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Neurocrine Biosciences (NBIX) Q2 FY26 earnings call: guidance and Q&A

Earnings call· Jun 2026 (Q2 FY26)· Health Care· Jul 30, 2026

Source: earnings call transcript

Executive summary

Neurocrine Biosciences Q2 FY26 — Record Sales and Pipeline Advancement

Neurocrine Biosciences delivered a record second quarter, driven by strong performance across its diversified commercial portfolio, including INGREZZA, CRENESITY, and the newly acquired VYKAT XR. The company is successfully executing its strategy of commercial growth, pipeline advancement, and disciplined capital deployment, positioning it for long-term value creation. Integration of VYKAT XR is progressing, with expectations for sequential growth exiting 2026, while key Phase III data readouts for osavampator and direclidine are anticipated in 2027.

Highlights

5
  • Net product sales exceeded $950 million, representing nearly 40% year-over-year growth.

  • INGREZZA net sales were $716 million, up 15% year-over-year, driven by record new patient additions and sustained demand.

  • Full-year INGREZZA guidance raised from $2.7B-$2.8B to $2.825B-$2.875B.

  • CRENESITY net sales were $184 million, with prescriber base nearly tripling year-over-year and 15% estimated diagnosed patient population prescribed.

  • VYKAT XR pro forma net sales were $94 million, with Neurocrine recognizing $54 million from May 18, immediately accretive to non-GAAP earnings.

Concerns

2
  • Approximately $150 million of acquisition-related costs for Soleno acquisition, with $130 million recognized in Q2.

  • VYKAT XR discontinuation rates tracked in line with expectations following initial launch bolus, requiring continued market development.

Guidance & targets

CategoryTargetConfidence
Full-year INGREZZA net sales
$2.825 billion to $2.875 billion
high materiality
High
VYKAT XR sequential quarterly growth
Sequential quarterly growth
medium materiality
High
osavampator Phase III top-line data readout
Top-line data readout
high materiality
High
direclidine first Phase III study readout
First Phase III study readout
high materiality
High
direclidine second Phase III study readout
Second Phase III study readout
high materiality
High
NBIP-01435 Phase II study start
Start Phase II study
medium materiality
High
NBI-2118 (CRF2 agonist) signal-seeking study readout
Signal-seeking study readout
medium materiality
High
Friedreich's ataxia gene therapy clinical development
Starting clinical development
medium materiality
High
Friedreich's ataxia gene therapy data in patients
Actual data in patients
medium materiality
High

Segment performance

SegmentRevenueYoYQoQMargin
INGREZZA
Strong performance driven by record new patient additions and sustained underlying demand, leading to raised full-year guidance.
New patient additions: Record highTotal prescriptions: All-time high
$716 million15%——
CRENESITY
Continued strong launch execution with consistent new patient starts, expanding prescriber adoption, and high persistence and compliance.
Estimated diagnosed patient population prescribed: 15%Prescriber base: Nearly tripled compared to 1 year ago
$184 million———
VYKAT XR
Neurocrine recognized sales from May 18, 2026, following the Soleno acquisition. Integration is progressing, with expectations for sequential growth exiting 2026.
Pro forma net sales (Q2 FY26): $94 millionNew patient demand: Fairly consistent with Q1 FY26Discontinuation rates: In line with expectations following initial launch bolus
$54 million———

Deals & partnerships

Soleno Therapeutics Acquisition of Soleno Therapeutics, adding VYKAT XR to Neurocrine's portfolio. $2.9 billion

Neurocrine financed the transaction with cash on hand, ending Q2 with approximately $500 million in cash and no debt. VYKAT XR is a first-in-class, first-in-disease medicine for Prader-Willi syndrome with IP extending to mid-2040s.

Risks & headwinds

IRA implementation impact on INGREZZA 2029

Not yet quantified

Mitigation:Ongoing discussions with payers; expectation of continued strong access for MFP-adjacent products; leveraging market leadership in VMAT2 category.

VYKAT XR integration and discontinuation rates Near-term

Discontinuation rates tracked in line with expectations following initial launch bolus

Mitigation:Improving messaging and education for caregivers, patients, and physicians; focusing on appropriate patient selection, titration, and setting realistic efficacy expectations; leveraging Neurocrine's resources and support for the VYKAT team.

Competitive landscape in CAH Future

Vertex acquired a potential future competitor (atumelnant)

Mitigation:CRENESITY has a high bar with strong efficacy, safety, multiple formulations, wide age range, and multiple years of clinical data; continued focus on growing CRENESITY as the standard of care.

What to watch in Q3 FY26

VYKAT XR sequential growth

Q3 FY26 and beyond
Current Q2 FY26 sales of $54M (Neurocrine recognized)
Target Sequential growth

Why it matters

To confirm successful integration of the acquired asset and its contribution to overall revenue growth.

Integration has progressed well and expect to drive sequential quarterly growth exiting 2026.

Find out whether NBIX delivers this. Inve re-checks your case every morning.

Q&A highlights

What is the visibility on INGREZZA pricing dynamics for next year, especially with AUSTEDO MFP, and how much additional cost might be incurred to maintain access?

Management stated that 70% of Medicare lives are covered in 2026 with consistent pricing expected. They anticipate ample opportunity for strong access in 2027 and 2028 for MFP-adjacent products. It's too early to quantify additional costs for maintaining access next year.

“I think where we are right now is we do see a process and the path moving forward is not just us but others that there'll be a place for MFP adjacent products for Medicare beneficiaries.”

asked by Paul Matteis · answered by Kyle Gano

2 min read 6 chapters

Detailed narrative

Commercial Portfolio Strength and Diversification

Neurocrine's commercial portfolio, comprising INGREZZA, CRENESITY, and VYKAT XR, achieved record net product sales exceeding $950 million in Q2 FY26, marking nearly 40% year-over-year growth. This performance underscores the company's successful transition from a single-product focus to a diversified commercial engine. The strong sales provide financial flexibility to invest in innovation and strategic opportunities, reinforcing Neurocrine's leadership in rare disease and endocrinology.

VYKAT XR Acquisition and Integration

The acquisition of Soleno and its product VYKAT XR for approximately $2.9 billion was financed with cash on hand, adding a first-in-class medicine for Prader-Willi syndrome to Neurocrine's portfolio. VYKAT XR contributed $54 million in sales from May 18, 2026, and is immediately accretive to non-GAAP earnings.

Integration efforts are progressing, with management optimistic about driving sequential quarterly growth exiting 2026 and confident in VYKAT XR's potential to become a third blockbuster product.

Pipeline Advancement and Future Milestones

The company's pipeline continues to advance, with significant clinical milestones expected in 2027. These include Phase III top-line data readouts for osavampator in major depressive disorder and direclidine in schizophrenia. Neurocrine is also progressing its next-generation CRENESITY asset (NBIP-01435) towards a Phase II study and has multiple muscarinic and obesity programs in development, including a CRF2 agonist (NBI-2118) with a signal-seeking study readout expected next year.

INGREZZA Performance and Market Dynamics

INGREZZA delivered $716 million in net sales, up 15% year-over-year, driven by record new patient additions and sustained demand. The full-year guidance for INGREZZA was raised to $2.825 billion to $2.875 billion. Management expects continued strong access for INGREZZA in 2027 and 2028 despite potential IRA/MFP impacts, noting the overall VMAT2 market continues to grow double-digit year-over-year.

CRENESITY Launch Trajectory and Long-Term Data

CRENESITY generated $184 million in net sales, reflecting strong launch execution, consistent new patient starts, and expanding prescriber adoption. Approximately 15% of the estimated diagnosed patient population has been prescribed CRENESITY, and its prescriber base has nearly tripled year-over-year. Two-year data from the CAHtalyst open-label studies demonstrated meaningful and durable improvements in cardiometabolic outcomes, bone health, quality of life, and pediatric growth, reinforcing its favorable long-term safety profile.

Muscarinic Franchise Strategy

Neurocrine is building a robust muscarinic franchise with four distinct assets. Direclidine (NBI-568) is in Phase III for schizophrenia and Phase II for bipolar mania. NBI-570, an M4-preferring M1/M4 dual, is in Phase II for schizophrenia with potential for a long-acting injectable.

NBI-569, another M1/M4 dual, is in an early study for Alzheimer's disease psychosis, and NBI-567 will soon start a Phase II study for Alzheimer's cognition. All are orthosteric agonists designed to be selective and avoid add-back medications for side effect management.

Summary of the company's earnings call; see how call summaries are prepared. Not investment advice.