Welcome to our dedicated page for Abvc Biopharma SEC filings (Ticker: ABVC), a comprehensive resource for investors and traders seeking official regulatory documents including 10-K annual reports, 10-Q quarterly earnings, 8-K material events, and insider trading forms.
Clinical-stage biotech filings tell a story beyond the financials. ABVC BioPharma's SEC documents reveal how this Fremont-based company allocates capital across its oncology, neurology, and ophthalmology programs while managing the cash runway challenges typical of development-stage pharmaceuticals.
The 10-K and 10-Q filings break down research and development spending across ABVC's therapeutic candidates: ABV-1501 for triple-negative breast cancer, ABV-1504 and ABV-1505 for neurological conditions, and the Vitargus medical device program. These disclosures help investors understand which programs receive priority funding and how clinical milestones affect resource allocation.
Form 8-K filings capture material events that move clinical-stage biotechs: partnership announcements, licensing agreements, patent grants, and funding developments. For ABVC BioPharma, these filings document collaboration arrangements with partners like RGene Corporation and BioFirst Corporation, providing transparency into how the company structures its development partnerships.
Our AI-powered summaries translate the technical disclosures in ABVC BioPharma's filings into clear explanations. Track Form 4 insider transactions to monitor executive confidence during clinical development stages, and access proxy statements for compensation structures and governance details. Whether analyzing cash burn rates, understanding pipeline progress, or following insider activity, these tools help you extract meaningful insights from regulatory filings.
ABVC BioPharma filed Prospectus Supplement No. 4 to its July 12, 2024 prospectus, registering 1,000,000 shares of common stock underlying a common stock purchase warrant. The supplement also attaches the company’s Q3 2025 Form 10‑Q. Shares outstanding were 24,301,089 as of October 30, 2025; this is a baseline figure, not the amount being offered.
For the nine months ended September 30, 2025, ABVC reported revenue of $795,950 and a net loss of $4,564,546. The company disclosed a working capital deficit of $2,434,951 and noted substantial doubt about its ability to continue as a going concern. Cash and cash equivalents were $192,068 with restricted cash of $661,843. Total assets rose to $21.18 million, reflecting land acquisitions and other noncurrent items.
ABVC BioPharma filed Prospectus Supplement No. 5 updating its April 5, 2024 prospectus covering 11,714,683 shares of common stock. The supplement appends the company’s Form 10-Q for the quarter ended September 30, 2025.
For Q3 2025, revenue was $795,950 and loss from operations was $1,168,410, leading to a net loss attributable to ABVC of $1,246,513. For the nine months, net loss attributable to ABVC was $4,345,610. Cash and cash equivalents were $192,068 with restricted cash of $661,843 as of September 30, 2025. The company disclosed substantial doubt about its ability to continue as a going concern, citing a working capital deficit of $2,434,951 and net cash outflows from operating activities of $1,567,264 for the nine months. Shares outstanding were 24,301,089 as of October 30, 2025; this is a baseline figure, not the amount being offered.
ABVC BioPharma filed Prospectus Supplement No. 5 covering 225,500 shares of common stock and updating its May 22, 2024 prospectus with the company’s Form 10‑Q for the quarter ended September 30, 2025.
For Q3 2025, revenue was $795,950 and net loss attributed to ABVC and subsidiaries was $1,246,513. For the nine months ended September 30, 2025, net loss was $4,564,546. Cash and cash equivalents were $192,068 and restricted cash was $661,843. The filing notes a working capital deficit of $2,434,951 and states there is substantial doubt about the company’s ability to continue as a going concern.
Shares outstanding were 24,301,089 as of October 30, 2025. The company also disclosed restatements affecting 2023 and certain 2024 interim figures, primarily related to stock‑based compensation, convertible note accounting, and noncontrolling interests.
ABVC BioPharma furnished an 8-K to announce its financial results for the third quarter ended September 30, 2025. The company reported these results via a press release attached as Exhibit 99.1.
The disclosure under Item 2.02 is being furnished and is not deemed filed for purposes of Section 18 of the Exchange Act. The filing also includes Exhibit 104, the cover page interactive data file formatted in Inline XBRL. The notice states it is not an offer to sell or solicit purchases of securities.
ABVC BioPharma filed its Q3 2025 Form 10‑Q, reporting revenues of $795,950 for the quarter and $795,950 for the nine months. The company posted a net loss of $1,287,523 for Q3 and $4,564,546 for the nine months, with basic and diluted net loss per share of $0.05 and $0.23, respectively.
Total assets were $21,176,299 as of September 30, 2025, up from $7,539,907 at December 31, 2024, largely reflecting property and equipment, net, of $12,055,642, including land acquisitions in Taiwan. Cash and cash equivalents were $192,068, with restricted cash of $661,843. The company reported a working capital deficit of $2,434,951 and stated that these conditions give rise to substantial doubt about its ability to continue as a going concern.
Operating cash outflow was $1,567,264 for the nine months, offset by $3,488,478 provided by financing activities. The company recognized collaboration revenues from related‑party licensing, including $595,950 from an OncoX agreement and $200,000 from a FEYE amendment during the nine months. ABVC restated prior periods to correct share‑based payment accounting, interest recognition on a convertible note, and non‑controlling interest presentation. Shares outstanding were 24,301,089 as of October 30, 2025.
ABVC BioPharma (ABVC) approved a performance incentive plan for directors, officers, and select employees. The plan will only take effect after the company achieves a $1B market cap for 30 consecutive trading days on or before December 31, 2027, of which there is no guarantee.
If implemented, awards will equal 1% of the company’s common stock outstanding on the implementation date, sourced from the Amended and Restated 2016 Equity Incentive Plan. The plan is capped at $10 million in total awards, with a $1 million cap per recipient. Grants will be tied to defined milestones and require allocation by the Compensation Committee, endorsement by a majority of independent directors, and final approval by the full Board. The structure is intended to align leadership incentives with shareholder value creation.
ABVC BioPharma, Inc. reported continued operating losses and a strained liquidity position while advancing multiple clinical programs and licensing arrangements. For the periods shown, the company recorded net losses of $2.33 million and $3.28 million (two comparable periods), with net loss attributable to ABVC of $2.26 million and $3.10 million in the comparable reporting periods. Basic and diluted net loss per share ranged from $(0.08) to $(0.36) depending on period and share count. Current liabilities totaled $6.53 million with a working capital deficit near $(3.76) million. Cash flows show investing uses of $(665,779) and financing proceeds of $2.54 million in the reporting period. Long-term investments and prepayments total several million, and the company discloses substantial related-party loans and short-term borrowings. Clinical pipeline progress includes completed Phase II for ABV-1504 (MDD), ongoing Phase II Part 2 for ABV-1505 (ADHD), planned Phase I for ABV-1601, and initiated Phase II for ABV-1701 Vitargus (medical device). License/milestone schedule includes $1M for IND, $1M for Phase II completion, $3M for Phase III initiation, and $4M for NDA submission.
ABVC BioPharma reported a loss and continuing financing reliance. The filing shows significant operating losses and negative working capital while the company advances multiple clinical and device programs.
For the period presented, net loss attributable to ABVC was $2,257,022 for the quarter and $3,099,097 for the six-month period, with basic and diluted net loss per share of $(0.13) and $(0.19) for the comparable periods. Current liabilities totaled $6,532,514 producing a working capital deficit of $(3,762,113). Long-term investments were $2,837,922 and property and equipment, net was reported at $8,215,366. Cash flow from financing activities provided $2,536,083 while investing used $(665,779). The company disclosed related-party loans and short-term borrowings, loaned funds to affiliates (BioFirst) and a warrant exercise arrangement with Lind to raise equity proceeds. The business continues multiple clinical programs (ABV-1504, ABV-1505, ABV-1601, ABV-1701, ABV-1519, ABV-1703) and milestone-based license payments tied to IND, Phase II, Phase III and NDA events.
ABVC BioPharma, Inc. reported continued operating losses and negative working capital while advancing multiple clinical programs and relying on financing and related-party support. For the six months ended June 30, 2025 the company recorded a net loss of $2.332 million versus a loss of $1.047 million in the prior period. Basic and diluted net loss per share for the quarter/period presented include $(0.13) and (figures shown in the report). Total current liabilities were $6.533 million with a working capital deficit of $(3.762 million). Total assets included cash/current assets and long-term investments that aggregate to reported totals (long-term investments noted at $2.838 million). Cash flows show cash used in investing activities of $(665,779) and cash provided by financing activities of $2.536 million. The company discloses material related-party loans, convertible debt exercises and warrant exercises as financing sources and milestone payment schedules tied to development and licensing (e.g., IND/Phase II/III/NDA payments totaling up to $10 million under a development agreement). The filing lists multiple clinical assets (ABV-1504, ABV-1505, ABV-1601, ABV-1519, ABV-1701, ABV-1703) at various Phase I/II/II-part stages and strategic licensing objectives.