BrightSpring Announces Secondary Offering of Common Stock and Concurrent Share Repurchase

BrightSpring Announces Secondary Offering of Common Stock and Concurrent Share Repurchase




BrightSpring Announces Secondary Offering of Common Stock and Concurrent Share Repurchase

LOUISVILLE, Ky., March 02, 2026 (GLOBE NEWSWIRE) — BrightSpring Health Services, Inc. (NASDAQ: BTSG) (“BrightSpring” or the “Company”), a leading provider of home and community-based health services for complex populations, today announced that certain of its stockholders (the “Selling Stockholders”), including an affiliate of Kohlberg Kravis Roberts & Co. L.P. and certain members of management, intend to offer for sale in a secondary offering an aggregate of 20,000,000 shares of common stock of BrightSpring. No shares are being sold by BrightSpring in the offering. The Selling Stockholders will receive all of the proceeds from this offering.

In addition, the Company has authorized, subject to the completion of the offering, the concurrent purchase from the underwriter, out of the 20,000,000 shares of common stock being sold as part of the secondary public offering, a number of shares having an aggregate purchase price of up to the lesser of 10% of the shares sold in the offering or $60.0 million at a price per share equal to the price per share to be paid by the underwriter to the Selling Stockholders. The underwriter will not receive any underwriting fees for the shares being repurchased by the Company. The closing of the share repurchase is conditioned on, and expected to occur simultaneously with, the closing of the offering. The offering is not conditioned upon the completion of the share repurchase.

Goldman Sachs & Co. LLC is acting as the sole book-running manager for the proposed offering.

A shelf registration statement (including a prospectus) on Form S-3 relating to these securities was filed with the Securities and Exchange Commission on June 10, 2025 and became automatically effective upon filing. This press release shall not constitute an offer to sell or a solicitation of an offer to buy these securities, nor shall there be any sale of these securities in any state or jurisdiction in which such offer, solicitation or sale would be unlawful prior to registration or qualification under the securities laws of any such state or jurisdiction.

The offering of these securities will be made only by means of a preliminary prospectus supplement and accompanying prospectus. Copies of the preliminary prospectus supplement and accompanying prospectus for the offering may be obtained from Goldman Sachs & Co. LLC, Prospectus Department, 200 West Street, New York, NY 10282, telephone: 1-866-471-2526, facsimile: 212-902-9316 or by emailing Prospectus-ny@ny.email.gs.com.

Forward Looking Statements

The statements contained in this press release that are not historical facts are “forward-looking statements” within the meaning of the Private Securities Litigation Reform Act of 1995. These forward-looking statements are based on BrightSpring’s current expectations and are not guarantees of future performance. The forward-looking statements are subject to various risks, uncertainties, assumptions, or changes in circumstances that are difficult to predict or quantify. These expectations, beliefs, and projections are expressed in good faith and BrightSpring believes there is a reasonable basis for them. However, there can be no assurance that these expectations, beliefs, and projections will result or be achieved. Actual results may differ materially from these expectations due to changes in global, regional, or local economic, business, competitive, market, regulatory, and other factors, many of which are beyond BrightSpring’s control. Important factors that could cause actual results to differ materially from those in the forward-looking statements are set forth in BrightSpring’s filings with the SEC under caption “Risk Factors,” including its Annual Report on Form 10-K for the fiscal year ended December 31, 2025, and subsequent other filings BrightSpring makes with the SEC from time to time. Any forward-looking statement in this press release speaks only as of the date of this release. BrightSpring undertakes no obligation to publicly update or review any forward-looking statement, whether as a result of new information, future developments or otherwise, except as may be required by any applicable securities laws.

Contacts

Investor Relations:
David Deuchler, CFA
Gilmartin Group LLC
ir@brightspringhealth.com

or

Media Contact:
Leigh White
leigh.white@brightspringhealth.com
502.630.7412

Entrada Therapeutics Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)

Entrada Therapeutics Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)




Entrada Therapeutics Announces Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)

BOSTON, March 02, 2026 (GLOBE NEWSWIRE) — Entrada Therapeutics, Inc. (Nasdaq: TRDA) today announced that the Company granted an aggregate of 12,990 restricted stock units (“RSUs”) to two newly-hired non-executive employees under the Company’s 2025 Inducement Equity Plan (the “Inducement Plan”), effective as of March 1, 2026. The inducement grants were previously approved by the Compensation Committee of the Company’s Board of Directors, as a material inducement to the new employees’ entry into employment with the Company in accordance with Nasdaq Listing Rule 5635(c)(4).

One-fourth of the RSUs will vest on the one-year anniversary of the vesting commencement date, and 6.25% shall vest quarterly thereafter on each subsequent vesting date, with such vesting dates of March 1, June 1, September 1 and December 1 of each subsequent year, in each case, subject to each employee’s continuous service with the Company through each vesting date. The RSUs are subject to the terms and conditions of the Inducement Plan approved by the Company’s Board of Directors in March 2025 and the terms and conditions of award agreements covering the grants.

About Entrada Therapeutics
Entrada Therapeutics is a clinical-stage biopharmaceutical company aiming to transform the lives of patients by establishing a new class of genetic medicines that engage intracellular targets that have long been considered inaccessible. Through proprietary, versatile and modular approaches, Entrada is advancing a robust development portfolio of genetic medicines for the potential treatment of neuromuscular and inherited retinal diseases, among others. The Company’s lead oligonucleotide programs are in development for the potential treatment of people living with Duchenne muscular dystrophy who are exon 44, 45, 50 and 51 skipping amenable. Entrada has partnered to develop a clinical-stage program, VX-670, for myotonic dystrophy type 1.

For more information about Entrada, please visit our website, www.entradatx.com, and follow us on LinkedIn.

Investor Contact
Karla MacDonald
Chief Corporate Affairs Officer
kmacdonald@entradatx.com

Invivyd Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)

Invivyd Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)




Invivyd Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)

NEW HAVEN, Conn., March 02, 2026 (GLOBE NEWSWIRE) — Invivyd, Inc. (Nasdaq: IVVD) today announced that on March 1, 2026, Invivyd granted four newly hired non-executive employees options to purchase an aggregate of 192,000 shares of its common stock, each as a material inducement for each employee’s entry into employment with Invivyd. The options were granted in accordance with Nasdaq Listing Rule 5635(c)(4) and pursuant to the Invivyd, Inc. 2026 Inducement Plan.

The options have a per share exercise price of $1.69, representing the closing price of Invivyd’s common stock on February 27, 2026, the last trading date prior to the date of grant. Each option vests over four years, with 25% of the shares subject to such option vesting on the first anniversary of the employee’s start date and the remaining shares vesting in equal monthly installments thereafter, in each case, subject to the employee’s continuous service with Invivyd. The options have a 10-year term and are subject to the terms of the Invivyd, Inc. 2026 Inducement Plan.

About Invivyd

Invivyd, Inc. (Nasdaq: IVVD) is a biopharmaceutical company devoted to delivering protection from serious viral infectious diseases, beginning with SARS-CoV-2. Invivyd deploys a proprietary integrated technology platform unique in the industry designed to assess, monitor, develop, and adapt to create best in class antibodies. In March 2024, Invivyd received emergency use authorization (EUA) from the U.S. FDA for a monoclonal antibody (mAb) in its pipeline of innovative antibody candidates. Visit https://invivyd.com/ to learn more. 

This press release contains hyperlinks to information that is not deemed to be incorporated by reference in this press release.

Contacts:

Media Relations
(781) 208-0160
media@invivyd.com

Investor Relations
(781) 208-1747
investors@invivyd.com

Invivyd Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)

Invivyd Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)




Invivyd Reports Inducement Grants Under Nasdaq Listing Rule 5635(c)(4)

NEW HAVEN, Conn., March 02, 2026 (GLOBE NEWSWIRE) — Invivyd, Inc. (Nasdaq: IVVD) today announced that on March 1, 2026, Invivyd granted four newly hired non-executive employees options to purchase an aggregate of 192,000 shares of its common stock, each as a material inducement for each employee’s entry into employment with Invivyd. The options were granted in accordance with Nasdaq Listing Rule 5635(c)(4) and pursuant to the Invivyd, Inc. 2026 Inducement Plan.

The options have a per share exercise price of $1.69, representing the closing price of Invivyd’s common stock on February 27, 2026, the last trading date prior to the date of grant. Each option vests over four years, with 25% of the shares subject to such option vesting on the first anniversary of the employee’s start date and the remaining shares vesting in equal monthly installments thereafter, in each case, subject to the employee’s continuous service with Invivyd. The options have a 10-year term and are subject to the terms of the Invivyd, Inc. 2026 Inducement Plan.

About Invivyd

Invivyd, Inc. (Nasdaq: IVVD) is a biopharmaceutical company devoted to delivering protection from serious viral infectious diseases, beginning with SARS-CoV-2. Invivyd deploys a proprietary integrated technology platform unique in the industry designed to assess, monitor, develop, and adapt to create best in class antibodies. In March 2024, Invivyd received emergency use authorization (EUA) from the U.S. FDA for a monoclonal antibody (mAb) in its pipeline of innovative antibody candidates. Visit https://invivyd.com/ to learn more. 

This press release contains hyperlinks to information that is not deemed to be incorporated by reference in this press release.

Contacts:

Media Relations
(781) 208-0160
media@invivyd.com

Investor Relations
(781) 208-1747
investors@invivyd.com

Senseonics Holdings, Inc. Reports Fourth Quarter and Full Year 2025 Financial Results

Senseonics Holdings, Inc. Reports Fourth Quarter and Full Year 2025 Financial Results




Senseonics Holdings, Inc. Reports Fourth Quarter and Full Year 2025 Financial Results

Generated Q4 revenue of $14.3 million, an increase of 72% year-over-year

Received CE Mark approval for commercialization of Eversense 365 in Europe

Launched first Eversense 365 AID system integration, with twiist in the US

GERMANTOWN, Md., March 02, 2026 (GLOBE NEWSWIRE) — Senseonics Holdings, Inc. (NASDAQ: SENS) a medical technology company focused on the development, manufacturing and commercialization of long-term, implantable continuous glucose monitoring (CGM) systems for people with diabetes, today announced fourth quarter 2025 financial results and provided a business update.

Recent Highlights & Accomplishments

  • Generated fourth quarter 2025 revenue of $14.3 million, an increase of approximately 72% year-over-year, and full year 2025 revenue of $35.3 million, an increase of approximately 57% year-over-year
  • Achieved 103% new patient growth in the U.S. in 2025 versus 2024, driven largely by positive returns from direct-to-consumer (DTC) marketing efforts
  • Further development of the Eon Care inserter network to 60 providers performing approximately 24% of all U.S. insertions in 2025
  • Continued growth of the HCP channel, with the number of active prescribers growing over 80% from 2024 to 2025
  • Received CE Mark approval for Eversense 365 in the European Union (EU)
  • Secured Investigational Device Exemption (IDE) approval from the FDA to commence a pivotal trial for the self-powered battery enabled Gemini sensor and enrolled the first patients in the trial, which the Company expects to complete in the second half of 2026
  • Launched the combination of the twiist™ Automated Insulin Delivery (AID) System integrated with the Eversense® 365 CGM system across the U.S.
  • Executed agreements with Ascensia Diabetes Care to take back commercialization and distribution of Eversense beginning January 1, 2026

Tim Goodnow, PhD, President and Chief Executive Officer of Senseonics said, “In 2025, we took strategic actions to set the Company up for long term growth. Successfully bringing commercial operations in-house and investing heavily in DTC marketing, we built the foundations necessary to achieve the full potential of the world’s first and only year-long CGM. We delivered encouraging commercial results last year, and expect this momentum to continue. In 2026 we plan to expand Eversense 365 compatibility with AID systems, launch in Europe and complete the Gemini pivotal trial, an important milestone for our exciting innovation pipeline. These efforts, coupled with improved margins, set Senseonics up for continued strong performance this year and beyond. We expect these efforts, coupled with improved margins, will set Senseonics up for continued strong performance this year and beyond.”

Fourth Quarter 2025 Results:
Total revenue for the fourth quarter of 2025 was $14.3 million compared to $8.3 million for the fourth quarter of 2024. U.S. revenue was $12.1 million for the fourth quarter of 2025 compared to $6.2 million for the fourth quarter of 2024, and revenue outside the U.S. was $2.2 million in the fourth quarter of 2025 compared to $2.1 million in the prior year period.

Fourth quarter 2025 gross profit was $7.7 million compared to a gross profit of $4.0 million for the fourth quarter of 2024. The increase in gross profit was partially due to the one-time charges incurred in the prior year as the result of the transition from Eversense E3 to Eversense 365. The additional improvement in the gross profit is due to several factors, including favorable margins on the 365-day product sales, lower fixed manufacturing costs, and one-time impacts such as VAT recoveries.

Fourth quarter 2025 research and development expenses decreased by $0.6 million year-over-year to $8.8 million from $9.4 million for the fourth quarter of 2024. The decrease was primarily due to the completion of the Eversense 365 clinical trials and development efforts as well as a reduction in headcount.

Fourth quarter 2025 selling, general and administrative expenses increased by $10.9 million year-over-year to $19.8 million from $8.9 million for the fourth quarter of 2024. The increase was primarily driven by higher selling and marketing personnel costs, promotional expenses mainly due to direct-to-consumer campaign investments, sales commission expenses as we increased consignment sales, and other general and administrative costs.

Net loss was $20.8 million, or a $0.46 loss per share, in the fourth quarter of 2025 compared to net loss of $15.5 million, or a $0.46 loss per share, in the fourth quarter of 2024. Net loss increased by $5.3 million primarily due to increased expenses due to increased consignment sales and other costs related to taking over the commercialization and distribution of Eversense.

Full Year 2025 Results:
Total revenue for 2025 was $35.3 million compared to $22.5 million in 2024. U.S. revenue was $27.9 million in 2025 compared to $15.3 million in 2024, and revenue outside the U.S. was $7.4 million in 2025 compared to $7.2 million in 2024.

Gross profit for 2025 was $15.8 million, an increase from $0.5 million in 2024. The increase in gross profit was primarily driven by $4.8 million in one-time charges incurred in the prior year as the result of the transition from Eversense E3 to Eversense 365. In addition, gross profit improved as the result of favorable margins on the 365-day product sales, lower fixed manufacturing costs, and one-time impacts such as VAT recoveries.

Research and development expenses for 2025 decreased by $9.5 million year-over-year, to $31.6 million. The decrease was primarily due to the completion of the Eversense 365 clinical trials and development efforts including the impact of inventory costs incurred prior to 365-day product regulatory approval as well as a reduction in headcount.

Selling, general and administrative expenses for 2025 increased by $18.3 million year-over-year, to $52.5 million. The increase was primarily driven by direct-to-consumer campaign investments, increased sales commission expenses as we increased consignment sales, and other general and administrative costs partially driven by activities to take back Eversense commercialization and distribution.

Net loss was $69.1 million, or a $1.66 loss per share, in 2025 compared to net loss of $78.6 million, or a $2.50 loss per share, in 2024. Net loss decreased by $9.5 million primarily due to the increase in gross profit margin offset by higher selling, general, and administrative costs to support our sales growth.

Cash, cash equivalents and investments were $94.3 million and outstanding indebtedness was $35.3 million as of December 31, 2025.

Full Year 2026 Financial Outlook

Senseonics expects full-year 2026 global net revenue to be approximately $58-$62 million, representing year-over-year growth of 65% to 76%, as the Company completes the transition of Eversense commercialization from Ascensia and brings the entire sales and marketing infrastructure in-house. Gross margins are expected to be approximately 50% for the full year. The financial outlook takes into consideration the following factors: (i) refined plans for commercial transition from Ascensia to Senseonics and the roll-out of Eversense 365 outside the United States, (ii) plans with respect to spending on the DTC marketing campaigns to generate leads, (iii) the status of other sales and marketing initiatives, and (iv) utilization of the patient assistance programs for Eversense 365.

Conference Call Information

Management will hold a conference call to review the Company’s fourth quarter and full year 2025 performance starting today at 4:30 p.m. (Eastern Time). The conference call will be concurrently webcast. The link to the webcast will be available on Senseonics’ website at www.senseonics.com by navigating to “Investor Relations,” and then “Events & Publications,” and will be archived there for future reference. To listen to the conference call, please dial 1-800-343-5172 (US/Canada) or 1-203-518-9856 (International), passcode SENSQ4, approximately five to ten minutes prior to start time.

About Senseonics

Senseonics Holdings, Inc. (“Senseonics”) is a medical technology company focused on the development and manufacturing of glucose monitoring products designed to transform lives in the global diabetes community with differentiated, long-term implantable glucose management technology. Senseonics’ CGM systems Eversense® 365 and Eversense® E3 include a small sensor inserted completely under the skin that communicates with a smart transmitter worn over the sensor. The glucose data are automatically sent every 5 minutes to a mobile app on the user’s smartphone.

About Eversense

The Eversense® Continuous Glucose Monitoring (CGM) Systems are indicated for continually measuring glucose levels for up to 365 days for Eversense® 365 and 180 days for Eversense® E3 in persons with diabetes age 18 and older. The systems are indicated for use to replace fingerstick blood glucose (BG) measurements for diabetes treatment decisions. Fingerstick BG measurements are still required for calibration primarily one time per week after day 14 for Eversense® 365 and one time per day after day 21 for Eversense® E3, and when symptoms do not match CGM information or when taking medications of the tetracycline class. The sensor insertion and removal procedures are performed by a health care provider. The Eversense CGM Systems are prescription devices; patients should talk to their health care provider to learn more. For important safety information, see https://www.eversensediabetes.com/safety-info/.

Forward Looking Statements

Any statements in this press release about future expectations, plans and prospects for Senseonics, including the revenue and gross margin projections under the heading “Full Year 2026 Financial Outlook,” statements regarding the ongoing transition of Eversense commercial operations from Ascensia, the commercial launch of Eversense 365 in the European Union, the expanded compatibility of Eversense 365 with automated insulin delivery systems, the anticipated timing of the completion of the Gemini trial, the future demand for Eversense, and other statements containing the words “believe,” “expect,” “intend,” “may,” “projects,” “will,” “planned,” and similar expressions, constitute forward-looking statements within the meaning of The Private Securities Litigation Reform Act of 1995. Actual results may differ materially from those indicated by such forward-looking statements as a result of various important factors, including: risks and uncertainties related to the transition of commercial responsibility for Eversense from Ascensia, including the negotiation, finalization and execution of the local purchase agreements related to the Eversense commercial operations in the European Union; uncertainties in insurer, regulatory and administrative processes and decisions; uncertainties in the development and registration and roll-out of new technology and solutions; uncertainties in finalizing integration and commercial terms and coordination with health systems and other new collaboration partners and third parties; uncertainties inherent in the ongoing commercialization and expansion of the Eversense product and Senseonics’ and its partners’ activities; uncertainties relating to the current economic and regulatory/political environment, including the effects of tariffs; and such other factors as are set forth in the risk factors detailed in Senseonics’ Annual Report on Form 10-K for the year ended December 31, 2025 and quarterly reports on Form 10-Q filed with the SEC under the heading “Risk Factors.” The forward-looking statements included in this press release represent Senseonics’ views as of the date hereof. Senseonics anticipates that subsequent events and developments will cause Senseonics’ views to change. However, while Senseonics may elect to update these forward-looking statements at some point in the future, Senseonics specifically disclaims any obligation to do so except as required by law. These forward-looking statements should not be relied upon as representing Senseonics’ views as of any date subsequent to the date hereof.

Senseonics Investor Contact
Jeremy Feffer
LifeSci Advisors
investors@senseonics.com

 
Senseonics Holdings, Inc.
Unaudited Consolidated Balance Sheets
(in thousands, except for share and per share data)
             
    December 31,
    2025     2024  
Assets            
Current assets:            
Cash and cash equivalents   $ 40,234     $ 74,597  
Restricted cash     315       315  
Short term investments, net     53,796       —  
Accounts receivable, net     6,807       1,365  
Accounts receivable, net – related parties     5,312       4,921  
Inventory, net     6,703       4,421  
Prepaid expenses and other current assets     4,366       5,819  
Total current assets     117,533       91,438  
             
Deposits and other assets     4,536       4,926  
Property, equipment and intangible assets, net     4,200       4,074  
Total assets   $ 126,269     $ 100,438  
             
Liabilities and Stockholders’ (Deficit) Equity            
Current liabilities:            
Accounts payable   $ 4,059     $ 3,205  
Accrued expenses and other current liabilities     15,091       13,636  
Accrued expenses and other current liabilities, related parties     5,198       1,870  
Note payable, current portion, net     —       20,138  
Total current liabilities     24,348       38,849  
             
Long-term debt and notes payables, net     35,586       34,703  
Non-current operating lease liabilities     5,289       5,785  
Total liabilities     65,223       79,337  
             
Commitments and contingencies            
             
Preferred stock and additional paid-in-capital, subject to possible redemption: $0.001 par value per share; 0 shares and 12,000 shares issued and outstanding as of December 31, 2025 and December 31, 2024     —       37,656  
Total temporary equity     —       37,656  
             
Stockholders’ equity (deficit):            
Common stock, $0.001 par value per share; 70,000,000 shares authorized as of December 31, 2025 and December 31, 2024; 41,265,778 shares and 29,767,561 shares issued and outstanding as of December 31, 2025 and December 31, 2024     41       30  
Additional paid-in capital     1,077,923       931,289  
Accumulated other comprehensive income     69       —  
Accumulated deficit     (1,016,987 )     (947,874 )
Total stockholders’ equity (deficit)     61,046       (16,555 )
Total liabilities, temporary equity and stockholders’ equity (deficit)   $ 126,269     $ 100,438  
                 


 
Senseonics Holdings, Inc.

Unaudited Consolidated Statements of Operations and Comprehensive Loss
(in thousands, except for share and per share data)

 
    Years Ended
    December 31,
    2025     2024  
             
             
Revenue, net   $ 17,084     $ 3,973  
Revenue, net – related parties     18,173       18,499  
Total revenue     35,257       22,472  
Cost of sales     19,494       21,939  
Gross profit     15,763       533  
             
Expenses:            
Research and development expenses     31,592       41,144  
Selling, general and administrative expenses     52,508       34,231  
Operating loss     (68,337 )     (74,842 )
Other income (expense), net:            
Interest income     4,198       4,502  
Interest expense     (4,951 )     (8,437 )
Gain on change in fair value of derivatives     —       102  
Other expense ( income)     (23 )     59  
Total other expense, net     (776 )     (3,774 )
             
Net Loss     (69,113 )     (78,616 )
Other comprehensive income            
Unrealized gain on marketable securities     69       11  
Total other comprehensive income     69       11  
Total comprehensive loss   $ (69,044 )   $ (78,605 )
             
Basic net loss per common share   $ (1.66 )   $ (2.50 )
Basic weighted-average shares outstanding     41,727,983       31,486,079  
             
Diluted net loss per common share   $ (1.66 )   $ (2.50 )
Diluted weighted-average shares outstanding     41,727,983       31,486,079  

Senseonics Holdings, Inc. Reports Fourth Quarter and Full Year 2025 Financial Results

Senseonics Holdings, Inc. Reports Fourth Quarter and Full Year 2025 Financial Results




Senseonics Holdings, Inc. Reports Fourth Quarter and Full Year 2025 Financial Results

Generated Q4 revenue of $14.3 million, an increase of 72% year-over-year

Received CE Mark approval for commercialization of Eversense 365 in Europe

Launched first Eversense 365 AID system integration, with twiist in the US

GERMANTOWN, Md., March 02, 2026 (GLOBE NEWSWIRE) — Senseonics Holdings, Inc. (NASDAQ: SENS) a medical technology company focused on the development, manufacturing and commercialization of long-term, implantable continuous glucose monitoring (CGM) systems for people with diabetes, today announced fourth quarter 2025 financial results and provided a business update.

Recent Highlights & Accomplishments

  • Generated fourth quarter 2025 revenue of $14.3 million, an increase of approximately 72% year-over-year, and full year 2025 revenue of $35.3 million, an increase of approximately 57% year-over-year
  • Achieved 103% new patient growth in the U.S. in 2025 versus 2024, driven largely by positive returns from direct-to-consumer (DTC) marketing efforts
  • Further development of the Eon Care inserter network to 60 providers performing approximately 24% of all U.S. insertions in 2025
  • Continued growth of the HCP channel, with the number of active prescribers growing over 80% from 2024 to 2025
  • Received CE Mark approval for Eversense 365 in the European Union (EU)
  • Secured Investigational Device Exemption (IDE) approval from the FDA to commence a pivotal trial for the self-powered battery enabled Gemini sensor and enrolled the first patients in the trial, which the Company expects to complete in the second half of 2026
  • Launched the combination of the twiist™ Automated Insulin Delivery (AID) System integrated with the Eversense® 365 CGM system across the U.S.
  • Executed agreements with Ascensia Diabetes Care to take back commercialization and distribution of Eversense beginning January 1, 2026

Tim Goodnow, PhD, President and Chief Executive Officer of Senseonics said, “In 2025, we took strategic actions to set the Company up for long term growth. Successfully bringing commercial operations in-house and investing heavily in DTC marketing, we built the foundations necessary to achieve the full potential of the world’s first and only year-long CGM. We delivered encouraging commercial results last year, and expect this momentum to continue. In 2026 we plan to expand Eversense 365 compatibility with AID systems, launch in Europe and complete the Gemini pivotal trial, an important milestone for our exciting innovation pipeline. These efforts, coupled with improved margins, set Senseonics up for continued strong performance this year and beyond. We expect these efforts, coupled with improved margins, will set Senseonics up for continued strong performance this year and beyond.”

Fourth Quarter 2025 Results:
Total revenue for the fourth quarter of 2025 was $14.3 million compared to $8.3 million for the fourth quarter of 2024. U.S. revenue was $12.1 million for the fourth quarter of 2025 compared to $6.2 million for the fourth quarter of 2024, and revenue outside the U.S. was $2.2 million in the fourth quarter of 2025 compared to $2.1 million in the prior year period.

Fourth quarter 2025 gross profit was $7.7 million compared to a gross profit of $4.0 million for the fourth quarter of 2024. The increase in gross profit was partially due to the one-time charges incurred in the prior year as the result of the transition from Eversense E3 to Eversense 365. The additional improvement in the gross profit is due to several factors, including favorable margins on the 365-day product sales, lower fixed manufacturing costs, and one-time impacts such as VAT recoveries.

Fourth quarter 2025 research and development expenses decreased by $0.6 million year-over-year to $8.8 million from $9.4 million for the fourth quarter of 2024. The decrease was primarily due to the completion of the Eversense 365 clinical trials and development efforts as well as a reduction in headcount.

Fourth quarter 2025 selling, general and administrative expenses increased by $10.9 million year-over-year to $19.8 million from $8.9 million for the fourth quarter of 2024. The increase was primarily driven by higher selling and marketing personnel costs, promotional expenses mainly due to direct-to-consumer campaign investments, sales commission expenses as we increased consignment sales, and other general and administrative costs.

Net loss was $20.8 million, or a $0.46 loss per share, in the fourth quarter of 2025 compared to net loss of $15.5 million, or a $0.46 loss per share, in the fourth quarter of 2024. Net loss increased by $5.3 million primarily due to increased expenses due to increased consignment sales and other costs related to taking over the commercialization and distribution of Eversense.

Full Year 2025 Results:
Total revenue for 2025 was $35.3 million compared to $22.5 million in 2024. U.S. revenue was $27.9 million in 2025 compared to $15.3 million in 2024, and revenue outside the U.S. was $7.4 million in 2025 compared to $7.2 million in 2024.

Gross profit for 2025 was $15.8 million, an increase from $0.5 million in 2024. The increase in gross profit was primarily driven by $4.8 million in one-time charges incurred in the prior year as the result of the transition from Eversense E3 to Eversense 365. In addition, gross profit improved as the result of favorable margins on the 365-day product sales, lower fixed manufacturing costs, and one-time impacts such as VAT recoveries.

Research and development expenses for 2025 decreased by $9.5 million year-over-year, to $31.6 million. The decrease was primarily due to the completion of the Eversense 365 clinical trials and development efforts including the impact of inventory costs incurred prior to 365-day product regulatory approval as well as a reduction in headcount.

Selling, general and administrative expenses for 2025 increased by $18.3 million year-over-year, to $52.5 million. The increase was primarily driven by direct-to-consumer campaign investments, increased sales commission expenses as we increased consignment sales, and other general and administrative costs partially driven by activities to take back Eversense commercialization and distribution.

Net loss was $69.1 million, or a $1.66 loss per share, in 2025 compared to net loss of $78.6 million, or a $2.50 loss per share, in 2024. Net loss decreased by $9.5 million primarily due to the increase in gross profit margin offset by higher selling, general, and administrative costs to support our sales growth.

Cash, cash equivalents and investments were $94.3 million and outstanding indebtedness was $35.3 million as of December 31, 2025.

Full Year 2026 Financial Outlook

Senseonics expects full-year 2026 global net revenue to be approximately $58-$62 million, representing year-over-year growth of 65% to 76%, as the Company completes the transition of Eversense commercialization from Ascensia and brings the entire sales and marketing infrastructure in-house. Gross margins are expected to be approximately 50% for the full year. The financial outlook takes into consideration the following factors: (i) refined plans for commercial transition from Ascensia to Senseonics and the roll-out of Eversense 365 outside the United States, (ii) plans with respect to spending on the DTC marketing campaigns to generate leads, (iii) the status of other sales and marketing initiatives, and (iv) utilization of the patient assistance programs for Eversense 365.

Conference Call Information

Management will hold a conference call to review the Company’s fourth quarter and full year 2025 performance starting today at 4:30 p.m. (Eastern Time). The conference call will be concurrently webcast. The link to the webcast will be available on Senseonics’ website at www.senseonics.com by navigating to “Investor Relations,” and then “Events & Publications,” and will be archived there for future reference. To listen to the conference call, please dial 1-800-343-5172 (US/Canada) or 1-203-518-9856 (International), passcode SENSQ4, approximately five to ten minutes prior to start time.

About Senseonics

Senseonics Holdings, Inc. (“Senseonics”) is a medical technology company focused on the development and manufacturing of glucose monitoring products designed to transform lives in the global diabetes community with differentiated, long-term implantable glucose management technology. Senseonics’ CGM systems Eversense® 365 and Eversense® E3 include a small sensor inserted completely under the skin that communicates with a smart transmitter worn over the sensor. The glucose data are automatically sent every 5 minutes to a mobile app on the user’s smartphone.

About Eversense

The Eversense® Continuous Glucose Monitoring (CGM) Systems are indicated for continually measuring glucose levels for up to 365 days for Eversense® 365 and 180 days for Eversense® E3 in persons with diabetes age 18 and older. The systems are indicated for use to replace fingerstick blood glucose (BG) measurements for diabetes treatment decisions. Fingerstick BG measurements are still required for calibration primarily one time per week after day 14 for Eversense® 365 and one time per day after day 21 for Eversense® E3, and when symptoms do not match CGM information or when taking medications of the tetracycline class. The sensor insertion and removal procedures are performed by a health care provider. The Eversense CGM Systems are prescription devices; patients should talk to their health care provider to learn more. For important safety information, see https://www.eversensediabetes.com/safety-info/.

Forward Looking Statements

Any statements in this press release about future expectations, plans and prospects for Senseonics, including the revenue and gross margin projections under the heading “Full Year 2026 Financial Outlook,” statements regarding the ongoing transition of Eversense commercial operations from Ascensia, the commercial launch of Eversense 365 in the European Union, the expanded compatibility of Eversense 365 with automated insulin delivery systems, the anticipated timing of the completion of the Gemini trial, the future demand for Eversense, and other statements containing the words “believe,” “expect,” “intend,” “may,” “projects,” “will,” “planned,” and similar expressions, constitute forward-looking statements within the meaning of The Private Securities Litigation Reform Act of 1995. Actual results may differ materially from those indicated by such forward-looking statements as a result of various important factors, including: risks and uncertainties related to the transition of commercial responsibility for Eversense from Ascensia, including the negotiation, finalization and execution of the local purchase agreements related to the Eversense commercial operations in the European Union; uncertainties in insurer, regulatory and administrative processes and decisions; uncertainties in the development and registration and roll-out of new technology and solutions; uncertainties in finalizing integration and commercial terms and coordination with health systems and other new collaboration partners and third parties; uncertainties inherent in the ongoing commercialization and expansion of the Eversense product and Senseonics’ and its partners’ activities; uncertainties relating to the current economic and regulatory/political environment, including the effects of tariffs; and such other factors as are set forth in the risk factors detailed in Senseonics’ Annual Report on Form 10-K for the year ended December 31, 2025 and quarterly reports on Form 10-Q filed with the SEC under the heading “Risk Factors.” The forward-looking statements included in this press release represent Senseonics’ views as of the date hereof. Senseonics anticipates that subsequent events and developments will cause Senseonics’ views to change. However, while Senseonics may elect to update these forward-looking statements at some point in the future, Senseonics specifically disclaims any obligation to do so except as required by law. These forward-looking statements should not be relied upon as representing Senseonics’ views as of any date subsequent to the date hereof.

Senseonics Investor Contact
Jeremy Feffer
LifeSci Advisors
investors@senseonics.com

 
Senseonics Holdings, Inc.
Unaudited Consolidated Balance Sheets
(in thousands, except for share and per share data)
             
    December 31,
    2025     2024  
Assets            
Current assets:            
Cash and cash equivalents   $ 40,234     $ 74,597  
Restricted cash     315       315  
Short term investments, net     53,796       —  
Accounts receivable, net     6,807       1,365  
Accounts receivable, net – related parties     5,312       4,921  
Inventory, net     6,703       4,421  
Prepaid expenses and other current assets     4,366       5,819  
Total current assets     117,533       91,438  
             
Deposits and other assets     4,536       4,926  
Property, equipment and intangible assets, net     4,200       4,074  
Total assets   $ 126,269     $ 100,438  
             
Liabilities and Stockholders’ (Deficit) Equity            
Current liabilities:            
Accounts payable   $ 4,059     $ 3,205  
Accrued expenses and other current liabilities     15,091       13,636  
Accrued expenses and other current liabilities, related parties     5,198       1,870  
Note payable, current portion, net     —       20,138  
Total current liabilities     24,348       38,849  
             
Long-term debt and notes payables, net     35,586       34,703  
Non-current operating lease liabilities     5,289       5,785  
Total liabilities     65,223       79,337  
             
Commitments and contingencies            
             
Preferred stock and additional paid-in-capital, subject to possible redemption: $0.001 par value per share; 0 shares and 12,000 shares issued and outstanding as of December 31, 2025 and December 31, 2024     —       37,656  
Total temporary equity     —       37,656  
             
Stockholders’ equity (deficit):            
Common stock, $0.001 par value per share; 70,000,000 shares authorized as of December 31, 2025 and December 31, 2024; 41,265,778 shares and 29,767,561 shares issued and outstanding as of December 31, 2025 and December 31, 2024     41       30  
Additional paid-in capital     1,077,923       931,289  
Accumulated other comprehensive income     69       —  
Accumulated deficit     (1,016,987 )     (947,874 )
Total stockholders’ equity (deficit)     61,046       (16,555 )
Total liabilities, temporary equity and stockholders’ equity (deficit)   $ 126,269     $ 100,438  
                 


 
Senseonics Holdings, Inc.

Unaudited Consolidated Statements of Operations and Comprehensive Loss
(in thousands, except for share and per share data)

 
    Years Ended
    December 31,
    2025     2024  
             
             
Revenue, net   $ 17,084     $ 3,973  
Revenue, net – related parties     18,173       18,499  
Total revenue     35,257       22,472  
Cost of sales     19,494       21,939  
Gross profit     15,763       533  
             
Expenses:            
Research and development expenses     31,592       41,144  
Selling, general and administrative expenses     52,508       34,231  
Operating loss     (68,337 )     (74,842 )
Other income (expense), net:            
Interest income     4,198       4,502  
Interest expense     (4,951 )     (8,437 )
Gain on change in fair value of derivatives     —       102  
Other expense ( income)     (23 )     59  
Total other expense, net     (776 )     (3,774 )
             
Net Loss     (69,113 )     (78,616 )
Other comprehensive income            
Unrealized gain on marketable securities     69       11  
Total other comprehensive income     69       11  
Total comprehensive loss   $ (69,044 )   $ (78,605 )
             
Basic net loss per common share   $ (1.66 )   $ (2.50 )
Basic weighted-average shares outstanding     41,727,983       31,486,079  
             
Diluted net loss per common share   $ (1.66 )   $ (2.50 )
Diluted weighted-average shares outstanding     41,727,983       31,486,079  

Black Diamond Therapeutics to Participate in Upcoming Investor Conferences

Black Diamond Therapeutics to Participate in Upcoming Investor Conferences




Black Diamond Therapeutics to Participate in Upcoming Investor Conferences

CAMBRIDGE, Mass., March 02, 2026 (GLOBE NEWSWIRE) — Black Diamond Therapeutics, Inc. (Nasdaq: BDTX), a clinical-stage oncology company developing MasterKey therapies that target families of oncogenic mutations in patients with cancer, today announced its participation in upcoming investor conferences. Presentation details with President and Chief Executive Officer, Mark Velleca, M.D., Ph.D. and Chief Scientific Officer Elizabeth Buck, Ph.D., are as follows:

  • 46th Annual TD Cowen Healthcare Conference presentation at 1:10pm ET on Wednesday, March 4, 2026
  • 25th Annual Needham Virtual Healthcare Conference presentation at 3:00pm ET on Wednesday, April 15, 2026

Webcasts will be available at the start of the presentations on the investor relations section of the Company’s website, www.blackdiamondtherapeutics.com. Replays of the presentations will also be available and archived on the site for 90 days. The Company will also meet with investors at the Raymond James BioPharma Conference on Tuesday, April 14, 2026.

About Black Diamond Therapeutics

Black Diamond Therapeutics is a clinical-stage oncology company developing MasterKey therapies that target families of oncogenic mutations in patients with cancer. The Company’s MasterKey therapies are designed to address a broad spectrum of genetically defined tumors, overcome resistance, minimize wild-type mediated toxicities, and be brain penetrant to treat central nervous system disease. The Company is advancing silevertinib, a brain-penetrant fourth-generation EGFR MasterKey inhibitor targeting EGFR-mutant NSCLC and GBM. For more information, please visit www.blackdiamondtherapeutics.com.

Contacts

For Investors:
investors@bdtx.com

For Media:
media@bdtx.com

Black Diamond Therapeutics to Participate in Upcoming Investor Conferences

Black Diamond Therapeutics to Participate in Upcoming Investor Conferences




Black Diamond Therapeutics to Participate in Upcoming Investor Conferences

CAMBRIDGE, Mass., March 02, 2026 (GLOBE NEWSWIRE) — Black Diamond Therapeutics, Inc. (Nasdaq: BDTX), a clinical-stage oncology company developing MasterKey therapies that target families of oncogenic mutations in patients with cancer, today announced its participation in upcoming investor conferences. Presentation details with President and Chief Executive Officer, Mark Velleca, M.D., Ph.D. and Chief Scientific Officer Elizabeth Buck, Ph.D., are as follows:

  • 46th Annual TD Cowen Healthcare Conference presentation at 1:10pm ET on Wednesday, March 4, 2026
  • 25th Annual Needham Virtual Healthcare Conference presentation at 3:00pm ET on Wednesday, April 15, 2026

Webcasts will be available at the start of the presentations on the investor relations section of the Company’s website, www.blackdiamondtherapeutics.com. Replays of the presentations will also be available and archived on the site for 90 days. The Company will also meet with investors at the Raymond James BioPharma Conference on Tuesday, April 14, 2026.

About Black Diamond Therapeutics

Black Diamond Therapeutics is a clinical-stage oncology company developing MasterKey therapies that target families of oncogenic mutations in patients with cancer. The Company’s MasterKey therapies are designed to address a broad spectrum of genetically defined tumors, overcome resistance, minimize wild-type mediated toxicities, and be brain penetrant to treat central nervous system disease. The Company is advancing silevertinib, a brain-penetrant fourth-generation EGFR MasterKey inhibitor targeting EGFR-mutant NSCLC and GBM. For more information, please visit www.blackdiamondtherapeutics.com.

Contacts

For Investors:
investors@bdtx.com

For Media:
media@bdtx.com

Cytokinetics to Participate in March Investor Conferences

Cytokinetics to Participate in March Investor Conferences




Cytokinetics to Participate in March Investor Conferences

SOUTH SAN FRANCISCO, Calif., March 02, 2026 (GLOBE NEWSWIRE) — Cytokinetics, Incorporated (Nasdaq: CYTK) today announced that members of the Company management team will participate in the following investor conferences in March:

  • Leerink 2026 Global Healthcare Conference: Fireside chat on Monday, March 9, 2026 at 9:20 AM Eastern Time in Miami Beach, FL.
  • Citizens 2026 Life Sciences Conference: Fireside chat on Tuesday, March 10, 2026 at 9:00 AM Eastern Time in Miami Beach, FL.
  • 2026 Jefferies Biotech on the Beach Summit: One-on-one meetings on Wednesday, March 11, 2026 in Miami Beach, FL.
  • Barclays 28th Annual Global Healthcare Conference: Fireside chat on Wednesday, March 11, 2026 at 2:30 PM Eastern Time in Miami Beach, FL.

Interested parties may access the live webcasts of the fireside chats by visiting the Investors & Media section of the Cytokinetics website at http://www.cytokinetics.com. The webcast replays will be archived on the Cytokinetics website for 90 days following the conclusion of the event.

About Cytokinetics

Cytokinetics is a specialty cardiovascular biopharmaceutical company, building on its over 25 years of pioneering scientific innovations in muscle biology, and advancing a pipeline of potential new medicines for patients suffering from diseases of cardiac muscle dysfunction. Cytokinetics’ MYQORZO™ (aficamten) is a cardiac myosin inhibitor approved in the U.S., Europe and China for the treatment of adults with symptomatic obstructive hypertrophic cardiomyopathy (oHCM). Aficamten is also being studied for the potential treatment of non-obstructive HCM. Cytokinetics is also developing omecamtiv mecarbil, an investigational cardiac myosin activator for the potential treatment of patients with heart failure with severely reduced ejection fraction and ulacamten, an investigational cardiac myosin inhibitor for the potential treatment of heart failure with preserved ejection fraction, while continuing pre-clinical research and development in muscle biology.

For additional information about Cytokinetics, visit www.cytokinetics.com and follow us on X, LinkedIn, Facebook and YouTube.

Disclaimer 

Omecamtiv mecarbil and ulacamten are investigational medicines. They have not been approved nor determined to be safe or efficacious for any disease state or any indication by FDA or any other regulatory agency.

Forward-Looking Statements

This press release contains forward-looking statements for purposes of the Private Securities Litigation Reform Act of 1995 (the “Act”). Cytokinetics disclaims any intent or obligation to update these forward-looking statements and claims the protection of the Act’s Safe Harbor for forward-looking statements. Examples of such statements include, but are not limited to, statements relating to Cytokinetics’ and its partners’ research and development activities of Cytokinetics’ product candidates. Such statements are based on management’s current expectations, but actual results may differ materially due to various risks and uncertainties, including, but not limited to the risks related to Cytokinetics’ business outlines in Cytokinetics’ filings with the Securities and Exchange Commission. Forward-looking statements are not guarantees of future performance, and Cytokinetics’ actual results of operations, financial condition and liquidity, and the development of the industry in which it operates, may differ materially from the forward-looking statements contained in this press release. Any forward-looking statements that Cytokinetics makes in this press release speak only as of the date of this press release. Cytokinetics assumes no obligation to update its forward-looking statements whether as a result of new information, future events or otherwise, after the date of this press release.

CYTOKINETICS® and the CYTOKINETICS C-shaped logo are registered trademarks of Cytokinetics in the U.S. and certain other countries.

Contact:
Cytokinetics
Diane Weiser
Senior Vice President, Corporate Affairs
(415) 290-7757

Beiersdorf Aktiengesellschaft: Guidance 2026 –– New Share Buyback Program

Beiersdorf Aktiengesellschaft / Key word(s): Forecast / Full year/Capital measures / Share buybacks

Beiersdorf Aktiengesellschaft: Guidance 2026 –– New Share Buyback Program

02-March-2026 / 19:50 CET/CEST

Disclosure of an inside information acc. to Article 17 MAR of the Regulation (EU) No 596/2014, transmitted by EQS News – a service of EQS Group.

The issuer is solely responsible for the content of this announcement.


Guidance 2026 –– New Share Buyback Program

 

 

The Executive Board of Beiersdorf Aktiengesellschaft, Hamburg, today resolved – with the approval of the Supervisory Board – the business plan for the financial year 2026.

 

The slowing skin care market and the volatile economic environment have a negative impact on the short-term growth outlook for Beiersdorf’s Consumer business segment. Despite these challenges, Beiersdorf will continue to pursue important planned strategic investments in its brands to secure mid- and long-term value generation. Against this backdrop, the Executive Board expects the Consumer business segment’s sales for the 2026 financial year to be flat to slightly growing organically and the EBIT margin (excluding special factors) to be slightly below previous year’s level.

 

For the tesa business segment, sales are expected to be flat to slightly growing organically for the 2026 financial year and – also due to investments in strategic growth areas – the EBIT margin (excluding special factors) is expected to be slightly below previous year’s level. On this basis, the Executive Board expects the Group to achieve flat to slightly growing organic sales in the 2026 financial year and an operating EBIT margin (excluding special factors) slightly below previous year’s level.

 

In the previous year 2025, organic sales growth was 2.4% with an operating EBIT margin (excluding special factors) of 14.0% at the Group level. In line with market expectations, the Consumer business segment achieved an organic sales growth of 2.5% with an operating EBIT margin (excluding special factors) of 13.6% and the tesa business segment an organic sales growth of 1.8% with an operating EBIT margin (excluding special items) of 16.1%.

 

Furthermore, the Executive Board today resolved – with the approval of the Supervisory Board – to buy back shares in the Company in the amount of up to €750 million over the next two years. This follows the successful completion of the share buyback programs in 2024 and 2025.
 

The Company will announce further details on the new share buyback program in accordance with the statutory provisions before the start of the share buyback program. Treasury shares held by the Company will be cancelled to the extent necessary to carry out the share buyback program.

 

Contact:
Christopher Sheldon
Head of Investor Relations
Tel.: +49 (40) 4909 5000
E-Mail: Investor.Relations@Beiersdorf.com

Florian Dieckmann
Head of Corporate Communications
Tel.: +49 (40) 4909 2001
E-Mail: cc@beiersdorf.com

End of Inside Information


02-March-2026 CET/CEST The EQS Distribution Services include Regulatory Announcements, Financial/Corporate News and Press Releases.


Language: English
Company: Beiersdorf Aktiengesellschaft
Beiersdorfstraße 1 – 9
22529 Hamburg
Germany
Phone: +49 (0)40 4909-0
Fax: +49 (0)40 4909-34 34
E-mail: kontakt@Beiersdorf.com
Internet: www.Beiersdorf.com
ISIN: DE0005200000
WKN: 520000
Indices: DAX
Listed: Regulated Market in Frankfurt (Prime Standard), Hamburg; Regulated Unofficial Market in Dusseldorf, Hanover, Munich, Stuttgart, Tradegate BSX
EQS News ID: 2284106

 
End of Announcement EQS News Service

2284106  02-March-2026 CET/CEST