Loading...
Access earnings results, analyst expectations, report, slides, earnings call, and transcript.
The earnings call summary and Q&A session indicate positive sentiment. The company has strong revenue guidance for 2025, plans for profitability by 2026, and reduced cash usage. The Q&A revealed management's confidence in overcoming challenges, such as prescription growth and advertising cuts. The strategic focus on gastroenterology practices and the expected inflection point in sales suggest positive momentum. While there are some uncertainties, the overall outlook is optimistic, leading to a positive sentiment rating.
Net Revenue for Q3 $49.5 million, representing 25% growth quarter-over-quarter. This growth was ahead of expectations and driven by covered prescriptions, which grew approximately 23% during the quarter.
Cash Operating Expenses for Q3 $49.3 million, significantly better than the target of below $60 million. This represents a nearly 50% reduction since Q1 2025, driven by reductions in advertising spend, headcount, and vendor costs.
Cash Usage for Q3 Less than $15 million, down 77% compared to Q2 2025. This reduction was attributed to disciplined cost management and reduced operating expenses.
Gross Profit Margin for Q3 Approximately 87%, consistent with previous quarters. This includes product costs and licensing royalties.
Filled Prescriptions in Q3 221,000 filled prescriptions, a 36% growth since Q2 2025. Of these, 144,000 were covered prescriptions (23% growth quarter-over-quarter) and 77,000 were cash prescriptions (38% growth quarter-over-quarter).
Year-to-Date Cash and Cash Equivalents (as of September 30, 2025) $135 million, reflecting a $14 million reduction in net cash, which is a 77% reduction in cash usage compared to the previous quarter.
VOQUEZNA prescriptions: Achieved 790,000 filled prescriptions as of October 17, representing 36% growth since Q2. Q3 had 221,000 filled prescriptions, with 144,000 covered scripts growing 23% quarter-over-quarter and 77,000 cash prescriptions growing 38%.
EoE Phase II trial: Initiated Phase II clinical trial in Eosinophilic Esophagitis with patient screening underway. First subject enrollment expected in Q4, with top-line results anticipated in 2027.
Gastroenterology market focus: Shifted focus to gastroenterology prescribers, targeting depth rather than breadth. Realigned sales territories to better target 24,000 gastroenterology writers, aiming to convert 20%-30% of the 20 million PPI prescriptions annually.
Revenue growth: Net revenue for Q3 was $49.5 million, a 25% quarter-over-quarter growth, exceeding expectations.
Cost reduction: Reduced operating expenses by 43% in Q3 compared to Q2, achieving below $60 million cash OpEx target early. Cash usage decreased by 77% quarter-over-quarter.
Sales strategy realignment: Realigned sales territories to focus on gastroenterology, increasing sales representatives to 300 by Q1 2026. Adjusted incentive plans to prioritize gastroenterology prescriptions.
Regulatory exclusivity: Updated FDA Orange Book indicates exclusivity for VOQUEZNA through May 2032, effectively extending to 2033 due to ANDA filing restrictions.
Regulatory Exclusivity: The company faces potential challenges in maintaining regulatory exclusivity for its product VOQUEZNA, which is currently set to expire in May 2032. Although generic entry is unlikely until 2033, this timeline could impact long-term revenue projections.
Supply Chain Disruption: There is a risk of disruption to the availability of the clarithromycin component in the VOQUEZNA TRIPLE PAK due to supplier issues. While no disruption has occurred yet, the uncertainty remains a concern.
Sales Force Realignment: The recent restructuring of sales territories to focus on gastroenterology could cause temporary disruptions in Q4, potentially impacting short-term revenue.
Clinical Trial Costs: The initiation of the Phase II EoE trial will increase operating expenses in Q4, which could strain financial resources despite the company's cost management efforts.
Market Penetration: The company has only captured approximately 3% of the gastroenterology PPI prescribing market, indicating significant room for growth but also highlighting the challenge of increasing market share in a competitive landscape.
Revenue Guidance: The company has updated its full-year revenue guidance to $170 million to $175 million, reflecting strong Q3 performance and anticipated Q4 results.
Gross to Net Range: The gross to net range for Q4 has been tightened to 55% to 60%, based on Q3 results and expectations for the rest of the year.
Operating Expenses: Q4 operating expenses are expected to be somewhat higher than Q3 due to the initiation of the Phase II EoE trial but will remain below $55 million, excluding stock-based compensation. Full-year 2025 non-GAAP operating expenses are refined to $280 million to $290 million.
Cash Position and Profitability: The company expects its current cash balance of $135 million to support operations through the anticipated point of achieving operating profitability in 2026, excluding stock-based compensation, without the need for additional equity financing.
Sales Force Realignment: The company has realigned its sales force to focus on gastroenterology target prescribers, which may temporarily impact Q4 revenue but is expected to accelerate growth in 2026.
EoE Phase II Trial: The Phase II clinical trial for Eosinophilic Esophagitis has been initiated, with patient screening underway and the first subject enrollment expected in Q4. Top-line results are anticipated in 2027.
Regulatory Exclusivity: Regulatory exclusivity for VOQUEZNA is updated to extend through May 2032, with generic entry unlikely until 2033.
The selected topic was not discussed during the call.
The earnings call summary and Q&A session indicate positive sentiment. The company has strong revenue guidance for 2025, plans for profitability by 2026, and reduced cash usage. The Q&A revealed management's confidence in overcoming challenges, such as prescription growth and advertising cuts. The strategic focus on gastroenterology practices and the expected inflection point in sales suggest positive momentum. While there are some uncertainties, the overall outlook is optimistic, leading to a positive sentiment rating.
The earnings call summary presents mixed signals: strong gross margins and a strategic focus on GI market growth are positives, while increased expenses and unclear revenue guidance pose concerns. The Q&A reveals management's cautious optimism but lack of precise timelines for revenue acceleration and cost reductions, which may create uncertainty. The company's focus on the U.S. market and cost-cutting measures are prudent, yet the potential delay in revenue growth and increased expenses temper positive sentiment, leading to a neutral stock price prediction.
Despite potential growth avenues like the VOQUEZNA launch and cost-saving initiatives, Phathom faces financial instability with significant losses and competitive pressures. The Q&A revealed uncertainties in FDA interactions and unclear management responses, adding to investor concerns. While there is a focus on profitability by 2026, the lack of immediate positive catalysts and the financial performance suggest a negative sentiment, likely leading to a stock price decline in the short term.
The earnings call reveals several concerns: a slight revenue decline, increased SG&A expenses, and significant operational losses. Although the company aims for profitability by 2026, guidance on cash flow breakeven is vague, and there's uncertainty around the FDA's CP decision. Additionally, competitive pressures and reduced advertising spending pose risks. The Q&A session highlighted management's evasiveness on critical issues, further dampening sentiment. These factors, combined with financial challenges and operational risks, suggest a negative stock reaction in the short term.
All transcripts are sourced directly from the official live webcast or the company’s official investor relations website. We use the exact words spoken during the call with no paraphrasing of the core discussion.
Full verbatim transcripts are typically published within 4–12 hours after the call ends. Same-day availability is guaranteed for all S&P 500 and most mid-cap companies.
No material content is ever changed or summarized in the “Full Transcript” section. We only correct obvious spoken typos (e.g., “um”, “ah”, repeated 10 times”, or clear misspoken ticker symbols) and add speaker names/titles for readability. Every substantive sentence remains 100% as spoken.
When audio quality is poor or multiple speakers talk over each other, we mark the section instead of guessing. This ensures complete accuracy rather than introducing potential errors.
They are generated by a specialized financial-language model trained exclusively on 15+ years of earnings transcripts. The model extracts financial figures, guidance, and tone with 97%+ accuracy and is regularly validated against human analysts. The full raw transcript always remains available for verification.