Axsome Boston Consulting Group Matrix

Axsome Boston Consulting Group Matrix

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Unlock the strategic potential of Axsome's product portfolio with a glimpse into their BCG Matrix. See where their key offerings might be positioned as Stars, Cash Cows, Dogs, or Question Marks. For a comprehensive understanding and actionable strategic insights, dive into the full BCG Matrix report.

Stars

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Auvelity (Major Depressive Disorder)

Auvelity is a standout performer for Axsome, positioned as a star in the company's portfolio due to its remarkable sales trajectory. The drug's significant year-over-year growth underscores its strong market penetration in the major depressive disorder treatment landscape.

In the fourth quarter of 2024, Auvelity achieved net product sales of approximately $92.6 million. For the entirety of 2024, sales reached an impressive $291.4 million, marking an 89% and 124% increase respectively compared to the previous year.

This robust financial performance, coupled with a consistent rise in prescription volume, solidifies Auvelity's status as a high-growth product in a dynamic and expanding market for depression therapies.

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Symbravo (Acute Migraine Treatment)

Symbravo, approved by the FDA in January 2025 for acute migraine treatment, is positioned as a potential blockbuster by Axsome. Its anticipated June 2025 commercial launch targets a significant market opportunity, driven by a novel mechanism and superior efficacy compared to current options.

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AXS-05 (Alzheimer's Disease Agitation)

AXS-05, targeting agitation associated with Alzheimer's disease, has successfully concluded its Phase 3 trials, demonstrating promising outcomes. The U.S. Food and Drug Administration (FDA) has recognized its potential by granting it Breakthrough Therapy designation, highlighting the significant unmet need in this therapeutic area.

Axsome Therapeutics anticipates submitting a supplemental New Drug Application (sNDA) for AXS-05 in the third quarter of 2025. This strategic move aims to establish AXS-05 as a leading treatment option for Alzheimer's disease agitation, a market segment with substantial growth potential and a clear need for innovative therapies.

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AXS-12 (Narcolepsy with Cataplexy)

AXS-12 is positioned as a potential Star in Axsome's portfolio, reflecting its strong performance and market prospects. The drug has achieved positive topline results in Phase 3 trials for narcolepsy with cataplexy. Axsome Therapeutics anticipates submitting a New Drug Application (NDA) for AXS-12 in the latter half of 2025.

The narcolepsy market is experiencing significant growth, and AXS-12's demonstrated efficacy suggests it could capture a substantial portion of this expanding market. This positions AXS-12 favorably for future success, potentially becoming a leading treatment option.

  • AXS-12 Phase 3 Results: Positive topline data has been reported for narcolepsy with cataplexy.
  • NDA Submission Timeline: Axsome expects to file an NDA in the second half of 2025.
  • Market Potential: The growing narcolepsy market and AXS-12's efficacy indicate strong market share potential.
  • Star Classification: These factors support AXS-12's classification as a Star within the BCG matrix.
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Solriamfetol (ADHD in Adults)

Solriamfetol, currently a Question Mark for Axsome in the ADHD market, showed promising results in the Q1 2025 FOCUS Phase 3 trial for adult ADHD.

Positive trial outcomes and successful market entry could elevate solriamfetol to Star status, capitalizing on a potentially significant unmet need in adult ADHD treatment.

The ADHD drug market is substantial, with global sales projected to reach over $25 billion by 2030, offering a lucrative opportunity for new entrants with demonstrated efficacy.

Axsome's strategic positioning of solriamfetol hinges on its ability to secure regulatory approval and differentiate itself in a competitive landscape, potentially capturing a notable market share.

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Axsome's Top Performers: High Growth, High Stakes

Stars in Axsome's portfolio represent products with high market share and high growth potential, demanding significant investment to maintain their leading position. Auvelity exemplifies this, showing substantial revenue growth and market penetration. AXS-12 also fits this category, with positive trial data and a strong market outlook in narcolepsy.

Product Market Growth Market Share 2024 Sales Growth vs. Prior Year
Auvelity High High $291.4 million 124%
AXS-12 High Projected High N/A (Pre-launch) N/A

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Cash Cows

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Sunosi (Excessive Daytime Sleepiness in Narcolepsy or OSA)

Sunosi, a treatment for excessive daytime sleepiness in narcolepsy or obstructive sleep apnea, is a key Cash Cow for Axsome. It consistently brings in revenue, with Q4 2024 net product revenue reaching approximately $25.7 million.

For the entirety of 2024, Sunosi generated $93.8 million in net product revenue, demonstrating its reliable performance. While its growth may not match newer products, its established market position ensures steady cash flow for the company.

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Established Payer Coverage for Sunosi

Sunosi demonstrates robust payer coverage, reaching approximately 83% of all covered lives across various healthcare channels. This widespread access, particularly the 95% coverage within the commercial sector, solidifies its position as a Cash Cow by ensuring a consistent and reliable revenue stream.

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Consistent Prescription Numbers for Sunosi

Sunosi demonstrates consistent prescription performance, nearing 46,000 prescriptions in the first quarter of 2025. This steady demand, within a well-established market, solidifies its role as a dependable revenue stream for Axsome.

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Lower Investment Needs for Sunosi

Sunosi, as a product in a mature market, typically demands less investment in marketing and distribution compared to newer, high-growth offerings. This strategic positioning allows Axsome to capitalize on its existing market share without significant incremental spending.

This lower investment requirement enables Axsome to effectively 'milk' the revenue generated by Sunosi. The company can then reallocate these freed-up capital resources to nurture and advance its promising pipeline assets, fostering future growth.

  • Mature Market Position: Sunosi operates in a well-established market, meaning its promotional and placement costs are generally lower than those for products entering high-growth sectors.
  • Passive Revenue Generation: Axsome can leverage Sunosi to generate consistent revenue with minimal ongoing investment, a classic 'cash cow' strategy.
  • Resource Reallocation: The cash flow from Sunosi can be strategically channeled into research and development for Axsome's pipeline, supporting future innovation and market expansion.
  • 2024 Financial Context: While specific 2024 figures for Sunosi's investment needs are proprietary, Axsome's overall R&D expenditure in 2023 was $459 million, highlighting the company's commitment to pipeline development, which cash flow from established products like Sunosi helps to support.
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Support for Pipeline Development

Sunosi, a key product for Axsome Therapeutics, serves as a vital Cash Cow, generating consistent revenue that underpins the company's growth strategy.

The reliable cash flow from Sunosi is instrumental in financing Axsome's ongoing research and development, particularly for its promising late-stage pipeline candidates. This financial backing is crucial for advancing potential future Stars and Question Marks, showcasing the essential role of a Cash Cow in a diversified portfolio.

  • Sunosi's Revenue Contribution: In the first quarter of 2024, Axsome reported $59.4 million in net sales for Sunosi, a significant increase from $34.5 million in the same period of 2023, highlighting its growing market presence and cash-generating ability.
  • R&D Investment: Axsome's total R&D expenses for Q1 2024 were $169.6 million, a substantial portion of which is supported by the stable income from established products like Sunosi.
  • Pipeline Support: The financial stability provided by Sunosi enables Axsome to commit resources to developing novel treatments, such as its pipeline candidates for Alzheimer's disease and migraine, positioning them for future growth.
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Sunosi: Axsome's Steady Revenue Stream & Strategic Investment Driver

Sunosi continues to be a cornerstone Cash Cow for Axsome, demonstrating consistent financial performance and market stability. Its role is crucial in funding the company's innovative pipeline.

The product's established market presence and strong payer coverage, reaching approximately 83% of covered lives, ensure a predictable and substantial revenue stream. This allows Axsome to strategically invest in future growth opportunities.

Sunosi's ability to generate passive revenue with lower investment needs allows Axsome to effectively reallocate capital towards its promising drug candidates, supporting overall portfolio development.

Product BCG Category 2024 Net Product Revenue (Approx.) Q1 2025 Prescriptions (Approx.) Payer Coverage (Approx.)
Sunosi Cash Cow $93.8 million ~46,000 ~83%

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Axsome BCG Matrix

The preview you see is the exact Axsome BCG Matrix report you will receive after purchase, offering a complete and uncompromised strategic analysis. This document is fully formatted and ready for immediate application in your business planning and decision-making processes. You can trust that no watermarks or demo content will be present in the final file delivered to you. This comprehensive report is designed to provide actionable insights into Axsome's product portfolio, enabling you to identify growth opportunities and manage resources effectively.

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Dogs

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Products with Limited Market Potential or Stalled Development

Within Axsome's product portfolio, those fitting the "Dogs" quadrant of the BCG matrix would be product candidates that have demonstrated limited market potential or have stalled in their development. While specific Axsome products are not publicly categorized as such, any drug candidate failing to meet primary endpoints in clinical trials or facing insurmountable regulatory challenges would be placed here. For instance, if a promising candidate like AXS-07 for migraine, which has experienced some setbacks in its regulatory journey, were to ultimately be de-prioritized due to persistent issues, it could be considered a Dog.

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Legacy Assets with Declining Relevance

Axsome Therapeutics, as of mid-2024, does not appear to have significant legacy assets with consistently declining market share or revenue that would be classified as Dogs in a BCG matrix. The company's current focus is on the growth and expansion of its recently launched and established commercial products.

Instead of legacy products, Axsome's portfolio is characterized by products demonstrating strong growth trajectories. For instance, AXS-07, a treatment for migraine, has shown promising market uptake since its approval. The company's pipeline also features assets with high growth potential, suggesting a strategic shift away from products that might fall into the Dog category.

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Investigational Candidates Not Meeting Efficacy or Safety Endpoints

Investigational candidates that falter in clinical trials, either by not showing enough effectiveness or by presenting concerning safety issues, are categorized as Dogs in the BCG framework. These are products that have consumed resources but are unlikely to yield future returns.

While Axsome Therapeutics has seen positive developments in areas like its migraine treatments, any investigational product that fails to meet its efficacy or safety endpoints would be relegated to this Dog category. The company's recent focus has been on successful trial outcomes, such as the positive Phase 3 trial results for AXS-07 in migraine, announced in 2023, which would place it in a different quadrant.

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Products Facing Significant Patent Expiration or Generic Competition

While Axsome has successfully navigated patent challenges for Sunosi, with generic competition not anticipated until 2040, any drug facing imminent patent expiration without new formulations or expanded indications risks becoming a Question Mark or even a Dog. This occurs as generic versions can rapidly erode market share and profitability.

Currently, Axsome's key commercialized products benefit from robust patent protection, mitigating immediate risks of generic competition. However, the pharmaceutical landscape necessitates continuous innovation to avoid products becoming Dogs.

  • Sunosi Patent Resolution: Axsome has resolved patent litigation for Sunosi, pushing generic entry to 2040.
  • Risk of Generic Erosion: Products without new formulations or indications facing near-term patent expiry are vulnerable to significant market share loss.
  • Current Portfolio Status: Axsome's primary commercial products are currently under patent protection.
  • Strategic Imperative: Ongoing innovation is crucial to prevent products from transitioning into the Dog category due to competitive pressures.
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Programs Divested Due to Underperformance

If Axsome were to divest any programs or assets that are deemed underperforming or no longer strategically aligned with its core focus, those divested assets would be considered Dogs in the BCG Matrix. This classification signifies products or business units with low market share and low market growth, typically generating minimal revenue and often requiring significant investment to maintain. As of recent reports, Axsome has not explicitly mentioned any such divestments.

For context, a company might divest underperforming assets to reallocate capital towards more promising areas. For example, if a particular drug candidate in Axsome's pipeline showed consistently poor clinical trial results and low projected market penetration, it could be a candidate for divestment. This would free up resources for pipeline candidates with higher growth potential.

  • Dogs: Underperforming assets with low market share and low market growth.
  • Strategic Reallocation: Divestment allows for capital to be shifted to more promising ventures.
  • No Explicit Divestments: Axsome has not publicly announced any divestments of underperforming programs.
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Failed Assets: The Dogs in the Portfolio

Dogs in Axsome's portfolio represent investigational assets that have failed to meet efficacy or safety thresholds in clinical trials, consuming resources without future return potential. While Axsome's current focus is on growth products like Sunosi and its migraine treatments, any candidate that falters in development, such as a hypothetical scenario where AXS-07 faced insurmountable regulatory hurdles, would be classified as a Dog. The company's strategy emphasizes advancing high-potential candidates, aiming to avoid the creation of new Dogs.

Question Marks

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AXS-14 (Fibromyalgia)

AXS-14, being developed for fibromyalgia, would likely be positioned as a question mark in Axsome's BCG Matrix. The company submitted an NDA to the FDA, with a decision on acceptance expected in Q2 2025.

While there is an existing market for fibromyalgia treatments, AXS-14 is a new entrant. Its market share and overall success are contingent on securing regulatory approval and executing a strong commercial launch strategy.

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Solriamfetol (Major Depressive Disorder with EDS)

Solriamfetol's position within Axsome's portfolio, particularly for Major Depressive Disorder with Excessive Daytime Sleepiness (EDS), is currently in a developmental stage, reflecting a potential growth opportunity. Axsome reported topline results from their PARADIGM Phase 3 trial in 2024, showing numerically greater improvements in a specific subgroup of patients.

Despite these promising numerical trends, the company has indicated plans to launch another Phase 3 trial in 2025. This suggests Axsome views the MDD with EDS market as a significant growth area, warranting further investment. However, the ultimate market share and success of solriamfetol in this indication remain to be determined, placing it in a position of uncertainty within the BCG matrix, likely a question mark or early-stage star depending on evolving data and market reception.

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Solriamfetol (Binge Eating Disorder)

Solriamfetol, currently being investigated for binge eating disorder (BED) in Axsome's ENGAGE Phase 3 trial, positions itself as a potential challenger in a market with unmet needs. Topline results for this trial are expected in 2026, which will be crucial in determining its future market standing.

While the potential for a new indication in a growing market is evident, solriamfetol's actual market share and commercial viability for BED remain uncertain. This uncertainty places it in a position where its future success is not guaranteed, requiring careful observation of trial outcomes and market reception.

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Solriamfetol (Shift Work Disorder)

Solriamfetol, currently being investigated for Shift Work Disorder (SWD) through Axsome's SUSTAIN Phase 3 trial, represents a potential "Question Mark" in the BCG Matrix. The trial's topline results are expected in 2026, and successful outcomes are crucial for market entry.

Similar to its development for binge eating disorder, establishing solriamfetol in the SWD market will demand substantial investment in clinical trials, regulatory approvals, and market penetration strategies. The company's ability to navigate these challenges and achieve commercial success will determine its future standing.

  • Potential Market: The global market for sleep disorder treatments, including SWD, is projected to grow significantly, with some estimates suggesting a compound annual growth rate (CAGR) of around 6-7% leading up to 2030, indicating substantial untapped potential.
  • Development Stage: Solriamfetol is in Phase 3 trials for SWD, a critical juncture that requires continued R&D expenditure and carries inherent risks of trial failure or regulatory hurdles.
  • Investment Needs: Successful commercialization will necessitate substantial marketing and sales efforts to compete against existing treatments and raise awareness for a new indication, demanding considerable financial resources.
  • Competitive Landscape: While specific direct competitors for solriamfetol in SWD are still emerging, the broader sleep aid market is competitive, requiring a strong value proposition.
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AXS-05 (Smoking Cessation)

AXS-05, being explored for smoking cessation, is positioned as a potential question mark in Axsome's BCG Matrix. Axsome intends to launch a pivotal Phase 2/3 trial for this indication in 2025, marking an expansion for a compound already established in other therapeutic areas.

The smoking cessation market is highly competitive, and AXS-05's ability to capture significant market share remains uncertain. This uncertainty, coupled with the substantial investment required for clinical trials and market penetration, places it squarely in the question mark category, demanding careful strategic evaluation.

  • AXS-05 Smoking Cessation Trial: Planned initiation of a pivotal Phase 2/3 trial in 2025.
  • Market Potential: Success in the competitive smoking cessation market is unproven.
  • Investment Needs: Substantial investment will be necessary for development and market entry.
  • BCG Classification: Positioned as a question mark due to high potential but uncertain market acceptance and significant investment requirements.
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Axsome's Question Marks: High Risk, High Reward!

Question marks in Axsome's portfolio represent products with low market share in high-growth markets, requiring significant investment to achieve their full potential.

These products are in the developmental stages, with success contingent on regulatory approvals, clinical trial outcomes, and market acceptance.

Axsome's strategic focus on these question marks, such as AXS-14 for fibromyalgia and solriamfetol for various indications, highlights a commitment to future growth opportunities.

However, the substantial investment needed and the inherent uncertainties in these markets place them in a high-risk, high-reward position within the BCG matrix.

Product Indication Market Growth Current Market Share BCG Classification Key Development/Consideration
AXS-14 Fibromyalgia High Low (New Entrant) Question Mark NDA submission expected Q2 2025; success depends on approval and launch.
Solriamfetol MDD with EDS High Low (Developmental) Question Mark/Star Phase 3 PARADIGM results in 2024; another Phase 3 planned for 2025.
Solriamfetol Binge Eating Disorder (BED) High Low (Developmental) Question Mark ENGAGE Phase 3 trial topline results expected 2026.
Solriamfetol Shift Work Disorder (SWD) High (6-7% CAGR to 2030) Low (Developmental) Question Mark SUSTAIN Phase 3 trial topline results expected 2026; requires significant investment.
AXS-05 Smoking Cessation High Low (Unproven) Question Mark Pivotal Phase 2/3 trial planned for 2025; competitive market.

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