Recent Updates
Recently added Catalysts
ABVC Positive Sentiment Score: 75/100

ABVC BioPharma Announces Fiscal Year 2022 Financial and Operational Results FREMONT, CA

Key Takeaway: ABVC BioPharma has announced its financial and operational results for the fiscal year 2022. The company is advancing its clinical pipeline with planned Phase II trials for its biodegradable vitreous substitute, Vitargus, expected to conclude in 2023. Additionally, ABV-1505 for ADHD and ABV-1601 for cancer patient depression are both in ongoing clinical studies. ABVC is optimistic about expanding its product pipeline and aims to seek partnerships following the progress of its trials.

Market Sentiment Analysis

POSITIVE FACTORS

  • ABVC expects significant progress in its clinical trials across multiple studies.
  • The company is preparing for potential distribution agreements following successful trial completions.
  • ABVC's innovative approach aims to improve patient experience and outcomes in critical medical conditions.

Full Press Release Details

ABVC BioPharma Announces Fiscal Year 2022 Financial
and Operational Results
FREMONT, CA, March 31, 2023 -- ABVC BioPharma,
Inc. (Nasdaq: ABVC), a biotechnology company specializing in botanically based solutions that seeks to deliver high efficacy and low toxicity
to improve health outcomes, today announced its financial and operating results for the fiscal year ended December 31, 2022.
Year 2022 Financial Results
All comparisons are made on a year-over-year basis.
is intended to be the first biodegradable vitreous substitute to facilitate retina reattachment surgery. The company expects to complete
Phase II trials of Vitargus in Thailand, Australia and Taiwan by the end of 2023, the successful completion of which is expected to lead
to distribution agreements in Asia soon thereafter. ABVC expects
the study to further demonstrate that Vitargus has properties that eliminate the need for post-surgery patient face-down positioning and
can provide greater patient comfort and visual acuity during the surgical recovery period.
The company's ADHD medicine
ABV-1505, is currently in Phase II, part 2, clinical trials at five prestigious medical centers in Taiwan. A Phase II, part 2 study
will begin at the University of California, San Francisco (UCSF) Medical Center in the next few months. This study is expected to
eventually enroll approximately 100 patients in Taiwan and the United States.
Following the May 2022 reports of the
first subject treated in Taiwan, 42 subjects have been enrolled in the study from a total of 64 subjects screened. 36 of the enrolled
participants have already completed the 8-week treatment in accordance with the study design.
ABV-1601 Cancer Patient Depression:
A Phase I study of ABV-1601 for treating
depression in cancer patients is expected to begin in the first quarter of 2023 at the Cedars-Sinai Medical Center (CSMC, West Hollywood
CA). The Phase I study is open label and will be conducted with 12 cancer patients with moderate to severe depressive symptoms. The main
objective of the study is to evaluate the safety of PDC-1421, the primary active ingredient in ABV-1601 in cancer patients. The Phase
II study is to determine the most effective dosages using a randomized, double-blind, non-inferiority protocol of PDC-1421 vs Wellbutrin
XL. ABVC expects to initiate the Phase II study in the fourth quarter of 2023 and then compare the results to Wellbutrin XL, a commonly
used medicine to treat cancer patients suffering with depression.
ABV-1504 Major Depressive Disorder:
MDD medicine, ABV-1504, has successfully completed Phase II at the Stanford University Medical Center and five major medical centers
in Taiwan. Later this year, with the help of Dr. Maurizio Fava and Dr. Thomas Laughren,
the company expects to conclude discussions with the US FDA on acceptable protocols for Phase III trials for MDD, allowing ABVC to seek
potential distribution partners active in manufacturing and distributing Central Nervous System (CNS) medicines.
with our remarkable accomplishments and meaningful progress in 2022," said Dr. Howard Doong, M.D., Ph.D., Chief Executive Officer
of ABVC BioPharma. "I am pleased that ABV-1504 ADHD Phase II, part II study is making substantial progress at five Taiwan study
sites and UCSF and expecting to be completed in 2023, that Phase I studies of ABV-1601 for treating depression in cancer patients is
being initiated at CSMC in US, and with the progress of End-of-Phase II meeting preparation for ABV-1504 (MDD) with Dr. Maurizio Fava
and Dr. Thomas Laughren of Clinical Trials Network and Institute, (CTNI). In addition, ABV-1701 Vitargus, a hydrogel we developed to
make retina reattachment surgery more comfortable and successful for patients, has shown advantages over existing devices available to
surgeons in Phase I clinical study completed in Australia in 2018, prompting us to start a Phase II trial in Australia and Thailand in
2022. The study has received the approvals from both Australian TGA and Thai FDA with patient enrollment planned in early Q2 of 2023.
We remain excited about our ongoing research initiatives and look forward to expanding our product pipeline in the future."
About ABVC BioPharma
ABVC BioPharma is a clinical-stage
biopharmaceutical company with an active pipeline of six drugs and one medical device (ABV-1701/Vitargus ) under development. For
its drug products, the company utilizes in-licensed technology from its network of world-renowned research institutions to conduct proof-of-concept
trials through Phase II of clinical development. The company's network of research institutions includes Stanford University, University
of California at San Francisco, and Cedars-Sinai Medical Center. For Vitargus , the company intends to conduct global clinical trials
Forward-Looking Statements
Clinical trials are in
early stages, and there is no guarantee that any specific outcome will be achieved. 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. None of the outcomes expressed herein are guaranteed. 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 to 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
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.
ABVC BIOPHARMA, INC. AND SUBSIDIARIES
CONSOLIDATED BALANCE SHEETS
December 31, December 31,
2022 2021
ASSETS
Current Assets
Cash and cash equivalents $ 85,265 $ 5,828,548
Restricted cash and cash equivalents 1,306,463 736,667
Accounts receivable, net 98,325 280,692
Accounts receivable - related parties, net 757,343 145,399
Due from related parties 513,819 -
Inventories, net - 25,975
Short-term investments 75,797 108,147
Prepaid expense and other current assets 150,235 528,354
Total Current Assets 2,987,247 7,653,782
Property and equipment, net 573,978 525,881
Operating lease right-of-use assets 1,161,141 1,471,899
Long-term investments 842,070 932,755
Deferred tax assets, net 117,110 981,912
Prepaid expenses - noncurrent 135,135 119,309
Security deposits 58,838 41,157
Prepayment for long-term investments 2,838,578 1,153,155
Due from related parties - noncurrent 1,141,378 818,183
Total Assets $ 9,855,475 $ 13,698,033
LIABILITIES AND EQUITY
Current Liabilities
Short-term bank loans $ 1,893,750 $ 1,640,000
Accrued expenses and other current liabilities 2,909,587 1,300,803
Advance from customers 10,985 10,985
Operating lease liability - current portion 369,314 347,100
Due to related parties 635,893 393,424
Total Current Liabilities 5,819,529 3,692,312
Tenant security deposit 7,980 10,580
Operating lease liability - noncurrent portion 791,827 1,124,799
Total Liabilities 6,619,336 4,827,691
COMMITMENTS AND CONTINGENCIES
Equity
Preferred stock, $0.001 par value, 20,000,000 authorized, nil shares issued and outstanding - -
Common stock, $0.001 par value, 100,000,000 authorized, 32,857,329 and 28,926,322 shares issued and outstanding as of December 31, 2022 and 2021, respectively 32,857 28,926
Additional paid-in capital 67,907,479 58,113,667
Stock subscription receivable (1,354,440 ) (2,257,400 )
Accumulated deficit (54,904,439 ) (38,481,200 )
Accumulated other comprehensive income 517,128 539,660
Treasury stock (9,100,000 ) (9,100,000 )
Total Stockholders' equity 3,098,585 8,843,653
Noncontrolling Interest 517,128 26,689
Total Equity 3,236,139 8,870,342
Total Liabilities and Equity $ 9,855,475 $ 13,698,033
ABVC BIOPHARMA, INC. AND SUBSIDIARIES
CONSOLIDATED STATEMENTS OF OPERATIONS AND COMPREHENSIVE LOSS
Year Ended December 31,
2022 2021
Revenue $ 969,783 $ 355,797
Cost of revenue 286,415 5,086
Gross profit 683,368 350,711
Operating expenses
Selling, general and administrative expenses 6,067,545 5,746,119
Research and development expenses 2,693,457 1,003,805
Stock based compensation 7,036,778 5,306,755
Total operating expenses 15,797,780 12,056,679
Loss from operations (15,114,412 ) (11,705,968 )
Other income (expense)
Interest income 187,817 43,196
Interest expense (293,968 ) (227,210 )
Operating sublease income 107,150 134,576
Operating sublease income - related parties - 4,800
Impairment loss (110,125 ) -
Investment loss (7,446 ) -
Gain/Loss on foreign exchange changes (259,463 ) 426,316
Gain/Loss on investment in equity securities - (269,844 )
Other income (expense) (24,149 ) 22,409
Government grant income - 360,898
Total other income (expenses) (400,184 ) 495,141
Loss before provision for income tax (15,514,596 ) (11,210,827 )
Provision for income tax expense 797,778 825,024
Net loss (16,312,374 ) (12,035,851 )
Net loss attributable to noncontrolling interests 110,865 802,962
Net loss attributed to ABVC and subsidiaries (16,423,239 ) (12,838,813 )
Foreign currency translation adjustment (22,532 ) (25,200 )
Comprehensive loss $ (16,445,771 ) $ (12,864,013 )
Net loss per share:
Basic and diluted $ (0.52 ) $ (0.51 )
Weighted average number of common shares outstanding:
Basic and diluted 31,664,660 25,053,522
ABVC BIOPHARMA, INC. AND SUBSIDIARIES
CONSOLIDATED STATEMENTS OF CASH FLOWS
FOR THE YEAR ENDED DECEMBER 31, 2022 AND 2021
2022 2021
Cash flows from operating activities
Net loss $ (16,312,374 ) $ (12,035,851 )
Adjustments to reconcile net loss to net cash used in operating activities:
Depreciation 23,799 11,993
Stock based compensation 7,036,778 5,306,755
Loss on investment in equity securities - 269,844
Inventory allowance for valuation losses 25,975 -
Provision for doubtful accounts, net of recovery 184,589 -
Government grant income - (360,898 )
Other non-cash income and expenses 32,350 -
Impairment of prepaid expenses 110,125 -
Deferred tax 864,802 824,199
Changes in operating assets and liabilities:
Decrease (increase) in accounts receivable (614,166 ) (120,980 )
Decrease (increase) in prepaid expenses and other current assets 238,092 (357,276 )
Decrease (increase) in due from related parties (837,014 ) (595,037 )
Decrease (increase) in inventories - (25,830 )
Increase (decrease) in accounts payable - (23,044 )
Increase (decrease) in accrued expenses and other current liabilities 1,608,784 (173,151 )
Increase (decrease) in advanced from customers - (1,085 )
Increase (decrease) in tenant security deposit received (2,600 ) -
Increase (decrease) in due to related parties 242,469 (317,358 )
Net cash used in operating activities (7,398,391 ) (7,597,719 )
Cash flows from investing activities
Purchase of investments - (107,547 )
Purchase of equipment (119,692 ) (17,503 )
Prepayment for equity investment (1,601,992 ) (680,916 )
Net cash used in investing activities (1,721,684 ) (805,966 )
Cash flows from financing activities
Issuance of common stock 3,663,925 11,119,452
Payment for offering costs - (850,429 )
Repayment of convertible notes - (306,836 )
Repayment of short-term loan - (100,000 )
Repayment of notes payable - (107,400 )
Proceeds from long-term loan - 236,498
Proceeds from short term loan 350,000 -
Proceeds from short term borrowings from third parties - 4,265
Net cash provided by financing activities 4,013,925 9,995,550
Effect of exchange rate changes on cash and cash equivalents and restricted cash (67,337 ) (28,021 )
Net increase in cash and cash equivalents and restricted cash (5,173,487 ) 1,563,844
Cash and cash equivalents and restricted cash
Beginning 6,565,215 5,001,371
Ending $ 1,391,728 $ 6,565,215
Supplemental disclosure of cash flows
Cash paid during the year for:
Interest expense paid $ 285,465 $ 333,873
Income taxes paid $ 1,600 $ -
Non-cash financing and investing activities
Common shares issued for debt conversion $ - $ 2,693,548

Frequently Asked Questions

What is ABVC BioPharma's focus area?

ABVC BioPharma specializes in botanically based solutions for health care.

Where is the Phase II trial for Vitargus being conducted?

The Phase II trial for Vitargus is being conducted in Thailand, Australia, and Taiwan.

What is the objective of the ABV-1601 study?

The ABV-1601 study aims to evaluate the safety of treating depression in cancer patients.

How many patients are involved in the ABV-1505 trials?

Approximately 100 patients will be enrolled in the ABV-1505 trials across Taiwan and the US.

What is the current status of ABV-1504 for Major Depressive Disorder?

ABV-1504 has completed Phase II trials and is in discussions for Phase III protocols.

Last updated: Mar 31, 2023