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.