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Correspondence 0001493152-24-052565 from Scienture Holdings, Inc. (SCNX)

Scienture Holdings, Inc.
Date: Dec. 30, 2024 · CIK: 0001382574 · Accession: 0001493152-24-052565

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File numbers found in text: 001-39199

Date
Dec. 30, 2024
Author
Gossett PLLC
Form
CORRESP
Company
Scienture Holdings, Inc.

Letter

Division of Corporate Finance Office of Life Sciences Attention: Tracie Mariner and Sasha Parikh Re: Scienture Holdings, Inc. Form 10-K for Fiscal Year Ended December 31, 2023 Form 10-Q for Fiscal Quarter Ended September 30, 2024 File No. 001-39199

Dear Ms. Mariner, and Ms. Parikh:

This response letter (this “Response”) is submitted on behalf of Scienture Holdings, Inc. (the “Company”) in response to the comments that the Company received from the staff of the Division of Corporation Finance (the “Staff”) of the U.S. Securities and Exchange Commission (the “SEC”) in a letter addressed to Mr. Ajjarapu, dated December 20, 2024 (the “Comment Letter”), with respect to the Company’s Form 10-K for the year ended December 31, 2023 (the “Form 10-K”), and Form 10-Q for the quarter ended September 30, 2024 (the “Form 10-Q”). For ease of reference, each of the Staff’s numbered comments from the Comment Letter is set forth in bold text below, followed by the Company’s response to each comment

The Company hopes that this letter is helpful and responsive to your request. The responses below are based on information provided by the Company to Dykema Gossett PLLC, the Company’s counsel.

Form 10-K for Fiscal Year Ended December 31, 2023

Financial Statements

Note 1- Organization and Basis of Presentation

Intangible Assets and Goodwill, page 65

1. You state that you recognized a goodwill impairment loss of $5.1 million for the year ended December 31, 2023 resulting from the acquisition of Superlatus which was subsequently determined to be impaired based on the facts and circumstances surrounding the sale of Superlatus on March 5, 2024. Please explain in detail in your response why you did not impair the $9.5 million of intangible assets as of December 31, 2023 that were acquired from Superlatus, in light of the significant reduction in the initial purchase price and the sale of Superlatus for $1. In future filings, as applicable, please revise your risk factor “Our acquisitions and investments in new businesses...”, on page 20, to disclose the $5.1 million goodwill impairment loss in your discussion regarding the divesture of Superlatus and the resulting loss on the disposition.

Response: In response to the Staff’s comments, the Company respectfully advises the Staff that its decision to sell Superlatus occurred in the first quarter of 2024. Given that intangible impairment is treated prospectively, the Company did not impair the intangible assets for the preceding period ending December 31, 2023. Due to limited information, the Company was not able to accurately calculate the fair value of the reporting unit including goodwill. Management did not believe that the fair value of the reporting unit was greater than the carrying value. Thus, as of December 31, 2023 the Company wrote off the entirety of the goodwill.

The intangible assets of Sapientia, Inc., a wholly-owned subsidiary of Superlatus, consisting of developed technology, had been recently appraised, with the valuation specialist issuing its report on November 4, 2023, with an effective date of July 31, 2023. Considering the significance of the dollar value of such valuation and there being a recent fair value measurement with no significant adverse changes that had occurred since that date, the Company’s management determined that impairment was not necessary as of December 31, 2023. Subsequently the company disposed of Superlatus for $1 due to operational difficulties.

The Company will supplement its disclosures in future filings to disclose the $5.1 goodwill impairment loss resulting from the acquisition of Superlatus in the risk factor, “Our acquisitions and investments in new businesses and new products, services, and technologies is inherently risky, and could disrupt our ongoing businesses” as shown below:

Our acquisitions and investments in new businesses and new products, services, and technologies is inherently risky, and could disrupt our ongoing businesses.

We have invested and expect to continue to invest in new businesses, products, services, and technologies. Such endeavors may involve significant risks and uncertainties, including insufficient revenues from such investments to offset any new liabilities assumed and expenses associated with these new investments, inadequate return of capital on our investments, distraction of management from current operations, and unidentified issues not discovered in our due diligence of such strategies and offerings that could cause us to fail to realize the anticipated benefits of such investments and incur unanticipated liabilities. Because these new ventures are inherently risky, no assurance can be given that such strategies and offerings will be successful and will not adversely affect our reputation, financial condition, and operating results. To date we have taken losses and/or write-downs on several businesses, products, services, and technologies. For example:

a) We had $725,973 of loss on impairment of goodwill for the fiscal year ended December 31, 2020, in connection with the acquisition of Community Specialty Pharmacy, LLC;

b) We designed and invested resources into the “Bonum Health Hub”, a self-enclosed, free standing virtual examination room, which was launched by the Company’s wholly-owned Bonum Health, LLC, in November 2019 and was expected to be operational in April 2020; however, the Company does not anticipate installations moving forward, and took a write off of the hubs purchased at June 30, 2021 in the amount of $143,891, which was included under loss on inventory investments in the statement of operations for the year ended December 31, 2021;

c) We also used resources and funding to create a Health Passport application during 2020 and 2021, which was planned to store a user’s health and vaccination status and allow confirmation thereof via a QR code; however, we did not generate any revenue from this product and the product was discontinued at the end of December 2021;

d) We had $792,500 of loss on impairment of intangible assets related to our investment in the joint venture SOSRx, LLC formed in February of 2022. The subsidiary did not generate material revenue and in February of 2023 the Company voluntarily withdrew from the joint venture agreement. The asset impairment is reflected in the statement of operations for the year ended December 31, 2022 as impairment of intangible asset. Additionally, the Company contributed a cash investment of $275,000 in February of 2022 when the joint venture was formed, the Company did not recover this investment as part of the withdrawal settlement;

e) We recorded a loss of $875,250 in connection with CSP Test Kits purchased for our Community Specialty Pharmacy that were later deemed inappropriate for distribution by the FDA. The inventory was written down and was recorded as loss on inventory investment in the statement of operations during the year ended December 31, 2022; and

d) During the year ended December 31, 2023 we acquired Superlatus through a merger transaction, however, due to various complications with the post-closing integration we elected to divest Superlatus in March 2024 for $1. As a result of this divestiture, the Company recognized a goodwill impairment loss of $5.1 million for the year ended December 31, 2023.

The use of resources for new businesses and new products, services, and technologies, to the extent such new businesses and new products, services, and technologies do not generate revenues or profits may take management’s focus and time away from more profitable endeavors, may require the Company to take significant write-downs or write-offs, may take funding away from the Company’s other operations or growth opportunities, which may ultimately be more profitable, and may have a material adverse effect on the Company’s cash flows, liquidity and revenues, any or all of which may cause the value of the Company’s securities to decline in value or become worthless.

Form 10-Q for Fiscal Quarter Ended September 30, 2024

Management’s Discussion and Analysis of Financial Condition and Results of Operations Results of Operations, page 33

2. We note a significant increase in your research and development expense from the prior periods. In future filings, please expand your disclosure to discuss the costs incurred during each period presented for each of your key research and development product candidates separately. If you do not track your research and development costs by project or program, please disclose that fact, and explain why you do not maintain and evaluate research and development costs by project or program. For amounts that are not tracked by product candidate or program, provide other quantitative or qualitative disclosure that provides more transparency as to the type of research and development expenses incurred (i.e. by nature or type of expense), which should reconcile to total research and development expense on the statements of operations. Provide draft disclosure with your response.

Response: In response to the Staff’s comments, the Company respectfully advises the Staff that it will supplement its disclosures in future filings to expand to discuss the costs incurred during each period presented for each of the Company’s key research and development product candidates separately. Using information on the Company’s research and development expenses for the three and nine month periods ending September 30, 2024 and 2023, as an example, the Company expects to set forth the costs incurred for each product candidate substantially as follows:

Research and development expenses were $1,253,983 million for the three and nine months ended September 30, 2024. The Company did not incur research and development expenses for the three and nine months ended September 30, 2023, as such periods predated the Company’s acquisition of former Scienture, Inc.:

Three Months Ended

September 30,

Project Codes Product Name

SCN-102 Losartan $ 322,245 $ -

SCN-104 DHE $ 870,888 $ -

SCN-106 Alteplase $ 3,441 $ -

SCN-107 Bupivacaine $ 36,245 $ -

SCN-105 Apomorphine $ 21,164 $ -

Total

$ 1,253,983 $ -

Nine Months Ended

September 30,

Project Codes Product Name

SCN-102 Losartan $ 322,245 $ -

SCN-104 DHE $ 870,888 $ -

SCN-106 Alteplase $ 3,441 $ -

SCN-107 Bupivacaine $ 36,245 $ -

SCN-105 Apomorphine $ 21,164 $ -

Total

$ 1,253,983 $ -

Critical Accounting Policies

Revenue Recognition, page 36

3. We note your disclosure stating that IPS is a licensed wholesaler of brand, generic, and non-drug products to customers. IPS takes orders for products, creates invoices for each order, and recognizes revenue at the time the customer receives the product. However, on page 18, you disclose that revenue for your products is recognized when the product is shipped to the customer. In future filings, please revise your disclosures as necessary to resolve the discrepancy.

Response: In response to the Staff’s comments, the Company respectfully advises the Staff that it will revise its disclosures in future filings to clarify that IPS recognizes revenue when the product is shipped to the customer.

Thank you for your review and consideration of the matters set forth in this Response and in Amendment No. 1. If you have any questions, please contact the undersigned at (414) 488-7333 or KBechen@dykema.com.

Sincerely,
Dykema
Gossett PLLC

Show Raw Text
CORRESP
1
filename1.htm

    Dykema
    Gossett PLLC

    111
    E. Kilbourn Ave.

    Suite
    1050

    Milwaukee,
    WI 53202

    www.dykema.com

    Tel:
    414-488-7300

    Kate
    Bechen

    Direct
    Dial: (414) 488-7333

    Email:
    KBechen@dykema.com

December
30, 2024

U.S.
Securities and Exchange Commission

Division
of Corporate Finance

Office
of Life Sciences

100
F Street, N.E.

Washington,
D.C. 20549

Attention:
Tracie Mariner and Sasha Parikh

    Re:
    Scienture
    Holdings, Inc.

    Form
    10-K for Fiscal Year Ended December 31, 2023

    Form
    10-Q for Fiscal Quarter Ended September 30, 2024

    File
    No. 001-39199

Dear
Ms. Mariner, and Ms. Parikh:

This
response letter (this “Response”) is submitted on behalf of Scienture Holdings, Inc. (the “Company”)
in response to the comments that the Company received from the staff of the Division of Corporation Finance (the “Staff”)
of the U.S. Securities and Exchange Commission (the “SEC”) in a letter addressed to Mr. Ajjarapu, dated December 20,
2024 (the “Comment Letter”), with respect to the Company’s Form 10-K for the year ended December 31, 2023 (the
“Form 10-K”), and Form 10-Q for the quarter ended September 30, 2024 (the “Form 10-Q”). For ease
of reference, each of the Staff’s numbered comments from the Comment Letter is set forth in bold text below, followed by the Company’s
response to each comment

The
Company hopes that this letter is helpful and responsive to your request. The responses below are based on information provided by the
Company to Dykema Gossett PLLC, the Company’s counsel.

Form
10-K for Fiscal Year Ended December 31, 2023

Financial
Statements

Note
1- Organization and Basis of Presentation

Intangible
Assets and Goodwill, page 65

    1.
    You
    state that you recognized a goodwill impairment loss of $5.1 million for the year ended December 31, 2023 resulting from the acquisition
    of Superlatus which was subsequently determined to be impaired based on the facts and circumstances surrounding the sale of Superlatus
    on March 5, 2024. Please explain in detail in your response why you did not impair the $9.5 million of intangible assets as of December
    31, 2023 that were acquired from Superlatus, in light of the significant reduction in the initial purchase price and the sale of
    Superlatus for $1. In future filings, as applicable, please revise your risk factor “Our acquisitions and investments in new
    businesses...”, on page 20, to disclose the $5.1 million goodwill impairment loss in your discussion regarding the divesture
    of Superlatus and the resulting loss on the disposition.

Response:
In response to the Staff’s comments, the Company respectfully advises the Staff that its decision to sell Superlatus occurred
in the first quarter of 2024. Given that intangible impairment is treated prospectively, the Company did not impair the intangible assets
for the preceding period ending December 31, 2023. Due to limited information, the Company was not able to accurately calculate the fair
value of the reporting unit including goodwill. Management did not believe that the fair value of the reporting unit was greater than
the carrying value. Thus, as of December 31, 2023 the Company wrote off the entirety of the goodwill.

The
intangible assets of Sapientia, Inc., a wholly-owned subsidiary of Superlatus, consisting of developed technology, had been recently
appraised, with the valuation specialist issuing its report on November 4, 2023, with an effective date of July 31, 2023. Considering
the significance of the dollar value of such valuation and there being a recent fair value measurement with no significant adverse changes
that had occurred since that date, the Company’s management determined that impairment was not necessary as of December 31, 2023.
Subsequently the company disposed of Superlatus for $1 due to operational difficulties.

The
Company will supplement its disclosures in future filings to disclose the $5.1 goodwill impairment loss resulting from the acquisition
of Superlatus in the risk factor, “Our acquisitions and investments in new businesses and new products, services, and technologies
is inherently risky, and could disrupt our ongoing businesses” as shown below:

Our
acquisitions and investments in new businesses and new products, services, and technologies is inherently risky, and could disrupt our
ongoing businesses.

We
have invested and expect to continue to invest in new businesses, products, services, and technologies. Such endeavors may involve significant
risks and uncertainties, including insufficient revenues from such investments to offset any new liabilities assumed and expenses associated
with these new investments, inadequate return of capital on our investments, distraction of management from current operations, and unidentified
issues not discovered in our due diligence of such strategies and offerings that could cause us to fail to realize the anticipated benefits
of such investments and incur unanticipated liabilities. Because these new ventures are inherently risky, no assurance can be given that
such strategies and offerings will be successful and will not adversely affect our reputation, financial condition, and operating results.
To date we have taken losses and/or write-downs on several businesses, products, services, and technologies. For example:

    a)
    We
    had $725,973 of loss on impairment of goodwill for the fiscal year ended December 31, 2020, in connection with the acquisition of
    Community Specialty Pharmacy, LLC;

    b)
    We
    designed and invested resources into the “Bonum Health Hub”, a self-enclosed, free standing virtual examination room,
    which was launched by the Company’s wholly-owned Bonum Health, LLC, in November 2019 and was expected to be operational in
    April 2020; however, the Company does not anticipate installations moving forward, and took a write off of the hubs purchased at
    June 30, 2021 in the amount of $143,891, which was included under loss on inventory investments in the statement of operations for
    the year ended December 31, 2021;

    c)
    We
    also used resources and funding to create a Health Passport application during 2020 and 2021, which was planned to store a user’s
    health and vaccination status and allow confirmation thereof via a QR code; however, we did not generate any revenue from this product
    and the product was discontinued at the end of December 2021;

    d)
    We
    had $792,500 of loss on impairment of intangible assets related to our investment in the joint venture SOSRx, LLC formed in February
    of 2022. The subsidiary did not generate material revenue and in February of 2023 the Company voluntarily withdrew from the joint
    venture agreement. The asset impairment is reflected in the statement of operations for the year ended December 31, 2022 as impairment
    of intangible asset. Additionally, the Company contributed a cash investment of $275,000 in February of 2022 when the joint venture
    was formed, the Company did not recover this investment as part of the withdrawal settlement;

    e)
    We
    recorded a loss of $875,250 in connection with CSP Test Kits purchased for our Community Specialty Pharmacy that were later deemed
    inappropriate for distribution by the FDA. The inventory was written down and was recorded as loss on inventory investment in the
    statement of operations during the year ended December 31, 2022; and

    d)
    During
    the year ended December 31, 2023 we acquired Superlatus through a merger transaction, however, due to various complications with
    the post-closing integration we elected to divest Superlatus in March 2024 for $1. As a result of this divestiture, the Company recognized
    a goodwill impairment loss of $5.1 million for the year ended December 31, 2023.

The
use of resources for new businesses and new products, services, and technologies, to the extent such new businesses and new products,
services, and technologies do not generate revenues or profits may take management’s focus and time away from more profitable endeavors,
may require the Company to take significant write-downs or write-offs, may take funding away from the Company’s other operations
or growth opportunities, which may ultimately be more profitable, and may have a material adverse effect on the Company’s cash
flows, liquidity and revenues, any or all of which may cause the value of the Company’s securities to decline in value or become
worthless.

Form
10-Q for Fiscal Quarter Ended September 30, 2024

Management’s
Discussion and Analysis of Financial Condition and Results of Operations Results of Operations, page 33

    2.
    We
    note a significant increase in your research and development expense from the prior periods. In future filings, please expand your
    disclosure to discuss the costs incurred during each period presented for each of your key research and development product candidates
    separately. If you do not track your research and development costs by project or program, please disclose that fact, and explain
    why you do not maintain and evaluate research and development costs by project or program. For amounts that are not tracked by product
    candidate or program, provide other quantitative or qualitative disclosure that provides more transparency as to the type of research
    and development expenses incurred (i.e. by nature or type of expense), which should reconcile to total research and development expense
    on the statements of operations. Provide draft disclosure with your response.

Response:
In response to the Staff’s comments, the Company respectfully advises the Staff that
it will supplement its disclosures in future filings to expand to discuss the costs incurred during each period presented for
each of the Company’s key research and development product candidates separately. Using information
on the Company’s research and development expenses for the three and nine month periods ending September 30, 2024 and 2023, as
an example, the Company expects to set forth the costs incurred for each product candidate substantially as follows:

Research
and development expenses were $1,253,983 million for the three and nine months ended September 30, 2024. The Company did not incur research
and development expenses for the three and nine months ended September 30, 2023, as such periods predated the Company’s acquisition
of former Scienture, Inc.:

    Three Months Ended

 September 30,

    Project Codes
    Product Name
    2024
    2023

    SCN-102
    Losartan
    $ 322,245
    $    -

    SCN-104
    DHE
    $ 870,888
    $ -

    SCN-106
    Alteplase
    $ 3,441
    $ -

    SCN-107
    Bupivacaine
    $ 36,245
    $ -

    SCN-105
    Apomorphine
    $ 21,164
    $ -

    Total

    $ 1,253,983
    $ -

    Nine Months Ended

 September 30,

    Project Codes
    Product Name
    2024
    2023

    SCN-102
    Losartan
    $ 322,245
    $    -

    SCN-104
    DHE
    $ 870,888
    $ -

    SCN-106
    Alteplase
    $ 3,441
    $ -

    SCN-107
    Bupivacaine
    $ 36,245
    $ -

    SCN-105
    Apomorphine
    $ 21,164
    $ -

    Total

    $ 1,253,983
    $ -

Critical
Accounting Policies

Revenue
Recognition, page 36

    3.
    We
    note your disclosure stating that IPS is a licensed wholesaler of brand, generic, and non-drug products to customers. IPS takes orders
    for products, creates invoices for each order, and recognizes revenue at the time the customer receives the product. However, on
    page 18, you disclose that revenue for your products is recognized when the product is shipped to the customer. In future filings,
    please revise your disclosures as necessary to resolve the discrepancy.

Response:
In response to the Staff’s comments, the Company respectfully advises the Staff that
it will revise its disclosures in future filings to clarify that IPS recognizes revenue when the product is shipped to the customer.

Thank
you for your review and consideration of the matters set forth in this Response and in Amendment No. 1. If you have any questions, please
contact the undersigned at (414) 488-7333 or KBechen@dykema.com.

    Sincerely,

    Dykema
    Gossett PLLC

    /s/
    Kate Bechen

    Kate
    Bechen, Esq.

    cc:
    Surendra
    Ajjarapu

    Chief
    Executive Officer

    Scienture
    Holdings, Inc.