ABVC BioPharma, Inc. Reports Strong Q2 2024 Financial Results and Strategic Achievements
ABVC BioPharma (NASDAQ: ABVC) reported strong Q2 2024 financial results and strategic achievements. Key highlights include:
1. Executed global licensing agreements potentially providing up to $292 million in income
2. Received $116,000 in cash milestone income
3. Improved EPS by 86.8% year-over-year to -$0.09
4. Increased revenue to $117,142, up from $6,109 in Q2 2023
5. Maintained $7.8 million in shareholders' equity
6. Obtained multiple patents and FDA approvals for treatments in major depressive disorder, ADHD, and ophthalmology
7. Completed Phase II trials for MDD and initiated Phase IIb trials for ADHD
ABVC is focusing on advancing its pipeline, expanding partnerships, and driving sustainable growth in oncology/hematology, CNS, and ophthalmology.
ABVC BioPharma (NASDAQ: ABVC) ha riportato solidi risultati finanziari per il secondo trimestre del 2024 e traguardi strategici. I punti salienti includono:
1. Esecuzione di accordi di licenza globali che potrebbero fornire fino a 292 milioni di dollari in entrate
2. Ricevuti 116.000 dollari in entrate da traguardi in contante
3. Miglioramento dell'utile per azione (EPS) del 86,8% anno su anno a -0,09 dollari
4. Aumento dei ricavi a 117.142 dollari, rispetto ai 6.109 dollari del secondo trimestre del 2023
5. Mantenimento di 7,8 milioni di dollari di patrimonio netto degli azionisti
6. Ottenimento di numerosi brevetti e approvazioni della FDA per trattamenti in caso di disturbo depressivo maggiore, ADHD e oftalmologia
7. Completamento delle sperimentazioni di Fase II per il disturbo depressivo maggiore e avvio delle sperimentazioni di Fase IIb per l'ADHD
ABVC sta concentrando i suoi sforzi sull'avanzamento del suo pipeline, sull'espansione delle partnership e sulla guida di una crescita sostenibile in oncologia/emato-oncologia, CNS e oftalmologia.
ABVC BioPharma (NASDAQ: ABVC) reportó sólidos resultados financieros para el segundo trimestre de 2024 y logros estratégicos. Los puntos destacados incluyen:
1. Ejecución de acuerdos de licencia globales que podrían proporcionar hasta 292 millones de dólares en ingresos
2. Recepción de 116.000 dólares en ingresos por hitos en efectivo
3. Mejora del EPS en un 86.8% año tras año a -0.09 dólares
4. Incremento de ingresos a 117.142 dólares, en comparación con 6.109 dólares en el segundo trimestre de 2023
5. Mantenimiento de 7.8 millones de dólares en capital contable de los accionistas
6. Obtención de múltiples patentes y aprobaciones de la FDA para tratamientos en trastorno depresivo mayor, TDAH y oftalmología
7. Finalización de ensayos de Fase II para el trastorno depresivo mayor y inicio de ensayos de Fase IIb para el TDAH
ABVC se está enfocando en avanzar en su pipeline, expandir asociaciones y promover un crecimiento sostenible en oncología/hematología, CNS y oftalmología.
ABVC BioPharma (NASDAQ: ABVC)는 2024년 2분기 강력한 재무 결과와 전략적 성과를 발표했습니다. 주요 내용은 다음과 같습니다:
1. 최대 2억 9천 2백만 달러의 수익을 제공할 수 있는 글로벌 라이선스 계약 체결
2. 116,000달러의 현금 마일스톤 수익 확보
3. 전년 대비 EPS가 86.8% 개선되어 -0.09달러
4. 2023년 2분기 6,109달러에서 증가한 117,142달러의 수익
5. 주주 자본 780만 달러 유지
6. 주요 우울 장애, ADHD 및 안과 치료를 위한 다수의 특허 및 FDA 승인 확보
7. MDD에 대한 2상 시험 완료 및 ADHD에 대한 2b상 시험 개시
ABVC는 파이프라인을 발전시키고 파트너십을 확장하며 종양학, 혈액학, CNS 및 안과 분야에서 지속 가능한 성장을 위해 노력하고 있습니다.
ABVC BioPharma (NASDAQ: ABVC) a annoncé de solides résultats financiers pour le deuxième trimestre de 2024 et des réalisations stratégiques. Les points saillants incluent :
1. Exécution d'accords de licence mondiaux pouvant potentiellement générer jusqu'à 292 millions de dollars de revenus
2. Réception de 116 000 dollars de revenus en espèces provenant d'étapes de réalisation
3. Amélioration du BPA de 86,8 % d'une année sur l'autre, atteignant -0,09 dollar
4. Augmentation des revenus à 117 142 dollars, contre 6 109 dollars au 2e trimestre 2023
5. Maintien de 7,8 millions de dollars de capitaux propres des actionnaires
6. Obtention de plusieurs brevets et approbations de la FDA pour des traitements du trouble dépressif majeur, du TDAH et de l'ophtalmologie
7. Achèvement des essais de phase II pour le trouble dépressif majeur et lancement des essais de phase IIb pour le TDAH
ABVC se concentre sur l'avancement de sa pipeline, l'expansion des partenariats et la promotion d'une croissance durable dans les domaines de l'oncologie/hématologie, du SNC et de l'ophtalmologie.
ABVC BioPharma (NASDAQ: ABVC) hat starke Finanzberichte für das zweite Quartal 2024 und strategische Errungenschaften veröffentlicht. Die wichtigsten Höhepunkte sind:
1. Durchführung globaler Lizenzverträge, die potenziell bis zu 292 Millionen Dollar Einkommen bringen können
2. Erhalt von 116.000 Dollar an Meilenstein-Einnahmen in bar
3. Verbesserung des EPS um 86,8 % im Jahresvergleich auf -0,09 Dollar
4. Umsatzsteigerung auf 117.142 Dollar, gegenüber 6.109 Dollar im 2. Quartal 2023
5. Beibehaltung von 7,8 Millionen Dollar im Eigenkapital der Aktionäre
6. Erwerb mehrerer Patente und FDA-Zulassungen für Behandlungen bei schwerer Depression, ADHS und Augenheilkunde
7. Abschluss der Phase-II-Studien für MDD und Beginn der Phase-IIb-Studien für ADHS
ABVC konzentriert sich darauf, sein Pipeline voranzutreiben, Partnerschaften auszubauen und nachhaltiges Wachstum in der Onkologie/Hämatologie, im CNS-Bereich und in der Augenheilkunde voranzutreiben.
- Executed global licensing agreements with potential income of up to $292 million
- Received $116,000 in cash milestone income
- Improved EPS by 86.8% year-over-year to -$0.09
- Increased revenue to $117,142, up from $6,109 in Q2 2023
- Obtained multiple patents and FDA approvals for various treatments
- Completed Phase II trials for MDD and initiated Phase IIb trials for ADHD
- Maintained $7.8 million in shareholders' equity
- EPS remains negative at -$0.09 despite improvement
Insights
ABVC BioPharma's Q2 2024 results show significant financial improvement. The company's EPS improved by
However, investors should note that while these licensing deals are promising, they are not guaranteed income. The company's shareholders' equity stands at
ABVC's strategic moves in Q2 2024 position it well in the competitive biotech landscape. The company has made significant progress across multiple therapeutic areas:
- Neurology: Completed Phase II trials for Major Depressive Disorder (MDD) and initiated Phase IIb trials for ADHD
- Ophthalmology: Advanced Vitargus®, a biodegradable hydrogel for retinal detachment surgery
- Oncology: Received FDA approval for multiple IND applications
The company's diverse pipeline and focus on unmet medical needs are promising. However, investors should be aware that drug development is a long and risky process. The multiple patents and FDA approvals received demonstrate the company's innovation capabilities and potential for future growth.
ABVC's market positioning has strengthened considerably with its recent licensing agreements and partnerships. The deals with ForSeeCon Eye for Vitargus® and OncoX BioPharma for oncology products could significantly boost the company's market value if successful. These agreements not only provide potential future revenue streams but also validate ABVC's technology and research.
The company's expansion into contract research, development and manufacturing (CRDMO) services through its subsidiary BioKey is a strategic diversification move. This could provide more stable revenue streams to offset the risks associated with drug development. However, investors should monitor how well ABVC can execute on these multiple fronts simultaneously, as managing diverse business lines can be challenging for smaller biotech firms.
• Executed Global Licensing Agreements that could provide up to
• Received Cash Milestone Incomes of
• Achieved Significant Improvements in Earnings
• Obtained Multiple Patents and FDA Approvals
FREMONT, CA, Aug. 15, 2024 (GLOBE NEWSWIRE) -- ABVC BioPharma, Inc. (NASDAQ: ABVC), a clinical-stage biopharmaceutical company developing therapeutic solutions in oncology/hematology, CNS, and ophthalmology, is pleased to announce its financial results and key operational highlights for the second quarter ended June 30, 2024.
Key Financial and Operational Highlights:
1. Significant Global Licensing Agreements:
- Vitargus® Licensing: Along with our subsidiary, BioFirst Corporation, we secured licensing agreements with ForSeeCon Eye Corporation that have the potential to provide up to a total of
- Oncology Products Licensing: Along with our subsidiary and affiliate, BioLite, Inc. and Rgene Corporation, we entered into a total of 8 licensing agreements with OncoX BioPharma, Inc., that have the potential to provide up to an aggregate of
2. Financial Performance:
- Earnings Per Share (EPS): Demonstrated a remarkable year-over-year improvement of approximately
- Revenue Growth: Revenue increased to
- Shareholders' Equity: As of June 30, 2024, shareholders' equity stood at
3. Strategic Partnerships and Market Positioning:
- ABVC has strategically aligned itself with promising partners that we believe will ultimately enhance the value of ABVC's equity holdings. These partnerships are pivotal in driving shareholder value as we believe they will help market valuations grow.
- We believe the Company is poised for significant market capitalization growth, leveraging its pipeline accomplishments and international partnerships to bring breakthrough therapies to market.
4. Operational and Regulatory Milestones:
- Patent and FDA Approvals: Received multiple patents and regulatory approvals across the US, Taiwan, and Australia for treatments targeting major depressive disorder, ADHD, and ophthalmology. These achievements highlight our continued progress in expanding our intellectual property portfolio and advancing clinical trials.
- Neurology and Oncology Advancements: Completed Phase II trials for MDD, initiated Phase IIb trials for ADHD, and received FDA approval for multiple IND applications, positioning us for continued growth and innovation in these critical therapeutic areas.
Management Commentary:
Dr. Uttam Patil, ABVC Chief Executive Officer, commented, "We are thrilled with the substantial progress we have made in Q2 2024. Our financial performance and strategic licensing agreements have enhanced our cash reserves and strengthened our position in the biopharmaceutical industry. We remain focused on advancing our pipeline, expanding our partnerships, and driving sustainable growth for the benefit of our shareholders."
Board of Directors Statement:
"We sincerely thank our shareholders for their continued support and confidence in ABVC. Our focus remains on advancing our licensing agreements and maximizing the value they bring. The execution of these agreements provides us with a solid foundation for future growth and stability. We are excited about these partnerships' prospects and are committed to driving our strategic goals forward."
Outlook:
We believe ABVC BioPharma is on a promising trajectory, focusing on sustainable growth, innovation, and value creation through strategic partnerships. Our improving financial strength and unwavering commitment to advancing healthcare solutions prepare us for future success. We sincerely thank our shareholders, partners, and dedicated team for their continued support and look forward to a prosperous future.
Recent Operational Highlights
Patents and FDA Approvals
The Company received a US patent (US 16/936,032), valid until September 04, 2040, a Taiwanese (TW I821593) Patent, valid until July 22, 2040, and an Australian (AU2021314052B2) Patent, valid until April 09, 2041, for Polygala extract for the treatment of major depressive disorder. The Company received a US (US17/120,965), valid until December 20, 2040, and Taiwanese (TW 110106546), valid until February 24, 2041, Patent for Polygala Extract for treating Attention Deficit Hyperactive Disorder. A Taiwanese Patent (TW I792427) for Storage Media for the Preservation of Corneal Tissue was obtained on February 11, 2023, and is valid till July 19, 2041. As we work towards expanding our patent map into global coverage, we eagerly await the results of patent applications in the European Union, China, Japan, and others.
On December 30, 2022, the Company received US FDA approval for the IND ABV-1519 to proceed with the Combination therapy for treating Advanced Inoperable or Metastatic EGFR Wild-type Non-Small Cell Lung Cancer was approved and the study can proceed. The IND was then submitted to the Taiwan FDA, and the approval was received on January 04, 2024. The United States Food & Drug Administration (US FDA) has approved four INDs, ABV-1501 for Triple Negative Breast Cancer (TNBC), ABV-1519 for Non-Small Cell Lung Cancer (NSCLC), ABV-1702 for Myelodysplastic Syndrome (MDS), and ABV-1703 for Pancreatic Cancer Therapy.
Neurology
The MDD Phase II trials for ABV-1504 were completed successfully with good tolerance to the drug, and no serious adverse effects were reported. The product is ready for an End-of-Phase 2 meeting with the FDA to finalize the protocol for Phase III trials. At the same time, we commenced the ADHD Phase IIb trials at the University of California, San Francisco (UCSF) and five other sites in Taiwan. The trials are heading for the interim report, which we expect to complete by the end of Q3 2024. ABV-1601 for MDD in cancer patients has completed Phase I study preparation, including the Site Initiation Visit (SIV). The study is set to initiate by the end of 2024.
On July 31, 2023, ABVC signed a legally binding term sheet with a Chinese pharmaceutical company, Xinnovation Therapeutics Co., Ltd, for the exclusive licensing of ABV-1504 for Major Depressive Disorder (MDD) and ABV-1505 for Attention-Deficit Hyperactivity Disorder in mainland China. Under this agreement, Xinnovation will hold exclusive rights to develop, manufacture, market, and distribute our innovative drugs for MDD and ADHD in the Chinese market and shall bear the costs for clinical trials and product registration in China. We are negotiating definitive agreements with Xinnovation and are excited that the licensing deal carries a possible aggregate income of
In November 2023, each of ABVC and one of its subsidiaries, BioLite, Inc. ("BioLite"), entered a multi-year, global licensing agreement with AIBL for the Company and BioLite's CNS drugs with the indications of MDD (Major Depressive Disorder) and ADHD (Attention Deficit Hyperactivity Disorder) (the "Licensed Products"). The potential license will cover the Licensed Products' clinical trial, registration, manufacturing, supply, and distribution rights. The Licensed Products for MDD and ADHD, owned by ABVC and BioLite, were valued at
Ophthalmology
Vitargus®, a vitreous substitute, is a groundbreaking, advanced-staged R&D product that we believe will be the first biodegradable hydrogel used in retinal detachment surgery. Vitargus® has completed the feasibility study in Australia and was approved by the Australian Therapeutic Goods Administration (TGA) to initiate the next trial phase in two participating sites. This is vital to obtaining final regulatory approval for Vitargus® in Australia.
The Science Park Administration in Taiwan approved ABVC's plan to set up a pilot Good Manufacturing Practice (GMP) facility to produce Vitargus® and to pursue the process development work for manufacturing optimization. We are undertaking this project, proposed by ABVC's Taiwan affiliate and co-development partner, BioFirst Corporation, to upgrade the Vitargus® manufacturing processes so it can ultimately handle the global market supply. ABVC and BioFirst Corporation expect to complete the facility's construction in Hsinchu Biomedical Science Park, Taiwan, in 2024.
Oncology/Hematology
The United States Food & Drug Administration (US FDA) approved the Investigational New Drug (IND) application for the proposed clinical investigation of BLEX 404, the primary active ingredient in ABV-1519, for advanced inoperable or metastatic EGFR wild-type non-small cell lung cancer. This treatment is being co-developed by BioKey, Inc. ("BioKey") and by the Rgene Corporation, Taiwan. The study received approval from the Taiwan FDA. This is the fourth IND approved by the US FDA for BLEX 404. The previous three INDs are for the combination therapies of triple-negative breast cancer, myelodysplastic syndromes (MDS), and pancreatic cancer.
CDMO
BioKey, a wholly-owned subsidiary of the Company based in Fremont, California, produces dietary supplements derived from the maitake mushroom in tablet and liquid forms. BioKey has entered the second year of the distribution agreement with Define Biotech Co. Ltd. BioKey is currently set to produce an additional
On the regulatory services front for our clients, we received two ANDA approvals from the US FDA. We have a three-year contract, worth up to
About ABVC BioPharma, Inc.
ABVC BioPharma, Inc. is a clinical-stage biopharmaceutical company focused on utilizing its licensed technology to conduct proof-of-concept trials through Phase II of the clinical development process at world-famous research institutions (such as Stanford University, University of California at San Francisco, and Cedars-Sinai Medical Center) and then out-licensing the products to international pharmaceutical companies for pivotal Phase III studies and, eventually, generating global sales. The Company has an active pipeline of six drugs and one medical device (ABV-1701/Vitargus®) under development.
Forward-looking Statements
This press release contains "forward-looking statements." Such statements may be preceded by the words "intends," "may," "will," "plans," "expects," "anticipates," "projects," "predicts," "estimates," "aims," "believes," "hopes," "potential" or similar words. Forward-looking statements are not guarantees of future performance, are based on certain assumptions and are subject to various known and unknown risks and uncertainties, many of which are beyond the Company's control, and cannot be predicted or quantified and consequently, actual results may differ materially from those expressed or implied by such forward-looking statements. Such risks and uncertainties include, without limitation, risks and uncertainties associated with (i) our inability to manufacture our product candidates on a commercial scale on our own, or in collaboration with third parties; (ii) difficulties in obtaining financing on commercially reasonable terms; (iii) changes in the size and nature of our competition; (iv) loss of one or more key executives or scientists; and (v) difficulties in securing regulatory approval to proceed to the next level of the clinical trials or market our product candidates. More detailed information about the Company and the risk factors that may affect the realization of forward-looking statements is set forth in the Company's filings with the Securities and Exchange Commission (SEC), including the Company's Annual Report on Form 10-K and its Quarterly Reports on Form 10-Q. Investors are urged to read these documents free of charge on the SEC's website at http://www.sec.gov. The Company assumes no obligation to publicly update or revise its forward-looking statements as a result of new information, future events or otherwise.
This press release does not constitute an offer to sell or the 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 that state or jurisdiction.
Contact:
Uttam Patil
Email: uttam@ambrivis.com
FAQ
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