuroinflammation in preclinical studies


InMed’s INM-901 is a small-molecule, orally-available drug candidate being developed for Alzheimer’s disease.


Promising studies demonstrate INM-901’s ability to reduce neuroinflammatory markers associated with Alzheimer’s disease. 


In a recent Alzheimer’s disease ex vivo preclinical study, INM-901 significantly reduced neuroinflammation, a recognized contributor to Alzheimer’s disease development and progression.


Key Findings from the Study:


INM-901 significantly reduced levels of NLRP3 and IL-1β, two inflammasome markers increasingly implicated in the pathogenesis of Alzheimer’s disease and other neuroinflammatory diseases.


INM-901 treatment resulted in a dose-dependent and statistically significant reduction in several key pro-inflammatory markers, including IL-6, IL-1β, KC/Gro, and IL-2.


INM-901 reduced key pro-inflammatory markers, independent of amyloid-beta or tau pathology, signifying potential to treat other dementia-related diseases.

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INM-901 - Targeting Initiation of Phase 1 Clinical Trial in Alzheimer’s Disease in 2027


InMed is accelerating development of its Alzheimer’s disease program.


2026 Development Priorities for INM-901 include:


  • Conduct a pre-IND meeting with the U.S. Food and Drug Administration in Q3/2026.


  • Continue to execute on IND-enabling pharmacology and toxicology studies.


  • Continued development and scale up of drug substance and product manufacturing activities to support IND enabling studies and submission.


  • Engage regulatory / clinical experts to map out topline clinical design for first in human clinical trials for the INM-901.


  • Subject to regulatory feedback and completion of IND-enabling activities, the Company targets submission of an IND and initiation of a Phase 1 clinical trial in 2027.


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What is Age-related Macular Degeneration?


Age-related macular degeneration (AMD) is an eye disease that causes damage to the macula which is part of the retina at the back of the eye.


The macula controls the sharp vision straight ahead of you, and damage to the macula affects a person’s central vision.


AMD is common amongst the elderly and is a leading cause of vision loss.


While it does not cause complete blindness, those with AMD will find it difficult to read, drive or do simple things around the home.


There two primary types of AMD – dry AMD and wet AMD.


Dry AMD is the most common form of AMD, accounting for 80% of AMD cases.


Dry AMD typically takes several years to progress and happens in three stages. The advanced stage of dry AMD is also referred to as geographic atrophy (GA).


InMed’s INM-089 is being studied for dry AMD.


INM-089 for Age-Related Macular Degeneration


InMed has selected INM-089, a small molecule drug candidate, for further preclinical development.


Recent preclinical studies of INM-089 demonstrated significant functional and pathological improvements in an AMD disease study model.


Results from several in vitro and in vivo studies demonstrate INM-089’s pharmacological effects in the potential treatment of dry AMD, as summarized:


  • INM-089 provides neuroprotection of photoreceptors and improves photoreceptor function
  • INM-089 improves the integrity of the retinal pigment epithelium (RPE)
  • INM-089 reduces extracellular autofluorescent (AF) deposits, a hallmark of dry AMD
  • INM-089 preserves retinal function in the back of the eye
  • INM-089 improves thickness of “outer nuclear layer” (ONL) of the retina where photoreceptors are located.


Based on widely accepted ocular research, the thickness of the outer nuclear layer is strongly correlated with photoreceptor preservation and visual acuity.


InMed is completing preclinical studies, including dose-ranging assessment studies, in preparation for a pre-IND meeting with the FDA in Q4 2026.


InMed's Pharmaceutical Pipeline

Grab Sources And Learn More Here: INM's Website. INM's Presentation.

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(Nasdaq: INM) Has 5 Potential Catalysts On Our Radar


#1. A Float Of This Size May Contribute To Increased Volatility.


Yahoo Finance is reporting INM to have a float of approximately 2.09Mn shares.


#2. Strategic FDA Pre-IND Engagement For INM-901 Could Signal Readiness To Advance Toward Clinical Trials.


InMed’s anticipated pre-IND meeting with the U.S. FDA in Q3 2026 represents a key milestone for its Alzheimer’s disease program.


This meeting could clarify the regulatory pathway, determine Phase 1 trial design, and validate the preclinical package that highlights INM-901’s unique neuroinflammation-targeting mechanism.


With Alzheimer’s treatments shifting toward multi-pathway approaches, the FDA’s preliminary feedback could draw serious attention, validate the drug’s commercial potential, and position InMed as a serious contender among next-generation neuroinflammation-focused therapeutics.


#3. INM-901 Phase 1 Clinical Trial Pathway Alignment Sets Stage For 2027 First-In-Human Study Launch.


Momentum is building around InMed’s target to initiate a Phase 1 clinical trial of INM-901 in Alzheimer’s disease in 2027, and confirmation of alignment between preclinical success and regulatory progress could be a pivotal catalyst.


#4. Groundbreaking INM-901 Neuroinflammation Data Reinforces Scientific Leadership In Multifactorial Alzheimer’s Therapeutics.


InMed’s release of new preclinical data showing robust anti-neuroinflammatory and neuroprotective activity for INM-901 could serve as a powerful catalyst, validating the company’s distinctive scientific platform.


Demonstrating measurable reductions in key inflammatory biomarkers (including IFN-γ, TNF-α, and IL-1β) alongside improvements in neuronal growth and behavioral outcomes strengthens INM-901’s profile as a multifactorial solution to Alzheimer’s disease.


These results not only diversify InMed’s scientific narrative beyond single-target mechanisms but also align with emerging research consensus.


#5. Advancement Of INM-089 Toward FDA Pre-IND Meeting Could Ignite Interest In The Ophthalmology Market.


InMed’s progress with INM-089, including successful dose-ranging studies and advancement toward a pre-IND meeting in Q4 2026, may attract increased attention from watchers of the dry age-related macular degeneration (AMD) space.


As current treatment options are limited, INM-089’s potential to address this underserved market positions InMed in a multi-Bn-dollar therapeutic category.


Clear evidence of dose proportionality and pharmacologically relevant exposure underpins regulatory readiness.


A strong FDA feedback outcome could establish a second clinical-ready asset for the company, diversifying risk and showcasing InMed’s expanding expertise beyond neurology into ophthalmology.

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The company’s 2026 milestones—ranging from IND-enabling studies and formulation scale-up to engagement with regulatory experts—are converging on this inflection point. 


A formally communicated timeline or partnership announcement for clinical execution could validate years of groundwork.


As the program transitions from laboratory to human trials, industry enthusiasm could surge around the company’s novel approach.


Coverage is now a "Go" on InMed Pharmaceuticals Inc. (Nasdaq: INM).


Updates will be coming out soon. Keep your eyes peeled.


All the best,

Dane James

Editor Market Pulse Today


(Remember: St-ock Prices Could Be Significantly Lower Now From The Original Dates I Provided.)


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