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Scienture Holdings Announces Cancelation of ELOC

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Scienture Holdings (NASDAQ: SCNX) has terminated its Equity Line of Credit (ELOC) facility effective May 22, 2025, and deregistered 310,488 unsold common stock shares. This strategic decision aligns with the company's preparation for the commercial launch of Arbli™, their first FDA-approved ready-to-use oral liquid losartan in the U.S. market, scheduled for Q3 2025. Arbli™ is indicated for treating hypertension in patients over 6 years old, reducing stroke risk in hypertensive patients with left ventricular hypertrophy, and treating diabetic nephropathy in certain type 2 diabetes patients. Management believes canceling the ELOC will allow them to focus on Arbli's commercialization and pursue more favorable financing options to support growth strategies.
Scienture Holdings (NASDAQ: SCNX) ha terminato la sua linea di credito azionaria (ELOC) con effetto dal 22 maggio 2025 e ha cancellato 310.488 azioni ordinarie non vendute. Questa decisione strategica è in linea con la preparazione dell'azienda al lancio commerciale di Arbli™, il loro primo losartan orale liquido pronto all'uso approvato dalla FDA, previsto per il terzo trimestre del 2025 sul mercato statunitense. Arbli™ è indicato per il trattamento dell'ipertensione in pazienti sopra i 6 anni, per ridurre il rischio di ictus in pazienti ipertesi con ipertrofia ventricolare sinistra e per il trattamento della nefropatia diabetica in alcuni pazienti con diabete di tipo 2. La direzione ritiene che la cancellazione dell'ELOC permetterà di concentrarsi sulla commercializzazione di Arbli e di perseguire opzioni di finanziamento più vantaggiose a supporto delle strategie di crescita.
Scienture Holdings (NASDAQ: SCNX) ha terminado su línea de crédito de capital (ELOC) con efecto a partir del 22 de mayo de 2025 y ha dado de baja 310,488 acciones comunes no vendidas. Esta decisión estratégica está alineada con la preparación de la compañía para el lanzamiento comercial de Arbli™, su primer losartán líquido oral listo para usar aprobado por la FDA en el mercado estadounidense, programado para el tercer trimestre de 2025. Arbli™ está indicado para el tratamiento de la hipertensión en pacientes mayores de 6 años, para reducir el riesgo de accidente cerebrovascular en pacientes hipertensos con hipertrofia ventricular izquierda y para tratar la nefropatía diabética en ciertos pacientes con diabetes tipo 2. La gerencia considera que cancelar la ELOC les permitirá enfocarse en la comercialización de Arbli y buscar opciones de financiamiento más favorables para apoyar las estrategias de crecimiento.
Scienture Holdings (NASDAQ: SCNX)는 2025년 5월 22일부로 자본 신용 한도(ELOC)를 종료하고, 미판매 보통주 310,488주를 등록 말소했습니다. 이 전략적 결정은 2025년 3분기 미국 시장에 출시 예정인 FDA 승인 첫 번째 즉시 사용 가능한 경구용 액상 로사르탄인 Arbli™의 상업적 출시 준비와 일치합니다. Arbli™는 6세 이상의 고혈압 환자 치료, 좌심실 비대가 있는 고혈압 환자의 뇌졸중 위험 감소, 일부 2형 당뇨병 환자의 당뇨병성 신병증 치료에 적응증이 있습니다. 경영진은 ELOC를 취소함으로써 Arbli의 상업화에 집중하고 성장 전략을 지원할 더 유리한 자금 조달 옵션을 모색할 수 있을 것으로 보고 있습니다.
Scienture Holdings (NASDAQ : SCNX) a mis fin à sa ligne de crédit en actions (ELOC) à compter du 22 mai 2025 et a radié 310 488 actions ordinaires invendues. Cette décision stratégique s'inscrit dans la préparation de l'entreprise au lancement commercial d'Arbli™, leur premier losartan oral liquide prêt à l'emploi approuvé par la FDA, prévu pour le troisième trimestre 2025 sur le marché américain. Arbli™ est indiqué pour le traitement de l'hypertension chez les patients de plus de 6 ans, pour réduire le risque d'accident vasculaire cérébral chez les patients hypertendus présentant une hypertrophie ventriculaire gauche, et pour traiter la néphropathie diabétique chez certains patients atteints de diabète de type 2. La direction estime que l'annulation de l'ELOC leur permettra de se concentrer sur la commercialisation d'Arbli et de rechercher des options de financement plus favorables pour soutenir leurs stratégies de croissance.
Scienture Holdings (NASDAQ: SCNX) hat seine Eigenkapitalkreditlinie (ELOC) mit Wirkung zum 22. Mai 2025 beendet und 310.488 unverkäufliche Stammaktien abgemeldet. Diese strategische Entscheidung steht im Einklang mit der Vorbereitung des Unternehmens auf die Markteinführung von Arbli™, ihrem ersten von der FDA zugelassenen gebrauchsfertigen oralen flüssigen Losartan in den USA, die für das dritte Quartal 2025 geplant ist. Arbli™ ist indiziert zur Behandlung von Bluthochdruck bei Patienten über 6 Jahre, zur Reduzierung des Schlaganfallrisikos bei hypertensiven Patienten mit linksventrikulärer Hypertrophie und zur Behandlung der diabetischen Nephropathie bei bestimmten Patienten mit Typ-2-Diabetes. Das Management ist der Ansicht, dass die Kündigung der ELOC es ihnen ermöglicht, sich auf die Kommerzialisierung von Arbli zu konzentrieren und günstigere Finanzierungsmöglichkeiten zur Unterstützung der Wachstumsstrategien zu verfolgen.
Positive
  • First and only FDA-approved ready-to-use oral liquid losartan in the U.S. market
  • Commercial launch of Arbli™ on track for Q3 2025
  • Strategic cancellation of ELOC to pursue more favorable financing terms
  • Multiple approved indications for Arbli™ covering large patient populations
Negative
  • Cancellation of financing facility may indicate need for additional capital
  • Company needs to secure new financing terms to support growth strategy

Insights

SCNX terminates its ELOC facility ahead of Arbli™ launch, suggesting confidence in securing better financing options.

Scienture Holdings' termination of its Equity Line of Credit (ELOC) facility represents a strategic financial repositioning ahead of the commercial launch of Arbli™, their FDA-approved oral liquid losartan product. The company has deregistered all 310,488 unsold shares that had been registered under this financing arrangement.

This decision signals management's confidence in securing more favorable financing terms to support both the imminent product launch and longer-term growth initiatives. The timing is particularly noteworthy as it comes just before their Q3 2025 commercial launch of Arbli™, the first and only FDA-approved ready-to-use oral liquid losartan in the U.S. market.

ELOCs typically provide companies with flexible but potentially dilutive financing options. By canceling this facility, Scienture appears to be prioritizing shareholder value while seeking alternative capital sources that better align with their commercialization phase. The move suggests management anticipates stronger market positioning following their product launch, potentially enabling them to negotiate better terms with lenders or investors.

With Arbli™ targeting multiple indications including hypertension treatment and stroke risk reduction, the commercial potential appears significant enough to warrant this financial strategy adjustment. The company's leadership is clearly pivoting from development-stage financing mechanisms toward commercialization-phase capital structures, which typically feature less dilutive terms when backed by revenue-generating products.

TAMPA, FL, June 17, 2025 (GLOBE NEWSWIRE) -- SCIENTURE HOLDINGS, INC. (NASDAQ: SCNX) (the “Company”), a holding company for existing and planned pharmaceutical operating companies focused on providing enhanced value to patients, physicians and caregivers through developing, bringing to market, and distributing novel specialty products to satisfy unmet market needs, announced it has terminated its Equity Line of Credit (“ELOC”) facility effective as of May 22, 2025.

In connection with cancellation of the ELOC, on June 16, 2025, the Company filed a post-effective amendment to the Registration Statement on Form S-1 (File No. 333-283591) filed with the Securities and Exchange Commission on December 3, 2025, declared effective on February 14, 2025. The post-effective amendment deregisters all 310,488 unsold shares of the Company’s common stock that had been registered under the registration statement.

This strategic financial decision comes as the Company prepares to commercially launch its first FDA-approved product candidate, Arbli, which is the first and only FDA-approved ready-to-use oral liquid losartan in the U.S. market.

"This move allows management to focus more on our planned commercialization of Arbli upcoming in summer 2025,” said Shankar Hariharan, Co-Chief Executive Officer and Executive Chairman. “We believe that it is in the Company’s best interest to cancel the ELOC facility as we prepare for the commercial launch of Arbli and seek more favorable financing terms to support the Company’s near and long-term growth strategy.”

"We are at a critical moment in our Company’s history as we quickly approach our target date for commercially lauunching Arbli this summer,” commented Naraismhan Mani, Co-Chief Executive Officer and President. “Cancelling the ELOC facility represents a commitment by our management to focus on the commercial launch and finding more favorable funding opportunities to support our strategic plans.”

The Company continues to expect that it will commercially launch Arbli by making it available to patients in the U.S. during Q3 2025. Arbli is indicated for the treatment of hypertension in patients greater than 6 years old, for the reduction of risk of stroke in patients with hypertension and left ventricular hypertrophy, and for the treatment of diabetic nephropathy in certain patients with type 2 diabetes.

About Arbli

Arbli is the first and only oral liquid formulation of losartan approved by the U.S. FDA. It comes in a 165 mL bottle as a peppermint flavored suspension that does not require refrigeration and has been approved for a shelf life of 18 months from the date of manufacture when stored at room temperature. Based on the additional stability data that has been obatined, the shelf-life of the product has been extended to 24-months at room temperature.

About Scienture Holdings, Inc.

SCIENTURE HOLDINGS, INC. (NASDAQ: “SCNX”), through its wholly owned subsidiaries, Scienture, LLC and Integra Pharma Solutions, LLC, is a comprehensive pharmaceutical product company focused on providing enhanced value to patients, physicians and caregivers by offering novel specialty products to satisfy unmet market needs. Integra Pharma Solutions, LLC, is a licensed pharmaceutical wholesaler and sells brand, generic and non-drug products to healthcare markets including government organizations, hospitals, clinics and independent pharmacies nationwide. Scienture, LLC is a branded, specialty pharmaceutical company consisting of a highly experienced team of industry professionals who are passionate about developing and bringing to market unique specialty products that provide enhanced value to patients and healthcare systems. The assets in development at Scienture are across therapeutics areas, indications and cater to different market segments and channels. For more information please visit www.scienture.com.

Cautionary Statements Regarding Forward-Looking Statements

This press release contains certain statements that may be deemed to be “forward-looking statements” within the federal securities laws, including the safe harbor provisions under the Private Securities Litigation Reform Act of 1995. Statements that are not historical are forward-looking statements within the meaning of Section 27A of the Securities Act of 1933 and Section 21E of the Securities Exchange Act of 1934. Forward-looking statements relate to future events or our future performance or future financial condition. These forward-looking statements are not historical facts, but rather are based on current expectations, estimates and projections about our company, our industry, our beliefs and our assumptions. Such forward-looking statements include, but are not limited to, statements regarding our or our management team’s expectations, hopes, beliefs, intentions or strategies regarding the future, including for the products we may launch and the success those products may have in the marketplace. In addition, any statements that refer to projections, forecasts or other characterizations of future events or circumstances, including any underlying assumptions, are forward-looking statements. In some cases, you can identify forward-looking statements by the following words: “anticipate,” “believe,” “continue,” “could,” “estimate,” “expect,” “intend,” “may,” “ongoing,” “plan,” “potential,” “predict,” “project,” “should,” or the negative of these terms or other similar expressions, but the absence of these words does not mean that a statement is not forward-looking. Forward-looking statements are subject to a number of risks and uncertainties (some of which are beyond our control) that may cause actual results or performance to be materially different from those expressed or implied by such forward-looking statements. Accordingly, readers should not place undue reliance on any forward-looking statements. These risks include risks relating to agreements with third parties; our ability to raise funding in the future, as needed, and the terms of such funding, including potential dilution caused thereby; our ability to continue as a going concern; security interests under certain of our credit arrangements; our ability to maintain the listing of our common stock on the Nasdaq Capital Market; claims relating to alleged violations of intellectual property rights of others; the outcome of any current legal proceedings or future legal proceedings that may be instituted against us; unanticipated difficulties or expenditures relating to our business plan; and those risks detailed in our most recent Annual Report on Form 10-K and subsequent reports filed with the SEC.

Forward-looking statements speak only as of the date they are made. Scienture Holdings, Inc. undertakes no obligation to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise that occur after that date, except as otherwise provided by law.

Contact:

SCIENTURE HOLDINGS, INC.
6308 Benjamin Rd, Suite 708
Tampa, Florida 33634
Phone: (866) 468-6535
Email: IR@Scienture.com


FAQ

When will Scienture Holdings (SCNX) launch Arbli?

Scienture Holdings plans to commercially launch Arbli in Q3 2025, making it available to patients in the U.S. market.

What is Arbli approved for by the FDA?

Arbli is approved for treating hypertension in patients over 6 years old, reducing stroke risk in hypertensive patients with left ventricular hypertrophy, and treating diabetic nephropathy in certain type 2 diabetes patients.

Why did SCNX cancel its ELOC facility?

Scienture Holdings canceled its ELOC facility to focus on Arbli's commercialization and pursue more favorable financing terms to support the company's growth strategy.

How many shares were deregistered by Scienture Holdings?

Scienture Holdings deregistered 310,488 unsold shares of common stock that had been registered under the registration statement.

What makes Arbli unique in the market?

Arbli is the first and only FDA-approved ready-to-use oral liquid losartan available in the U.S. market.
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