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Beta Bionics Reports Second Quarter 2025 Financial Results and Raises Full Year 2025 Guidance

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Beta Bionics (Nasdaq: BBNX) reported strong Q2 2025 financial results, with net sales reaching $23.2 million, up 54% year-over-year. The company's installed customer base grew 200% to 24,085 users, with 4,934 new patient starts in Q2. The company achieved significant growth in both DME and PBP channels, with PBP channel sales surging 498% to $4.6 million.

Key operational metrics showed improvement with gross margin reaching 53.8%. Despite growth, the company reported a net loss of $16.9 million. Beta Bionics raised its full-year 2025 guidance, projecting revenue of $88-93 million, up from previous guidance of $82-87 million.

Strategic highlights include securing formulary agreements with major PBMs and completing dosing in the glucagon PK-PD bridging trial for their bihormonal configuration development.

Beta Bionics (Nasdaq: BBNX) ha annunciato risultati finanziari solidi per il secondo trimestre 2025, con vendite nette pari a 23,2 milioni di dollari, in aumento del 54% rispetto all'anno precedente. La base clienti installata è cresciuta del 200%, raggiungendo 24.085 utenti, con 4.934 nuovi pazienti iniziati nel Q2. L'azienda ha registrato una crescita significativa sia nel canale DME che in quello PBP, con vendite nel canale PBP in aumento del 498%, raggiungendo 4,6 milioni di dollari.

I principali indicatori operativi hanno mostrato miglioramenti, con un margine lordo che ha raggiunto il 53,8%. Nonostante la crescita, l'azienda ha riportato una perdita netta di 16,9 milioni di dollari. Beta Bionics ha rivisto al rialzo le previsioni per l'intero anno 2025, stimando ricavi tra 88 e 93 milioni di dollari, rispetto alla precedente stima di 82-87 milioni.

I punti strategici includono la stipula di accordi di formulary con importanti PBM e il completamento della somministrazione nella sperimentazione PK-PD del glucagone per lo sviluppo della configurazione bihormonale.

Beta Bionics (Nasdaq: BBNX) reportó sólidos resultados financieros para el segundo trimestre de 2025, con ventas netas que alcanzaron los 23,2 millones de dólares, un aumento del 54% interanual. La base de clientes instalada creció un 200%, llegando a 24.085 usuarios, con 4.934 nuevos pacientes iniciados en el segundo trimestre. La compañía logró un crecimiento significativo en los canales DME y PBP, con ventas en el canal PBP que aumentaron un 498%, alcanzando los 4,6 millones de dólares.

Los principales indicadores operativos mostraron mejoras, con un margen bruto que alcanzó el 53,8%. A pesar del crecimiento, la empresa reportó una pérdida neta de 16,9 millones de dólares. Beta Bionics elevó su guía para todo el año 2025, proyectando ingresos de 88 a 93 millones de dólares, frente a la guía previa de 82 a 87 millones.

Los aspectos estratégicos incluyen la obtención de acuerdos de formulario con importantes PBM y la finalización de la dosificación en el ensayo de puente PK-PD de glucagón para el desarrollo de su configuración bihormonal.

Beta Bionics (나스닥: BBNX)는 2025년 2분기 강력한 재무 실적을 보고했으며, 순매출은 2,320만 달러로 전년 동기 대비 54% 증가했습니다. 회사의 설치된 고객 기반은 200% 증가하여 24,085명에 달했으며, 2분기에 4,934명의 신규 환자가 시작되었습니다. 회사는 DME 및 PBP 채널 모두에서 상당한 성장을 이루었으며, PBP 채널 매출은 498% 급증하여 460만 달러에 달했습니다.

주요 운영 지표도 개선되어 총 마진율은 53.8%에 도달했습니다. 성장에도 불구하고 회사는 1,690만 달러의 순손실을 보고했습니다. Beta Bionics는 2025년 전체 연간 가이던스를 상향 조정하여 매출을 이전 가이던스인 8,200만~8,700만 달러에서 8,800만~9,300만 달러로 전망했습니다.

전략적 하이라이트로는 주요 PBM과의 포뮬러리 계약 확보 및 이중호르몬 구성 개발을 위한 글루카곤 PK-PD 브리징 시험의 투여 완료가 포함됩니다.

Beta Bionics (Nasdaq : BBNX) a annoncé de solides résultats financiers pour le deuxième trimestre 2025, avec des ventes nettes atteignant 23,2 millions de dollars, en hausse de 54 % par rapport à l'année précédente. La base clients installée a augmenté de 200 % pour atteindre 24 085 utilisateurs, avec 4 934 nouveaux patients débutant au T2. L'entreprise a enregistré une croissance significative dans les canaux DME et PBP, les ventes du canal PBP ayant bondi de 498 % pour atteindre 4,6 millions de dollars.

Les principaux indicateurs opérationnels se sont améliorés, avec une marge brute atteignant 53,8 %. Malgré cette croissance, l'entreprise a enregistré une perte nette de 16,9 millions de dollars. Beta Bionics a relevé ses prévisions pour l'ensemble de l'année 2025, projetant un chiffre d'affaires de 88 à 93 millions de dollars, contre une précédente estimation de 82 à 87 millions.

Les points stratégiques incluent la conclusion d'accords de formulaire avec de grands PBM et l'achèvement du dosage dans l'essai de pontage PK-PD du glucagon pour le développement de leur configuration bihormonale.

Beta Bionics (Nasdaq: BBNX) meldete starke Finanzergebnisse für das zweite Quartal 2025 mit Nettoumsätzen von 23,2 Millionen US-Dollar, was einem Anstieg von 54 % im Jahresvergleich entspricht. Die installierte Kundenbasis des Unternehmens wuchs um 200 % auf 24.085 Nutzer, mit 4.934 neuen Patientenstarts im zweiten Quartal. Das Unternehmen verzeichnete ein erhebliches Wachstum in den Vertriebskanälen DME und PBP, wobei die Umsätze im PBP-Kanal um 498 % auf 4,6 Millionen US-Dollar stiegen.

Wichtige operative Kennzahlen verbesserten sich, wobei die Bruttomarge 53,8 % erreichte. Trotz des Wachstums meldete das Unternehmen einen Nettoverlust von 16,9 Millionen US-Dollar. Beta Bionics hob seine Prognose für das Gesamtjahr 2025 an und erwartet nun Umsätze von 88 bis 93 Millionen US-Dollar, gegenüber der vorherigen Prognose von 82 bis 87 Millionen.

Strategische Highlights umfassen den Abschluss von Formulierungsveträgen mit großen PBMs und den Abschluss der Dosierung in der Glucagon-PK-PD-Brückungsstudie für die Entwicklung ihrer bihormonalen Konfiguration.

Positive
  • Net sales increased 54% year-over-year to $23.2 million
  • Installed customer base grew 200% to 24,085 users
  • PBP channel sales surged 498% to $4.6 million
  • Gross margin improved to 53.8%
  • Secured formulary agreements with all major U.S. PBMs
  • Raised full-year 2025 revenue guidance to $88-93 million
  • Strong cash position with $280.9 million in cash and investments
Negative
  • Operating loss increased to $19.9 million (86% of sales)
  • Net loss grew to $16.9 million
  • Adjusted EBITDA remained negative at $14.5 million
  • Operating losses widened compared to Q2 2024

Insights

Beta Bionics shows strong revenue growth despite losses, raising full-year guidance amid expanding market penetration and pharmacy channel growth.

Beta Bionics delivered impressive top-line growth with Q2 revenue reaching $23.2 million, a 54% year-over-year increase. The company's two-pronged distribution strategy is showing clear differentiation in growth rates. While the traditional DME channel grew a solid 31%, the pharmacy benefit plan channel exploded with 498% growth, albeit from a smaller base.

The installed customer base tripled to 24,085 users, demonstrating the iLet Bionic Pancreas is gaining significant market traction. Particularly noteworthy is that 71% of new patients are converting from multiple daily injections rather than competing pump systems, indicating Beta Bionics is expanding the overall pump market rather than merely taking share from competitors.

On the profitability front, gross margin held steady at 53.8%, but operating losses widened to $19.9 million from $11.8 million year-over-year. This reflects the company's aggressive investment in scaling operations and market penetration. Despite these losses, the $280.9 million cash position provides substantial runway to achieve scale.

The company's strategic highlights reveal important progress: securing formulary agreements with all major PBMs creates a clear path to expanded insurance coverage, potentially accelerating adoption. The development of the \"Mint\" patch pump and progress on the glucagon component for a bihormonal system indicate a robust product pipeline that could drive future growth.

Management's decision to raise full-year guidance across all metrics signals confidence in continued execution, with pharmacy channel penetration expected to reach 25-28% of new starts by year-end, improving accessibility and potentially accelerating adoption rates.

IRVINE, Calif., July 29, 2025 (GLOBE NEWSWIRE) -- Beta Bionics, Inc. (Nasdaq: BBNX), a pioneering leader in the development of advanced diabetes management solutions, today reported its financial results for the quarter ended June 30, 2025 and raised its full year guidance for the year ending December 31, 2025.

Second Quarter 2025 Financial Results & Key Metrics

  • Net sales of $23.2 million, up 54% compared to $15.0 million in the second quarter of 2024.
    • Durable Medical Equipment (DME) channel net sales of $18.6 million, up 31% compared to $14.3 million in the second quarter of 2024.
    • Pharmacy Benefit Plan (PBP) channel net sales of $4.6 million, up 498% compared to $0.8 million in the second quarter of 2024.
  • Gross margin of 53.8%, up 7 basis points compared to 53.7% in the second quarter of 2024.
  • Installed customer base (calculated as all new patient starts over a rolling four-year period) of 24,085 users, up 200% compared to 8,034 in the second quarter of 2024.
  • 4,934 new patient starts, up 57% compared to 3,133 new patient starts in the second quarter of 2024.
    • 71% of new patient starts came from multiple daily injections (MDI).
    • High 20s percentage of new patient starts reimbursed through the PBP channel.
  • Loss from operations of $19.9 million, or negative 86% of sales, compared to $11.8 million or negative 78% of sales in the second quarter of 2024.
  • Net loss of $16.9 million, or negative 73% of sales, compared to $14.5 million or negative 96% of sales in the second quarter of 2024.
  • Adjusted EBITDA(1) of negative $14.5 million, or negative 63% of sales, compared to negative $10.0 million or negative 66% of sales in the second quarter of 2024.
  • $280.9 million in cash, cash equivalents, short-term investments, and long-term investments as of June 30, 2025.

(1) See “Non-GAAP Financial Measures” below for additional information. A reconciliation of the non-GAAP financial measure to its most directly comparable GAAP financial measure can be found in Table E.

Recent Strategic Highlights

  • Hosted the company’s first investor and analyst event on June 22, 2025 in conjunction with the 85th Scientific Sessions of the American Diabetes Association.
    • Presented real-world evidence from the first two years of real-world iLet usage including outcomes for iLet users coming from multiple daily injections, iLet users coming from competitive hybrid-closed loop systems, iLet users treated in endocrinology or primary care practices, and iLet users that use the pump in a “fully-closed loop” manner, defined as users who announced less than one meal per day on average over 21 days.
    • Announced “Mint” as the brand name for the patch pump in development, and provided a live demonstration of Mint’s key features as well as the change process for the disposable cartridge.
  • As of July 1, 2025, Beta Bionics has effective formulary agreements in place with all the major pharmacy benefit managers (PBMs) that operate in the United States
    • For the PBMs with whom Beta Bionics has an effective formulary agreement in place, Beta Bionics is actively working with the health plans that partner with those PBMs to drive coverage of iLet under their pharmacy benefit.
    • For plans that cover the iLet Bionic Pancreas under their pharmacy benefit, this decision significantly reduces the potentially large up-front cost of the pump for both the patient and the plan, while easing the administrative burden for the physician when prescribing the iLet Bionic Pancreas.
  • Completed dosing in July 2025 for the glucagon pharmacokinetic (PK)-pharmacodynamic (PD) bridging trial in Canada.
    • The trial is intended to enable Beta Bionics to bridge previous bihormonal clinical data, which tested prior formulations of glucagon in three pre-pivotal inpatient and six pre-pivotal outpatient clinical trials, to Beta Bionics’ glucagon candidate developed by Xeris Pharmaceuticals for use in the bihormonal configuration of the iLet.
    • Preliminary PD data are supportive of continued development of the Glucagon candidate.
    • Beta Bionics expects to have full results from the PK-PD bridging trial in the second half of 2025, which will inform the go-forward development strategy for the glucagon candidate.

2025 Full Year Guidance

  • Estimated total revenue of $88 million to $93 million (previously $82 million to $87 million).
  • Estimated 25% to 28% of new patient starts reimbursed through the PBP channel (previously 22% to 25%).
  • Estimated gross margin of 52% to 55% (previously 50% to 53%).

Webcast & Conference Call Details

Beta Bionics will host a conference call and concurrent webcast today at 4:30 pm Eastern Time (1:30 pm Pacific Time), to review the company’s second quarter 2025 performance. The link to the webcast will be available on the Company’s website in the “Investors—Events & Presentations” section at https://investors.betabionics.com, and will be archived there for future replay. To access the live call by phone, please use the following link, which will provide you with dial-in details and a personal pin: https://register-conf.media-server.com/register/BIc649100069fd4629a4ed5bf4826b8acb.

Non-GAAP Financial Measures

Beta Bionics, Inc. (the “Company”) prepares and presents the Company’s financial statements in accordance with U.S. Generally Accepted Accounting Principles (“GAAP”). The Company believes adjusted EBITDA as a non-GAAP measure is useful in evaluating the Company’s operating performance and uses adjusted EBITDA to evaluate ongoing operations and for internal planning and forecasting purposes. The Company believes that this non-GAAP financial measure, when taken together with the corresponding GAAP financial measures, provide meaningful supplemental information regarding the Company’s performance by excluding certain items that may not be indicative of the Company’s business, results of operations, or outlook. However, non-GAAP financial information is presented for supplemental informational purposes only, has limitations as an analytical tool and should not be considered in isolation or as a substitute for financial information presented in accordance with GAAP. In addition, other companies, including companies in the Company’s industry, may calculate similarly-titled non-GAAP measures differently or may use other measures to evaluate their performance, all of which could reduce the usefulness of the Company’s non-GAAP financial measures as tools for comparison. A reconciliation is provided below for adjusted EBITDA to the most directly comparable financial measure stated in accordance with GAAP in Table E below.

The Company calculates adjusted EBITDA as net loss adjusted to exclude (i) depreciation and amortization expense, (ii) stock-based compensation expense, (iii) interest income, (iv) provision for state taxes, (v) change in fair value of warrant liabilities, and (vi) litigation settlement and other related expense.

Some of the limitations of adjusted EBITDA include: (i) adjusted EBITDA does not properly reflect capital commitments to be paid in the future and (ii) although depreciation and amortization expense are non-cash charges, the underlying assets may need to be replaced and adjusted EBITDA does not reflect these capital expenditures. The Company’s adjusted EBITDA may not be comparable to similarly titled measures of other companies because they may not calculate adjusted EBITDA in the same manner as the Company calculates the measure, limiting its usefulness as a comparative measure. In evaluating adjusted EBITDA, you should be aware that in the future the Company will incur expenses similar to the adjustments in this presentation. The Company’s presentation of adjusted EBITDA should not be construed as an inference that the Company’s future results will be unaffected by these expenses or any unusual or non-recurring items. When evaluating the Company’s performance, you should consider adjusted EBITDA alongside other financial performance measures, including the Company’s net loss and other GAAP results.

Investors are encouraged to review the related GAAP financial measures and the reconciliation of this non-GAAP financial measure to its most directly comparable GAAP financial measure, and not to rely on any single financial measure to evaluate the Company’s business. This non-GAAP measure has limitations as an analytical tool and should not be construed as an inference that the Company’s future results will be unaffected by unusual or non-recurring items. Therefore, this non-GAAP financial measure should be considered in addition to, not as a substitute for, or in isolation from, measures prepared in accordance with GAAP.

About Beta Bionics

Beta Bionics, Inc. is a commercial-stage medical device company engaged in the design, development, and commercialization of innovative solutions to improve the health and quality of life of insulin-requiring people with diabetes (PWD) by utilizing advanced adaptive closed-loop algorithms to simplify and improve the treatment of their disease. The iLet Bionic Pancreas is the first FDA-cleared insulin delivery device that autonomously determines every insulin dose and offers the potential to substantially improve overall outcomes across broad populations of PWD. To learn more, visit www.betabionics.com.

Forward-Looking Statements

This press release contains forward-looking statements within the meaning of the Private Securities Litigation Reform Act of 1995. Statements in this press release that are not statements of historical fact are forward-looking statements. Such forward-looking statements include, without limitation, statements regarding: expectations of Beta Bionics, Inc. (the “Company”) regarding its regulatory development plans for the iLet and other product candidates; the markets and market opportunities for the iLet and other product candidates, if approved; the timing, likelihood or success of its business strategy, including commercialization and its multi-channel reimbursement strategy, as well as plans and objectives of management for future operations; its anticipated growth and other measures of future operating results and financial performance, including 2025 full year guidance regarding revenue, new patient starts through the PBP channel and gross margin; and its expectation to have full results from the pharmacokinetic-pharmacodynamic bridging trial in the second half of 2025, and for such results to inform the go-forward development strategy for the glucagon candidate . Words such as “believe,” “anticipate,” “plan,” “expect,” “intend,” “will,” “may,” “goal,” “potential” and similar expressions are intended to identify forward-looking statements, though not all forward-looking statements necessarily contain these identifying words. These forward-looking statements are based on the beliefs of the management of the Company as well as assumptions made by and information currently available to the Company. Such statements reflect the current views of the Company with respect to future events and are subject to known and unknown risks and uncertainties, including business, regulatory, economic and competitive risks and uncertainties about the Company, including, without limitation, risks inherent in developing product candidates, future results from the Company’s ongoing and future studies and clinical trials, the Company’s ability to obtain adequate financing to fund its product development and other expenses, risks that real-world data or future results may not be consistent with interim, initial or preliminary results or results from prior preclinical studies or clinical trials, trends in the industry, the Company’s relationships with its existing and future collaboration partners, the legal and regulatory framework for the industry, future expenditures and the potential impacts of global macroeconomic conditions. In light of these risks and uncertainties, the events or circumstances referred to in the forward-looking statements may not occur. The actual results may vary from the anticipated results and the variations may be material. Other factors that may cause the Company’s actual results to differ from current expectations are discussed in the Company’s filings with the Securities and Exchange Commission, including the section titled “Risk Factors” in the Company’s Quarterly Report on Form 10-Q for the quarter ended June 30, 2025. You are cautioned not to place undue reliance on these forward-looking statements, which speak only as of the date this press release is given. Except as required by law, the Company undertakes no obligation to publicly update any forward-looking statements, whether as a result of new information, future events or otherwise.

Beta Bionics, Inc.
Statements of Operations and Comprehensive Loss (unaudited)
Table A
             
  Three Months Ended  Six Months Ended
(In thousands, except number of shares and per share data)

 June 30, June 30,
 2025  2024  2025  2024 
             
Net sales $23,238  $15,046  $40,877  $27,979 
Cost of sales  10,735   6,962   19,403   12,694 
Gross profit  12,503    8,084    21,474    15,285  
Gross margin  53.8%  53.7%  52.5%  54.6%
Operating expenses:            
Research and development  8,873   6,350   16,463   11,829 
Sales and marketing  15,623   8,974   29,025   16,637 
General and administrative  7,879   4,544   14,500   8,056 
Total operating expenses  32,375   19,868   59,988   36,522 
Loss from operations  (19,872)  (11,784)  (38,514)  (21,237)
Other income (expense):            
Interest income  3,005   993   5,441   2,132 
Other income (expense), net  (2)  (2)  (2)  2 
Change in fair value of warrant liabilities     (3,670)  (12,450)  (7,809)
Total other income (expense), net  3,003   (2,679)  (7,011)  (5,675)
Net loss  $(16,869) $(14,463) $(45,525) $(26,912)
Other comprehensive income (loss):            
Unrealized gain (loss) on short-term investments  (91)  (26)  84   (158)
Comprehensive loss $(16,960) $(14,489) $(45,441) $(27,070)
Net loss per share attributable to common stockholders, basic and diluted $(0.39)  (2.37) $(1.23) $(4.44)
Weighted-average common shares outstanding, basic and diluted 43,390,652  6,105,813  37,087,726  6,063,848 
             
             
Beta Bionics, Inc.
Balance Sheets (unaudited)
Table B
             
(In thousands, except number of shares)

 June 30, December 31,
 2025  2024 
Assets        
Current assets:        
Cash and cash equivalents   $35,075  $30,432 
Short-term investments    214,645   73,143 
Accounts receivable, net    11,395   11,996 
Inventories, net    17,323   13,320 
Prepaid expenses and other current assets    7,637   4,032 
Total current assets    286,075   132,923 
Property and equipment, net    6,465   4,776 
Operating lease right-of-use asset    6,038   6,645 
Restricted cash    100   100 
Deferred offering costs       5,051 
Long-term investments    31,149    
Other long-term assets    144   150 
Total assets   $329,971   $149,645  
         
Liabilities, Convertible Preferred Stock and Stockholders’ Equity (Deficit)        
Current liabilities:        
Accounts payable   $3,424  $2,852 
Accrued expenses and other current liabilities    13,405   15,828 
Operating lease liabilities    1,519   1,529 
Deferred revenue    1,141   939 
Total current liabilities    19,489   21,148 
Operating lease liabilities, net of current portion    5,168   5,726 
Deferred revenue, net of current portion    2,670   1,860 
Warrant liabilities           44,898 
Other long-term liabilities    1,011    
Total liabilities    28,338   73,632 
Commitments and contingencies        
Convertible preferred stock (Series A, A-2, B, B-2, C, D and E), par value of $0.0001 per share; no and 34,966,547 shares authorized at June 30, 2025 and December 31, 2024, respectively; no and 17,228,954 shares issued and outstanding at June 30, 2025 and December 31, 2024, respectively; liquidation preference of no and $355,162 at June 30, 2025 and December 31, 2024, respectively       321,373 
Stockholders’ equity (deficit):        
Class A common stock, par value of $0.0001 per share; no and 5,790,000 shares authorized at June 30, 2025 and December 31, 2024, respectively; no and 2,939,085 shares issued and outstanding at June 30, 2025 and December 31, 2024, respectively       1 
Class B common stock, par value of $0.0001 per share; no and 70,000,000 shares authorized at June 30, 2025 and December 31, 2024, respectively; no and 3,679,790 shares issued and outstanding at June 30, 2025 and December 31, 2024, respectively        
Class C common stock, par value of $0.0001 per share; no and 96,910 shares authorized at June 30, 2025 and December 31, 2024, respectively; no and 48,918 shares issued and outstanding at June 30, 2025 and December 31, 2024, respectively        
Preferred stock, par value of $0.0001 per share; 10,000,000 and no shares authorized at June 30, 2025 and December 31, 2024, respectively; no shares issued or outstanding at June 30, 2025 and December 31, 2024        
Common stock, par value of $0.0001 per share; 700,000,000 and no shares authorized at June 30, 2025 and December 31, 2024, respectively; 43,465,136 and no shares issued and outstanding at June 30, 2025 and December 31, 2024, respectively    4    
Additional paid-in capital    643,742   51,311 
Accumulated other comprehensive income    149   65 
Accumulated deficit   (342,262)  (296,737)
Total stockholders’ equity (deficit)    301,633    (245,360)
Total liabilities, convertible preferred stock and stockholders’ equity (deficit)   $329,971   $149,645  
             
             
Beta Bionics, Inc.
Net Sales by Channel (unaudited)
Table C
             
  Three Months Ended Six Months Ended
(In thousands)

 June 30, June 30,
 2025  2024  2025  2024 
DME channel:            
iLet(1) $13,414  $11,690  $23,042  $22,063 
Single-use products  5,230   2,588   9,429   4,320 
Total DME channel  18,644   14,278   32,471   26,383 
             
PBP channel:            
iLet(1)  205   229   711   520 
Single-use products  4,389   539   7,695   1,076 
Total PBP channel  4,594   768   8,406   1,596 
Total net sales $23,238   $15,046   $40,877   $27,979  
(1)iLet includes the over-time recognition software updates and mobile app access.
             
             
Beta Bionics, Inc.
Key Business Metrics (unaudited)
Table D
             
  Three Months Ended Six Months Ended
  June 30, June 30,
 2025  2024  2025  2024 
New patient starts(1)  4,934    3,133    8,787    5,730  
New patient starts from MDI as a percentage of total new patient starts  71%  69%  71%  66%
Installed customer base(2)  24,085    8,034    24,085    8,034  
(1)In the three months ended June 30, 2024 a mid-single digit percentage of our new patient starts were reimbursed through the PBP channel. In the three months ended June 30, 2025 a high 20s percentage of our new patient starts were reimbursed through the PBP channel.
(2)The installed customer base represents all new patient starts, over a rolling four-year period basis. This period reflects our in-warranty customer base under the typical four-year reimbursement cycle and helps us understand the total number of patients using the iLet.
             
             
Beta Bionics, Inc.
Reconciliation of GAAP versus Non-GAAP Financial Results (unaudited)
Table E
             
  Three Months Ended Six Months Ended
(In thousands)

 June 30, June 30,
 2025  2024  2025  2024 
Net loss $(16,869) $(14,463) $(45,525) $(26,912)
Add:            
Depreciation expense  347   299   650   586 
Stock-based compensation expense  4,799   1,499   7,603   2,856 
Interest income  (3,005)  (993)  (5,441)  (2,132)
Income tax expense (benefit)  2   2   2   2 
Litigation settlement and other related expense  200      200    
Change in fair value of warrant liabilities     3,670   12,450   7,809 
Adjusted EBITDA $(14,526) $(9,986) $(30,061) $(17,791)
             

Investor Relations:
Blake Beber
Head of Investor Relations
ir@betabionics.com

Media and Public Relations:
Karen Hynes
Vice President of Marketing
media@betabionics.com

Source: Beta Bionics, Inc.


FAQ

What were Beta Bionics (BBNX) Q2 2025 earnings results?

Beta Bionics reported Q2 2025 net sales of $23.2 million (up 54% YoY), with a net loss of $16.9 million. The company achieved a gross margin of 53.8% and had 4,934 new patient starts.

How many users does Beta Bionics' iLet system have in 2025?

Beta Bionics reported an installed customer base of 24,085 users as of Q2 2025, representing a 200% increase from 8,034 users in Q2 2024.

What is Beta Bionics' revenue guidance for 2025?

Beta Bionics raised its full-year 2025 revenue guidance to $88-93 million, up from the previous guidance of $82-87 million.

What progress has BBNX made with pharmacy benefit managers?

As of July 1, 2025, Beta Bionics has secured effective formulary agreements with all major U.S. pharmacy benefit managers (PBMs), significantly reducing up-front costs for patients and plans.

What is Beta Bionics' cash position as of Q2 2025?

Beta Bionics maintained a strong financial position with $280.9 million in cash, cash equivalents, and investments as of June 30, 2025.

What percentage of Beta Bionics' new patients come from multiple daily injections?

71% of Beta Bionics' new patient starts came from multiple daily injections (MDI) in Q2 2025.
Beta Bionics, Inc.

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