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Earnings Call Transcripts·

GUGGENHEIM 3RD ANNUAL HEALTHCARE INNOVATION CONFERENCE - PHATHOM PHARMACEUTICALS INC

  • Financial Performance:

    • Q3 revenue run rate is approximately $380,000 prescriptions (75% from GI), driving full-year 2023 revenue guidance of $310–$325 million.
    • Revenue represents significant growth, approximately doubling from the previous year's $175 million.
    • Company achieved positive cash flow for the first time over the last two quarters.
    • Operating profitability (excluding stock comp) has been reached, with results very close to profitability even including stock comp.
    • Approximately 35% of current scripts are cash-filled (non-insured), with a strategic goal to reduce this percentage over time through improved prior authorization success.
    • Access program "BlinkRx" offers a $0 copay for covered patients, serving as a critical enabler for prescription fill confidence.
  • Guidance and Future Outlook:

    • Company projects 2023 growth of approximately 70% year-over-year.
    • Formal guidance for 2027 will be established during the Q4 earnings call; no specific numbers provided for 2027 yet.
    • Long-term revenue target includes two $1 billion opportunities: one derived from Gastroenterology (GI) and one from Primary Care.
    • Current GI penetration is estimated at 5% of the total PPI/H2 blocker script universe (20 million annual scripts); potential to reach $1B+ at 20–30% penetration.
    • Primary care expansion is expected to drive the second $1 billion as patients transition from GI to PCP for maintenance and as "as-needed" labeling opens new use cases.
  • Business Segments and Product Lines:

    • Core Product: Voquesna (Laqueuna), a potent acid-suppression therapy for GERD, marketed as a superior alternative to PPIs for patients with uncontrolled symptoms.
    • Sales Force Strategy: Pivot completed to focus on GI specialists (24,000 prescribers); 70% of sales calls target this group, yielding 75% of prescriptions.
    • Growth Drivers: Deepening utilization within existing GI practices (moving from severe to moderate cases) and expanding the primary care prescriber base.
    • Pipeline Developments:
      • As-Needed (PRN) Indication: Phase 3 trials currently active; data expected in H1 2028 with potential label approval filing in early 2029.
      • EoE Indication: Phase 2 trial underway (first of its kind for acid suppression as first-line EoE therapy); initial 12-week data release imminent, with full trial completion expected Q1 next year.
      • OTC Potential: Extensive planning for Over-the-Counter launch, leveraging the product's rapid onset and patient feedback; potential to be a billion-dollar+ franchise, likely timed near loss of exclusivity but under assessment for earlier launch.
    • H. Pylori Packs: Maintain exclusivity until May 2032 under the GAIN Act for H. pylori treatment packs.
  • Market and Competitive Landscape:

    • Market Opportunity: Enormous GERD market with 20 million annual PPI/H2 blocker scripts; significant patient demand for alternatives to daily chronic PPI therapy due to perceived long-term risks.
    • Competitive Positioning: Voquesna positioned to displace PPIs as first-line or second-line therapy in EoE and to replace daily PPIs with PRN usage.
    • Market Share: Currently capturing approximately 5% of the relevant script volume; competitive advantage lies in efficacy perception and patient satisfaction ("no ambiguity" in symptom relief).
    • Prescriber Sentiment: 97% of Gastroenterologists view Voquesna as effective and superior to PPIs for their patients.
  • Risks and Challenges:

    • Litigation: Ongoing litigation regarding the application of the GAIN Act to NCE exclusivity for Voquesna tablets; management views the FDA's June decision as robust and correct but acknowledges investor uncertainty due to legal unpredictability.
    • Access/Coverage: High cash-fill percentage (35%) highlights ongoing challenges with insurance prior authorizations; success depends on improving PA throughput and physician confidence in the BlinkRx partnership.
    • Patient Adherence: While patient feedback is positive, maintaining adherence through the transition from GI to primary care and ensuring consistent access remains a focus.
  • Management Commentary and Tone:

    • Tone: Highly confident and optimistic, emphasizing a clear path to profitability and sustained double-digit growth.
    • Strategic Focus: Management is pivoting sales efforts from efficacy education (which is already accepted) to access and affordability education ("Access First" initiative).
    • Confidence: Strong belief in the "patient-driven" nature of the therapy, noting patients rarely wish to switch back to PPIs once on Voquesna.
    • Financial Discipline: Highlighted as a key achievement, positioning the company as a leader in the GI space with a sustainable profit trajectory.
  • Analyst Questions and Answers:

    • Question: What drives Q3 growth and the trajectory into 2027?
      • Answer: Growth driven by depth in GI (maximizing existing 24k prescribers) and expansion into primary care; 2027 guidance to be set at Q4 earnings.
    • Question: What is the specific revenue opportunity in GI?
      • Answer: Current $300M run rate represents ~25% of the path to a $1B GI opportunity; achieving 20-30% penetration of the PPI market is the target.
    • Question: Can you clarify the "Access First" initiative and BlinkRx role?
      • Answer: Initiative focuses on educating physicians on BlinkRx for $0 copay access and cash backup; aims to remove friction in the prescribing/dispensing process.
    • Question: What is the timeline for EoE and PRN indications?
      • Answer: EoE data expected this quarter (12-week) and Q1 next year (full); PRN data expected H1 2028 with filing in early 2029.
    • Question: How does management view the litigation?
      • Answer: FDA has already ruled in favor of the May 2032 exclusivity date for tablets; management believes this is the correct application of policy despite the litigation noise.
  • Other Key Points:

    • The company is in its third year of commercialization and has successfully reached its milestone of operating profitability (excluding stock comp).
    • The "handoff" of patients from GI to Primary Care is expected to increase as the patient base expands and the "as-needed" label opens new treatment segments.
    • OTC potential is considered "enormous," potentially exceeding current PPI OTC revenues when adjusted for inflation and the product's dual-use profile (daily + PRN).
    • Management emphasizes that the primary barrier to growth is no longer efficacy awareness but rather the physician's confidence in patient access and affordability.
Company
PHATHOM PHARMACEUTICALS INC
Keywords
PHATHOM PHARMACEUTICALS INC