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SEC Comment Letter 0000000000-25-001252 to Cytonics Corp (CIK 0001421744)

Cytonics Corp (CIK 0001421744)
Date: Feb. 5, 2025 · CIK: 0001421744 · Accession: 0000000000-25-001252

AI Filing Summary & Sentiment

File numbers found in text: 024-12533

Date
February 5, 2025
Author
Not clearly detected
Form
UPLOAD
Company
Cytonics Corp (CIK 0001421744)

Letter

February 5, 2025 Anjun Bose Chief Executive Officer and President Cytonics Corporation 658 West Indiantown Road, Suite 214 Jupiter, FL 33458 Re:Cytonics Corporation Amendment No. 1 to Offering Statement on Form 1-A Filed January 24, 2025 File No. 024-12533 Dear Anjun Bose: We have reviewed your amended offering statement and have the following comments. Please respond to this letter by amending your offering statement and providing the requested information. If you do not believe a comment applies to your facts and circumstances or do not believe an amendment is appropriate, please tell us why in your response. After reviewing any amendment to your offering statement and the information you provide in response to this letter, we may have additional comments. Unless we note otherwise, any references to prior comments are to comments in our December 16, 2024 letter. Amendment No. 1 to Offering Statement on Form 1-A Offering Circular Summary The Company, page 6 1.We note your response to prior comment 2 and reissue in part. Please revise to briefly describe the additional steps necessary to commercialize your product candidate rather than providing a cross-reference. The Company's Business Regulatory Regimes, page 29 We note your response to prior comment 10 and reissue in part. Please revise to provide a more detailed discussion of the FDA's regulatory requirements for 2.

February 5, 2025 Page 2 marketing your products. For example, without limitation, discuss the clinical trial process, what data must be presented for each phase of clinical development and the requirements for filing a New Drug Application. Alpha-2-Macroglobulin ("A2M") and Variant CYT - 108, page 30 3.We note your response to prior comment 11 and do not see the revised disclosure regarding preclinical development under this heading. Please revise or otherwise advise. 4.We note your response to prior comment 12 and do not see the revised disclosure regarding the design of your Phase 1 clinical trial for CYT-108 and the primary and secondary endpoints. Please revise or otherwise advise. Material Agreements, page 31 5.We note your response to prior comment 14 and reissue in part. Please revise to disclose the termination provisions for the agreement with Christie Medical Holdings and the aggregate payments received to date pursuant to the agreement with Astaria Global, LLC. Intellectual Property, page 33 6.We note your response to prior comment 15 and reissue in part. Please revise to disclose the expected expiration dates for your pending patent applications. Management's Discussion and Analysis of Financial Condition and Results of Operations Results of Operations, page 43 7.We note your response to comment 16. As previously requested, revise your disclosure to separately quantify and explain the nature of the research and development expenses for each reporting period presented. To the extent you track your research and development costs by product candidate, revise to provide a breakdown of for each period presented. For research and development expenses not tracked by product candidate, provide a breakdown by nature or type of expenses such that the total reconciles to the research and development expense line item. Securities Being Offered Irrevocable Proxy, page 59 8.Please revise your disclosure in this section to clarify, if true, that the investor grant of the irrevocable proxy would (i) preclude investors from voting on mergers, acquisitions or dispositions involving your company for the duration of the proxy and (ii) allow the company to take actions that would disadvantage investors who are subject to the proxy. Please also revise your disclosure regarding the irrevocable proxy to reflect Section 5(a) of the Subscription Agreement which appears to indicate that the proxy will also terminate five years after execution of the Subscription Agreement. Alternatively, please advise. Note 8. Stockholders' Equity, page F-14 We note your response to comment 22 and that your response does not address 9.

February 5, 2025 Page 3 whether you have granted any stock options subsequent to June 30, 2024. Please revise your filing to disclose the extent to which you have granted stock options subsequent to June 30, 2024 and to disclose the number of stock options issued and terms of the stock options issued including the underlying exercise price. Within your response, please also explain to us how you determined the fair value of the common stock underlying these subsequent issuances and the reasons for any differences between the recent valuations of your common stock leading up to the $3 estimated offering price. This information will help facilitate our review of your accounting for equity issuances including stock compensation. Please discuss with the staff how to submit your response. General 10.We are continuing to evaluate your response to prior comment 6 and may have further comment. Please contact Tara Harkins at 202-551-3639 or Kevin Vaughn at 202-551-3494 if you have questions regarding comments on the financial statements and related matters. Please contact Daniel Crawford at 202-551-7767 or Alan Campbell at 202-551-4224 with any other questions. Sincerely, Division of Corporation Finance Office of Life Sciences cc:Andrew Stephenson, Esq.

Show Raw Text
February 5, 2025
Anjun Bose
Chief Executive Officer and President
Cytonics Corporation
658 West Indiantown Road, Suite 214
Jupiter, FL 33458
Re:Cytonics Corporation
Amendment No. 1 to Offering Statement on Form 1-A
Filed January 24, 2025
File No. 024-12533
Dear Anjun Bose:
            We have reviewed your amended offering statement and have the following
comments.
            Please respond to this letter by amending your offering statement and providing the
requested information. If you do not believe a comment applies to your facts and
circumstances or do not believe an amendment is appropriate, please tell us why in your
response.
            After reviewing any amendment to your offering statement and the information you
provide in response to this letter, we may have additional comments. Unless we note
otherwise, any references to prior comments are to comments in our December 16,
2024 letter.
Amendment No. 1 to Offering Statement on Form 1-A
Offering Circular Summary
The Company, page 6
1.We note your response to prior comment 2 and reissue in part. Please revise to briefly
describe the additional steps necessary to commercialize your product candidate rather
than providing a cross-reference.
The Company's Business
Regulatory Regimes, page 29
We note your response to prior comment 10 and reissue in part. Please revise to
provide a more detailed discussion of the FDA's regulatory requirements for 2.

February 5, 2025
Page 2
marketing your products. For example, without limitation, discuss the clinical trial
process, what data must be presented for each phase of clinical development and the
requirements for filing a New Drug Application.
Alpha-2-Macroglobulin ("A2M") and Variant CYT - 108, page 30
3.We note your response to prior comment 11 and do not see the revised disclosure
regarding preclinical development under this heading. Please revise or otherwise
advise.
4.We note your response to prior comment 12 and do not see the revised disclosure
regarding the design of your Phase 1 clinical trial for CYT-108 and the primary and
secondary endpoints. Please revise or otherwise advise.
Material Agreements, page 31
5.We note your response to prior comment 14 and reissue in part. Please revise to
disclose the termination provisions for the agreement with Christie Medical Holdings
and the aggregate payments received to date pursuant to the agreement with Astaria
Global, LLC.
Intellectual Property, page 33
6.We note your response to prior comment 15 and reissue in part. Please revise to
disclose the expected expiration dates for your pending patent applications.
Management's Discussion and Analysis of Financial Condition and Results of Operations
Results of Operations, page 43
7.We note your response to comment 16. As previously requested, revise your
disclosure to separately quantify and explain the nature of the research and
development expenses for each reporting period presented.  To the extent you track
your research and development costs by product candidate, revise to provide a
breakdown of for each period presented. For research and development expenses not
tracked by product candidate, provide a breakdown by nature or type of expenses such
that the total reconciles to the research and development expense line item.
Securities Being Offered
Irrevocable Proxy, page 59
8.Please revise your disclosure in this section to clarify, if true, that the investor grant of
the irrevocable proxy would (i) preclude investors from voting on mergers,
acquisitions or dispositions involving your company for the duration of the proxy and
(ii) allow the company to take actions that would disadvantage investors who are
subject to the proxy. Please also revise your disclosure regarding the irrevocable
proxy to reflect Section 5(a) of the Subscription Agreement which appears to indicate
that the proxy will also terminate five years after execution of the Subscription
Agreement. Alternatively, please advise.
Note 8. Stockholders' Equity, page F-14
We note your response to comment 22 and that your response does not address 9.

February 5, 2025
Page 3
whether you have granted any stock options subsequent to June 30, 2024.  Please
revise your filing to disclose the extent to which you have granted stock options
subsequent to June 30, 2024 and to disclose the number of stock options issued and
terms of the stock options issued including the  underlying exercise price. Within your
response, please also explain to us how you determined the fair value of the common
stock underlying these subsequent issuances and the reasons for any differences
between the recent valuations of your common stock leading up to the $3 estimated
offering price. This information will help facilitate our review of your accounting for
equity issuances including stock compensation. Please discuss with the staff how to
submit your response.
General
10.We are continuing to evaluate your response to prior comment 6 and may have further
comment.
            Please contact Tara Harkins at 202-551-3639 or Kevin Vaughn at 202-551-3494 if
you have questions regarding comments on the financial statements and related
matters. Please contact Daniel Crawford at 202-551-7767 or Alan Campbell at 202-551-4224
with any other questions.
Sincerely,
Division of Corporation Finance
Office of Life Sciences
cc:Andrew Stephenson, Esq.