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SEC Comment Letter for Veraxa Biotech AG - Post de-SPAC (VRXA) — Nov 20, 2025

Veraxa Biotech AG - Post de-SPAC
Date: Nov. 20, 2025 · CIK: 0002079109 · Accession: 0000000000-25-010891

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File numbers found in text: 333-289108

Date
November 20, 2025
Author
Tara Harkins
Form
UPLOAD
Company
Veraxa Biotech AG - Post de-SPAC

Letter

November 20, 2025 Christoph Antz Chief Executive Officer Veraxa Biotech Holding AG Talacker 35 8001 Zurich, Switzerland Adeel Rouf Chief Executive Officer Voyager Acquisition Corp./Cayman Islands 131 Concord Street Brooklyn, NY 11201 Re:Veraxa Biotech Holding AG Amendment No. 2 to Registration Statement on Form F-4 September 29, 2025 File No. 333-289108 Dear Christoph Antz and Adeel Rouf: We have reviewed your amended registration statement 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. Amendment 2 to Form F-4 filed on September 29, 2025 Our Dual-Targeting/AND-Gate Concept, page 231 1.We note your response to prior comment 24 and reissue in part. Please revise the graphic appearing on page 231 to remove the arrows implying that your product candidates will be safer and more effective than approved therapies.

November 20, 2025 Page 2 Our Pipeline, page 268 2.Please revise your pipeline table to condense the preclinical phases to no more than two columns. In addition, the progress arrow for VX-A901 indicates that Phase II in underway. However, disclosure elsewhere in the prospectus states that further evaluation in a Phase II study is planned, suggesting that Phase II has not yet commenced. Please revise the table as necessary so that the progress arrows accurately depict the current state of development for each product candidate. Please also revise to clarify if there is an active IND for this trial. 3.We note your response to prior comment 32 and reissue. Please further revise your statement claiming that your DAR 4 anti-HER2 ADC showed "efficacy" comparable to Enhertu, as it improperly implies this candidate will be successful in clinical trials. We would not object to disclosure presenting the objective data observed in the study without making conclusions as to the efficacy of your product candidate. Partnerships And Collaborations, page 277 4.We note in your response that you will file the Hemibody license agreement with Cherry Biolabs GmbH in a subsequent amendment. Please also revise this section to include a description of the Hemibody license agreement and ensure that you disclose the rights and obligations of both parties, any term and termination provisions, aggregate amounts paid or due under these agreements and any amounts paid to date. Company Management's Discussion and Analysis of Financial Condition and Results of Operations Results of Operations Research and Development Expenses, page 305 5.We note your response to comment 36. Please revise your filing to disclose if you track any of your research and development costs by product candidate. To the extent you track any your research and development costs by product candidate, revise to also provide a breakdown of the tracked amounts for each period presented. To the extent you do not track any of your research and development costs by product candidate, disclose that fact and explain why not. To the extent you begin tracking your costs by product candidate in future periods, confirm you will provide a breakdown at that point. 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 Tyler Howes at 202-551-3370 or Chris Edwards at 202-551-6761 with any other questions. Sincerely, Division of Corporation Finance Office of Life Sciences

November 20, 2025 Page 3 cc:Andrew Tucker, Esq. Michael J. Blankenship, Esq.

Show Raw Text
November 20, 2025
Christoph Antz
Chief Executive Officer
Veraxa Biotech Holding AG
Talacker 35
8001 Zurich, Switzerland
Adeel Rouf
Chief Executive Officer
Voyager Acquisition Corp./Cayman Islands
131 Concord Street
Brooklyn, NY 11201
Re:Veraxa Biotech Holding AG
Amendment No. 2 to Registration Statement on Form F-4
September 29, 2025
File No. 333-289108
Dear Christoph Antz and Adeel Rouf:
            We have reviewed your amended registration statement 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.
Amendment 2 to Form F-4 filed on September 29, 2025
Our Dual-Targeting/AND-Gate Concept, page 231
1.We note your response to prior comment 24 and reissue in part. Please revise the
graphic appearing on page 231 to remove the arrows implying that your product
candidates will be safer and more effective than approved therapies.

November 20, 2025
Page 2
Our Pipeline, page 268
2.Please revise your pipeline table to condense the preclinical phases to no more
than two columns. In addition, the progress arrow for VX-A901 indicates that Phase II
in underway. However, disclosure elsewhere in the prospectus states that further
evaluation in a Phase II study is planned, suggesting that Phase II has not yet
commenced. Please revise the table as necessary so that the progress arrows
accurately depict the current state of development for each product candidate. Please
also revise to clarify if there is an active IND for this trial.
3.We note your response to prior comment 32 and reissue. Please further revise your
statement claiming that your DAR 4 anti-HER2 ADC showed "efficacy" comparable
to Enhertu, as it improperly implies this candidate will be successful in clinical trials.
We would not object to disclosure presenting the objective data observed in the study
without making conclusions as to the efficacy of your product candidate.
Partnerships And Collaborations, page 277
4.We note in your response that you will file the Hemibody license agreement with
Cherry Biolabs GmbH in a subsequent amendment. Please also revise this section to
include a description of the Hemibody license agreement and ensure that you disclose
the rights and obligations of both parties, any term and termination provisions,
aggregate amounts paid or due under these agreements and any amounts paid to date.
Company Management's Discussion and Analysis of Financial Condition and Results of
Operations
Results of Operations
Research and Development Expenses, page 305
5.We note your response to comment 36.  Please revise your filing to disclose if you
track any of your research and development costs by product candidate. To the extent
you track any your research and development costs by product candidate, revise to
also provide a breakdown of the tracked amounts for each period presented. To the
extent you do not track any of your research and development costs by product
candidate, disclose that fact and explain why not. To the extent you begin tracking
your costs by product candidate in future periods, confirm you will provide a
breakdown at that point.
            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 Tyler Howes at 202-551-3370 or Chris Edwards at 202-551-6761
with any other questions.
Sincerely,
Division of Corporation Finance
Office of Life Sciences

November 20, 2025
Page 3
cc:Andrew Tucker, Esq.
Michael J. Blankenship, Esq.