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SEC Comment Letter 0000000000-24-013409 to Liminatus Pharma, Inc. (LIMN)

Liminatus Pharma, Inc.
Date: Dec. 5, 2024 · CIK: 0001971387 · Accession: 0000000000-24-013409

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File numbers found in text: 333-275409

Date
December 5, 2024
Author
Not clearly detected
Form
UPLOAD
Company
Liminatus Pharma, Inc.

Letter

December 5, 2024 Chris Kim Chief Executive Officer and Director Iris Parent Holding Corp. 6 Centerpointe Drive #625 La Palma, California 90623 Re:Iris Parent Holding Corp. Post-Effective Amendment No. 1 to Registration Statement on Form S-4 Filed November 8, 2024 File No. 333-275409 Dear Chris Kim: We have reviewed your post-effective amendment and have the following comments. Please respond to this letter by amending your registration 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 registration statement and the information you provide in response to this letter, we may have additional comments. Post-Effective Amendment No. 1 to Registration Statement on Form S-4 Cover Page 1.We note your revised disclosure that, after the completion of the Business Combination, Chris Kim will be deemed to beneficially own approximately 32.7% of the outstanding voting power of ParentCo Common Stock, assuming no redemptions (or 33.0% assuming maximum redemptions), and that ParentCo will be a "controlled company" within the meaning of the Nasdaq rules and could elect to take advantage of certain "controlled company" exemptions. Given the revised disclosure regarding the beneficial ownership percentages, please tell us why you continue to disclose that ParentCo will be a "controlled company" after the completion of the Business Combination and could elect to take advantage of certain "controlled company" exemptions, or revise your disclosure as appropriate.

December 5, 2024 Page 2 Questions and Answers About the Proposals for Stockholders, page viii 2.Please consider expanding this section to include a Q&A that explains why this business combination is still in the best interest of the stockholders in light of the TDT License Termination. Why am I receiving this proxy statement/prospectus?, page viii 3.We note your disclosure that ParentCo will apply to list, to be effective at the time of the Business Combination, its common stock and warrants on Nasdaq. In an appropriate location, please address where you stand with respect to meeting the quantitative listing standards for Nasdaq, and, if you currently do not meet such standards, what actions you intend to take to be eligible for listing. Summary of the Proxy Statement/Prospectus, page 1 4.We note your disclosure under the heading "Liminatus Pharma, LLC," and in the first risk factor on page 25, that you refer to Liminatus as a "clinical-stage" company. Please revise so that these statements are consistent with your other disclosure that Liminatus is a pre-clinical company. 5.We note your initial disclosure of the termination of the TDT license agreement included in the Explanatory Note. Please expand your disclosure of the license agreement termination here to include additional information/explanation on why the parties decided to terminate this license agreement, given its significance to the business plan of Liminatus. 6.Please remove suggestions that your product candidate, IBA-101, has a promising "safety profile," both here and throughout your prospectus. Determinations of safety and efficacy are in the sole jurisdiction of the FDA and given the pre-clinical stage of your current product candidate, these statements appear to be pre-mature. Also, where you continue to discuss your toxicity-related experiments, such as on page 185, please revise to indicate whether these results were statistically meaningful. 7.Please revise your statement here and throughout the prospectus that Liminatus' anti- CD47 antibody, IBA-101, potentially positions the company as a "frontrunner" in the CD47 space. Given the current stage of development of this product candidate such statements appear to be pre-mature. Termination, page 4 8.We note that Section 4.1(b) of the Business Combination Agreement has been amended so that it is now a condition to closing that Iris Acquisition Corporation shall have received "an acknowledgement from Viral Gene stating that the obligations of the parties thereto, including ParentCo and the Company, under, or pursuant to, the Viral Gene Assignment have been satisfied or terminated and that no obligations of any party thereto, including ParentCo and the Company, under the Viral Gene Assignment remain outstanding." Please update your disclosure for this new condition to closing, indicate whether the acknowledgment has been received, and, if not, whether this condition to closing is waivable. If this condition is waivable, please include appropriate risk factor disclosure.

December 5, 2024 Page 3 Lock-Up Agreement, page 6 9.We note your disclosure that on August 9, 2024, ParentCo and Sponsor agreed to grant a waiver of the lock-up restrictions contained in the Lock-Up Agreement with respect to an aggregate of 3.64 million ParentCo Shares. Please revise your disclosure so that it is clear how to reconcile this number of shares to the provisions of the Waiver and Consent filed as Exhibit 10.8, which indicates that the waiver applies to 5.1 million shares, or revise your disclosure as appropriate. Also indicate the business purpose for such waiver and whether there was any consideration paid to ParentCo or the Sponsor in connection with the waiver. The Iris Board's Reasons for Approving the Business Combination, page 10 10.We note the Iris Board's determinations and unanimous approvals in your disclosure in the first sentence of the first paragraph of this section and your disclosure, that on September 18, 2024, the Iris Board determined that notwithstanding the TDT License Termination, the Business Combination was advisable to and in the best interests of Iris and its stockholders. Similar to your disclosure in the first sentence, please also clarify if the Iris Board unanimously approved the Business Combination Agreement, as amended to date, and the transactions contemplated thereby, and recommended that Iris's stockholders approve the Business Combination Agreement, as amended to date, and the transactions contemplated thereby. Potential to Grow Globally, page 11 11.We note your reference in this section, and in other locations, to Liminatus' "strong intellectual property protection." Please balance these statements with your disclosure elsewhere that the anti-CD47 antibody is covered by three early-stage applications. Background of the Business Combination Target F (Liminatus), page 109 12.Please revise to provide more detailed disclosure of how the enterprise value associated with Liminatus was negotiated and changed from $250,000,000 to $175,000,000 following the TDT License Termination. Please ensure your disclosure addresses how Iris Acquisition Corp negotiated the revised merger consideration in light of the loss of Liminatus' clinical stage product candidate and that Liminatus is now a single-asset, pre-clinical company, and how the board determined the revised merger consideration was appropriate given those changes and determined that the transactions contemplated by the Business Combination Agreement were advisable and in the best interests of Iris and its stockholders. Business of Liminatus Pre-Clinical Development to Date, page 184 13.We note your pre-clinical development to date of the CD47 therapeutic candidate appears to have studied Hu3A5 in murine colon adenocarcinoma and that the anticipated clinical trials will focus on patients with lung cancer. Please disclose whether you will conduct additional pre-clinical studies that focus on lung cancer cells prior to the anticipated clinical trials.

December 5, 2024 Page 4 CD47, page 190 14.We note your disclosure that Magrolimab, a CD47-targeting drug candidate, is in Phase 3 clinical trials and that this drug is expected to be the first CD47-targeted treatment to gain approval. If the study of this drug has been wound down by the developer, please update your disclosure as appropriate. We remind you that the company and its management are responsible for the accuracy and adequacy of their disclosures, notwithstanding any review, comments, action or absence of action by the staff. Please contact Sasha Parikh at 202-551-3627 or Kevin Kuhar at 202-551-3662 if you have questions regarding comments on the financial statements and related matters. Please contact Tamika Sheppard at 202-551-8346 or Tim Buchmiller at 202-551-3635 with any other questions. Sincerely, Division of Corporation Finance Office of Life Sciences cc:Chauncey M. Lane, Esq.

Show Raw Text
December 5, 2024
Chris Kim
Chief Executive Officer and Director
Iris Parent Holding Corp.
6 Centerpointe Drive #625
La Palma, California 90623
Re:Iris Parent Holding Corp.
Post-Effective Amendment No. 1 to Registration Statement on Form S-4
Filed November 8, 2024
File No. 333-275409
Dear Chris Kim:
            We have reviewed your post-effective amendment and have the following comments.
            Please respond to this letter by amending your registration 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 registration statement and the information
you provide in response to this letter, we may have additional comments.
Post-Effective Amendment No. 1 to Registration Statement on Form S-4
Cover Page
1.We note your revised disclosure that, after the completion of the Business
Combination, Chris Kim will be deemed to beneficially own approximately 32.7% of
the outstanding voting power of ParentCo Common Stock, assuming no redemptions
(or 33.0% assuming maximum redemptions), and that ParentCo will be a "controlled
company" within the meaning of the Nasdaq rules and could elect to take advantage
of certain "controlled company" exemptions. Given the revised disclosure regarding
the beneficial ownership percentages, please tell us why you continue to disclose that
ParentCo will be a "controlled company" after the completion of the Business
Combination and could elect to take advantage of certain "controlled company"
exemptions, or revise your disclosure as appropriate.

December 5, 2024
Page 2
Questions and Answers About the Proposals for Stockholders, page viii
2.Please consider expanding this section to include a Q&A that explains why this
business combination is still in the best interest of the stockholders in light of the TDT
License Termination.
Why am I receiving this proxy statement/prospectus?, page viii
3.We note your disclosure that ParentCo will apply to list, to be effective at the time of
the Business Combination, its common stock and warrants on Nasdaq. In an
appropriate location, please address where you stand with respect to meeting the
quantitative listing standards for Nasdaq, and, if you currently do not meet such
standards, what actions you intend to take to be eligible for listing.
Summary of the Proxy Statement/Prospectus, page 1
4.We note your disclosure under the heading "Liminatus Pharma, LLC," and in the first
risk factor on page 25, that you refer to Liminatus as a "clinical-stage" company.
Please revise so that these statements are consistent with your other disclosure that
Liminatus is a pre-clinical company.
5.We note your initial disclosure of the termination of the TDT license agreement
included in the Explanatory Note. Please expand your disclosure of the license
agreement termination here to include additional information/explanation on why the
parties decided to terminate this license agreement, given its significance to the
business plan of Liminatus.
6.Please remove suggestions that your product candidate, IBA-101, has a promising
"safety profile," both here and throughout your prospectus. Determinations of safety
and efficacy are in the sole jurisdiction of the FDA and given the pre-clinical stage of
your current product candidate, these statements appear to be pre-mature. Also, where
you continue to discuss your toxicity-related experiments, such as on page 185, please
revise to indicate whether these results were statistically meaningful.
7.Please revise your statement here and throughout the prospectus that Liminatus' anti-
CD47 antibody, IBA-101, potentially positions the company as a "frontrunner" in the
CD47 space. Given the current stage of development of this product candidate such
statements appear to be pre-mature.
Termination, page 4
8.We note that Section 4.1(b) of the Business Combination Agreement has been
amended so that it is now a condition to closing that Iris Acquisition Corporation shall
have received "an acknowledgement from Viral Gene stating that the obligations of
the parties thereto, including ParentCo and the Company, under, or pursuant to, the
Viral Gene Assignment have been satisfied or terminated and that no obligations of
any party thereto, including ParentCo and the Company, under the Viral Gene
Assignment remain outstanding." Please update your disclosure for this new condition
to closing, indicate whether the acknowledgment has been received, and, if not,
whether this condition to closing is waivable. If this condition is waivable, please
include appropriate risk factor disclosure.

December 5, 2024
Page 3
Lock-Up Agreement, page 6
9.We note your disclosure that on August 9, 2024, ParentCo and Sponsor agreed to
grant a waiver of the lock-up restrictions contained in the Lock-Up Agreement with
respect to an aggregate of 3.64 million ParentCo Shares. Please revise your disclosure
so that it is clear how to reconcile this number of shares to the provisions of the
Waiver and Consent filed as Exhibit 10.8, which indicates that the waiver applies to
5.1 million shares, or revise your disclosure as appropriate. Also indicate the business
purpose for such waiver and whether there was any consideration paid to ParentCo or
the Sponsor in connection with the waiver.
The Iris Board's Reasons for Approving the Business Combination, page 10
10.We note the Iris Board's determinations and unanimous approvals in your disclosure
in the first sentence of the first paragraph of this section and your disclosure, that on
September 18, 2024, the Iris Board determined that notwithstanding the TDT License
Termination, the Business Combination was advisable to and in the best interests of
Iris and its stockholders. Similar to your disclosure in the first sentence, please also
clarify if the Iris Board unanimously approved the Business Combination Agreement,
as amended to date, and the transactions contemplated thereby, and recommended that
Iris's stockholders approve the Business Combination Agreement, as amended to date,
and the transactions contemplated thereby.
Potential to Grow Globally, page 11
11.We note your reference in this section, and in other locations, to Liminatus' "strong
intellectual property protection." Please balance these statements with your disclosure
elsewhere that the anti-CD47 antibody is covered by three early-stage applications.
Background of the Business Combination
Target F (Liminatus), page 109
12.Please revise to provide more detailed disclosure of how the enterprise value
associated with Liminatus was negotiated and changed from $250,000,000 to
$175,000,000 following the TDT License Termination. Please ensure your disclosure
addresses how Iris Acquisition Corp negotiated the revised merger consideration in
light of the loss of Liminatus' clinical stage product candidate and that Liminatus is
now a single-asset, pre-clinical company, and how the board determined the revised
merger consideration was appropriate given those changes and determined that the
transactions contemplated by the Business Combination Agreement were advisable
and in the best interests of Iris and its stockholders.
Business of Liminatus
Pre-Clinical Development to Date, page 184
13.We note your pre-clinical development to date of the CD47 therapeutic candidate
appears to have studied Hu3A5 in murine colon adenocarcinoma and that the
anticipated clinical trials will focus on patients with lung cancer. Please disclose
whether you will conduct additional pre-clinical studies that focus on lung cancer cells
prior to the anticipated clinical trials.

December 5, 2024
Page 4
CD47, page 190
14.We note your disclosure that Magrolimab, a CD47-targeting drug candidate, is in
Phase 3 clinical trials and that this drug is expected to be the first CD47-targeted
treatment to gain approval. If the study of this drug has been wound down by the
developer, please update your disclosure as appropriate.
            We remind you that the company and its management are responsible for the accuracy
and adequacy of their disclosures, notwithstanding any review, comments, action or absence
of action by the staff.
            Please contact Sasha Parikh at 202-551-3627 or Kevin Kuhar at 202-551-3662 if you
have questions regarding comments on the financial statements and related matters. Please
contact Tamika Sheppard at 202-551-8346 or Tim Buchmiller at 202-551-3635 with any
other questions.
Sincerely,
Division of Corporation Finance
Office of Life Sciences
cc:Chauncey M. Lane, Esq.