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HARMONY BIOSCIENCES REPORTS STRONG THIRD QUARTER 2024 FINANCIAL RESULTS AND HIGHLIGHTS CATALYST-RICH, LATE-STAGE PIPELINE POISED TO DELIVER ONE OR MORE NEW LAUNCHES EVERY YEAR OVER NEXT FIVE YEARS

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Harmony Biosciences (HRMY) reported Q3 2024 net revenue of $186.0 million, marking a 16% growth from Q3 2023. The company surpassed $2 billion in cumulative net revenue since WAKIX's launch in 2019. GAAP net income reached $46.1 million ($0.79 per diluted share), compared to $38.5 million in Q3 2023. The average number of WAKIX patients increased by 250 to approximately 6,800. The company maintains its 2024 net product revenue guidance of $700-720 million. Harmony's pipeline development includes advancing programs in idiopathic hypersomnia, rare epilepsies, and neurobehavioral disorders.

Harmony Biosciences (HRMY) ha riportato un fatturato netto per il terzo trimestre 2024 di 186,0 milioni di dollari, segnando una crescita del 16% rispetto al terzo trimestre 2023. L'azienda ha superato i 2 miliardi di dollari di fatturato netto cumulativo dalla lanciata di WAKIX nel 2019. L'utile netto GAAP ha raggiunto 46,1 milioni di dollari (0,79 dollari per azione diluita), rispetto ai 38,5 milioni di dollari del terzo trimestre 2023. Il numero medio di pazienti trattati con WAKIX è aumentato di 250, per un totale di circa 6.800. L'azienda mantiene le sue stime di fatturato netto da prodotto per il 2024 tra 700-720 milioni di dollari. Lo sviluppo del pipeline di Harmony include l'avanzamento di programmi in ipersomnia idiopatica, epilessie rare e disturbi neurocomportamentali.

Harmony Biosciences (HRMY) reportó ingresos netos del tercer trimestre de 2024 de 186,0 millones de dólares, marcando un crecimiento del 16% en comparación con el tercer trimestre de 2023. La compañía superó los 2 mil millones de dólares en ingresos netos acumulados desde el lanzamiento de WAKIX en 2019. La ganancia neta GAAP alcanzó 46,1 millones de dólares (0,79 dólares por acción diluida), en comparación con 38,5 millones de dólares en el tercer trimestre de 2023. El número promedio de pacientes de WAKIX aumentó en 250, alcanzando aproximadamente 6,800. La compañía mantiene su guía de ingresos netos por productos de 700-720 millones de dólares para 2024. El desarrollo de la cartera de Harmony incluye el avance de programas en hipersomnia idiopática, epilepsias raras y trastornos neuroconductuales.

하모니 바이오사이언스 (HRMY)는 2024년 3분기 순매출이 1억 8600만 달러에 달하며, 이는 2023년 3분기 대비 16% 성장한 수치입니다. 회사는 2019년 WAKIX 출시 이후 누적 순매출 20억 달러를 초과했습니다. GAAP 순이익은 4610만 달러 (희석 주당 0.79 달러)에 도달했으며, 이는 2023년 3분기 3850만 달러와 비교됩니다. WAKIX 치료를 받는 환자 수의 평균이 250명 증가하여 약 6800명이 되었습니다. 회사는 2024년 순제품 매출 전망을 7억-7억 2000만 달러로 유지하고 있습니다. 하모니의 파이프라인 개발에는 특발성 과수면증, 희귀간질, 신경행동장애와 관련된 프로그램의 진행이 포함됩니다.

Harmony Biosciences (HRMY) a annoncé un chiffre d'affaires net pour le troisième trimestre 2024 de 186,0 millions de dollars, marquant une croissance de 16 % par rapport au troisième trimestre 2023. L'entreprise a dépassé les 2 milliards de dollars de chiffre d'affaires net cumulé depuis le lancement de WAKIX en 2019. Le bénéfice net selon les normes GAAP a atteint 46,1 millions de dollars (0,79 dollar par action diluée), contre 38,5 millions de dollars au troisième trimestre 2023. Le nombre moyen de patients utilisant WAKIX a augmenté de 250, pour atteindre environ 6 800. L'entreprise maintient sa prévision de chiffre d'affaires net de produit pour 2024 entre 700 et 720 millions de dollars. Le développement de la pipeline de Harmony inclut l'avancement de programmes concernant l'hypersomnie idiopathique, les épilepsies rares et les troubles neurocomportementaux.

Harmony Biosciences (HRMY) hat im dritten Quartal 2024 einen Nettoumsatz von 186,0 Millionen US-Dollar gemeldet, was einem Wachstum von 16 % im Vergleich zum dritten Quartal 2023 entspricht. Das Unternehmen hat seit der Einführung von WAKIX im Jahr 2019 einen kumulierten Nettoumsatz von über 2 Milliarden US-Dollar überschritten. Der Nettogewinn nach GAAP belief sich auf 46,1 Millionen US-Dollar (0,79 US-Dollar pro verwässerter Aktie) im Vergleich zu 38,5 Millionen US-Dollar im dritten Quartal 2023. Die durchschnittliche Anzahl der WAKIX-Patienten ist um 250 auf ungefähr 6.800 angestiegen. Das Unternehmen hält an seiner Prognose für den Nettoumsatz von Produktverkäufen im Jahr 2024 von 700-720 Millionen US-Dollar fest. Die Entwicklung von Harmony's Pipeline umfasst Fortschritte bei Programmen zur idiopathischen Hypersomnie, seltenen Epilepsien und neurobehavioralen Störungen.

Positive
  • Net revenue grew 16% YoY to $186.0 million in Q3 2024
  • GAAP net income increased to $46.1 million from $38.5 million YoY
  • Patient base expanded by 250 to 6,800 patients in Q3
  • Cash position strengthened to $504.7 million from $425.6 million at year-end 2023
  • Surpassed $2 billion in cumulative net revenue since WAKIX launch
Negative
  • Operating expenses increased 29% YoY to $81.6 million
  • R&D expenses rose 45% YoY to $25.4 million
  • Sales and Marketing expenses increased 18% YoY to $27.6 million
  • G&A expenses grew 27% YoY to $28.6 million

Insights

A strong quarter for Harmony Biosciences with $186.0M in net revenue, up 16% year-over-year. The company surpassed $2B in cumulative revenue since WAKIX's launch, demonstrating exceptional market penetration. Patient count grew by 250 to 6,800, indicating steady market expansion.

Key financial metrics show robust health: $46.1M GAAP net income ($0.79 EPS), $504.7M cash position and maintained 2024 revenue guidance of $700-720M. Operating expenses increased 29% to $81.6M, primarily driven by R&D investment, signaling strong commitment to pipeline development.

The extensive late-stage pipeline, including expansion opportunities in IH and rare epilepsies, positions HRMY for sustainable growth beyond 2040. The company's self-funding status and $150M remaining in share buyback authority provide financial flexibility.

The clinical pipeline shows remarkable breadth and depth across CNS disorders. The IH program's long-term extension data reveals impressive efficacy with ~9-point ESS improvement sustained beyond one year. The enhanced Pitolisant-HD formulation and gastro-resistant Pitolisant-GR demonstrate strategic lifecycle management.

The novel orexin-2 agonist program (BP1.15205) shows best-in-class potential with superior potency and selectivity profiles. In rare epilepsies, EPX-100's validated serotonergic mechanism and dual Phase 3 programs in Dravet and Lennox-Gastaut syndromes represent significant market opportunities. Multiple catalysts through 2025-2026 could drive substantial value creation.

WAKIX (pitolisant) Net Revenue of $186.0 Million for Third Quarter 2024; Surpassed $2B in Cumulative Net Revenue in Less Than Five Years

On Track to Submit sNDA for Pitolisant in Idiopathic Hypersomnia (IH) in Q4 2024 Based on Updated Strong and Sustained Efficacy Data from Long-Term Extension Study

Next-Gen Pitolisant-GR and Pitolisant-HD Programs Advance; IND for Potential Best-In-Class, Novel Orexin-2 Agonist On Track for mid-2025, Extending Leadership in Sleep/Wake Beyond 2040s

Highlights Most Advanced Development Program and Proven Serotonergic (5-HT2) Mechanism of Action For EPX-100 in Rare Epilepsies; Pivotal Phase 3 Trial in Dravet Syndrome Ongoing; Phase 3 Registrational Trial in Lennox-Gastaut Syndrome to Initiate Before Year End

Next Major Clinical Catalyst: Topline Data From ZYN-002 Pivotal Phase 3 RECONNECT Trial in Fragile X Syndrome on Track For mid-2025

Reiterates 2024 Net Product Revenue Guidance of $700 - $720 Million

Conference Call and Webcast to be Held Today at 8:30 a.m. ET 

PLYMOUTH MEETING, Pa., Oct. 29, 2024 /PRNewswire/ -- Harmony Biosciences Holdings, Inc. (Nasdaq: HRMY), today reported a record $186.0 million in net revenue for the quarter ending on September 30, 2024, surpassing $2 billion in cumulative net revenues since the launch of WAKIX® in adult narcolepsy in November of 2019. In addition, the company recently hosted an Investor Day on October 1, during which it highlighted its transformation into an innovative, catalyst-rich, self-funding biotech company with a robust late-stage pipeline.

"Going into Q4, Harmony has great momentum. During our Investor Day, we shared new data in support of our confidence and excitement about the company's growth trajectory as we advance our robust, catalyst-rich, late-stage pipeline and expand into additional rare CNS therapeutic areas. We are building on our success in sleep/wake with a strategy focused on continuous innovation, patient impact, and long-term value creation for our shareholders, and, if successful, our current pipeline is poised to deliver over $3 billion in net revenue going forward," said Jeffrey M. Dayno, M.D., President and Chief Executive Officer of Harmony Biosciences. "We have been building a leading CNS biotech company and are committed to addressing unmet medical needs for people living with CNS disorders that have few or no treatment options and, when we deliver on this promise to patients, we have the potential to deliver significant value to our shareholders as well."

Key Franchise Highlights:

Sleep/Wake: Extending Leadership Position

WAKIX:

  • Net Sales for the quarter were $186.0M; with these quarterly sales, WAKIX surpassed $2B in cumulative net revenue in less than five years on the market
  • The average number of patients on WAKIX increased by approximately 250 patients sequentially to approximately 6,800 for the quarter ended September 30, 2024

Pitolisant in Idiopathic Hypersomnia (IH): 

  • New data from the Long-Term Extension study demonstrate robust and sustained efficacy of pitolisant in patients with idiopathic hypersomnia

Mean improvement in Epworth Sleepiness Scale (ESS) was ~9 points from baseline out beyond one year, with the majority of patients in the normal range as measured by the ESS

Sustained efficacy was also observed on the Idiopathic Hypersomnia Severity Scale (IHSS) and Sleep Inertia Questionnaire (SIQ) beyond one year

  • Data supports strong benefit/risk proposition; on track to submit sNDA in Q4 2024

Pitolisant-HD (high dose) program: 

  • Pitolisant-HD is an enhanced formulation of pitolisant designed with the following attributes:

A higher dose with an optimized pharmacokinetic profile to drive greater efficacy in EDS and cataplexy

Targeting a unique indication for fatigue in narcolepsy

A gastro-resistant coating with no need for a titration dose

  • Preliminary safety data up to 5x the current highest labeled dose of WAKIX are consistent with the established safety profile of WAKIX and establish safety margins for the pitolisant-HD development program
  • Pitolisant-HD on track for PDUFA in 2028 with the goal to extend the pitolisant franchise to mid-2040s
  • Provisional patents filed until 2044 with the opportunity to grow the pitolisant franchise by pursuing additional indications

Pitolisant-GR (gastro-resistant) program: 

  • Pitolisant-GR is a gastro-resistant formulation of pitolisant designed to minimize GI tolerability issues in patients with narcolepsy; approximately 90% of patients with narcolepsy experience GI symptoms partly related to the underlying disease mechanism
  • On track to initiate pivotal bioequivalence study and dosing optimization study (to remove the titration dose) in Q1 2025
  • PDUFA on track for 2026 with IP to the mid-2040s

Orexin-2 agonist program: 

  • BP1.15205 (formerly TPM-1116) potential to be best-in-class orexin-2 receptor agonist

Based on a novel chemical scaffold

Demonstrated greater potency compared to all publicly disclosed data on orexin-2 agonists; allows for dosing flexibility to target all central disorders of hypersomnolence. The potency was consistent across species along with an excellent selectivity of greater than 600x which translates to over 140-fold margin over orexin-1 receptors at the anticipated maximum human dose

In addition, BP1.15205 demonstrated over 1000-fold selectively over 150 other targets of interest

Preclinical PK data consistent with once-a-day dosing

Rare Epilepsy: Most Advanced Development Program in the 5-HT2 agonist class

EPX-100 (clemizole hydrochloride):

  • MoA: Proven serotonergic (5-HT2) mechanism of action in Developmental Epileptic Encephalopathies (DEEs) confirmed via a validated and highly predictive preclinical model (zebra fish model)
  • Most advanced development program for the DEEs:

EPX-100 in Phase 3 registration trial, ARGUS study, in patients with Dravet syndrome (DS); on track for topline data in 2026

  • EPX-100 Phase 3 registration trial for Lennox-Gastaut syndrome (LGS) on track to initiate later this year
  • Preliminary Safety and Tolerability data suggests favorable profile compared to select approved drugs for rare epilepsies (with no need for routine laboratory or cardiac monitoring)
  • Received Orphan Drug Designation (ODD) and Rare Pediatric Disease Designation (RPDD) by the FDA for DS and LGS

EPX-200 (lorcaserin hydrochloride):

  • MoA: Potent, selective 5HT2C agonist with proven mechanism of action in DEEs confirmed via non-clinical and clinical data
  • Currently in IND-enabling stage
  • Received ODD for DS, and ODD / RPDD for LGS by the FDA; and ODD for DS by the European Medicines Agency

Neurobehavioral: Next Major Clinical Catalyst

ZYN-002

  • Pivotal Phase 3 RECONNECT trial in Fragile X syndrome ongoing; topline data on track for mid-2025
  • Anticipate initiation of pivotal Phase 3 trial in 22q11.2 deletion syndrome (22q) in 2025

Third Quarter 2024 Financial Results

Net product revenues for the quarter ended September 30, 2024, were $186.0 million, compared to $160.3 million for the same period in 2023. The 16% growth versus the same period in 2023 is primarily attributed to strong commercial sales of WAKIX driven by continued organic demand tapping into a large market opportunity (approximately 80,000 patients diagnosed with narcolepsy in the U.S.) and the broad clinical utility of WAKIX across the approximately 9,000 HCPs that we call on (about 5,000 of whom do not participate in an oxybate REMS program). The average number of patients on WAKIX increased by approximately 250 sequentially to approximately 6,800 for the quarter ended September 30, 2024. 

GAAP net income for the quarter ended September 30, 2024, was $46.1 million, or $0.79 earnings per diluted share, compared to GAAP net income of $38.5 million, or $0.63 earnings per diluted share, for the same period in 2023. Non-GAAP adjusted net income was $59.6 million, or $1.03 earnings per diluted share, for the quarter ended September 30, 2024, compared to Non-GAAP adjusted net income of $58.8 million, or $0.97 per diluted share, for the same period in 2023.

Reconciliations of applicable GAAP financial measures to Non-GAAP financial measures are included at the end of this press release.

Harmony's operating expenses include the following:

  • Research and Development expenses were $25.4 million in the third quarter of 2024, as compared to $17.5 million for the same quarter in 2023, representing a 45% increase;
  • Sales and Marketing expenses were $27.6 million in the third quarter of 2024, as compared to $23.4 million for the same quarter in 2023, representing a 18% increase;
  • General and Administrative expenses were $28.6 million in the third quarter of 2024, as compared to $22.5 million for the same quarter in 2023, representing a 27% increase; and
  • Total Operating Expenses were $81.6 million in the third quarter of 2024, as compared to $63.5 million for the same quarter in 2023, representing a 29% increase.

As of September 30, 2024, Harmony had cash, cash equivalents and investments of $504.7 million, compared to $425.6 million as of December 31, 2023.

Reiterates 2024 Net Product Revenue Guidance

Expect full year 2024 net product revenue of $700 million to $720 million.

Share Repurchase Program

The remaining amount of common stock authorized for repurchases as of September 30, 2024, was $150 million.

Conference Call Today at 8:30 a.m. ET

We are hosting our third quarter 2024 financial results conference call and webcast today, beginning at 8:30 a.m. Eastern Time. The live and replay webcast of the call will be available on the investor relations page of our website at  https://ir.harmonybiosciences.com/. To participate in the live call by phone, dial (800) 245-3047 (domestic) or (203) 518-9765 (international), and reference passcode HRMYQ324.

Non-GAAP Financial Measures

In addition to our GAAP results, we present certain Non-GAAP metrics including Non-GAAP adjusted net income and Non-GAAP adjusted net income per share, which we believe provides important supplemental information to management and investors regarding our performance. These measurements are not a substitute for GAAP measurements, and the manner in which we calculate Non-GAAP adjusted net income and Non-GAAP adjusted net income per share may not be identical to the manner in which other companies calculate adjusted net income and adjusted net income per share. We use these Non-GAAP measurements as an aid in monitoring our financial performance from quarter-to-quarter and year-to-year and for benchmarking against comparable companies.

Non-GAAP financial measures should not be considered in isolation or as a substitute for comparable GAAP measures; should be read in conjunction with our consolidated financial statements prepared in accordance with GAAP; have no standardized meaning prescribed by GAAP; and are not prepared under any comprehensive set of accounting rules or principles. In addition, from time to time in the future there may be other items that we may exclude for purposes of our Non-GAAP financial measures; and we may in the future cease to exclude items that we have historically excluded for purposes of our Non-GAAP financial measures.

About WAKIX® (pitolisant) Tablets
WAKIX, a first-in-class medication, is approved by the U.S. Food and Drug Administration for the treatment of excessive daytime sleepiness (EDS) or cataplexy in adult patients with narcolepsy and for the treatment of EDS in pediatric patients 6 years of age and older with narcolepsy. It was granted orphan drug designation for the treatment of narcolepsy in 2010, and breakthrough therapy designation for the treatment of cataplexy in 2018. WAKIX is a selective histamine 3 (H₃) receptor antagonist/inverse agonist. The mechanism of action of WAKIX is unclear; however, its efficacy could be mediated through its activity at H₃ receptors, thereby increasing the synthesis and release of histamine, a wake promoting neurotransmitter. WAKIX was designed and developed by Bioprojet (France). Harmony has an exclusive license from Bioprojet to develop, manufacture and commercialize pitolisant in the United States.

Indications and Usage
WAKIX is indicated for the treatment of excessive daytime sleepiness (EDS) or cataplexy in adult patients with narcolepsy and for the treatment of excessive daytime sleepiness (EDS) in pediatric patients 6 years of age and older with narcolepsy.

Important Safety Information

Contraindications
WAKIX is contraindicated in patients with known hypersensitivity to pitolisant or any component of the formulation. Anaphylaxis has been reported. WAKIX is also contraindicated in patients with severe hepatic impairment.

Warnings and Precautions
WAKIX prolongs the QT interval. Avoid use of WAKIX in patients with known QT prolongation or in combination with other drugs known to prolong the QT interval. Avoid use in patients with a history of cardiac arrhythmias, as well as other circumstances that may increase the risk of the occurrence of torsade de pointes or sudden death, including symptomatic bradycardia, hypokalemia or hypomagnesemia, and the presence of congenital prolongation of the QT interval. 

The risk of QT prolongation may be greater in patients with hepatic or renal impairment due to higher concentrations of pitolisant; monitor these patients for increased QTc. Dosage modification is recommended in patients with moderate hepatic impairment and moderate or severe renal impairment. WAKIX is contraindicated in patients with severe hepatic impairment and not recommended in patients with end-stage renal disease (ESRD).

Adverse Reactions
In the placebo-controlled clinical trials conducted in patients with narcolepsy with or without cataplexy, the most common adverse reactions (≥5% and at least twice placebo) for WAKIX were insomnia (6%), nausea (6%), and anxiety (5%). Other adverse reactions that occurred at ≥2% and more frequently than in patients treated with placebo included headache, upper respiratory tract infection, musculoskeletal pain, heart rate increased, hallucinations, irritability, abdominal pain, sleep disturbance, decreased appetite, cataplexy, dry mouth, and rash.

In the placebo-controlled phase of the clinical trial conducted in pediatric patients 6 years and older with narcolepsy with or without cataplexy, the most common adverse reactions (≥5% and greater than placebo) for WAKIX were headache (19%) and insomnia (7%). The overall adverse reaction profile of WAKIX in the pediatric clinical trial was similar to that seen in the adult clinical trial program.

Drug Interactions
Concomitant administration of WAKIX with strong CYP2D6 inhibitors increases pitolisant exposure by 2.2-fold. Reduce the dose of WAKIX by half. 

Concomitant use of WAKIX with strong CYP3A4 inducers decreases exposure of pitolisant by 50%. Dosage adjustments may be required.

H1 receptor antagonists that cross the blood-brain barrier may reduce the effectiveness of WAKIX. Patients should avoid centrally acting H1 receptor antagonists. 

WAKIX is a borderline/weak inducer of CYP3A4. WAKIX may reduce the effectiveness of sensitive CYP3A4 substrates, including hormonal contraceptives. Patients using hormonal contraception should be advised to use an alternative non-hormonal contraceptive method during treatment with WAKIX and for at least 21 days after discontinuing treatment.

Use in Specific Populations

There is a pregnancy exposure registry that monitors pregnancy outcomes in women who are exposed to WAKIX during pregnancy. Patients should be encouraged to enroll in the WAKIX pregnancy registry if they become pregnant. To enroll or obtain information from the registry, patients can call 1-800-833-7460.

The safety and effectiveness of WAKIX have not been established for treatment of excessive daytime sleepiness in pediatric patients less than 6 years of age with narcolepsy.

The safety and effectiveness of WAKIX have not been established for treatment of cataplexy in pediatric patients with narcolepsy.

WAKIX is extensively metabolized by the liver. WAKIX is contraindicated in patients with severe hepatic impairment. Dosage adjustment is recommended in patients with moderate hepatic impairment.

WAKIX is not recommended in patients with end-stage renal disease. Dosage adjustment of WAKIX is recommended in patients with eGFR <60 mL/minute/1.73 m2.

Dosage reduction is recommended in patients known to be poor CYP2D6 metabolizers; these patients have higher concentrations of WAKIX than normal CYP2D6 metabolizers.

Please see the Full Prescribing Information for WAKIX for more information.

To report suspected adverse reactions, contact Harmony Biosciences at 1-800-833-7460 or the FDA at 1-800-FDA-1088 or www.fda.gov/medwatch.

About Narcolepsy
Narcolepsy is a rare, chronic, debilitating neurological disease of sleep-wake state instability that impacts approximately 170,000 Americans and is primarily characterized by excessive daytime sleepiness (EDS) and cataplexy – its two cardinal symptoms – along with other manifestations of REM sleep dysregulation (hallucinations and sleep paralysis), which intrude into wakefulness. EDS is the inability to stay awake and alert during the day and is the symptom that is present in all people living with narcolepsy. In most patients, narcolepsy is caused by the loss of hypocretin/orexin, a neuropeptide in the brain that supports sleep-wake state stability. This disease affects men and women equally, with typical symptom onset in adolescence or young adulthood; however, it can take up to a decade to be properly diagnosed.

About Idiopathic Hypersomnia
Idiopathic Hypersomnia (IH) is a rare and chronic neurological disease that is characterized by excessive daytime sleepiness (EDS) despite sufficient or even long sleep time. EDS in IH cannot be alleviated by naps, longer sleep or more efficient sleep. People living with IH experience significant EDS along with the symptoms of sleep inertia (prolonged difficulty waking up from sleep) and 'brain fog' (impaired cognition, attention, and alertness). The cause of IH is unknown, but it is likely due to alterations in areas of the brain that stabilize states of sleep and wakefulness. IH is one of the central disorders of hypersomnolence and, like narcolepsy, is a debilitating sleep disorder that can result in significant disruption in daily functioning.

About ZYN-002
ZYN-002 is the first-and-only pharmaceutically manufactured synthetic cannabidiol devoid of THC and formulated as a patent-protected permeation-enhanced gel for transdermal delivery through the skin and into the circulatory system. The product is manufactured through a synthetic process in a cGMP facility and is not extracted from the cannabis plant. ZYN-002 does not contain THC, the compound that causes the euphoric effect of cannabis, and has the potential to be a nonscheduled product if approved. Cannabidiol, the active ingredient in ZYN-002, has been granted orphan drug designation by the United States Food and Drug Administration (FDA) and the European Medicines Agency (EMA) for the treatment of FXS and for the treatment of 22q. Additionally, ZYN-002 has received FDA Fast Track designation for the treatment of behavioral symptoms in patients with FXS.

About Fragile X Syndrome
Fragile X syndrome (FXS) is a rare genetic disorder that is the leading known cause of both inherited intellectual disability and autism spectrum disorder. The disorder negatively affects synaptic function, plasticity and neuronal connections, and results in a spectrum of intellectual disabilities and behavioral symptoms, such as social avoidance and irritability. While the exact prevalence is unknown, upwards of 80,000 patients in the U.S. and 121,000 patients in the European Union and the UK are believed to have FXS, based on FXS prevalence estimates of approximately 1 in 4,000 to 7,000 in males and approximately 1 in 8,000 to 11,000 in females. There is a significant unmet medical need in patients living with FXS as there are currently no FDA approved treatments for this disorder.

FXS is caused by a mutation in FMR1, a gene which modulates a number of systems, including the endocannabinoid system, and most critically, codes for a protein called FMRP. The FMR1 mutation manifests as multiple repeats of a DNA segment, known as the CGG triplet repeat, resulting in deficiency or lack of FMRP. FMRP helps regulate the production of other proteins and plays a role in the development of synapses, which are critical for relaying nerve impulses, and in regulating synaptic plasticity. In people with full mutation of the FMR1 gene, the CGG segment is repeated more than 200 times, and in most cases causes the gene to not function. Methylation of the FMR1 gene also plays a role in determining functionality of the gene. In approximately 60% of patients with FXS, who have complete methylation of the FMR1 gene, no FMRP is produced, resulting in dysregulation of the systems modulated by FMRP.

About 22q11.2 Deletion Syndrome
22q11.2 deletion syndrome (22q) is a disorder caused by a small missing piece of the 22nd chromosome. The deletion occurs near the middle of the chromosome at a location designated q11.2. It is considered a mid-line condition, with physical symptoms including characteristic palate abnormalities, heart defects, immune dysfunction, and esophageal/ GI issues, as well as debilitating neuropsychiatric and behavioral symptoms, including anxiety, social withdrawal, ADHD, cognitive impairment and autism spectrum disorder. It is estimated that 22q occurs in one in 4,000 live births, suggesting that there are approximately 80,000 people living with 22q in the U.S. and 129,000 in the European Union and the UK. Patients with 22q deletion syndrome are managed by multidisciplinary care providers, and there are currently no FDA approved treatments for this disorder.

About Clemizole Hydrochloride (EPX-100)
EPX-100, clemizole hydrochloride, is under development for the treatment of Dravet syndrome (DS) and Lennox-Gastaut syndrome (LGS). EPX-100 acts by targeting central 5-hydroxytryptamine receptors to modulate serotonin signaling. The drug candidate is administered orally twice a day in a liquid formulation and has been developed based on a proprietary phenotype-based zebrafish drug screening platform. DS is caused by a loss of function mutation in the SCN1A gene, and scn1 mutant zebrafish replicate the genetic etiology and phenotype observed in the majority of DS patients. The scn1Lab mutant zebrafish model that expresses voltage gated sodium channels has been used for high-throughput screening of compounds that modulate Nav1.1 in the central nervous system.

About Lorcaserin (EPX-200)
EPX-200, liquid formulation of lorcaserin is under development for the treatment of DEEs (Developmental Epileptic Encephalopathies). EPX-200 is a selective 5-HT2C receptor agonist. The drug candidate is developed based on a proprietary phenotype-based zebrafish drug screening platform and clinical data in patients with DEEs1,2.

About Dravet Syndrome
Dravet syndrome (DS) is a severe and progressive epileptic encephalopathy that begins in infancy and causes significant impact on patient functioning. DS begins in the first year of life and is characterized by high seizure frequency and severity, intellectual disability, and a risk of sudden unexpected death in epilepsy. Approximately 85% of Dravet Syndrome cases are caused by de novo loss-of-function (LOF) mutations in a voltage-gated sodium channel gene, SCN1A1. DS has an estimated incidence rate of 1:15,700.

About Lennox-Gastaut Syndrome
Lennox-Gastaut Syndrome (LGS) is a rare and drug-resistant epileptic encephalopathy characterized by onset in children between 3-5 years of age. The underlying cause of LGS is unknown and can be related to a wide range of factors including genetic differences and structural differences in the brain. As a result, patients experience multiple seizure types, including atonic seizures, and developmental, cognitive, and behavioral issues. LGS affects approximately 48,000 patients in the U.S. 

About Harmony Biosciences
Harmony Biosciences is a pharmaceutical company dedicated to developing and commercializing innovative therapies for patients with rare neurological diseases who have unmet medical needs. Driven by novel science, visionary thinking, and a commitment to those who feel overlooked, Harmony Biosciences is nurturing a future full of therapeutic possibilities that may enable patients with rare neurological diseases to truly thrive. Established by Paragon Biosciences, LLC, in 2017 and headquartered in Plymouth Meeting, PA, we believe that when empathy and innovation meet, a better future can begin; a vision evident in the therapeutic innovations we advance, the culture we cultivate, and the community programs we foster. For more information, please visit www.harmonybiosciences.com.

Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. All statements contained in this press release that do not relate to matters of historical fact should be considered forward-looking statements, including statements regarding our full year 2024 net product revenue, expectations for the growth and value of WAKIX, plans to submit an sNDA for pitolisant in idiopathic hypersomnia; our future results of operations and financial position, business strategy, products, prospective products, product approvals, the plans and objectives of management for future operations and future results of anticipated products. These statements are neither promises nor guarantees, but involve known and unknown risks, uncertainties and other important factors that may cause our actual results, performance or achievements to be materially different from any future results, performance or achievements expressed or implied by the forward-looking statements, including, but not limited to, the following: our commercialization efforts and strategy for WAKIX; the rate and degree of market acceptance and clinical utility of pitolisant in additional indications, if approved, and any other product candidates we may develop or acquire, if approved; our research and development plans, including our plans to explore the therapeutic potential of pitolisant in additional indications; our ongoing and planned clinical trials; our ability to expand the scope of our license agreements with Bioprojet Société Civile de Recherche ("Bioprojet"); the availability of favorable insurance coverage and reimbursement for WAKIX; the timing of, and our ability to obtain, regulatory approvals for pitolisant for other indications as well as any other product candidates; our estimates regarding expenses, future revenue, capital requirements and additional financing needs; our ability to identify, acquire and integrate additional products or product candidates with significant commercial potential that are consistent with our commercial objectives; our commercialization, marketing and manufacturing capabilities and strategy; significant competition in our industry; our intellectual property position; loss or retirement of key members of management; failure to successfully execute our growth strategy, including any delays in our planned future growth; our failure to maintain effective internal controls; the impact of government laws and regulations; volatility and fluctuations in the price of our common stock; the significant costs and required management time as a result of operating as a public company; the fact that the price of Harmony's common stock may be volatile and fluctuate substantially; statements related to our intended share repurchases and repurchase timeframe and the significant costs and required management time as a result of operating as a public company. These and other important factors discussed under the caption "Risk Factors" in our Annual Report on Form 10-K filed with the Securities and Exchange Commission (the "SEC") on February 22, 2024, and our other filings with the SEC could cause actual results to differ materially from those indicated by the forward-looking statements made in this press release. Any such forward-looking statements represent management's estimates as of the date of this press release. While we may elect to update such forward-looking statements at some point in the future, we disclaim any obligation to do so, even if subsequent events cause our views to change.

HARMONY BIOSCIENCES HOLDINGS, INC. AND SUBSIDIARIES

UNAUDITED CONDENSED CONSOLIDATED

STATEMENTS OF OPERATIONS AND COMPREHENSIVE INCOME

(In thousands, except share and per share data)




Three Months Ended September 30, 


Nine Months Ended September 30, 



2024


2023


2024


2023

Net product revenue


$

186,038


$

160,268


$

513,467


$

413,610

Cost of product sold



42,778



32,296



102,406



78,084

Gross profit



143,260



127,972



411,061



335,526

Operating expenses:













Research and development



25,387



17,499



111,159



45,757

Sales and marketing



27,576



23,418



83,316



70,518

General and administrative



28,587



22,546



81,487



67,417

Total operating
expenses



81,550



63,463



275,962



183,692

Operating income



61,710



64,509



135,099



151,834

Loss on debt extinguishment





(9,766)





(9,766)

Other (expense) income, net



(124)



(5)



(228)



(34)

Interest expense



(4,348)



(7,012)



(13,287)



(18,961)

Interest income



4,932



4,106



14,065



10,634

Income before income taxes



62,170



51,832



135,649



133,707

Income tax expense



(16,077)



(13,371)



(39,631)



(31,461)

Net income


$

46,093


$

38,461


$

96,018


$

102,246

Unrealized (loss) income on
investments



733



6



497



(365)

Comprehensive income


$

46,826


$

38,467


$

96,515


$

101,881

 EARNINGS PER SHARE:













Basic


$

0.81


$

0.64


$

1.69


$

1.71

Diluted


$

0.79


$

0.63


$

1.66


$

1.68

Weighted average number
of shares of common stock
- basic



56,870,234



59,863,102



56,815,167



59,856,941

Weighted average number
of shares of common stock
- diluted



58,103,963



60,681,676



57,754,016



60,892,992

 

HARMONY BIOSCIENCES HOLDINGS, INC. AND SUBSIDIARIES

UNAUDITED CONDENSED CONSOLIDATED BALANCE SHEETS
(In thousands, except share and per share data)




September 30, 


December 31, 



2024


2023

ASSETS







CURRENT ASSETS:







Cash and cash equivalents


$

387,367


$

311,660

Investments, short-term



23,109



41,800

Trade receivables, net



81,502



74,140

Inventory, net



6,915



5,363

Prepaid expenses



16,057



12,570

Other current assets



7,455



5,537

Total current assets



522,405



451,070

NONCURRENT ASSETS:







Property and equipment, net



750



371

Restricted cash



270



270

Investments, long-term



94,222



72,169

Intangible assets, net



119,225



137,108

Deferred tax asset



185,016



144,162

Other noncurrent assets



6,247



6,298

Total noncurrent assets



405,730



360,378

TOTAL ASSETS


$

928,135


$

811,448

LIABILITIES AND STOCKHOLDERS' EQUITY







CURRENT LIABILITIES:







Trade payables


$

10,532


$

17,730

Accrued compensation



14,224



23,747

Accrued expenses



109,673



99,494

Current portion of long-term debt



15,000



15,000

Other current liabilities



11,850



7,810

Total current liabilities



161,279



163,781

NONCURRENT LIABILITIES:







Long-term debt, net



167,847



178,566

Other noncurrent liabilities



2,205



2,109

Total noncurrent liabilities



170,052



180,675

TOTAL LIABILITIES



331,331



344,456

COMMITMENTS AND CONTINGENCIES (Note 13)







STOCKHOLDERS' EQUITY:







Common stock—$0.00001 par value; 500,000,000 shares authorized at
September 30, 2024 and December 31, 2023, respectively; 57,030,897 and
56,769,081 shares issued and outstanding at September 30, 2024 and
December 31, 2023, respectively



1



1

Additional paid in capital



643,563



610,266

Accumulated other comprehensive (loss) income



499



2

Accumulated deficit



(47,259)



(143,277)

TOTAL STOCKHOLDERS' EQUITY



596,804



466,992

TOTAL LIABILITIES AND STOCKHOLDERS' EQUITY


$

928,135


$

811,448

 

HARMONY BIOSCIENCES HOLDINGS, INC. AND SUBSIDIARIES

RECONCILIATION OF GAAP TO NON-GAAP FINANCIAL RESULTS

(In thousands except share and per share data)




Three Months Ended


Nine Months Ended



September 30,


September 30,


September 30,


September 30,



2024


2023


2024


2023

GAAP net income


$

46,093


$

38,461


$

96,018


$

102,246

Non-GAAP Adjustments:













Non-cash interest expense (1)



175



2,221



531



3,061

Depreciation



7



144



261



350

Amortization (2)



5,961



5,962



17,883



17,884

Stock-based compensation expense



11,448



7,957



32,845



22,311

Licensing fee and milestone payments (3)



1,000



-



26,500



750

Loss on debt extinguishment (4)



-



9,766



-



9,766

Transaction related costs (5)



-



-



17,095



-

Income tax effect related to non-GAAP
adjustments (6)



(5,096)



(5,723)



(20,215)



(10,987)

Non-GAAP adjusted net income


$

59,596


$

58,788


$

170,926


$

145,381














GAAP reported net income per diluted share


$

0.79


$

0.63


$

1.66


$

1.68

Non-GAAP adjusted net income per diluted share


$

1.03


$

0.97


$

2.96


$

2.39














Weighted average number of shares of common
stock used in non-GAAP diluted per share



58,103,963



60,681,676



57,754,016



60,892,992


(1) Includes amortization of deferred finance charges.

(2) Includes amortization of intangible asset related to WAKIX. 

(3) Amount represents upfront licensing fee incurred upon closing the 2024 Bioprojet Sublicense Agreement, milestone payment related to HBS-102 in September 2024 and milestone payment related to HBS-102 in March 2023.

(4) Includes loss on extinguishment of the Blackstone Credit Agreement.

(5) Includes IPR&D charge related to the acquisition of Epygenix.

(6) Calculated using the reported effective tax rate for the periods presented less impact of discrete items.

Harmony Biosciences Investor Contact:
Brennan Doyle
484-539-9700
bdoyle@harmonybiosciences.com

Harmony Biosciences Media Contact:
Cate McCanless
202-641-6086
cmccanless@harmonybiosciences.com

Cision View original content to download multimedia:https://www.prnewswire.com/news-releases/harmony-biosciences-reports-strong-third-quarter-2024-financial-results-and-highlights-catalyst-rich-late-stage-pipeline-poised-to-deliver-one-or-more-new-launches-every-year-over-next-five-years-302289505.html

SOURCE Harmony Biosciences

FAQ

What was Harmony Biosciences (HRMY) Q3 2024 revenue?

Harmony Biosciences reported net revenue of $186.0 million for Q3 2024, representing a 16% increase from Q3 2023.

How many patients are currently using WAKIX from Harmony Biosciences (HRMY)?

As of Q3 2024, approximately 6,800 patients were using WAKIX, representing an increase of 250 patients from the previous quarter.

What is Harmony Biosciences' (HRMY) revenue guidance for 2024?

Harmony Biosciences maintains its full-year 2024 net product revenue guidance of $700 million to $720 million.

When will Harmony Biosciences (HRMY) submit sNDA for Pitolisant in Idiopathic Hypersomnia?

Harmony Biosciences is on track to submit the sNDA for Pitolisant in Idiopathic Hypersomnia in Q4 2024.

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