Simulations Plus, Inc (SLP.US) 2026财年第二季度业绩电话会
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会议摘要
Simulation Plus Inc. reported a 8% revenue increase to $24.3 million in Q2 FY2026, driven by software and services growth. The company highlights AI integration enhancing scientific engines, stable customer base, and cross-selling opportunities. Financial metrics include adjusted EBITDA of $8.7 million and EPS of $0.35. Guidance for the remainder of FY2026 is provided, emphasizing innovation, strategic partnerships, and cautious optimism about AI monetization and future growth.
会议速览
Conference call updates on Q2 FY2026 financials, including forward-looking statements and non-GAAP measures, followed by a Q&A session.
Company reports Q2 revenue of $24.3 million, strong software and service growth, and 36% adjusted EBITDA margin. Highlights AI's role in enhancing scientific engines, strategic collaborations with pharma giants, and ongoing market momentum.
Total revenue rose 8% to $24.3 million, with software revenue up 9% and services up 8%. Software highlights include a 19% increase in discovery revenue and a 12% rise in development revenue, while clinical operations revenue declined. The focus is on leveraging AI to enhance drug development efficiency and support clients' AI strategies.
The dialogue discusses trends in software renewal rates, emphasizing high logo retention among top pharma clients and the potential for cross-selling additional products, highlighting a strategic shift towards regional account management to deepen client relationships and expand revenue.
The company reported a 12% increase in development services revenue, attributing growth to biosimilars. Commercialization services saw a 66% rise over the trailing 12 months. Gross margins improved, particularly in software, driven by higher revenue and reduced amortization costs. Guidance for fiscal 2026 includes revenue growth of 0-4%, with adjusted EBITDA margins between 26-30%, reflecting a revised effective tax rate of 23-25%.
The company highlights its transition from modeling tools to an AI-driven biosimilar system, improving speed and interoperability for clients. By combining scientific engines with cloud capabilities and AI workflows, Simulations Plus aims to empower safer, more effective therapies, focusing on the full drug development lifecycle.
The dialogue reveals the strategic approach to AI development through collaborations with three large pharma customers, emphasizing tailored solutions and product development discussions for future financial agreements.
Discussed the acquisition of new logos from non-existing customers, exploring opportunities at the lower end of the client size spectrum. Highlighted the competitive conversion aspect, noting instances where clients moved from competing products. Emphasized the strategic approach in winning new business, particularly among emerging internal biosimilar capabilities.
Discusses the growth in commercial services backlog, driven by proficiency's service revenue, with a focus on software and services pipeline. Highlights stable software revenue contribution post-acquisition, anticipating reasonable future growth.
The dialogue explores the potential for cross-selling products to existing customers, emphasizing the importance of reorganizing the sales approach and focusing on an ecosystem strategy. It highlights the growth opportunities in moving customers from single to multiple products, the success of integrating acquired products, and the impact of cloud-based solutions on new and existing customer engagement. The discussion underscores the need for a quota system aligned with client needs rather than specific products, aiming to boost cross-selling efforts and revenue.
A company reassesses its guidance halfway through the year amidst a fragile economic environment, acknowledging positive momentum but maintaining a cautious outlook due to global uncertainties and macroeconomic issues. It highlights the distinction between macroeconomic recovery and sector-specific growth, emphasizing the importance of not prematurely declaring trends based on short-term results.
The dialogue highlights the growing support for AI in biosimilar methodologies, particularly in the pharmaceutical sector. There's a noted shift towards AI investment strategies, with large pharma companies increasingly focusing on internal AI implementation. The momentum for these advancements is strong, despite industry fragility due to external factors. Regulatory perspectives and industry partnerships are driving this trend.
Discussion on assessing advancements in client organizations, focusing on expanding influence beyond modeling departments, and understanding client engagement metrics.
Discusses leveraging AI budgets and collaborations to expand total addressable market (TAM) in clinical trial operations, emphasizing growth in modeling and simulation projects alongside AI investments.
The dialogue discusses the ongoing discussions on AI monetization, emphasizing low to minimal expectations for the current fiscal year. It highlights the importance of proving AI's incremental value, focusing on the groundwork established with clients and the path forward in monetization. The conversation also anticipates significant contributions from AI in fiscal year 27, contingent on the commercial delivery of the technology.
A discussion reveals that major AI entities, including Google DeepMind, utilize the company's software for drug discovery. The software, with its extensive data dictionaries and scientific engines, aids in property prediction and clinical development, generating revenue for the company in the AI market.
Discusses the apparent contradiction of a slight decrease in total projects year over year alongside an increase in backlog, questioning whether this is due to the nature of projects, customer types, or other underlying dynamics, aiming to clarify the factors contributing to these service metrics trends.
Speakers discuss how project workloads can fluctuate, impacting staff allocation, and explore expectations for shifts in software revenue segments due to new rollouts and sector interests.
Discusses current software usage trends in the pharmaceutical sector, highlighting monoliths and Admet predictor as key drivers. Anticipates increased adoption among large pharma clients, particularly in PKPB space, with potential shifts towards discovery and development solutions.
Closing remarks from a quarterly results call highlight upcoming investor conferences and express gratitude for participation, concluding with a call for disconnection and well-wishing for the day.
要点回答
Q:What were the financial results for Simulation Plus's second quarter fiscal year 2026?
A:Simulation Plus's second quarter fiscal year 2026 saw a revenue of $24.3 million, exceeding the top line guidance communicated in the previous quarter. Adjusted EBITDA was $8.7 million with a 36% margin, and adjusted diluted EPS was 35 cents, in line with internal expectations.
Q:How is the macro environment and regulatory landscape impacting Simulation Plus?
A:The macro environment continues to support Simulation Plus with global encouraging market conditions, ongoing most favored nation pricing agreements, reduced tariff concerns, and a more supportive funding environment for customers. On the regulatory front, the new Approaches Methodologies (Nams) guidance issued late last year was further clarified, leading to a pickup in client spending, solid software renewal rates, increased new logo activity, and strength in service bookings.
Q:How is Simulation Plus responding to the impact of AI on software companies and its own business?
A:Simulation Plus is responding to the AI impact by focusing on the practical application of AI across its ecosystem. At its investor day in January, the company outlined a roadmap for leveraging AI and continues to make progress executing against this plan. The company has announced strategic collaboration programs with major pharmaceutical companies to integrate AI into real-world drug development workflows, advancing software and services into a unified modeling ecosystem. These collaborations are intended to move beyond experimentation to practical implementation and support long-term growth plans.
Q:What were the revenue segments and client performance highlights for the quarter?
A:For the quarter, total revenue increased by 8% to $24.3 million, with software revenue up 9% (60% of total revenue) and services revenue up 8% (40% of total revenue). Discovery revenue, primarily from Admet predictor, grew 19% for the quarter and 6% for the trailing 12 months. Development revenue, primarily from Gastroplus and Monolith suite, increased 12% for the quarter and 3% for the trailing 12 month period. Clinical operations revenue, primarily from proficiency, declined 54% for the quarter and 58% for the trailing 12 month period. The company ended the quarter with 297 commercial clients, achieving an average revenue per client of $124,000 and a 91% renewal rate for the quarter. On a trailing 12-month basis, the average revenue per client was $148,000 and the renewal rate was 87%.
Q:What was the percentage growth in the number of clients purchasing multiple software products in fiscal 2025?
A:In fiscal 2025, 50% of clients with software revenue greater than $100,000 purchased two software products, 23% purchased three software products, and 15% purchased four or more products.
Q:What were the key highlights for services in the quarter mentioned?
A:For the quarter, development services increased 12% and commercialization services increased 66%. Total services revenue grew with projects worked on increasing to 199, and the ending backlog increased 18% to $24 million from $20.4 million the previous year.
Q:How did the gross margins for the second quarter compare to the prior period?
A:The gross margin for the second quarter was 66%, with software gross margin at 89% and services gross margin at 33%, compared to the prior period's gross margin of 59% with software gross margin at 81% and services gross margin at 25%.
Q:What were the changes in the company's income tax expenses and effective tax rates?
A:Income tax expense was $1.4 million compared to $0.4 million last year, with an effective tax rate of 23% compared to 12% last year. The increase in the tax rate is primarily due to discrete items in the prior year that did not recur, and a less favorable jurisdictional mix of earnings.
Q:What is the updated guidance for fiscal 2026 and the third quarter?
A:The updated guidance for fiscal 2026 is total revenue between $79 to $82 million year over year, revenue growth between 0 to 4%, software mix between 57% to 62%, adjusted EBITDA margin between 26% to 30%, and adjusted diluted earnings per share now ranging between 75 cents to 85 cents. For the third quarter of 2026, revenue is expected to be between $20 to $22 million, adjusted EBITDA margin of 27% to 33%, and adjusted diluted EPS between 20 to 27 cents.
Q:How is the company progressing with its integration of AI into drug development?
A:Simulations Plus is transitioning from a set of innovative modeling tools into an integrated AI-driven biosimulation company, supporting the full drug development life cycle from discovery through commercialization. The company is combining validated scientific engines with enhanced cloud capabilities, AI-powered workflows, and a coordinated roadmap to deliver greater speed, consistency, and interoperability to clients.
Q:What is the impact of new logo opportunities on the company's client base?
A:New logo opportunities are expected to contribute to the stability of the client base, particularly among the large top 20 and billion-dollar large pharma companies, which are considered to be at the lower end of the environment or size of the clients.
Q:What is the composition of the services backlog and how has it performed?
A:The services backlog is 75% service revenue-based in the development space and 25% in the communication space. It has performed well, with a good pipeline activity and closure, resulting in service revenue in the first quarter and continues to do so in the second quarter.
Q:How has the acquisition of proficiency influenced the company's revenue streams?
A:The acquisition of proficiency has contributed to the service revenue stream, with good performance in the first and second quarters. However, the run rate of software revenue contribution decreased in the back half of 2025 and has stabilized at a good starting point in the first half of the year. The company expects reasonable growth from proficiency going forward.
Q:What are the opportunities for upselling to existing customers?
A:There are opportunities for upselling at all levels, from getting single product customers to two or more products. The company has historically seen a good linkage between Avent predictor and Gastro plus, and the monolith acquired 55 years ago complements the PKPB space for clients. The opportunity for upselling is expected to accelerate with a reorganization of the business development organization and the development of the ecosystem which enhances the scientific engines and access for smaller and medium entities.
Q:How does the company view its current position halfway through the year relative to its expectations?
A:Halfway through the year, the company is performing better than its initial guidance at the end of the previous year, despite a cautious approach due to an environment that is still fragile with global political issues and specific client-related challenges. Momentum seems to be building, and the company has greater confidence in the guidance provided, although it remains cautious not to identify any single quarter as a trend.
Q:What factors contribute to the momentum the company is experiencing?
A:The momentum the company is experiencing is not just due to an overall recovery in the macro environment or biopharma spend but also to the growing interest in and adoption of NAND (not mentioned in the transcript but implied in the context). The animal testing announcement and the support for biosimilar and AI methodologies are anticipated to be positive factors in the future, although the timeline is a couple of years out.
Q:What are the signs of momentum building in AI within large pharma companies?
A:The momentum in AI within large pharma companies is building out of partnerships with AI discovery companies, which are now prompting pharma firms to reconsider their internal implementation of AI. The speaker indicates this is a broad-based trend.
Q:How are collaborations impacting AI budget and opportunity within client organizations?
A:Collaborations have expanded the budget and opportunity for AI within clients by leveraging strong modeling and simulation relationships into connections with AI leaders within these clients. This has led to new budget allocations outside of traditional modeling and simulation, specifically in the AI budgets of large pharmaceutical companies.
Q:What is the projected timeline for AI monetization to appear in the P&L?
A:AI monetization is not expected to contribute significantly to the P&L in fiscal year 26. Discussions are ongoing with collaborators to establish the economic model for monetization, and the groundwork for value and monetization is currently visible and accepted by clients. The exact mechanics and timing of monetization are still under discussion, but it is anticipated that this area will start contributing to the P&L in fiscal year 27.
Q:Can you confirm if the company has any large AI organizations like Google DeepMind as clients?
A:Yes, the company does have large AI organizations such as Google DeepMind among its clients, and these entities, including Recursion and DeepMind, are primarily focused on drug discovery and use AI technology.
Q:How is revenue from AI market licensing structured for these large AI organizations?
A:The revenue from AI market licensing for large AI organizations stems from the use of the company's software, which includes data dictionaries and models that enable these organizations to conduct their research. Additionally, AI organizations evolve into drug development companies that move into the clinic with the company's discovery platform, Ame predictor, which is valuable for property prediction. Other software solutions, like Monolith and GastroPlus, are also used in the development cycle of their drugs and could become preferred platforms for large pharmaceutical companies.
Q:How should the recent service metrics be interpreted, particularly the year-over-year comparison?
A:The year-over-year comparison in service metrics reflects the natural evolution and progression of projects, which can consume a high percentage of staff in certain quarters and shift to smaller and medium-sized projects in others. Growth in backlog is a positive indicator of the pipeline and is returning to prior-year levels.
Q:Are there any indications of shifts in the segment breakdown of software solutions over the next 12 months?
A:The segment breakdown of software solutions is expected to remain relatively stable over the next 12 months. However, there could be some shifts, particularly with the larger clients adopting monoliths for their preferred platform in the PKPB space, which could contribute to the growth of software revenue. Discovery, development, and clinical solutions are expected to continue to contribute to software revenue, but monoliths could see faster percentage growth.

Simulations Plus, Inc.
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