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                             March 19, 2021

       Christopher Gibson, Ph.D.
       Chief Executive Officer
       Recursion Pharmaceuticals, Inc.
       41 S Rio Grande Street
       Salt Lake City, UT 84101

                                                        Re: Recursion
Pharmaceuticals, Inc.
                                                            Amendment No. 1 to
Draft Registration Statement on Form S-1
                                                            Submitted March 3,
2021
                                                            CIK No. 0001601830

       Dear Dr. Gibson:

             We have reviewed your amended draft registration statement and
have the following
       comments. In some of our comments, we may ask you to provide us with
information so we
       may better understand your disclosure.

              Please respond to this letter by providing the requested
information and either submitting
       an amended draft registration statement or publicly filing your
registration statement on
       EDGAR. If you do not believe our comments apply to your facts and
circumstances or do not
       believe an amendment is appropriate, please tell us why in your
response.

             After reviewing the information you provide in response to these
comments and your
       amended draft registration statement or filed registration statement, we
may have additional
       comments.

       Amendment No. 1 to Draft Registration Statement on Form S-1

       Prospectus Summary
       Overview, page 1

   1.                                                   We note your revisions
in response to prior comment 1 and reissue. Please revise the first
                                                        paragraph in this
section to state that there is no guarantee that you will achieve similar
                                                        development timelines
with your future product candidates. Please revise the statements
                                                        on pages 141 and 216
that your strategy is to "rapidly" advance your Notable Products
                                                        through development and
toward regulatory submission and similar disclosure throughout
                                                        the prospectus to
remove any implication that you will be successful in obtaining
                                                        regulatory approval or
commercializing your product candidates in a rapid or accelerated
                                                        manner as such
statements are speculative. Please balance the disclosure on page 131 that
 Christopher Gibson, Ph.D.
FirstName  LastNameChristopher
Recursion Pharmaceuticals, Inc. Gibson, Ph.D.
Comapany
March      NameRecursion Pharmaceuticals, Inc.
       19, 2021
March2 19, 2021 Page 2
Page
FirstName LastName
         you    identify low-viability programs earlier in the research cycle,
     spend less per
         program    because of your approach, and    advance programs more
quickly from program
         start to the clinic    compared to industry averages to state that the
process of clinical
         development is inherently uncertain and there can be no guarantee that
you will achieve
         similar development timelines with your future product candidates.
The Recursion OS, page 5

2.       We note your response to prior comment 3 and reissue in part. Please
revise your
         Prospectus Summary to indicate the material challenges that your
inferential search
         approach presents to moving drug candidates into clinical trials,
including any challenges
         to obtaining IND approval if the mechanism of action is not
understood, and ensure that
         your Prospectus Summary presents balanced disclosure in this regard.
Influential Search Programs, page 9

3.       We note your response to prior comment 6 regarding the table on page
10 depicting 25
         additional programs. Please provide us with further analysis as to why
these additional
         programs are sufficiently material to investors for inclusion in the
prospectus summary
         and as to how your current disclosure presents balanced disclosure
given that you have not
         specified the disease genes or compounds being studied, and the
currently disclosed
         therapeutic areas may be overly broad, or revise your disclosure as
appropriate.
Class B common stock to be outstanding immediately after this offering, page 14

4.       We note that the second to last bullet point on page 15 only addresses
the shares of Class
         A common stock that are reserved for issuance under you 2021 Plan.
However, your
         disclosure on page 260 currently indicates that Class A and Class B
shares will be
         reserved for issuance under that plan. If Class B shares will be
reserved for issuance
         under the 2021 Plan, please revise your bullet point as appropriate.
Risks Related to Our Class A Common Stock and This Offering
The dual-class structure of our common stock will have the effect of
concentrating voting power,
page 83

5.       If appropriate, please revise this risk factor to disclose that future
issuances of your Class
         B common stock as well as mandatory and optional conversions of your
Class B common
         stock may be dilutive to holders of your Class A common stock. Please
also disclose the
         percentage of outstanding shares that Class B shareholders must
maintain to continue to
         control the outcome of matters submitted to shareholders for approval.
Use of Proceeds, page 97

6.       We note your revisions in response to prior comment 10. Please revise
to disclose how
         many product candidates you expect to be able to move from hit
screening through hit
         identification, hit identification through identification of
development candidates
 Christopher Gibson, Ph.D.
Recursion Pharmaceuticals, Inc.
March 19, 2021
Page 3
      and identification of development candidates through commercialization
using the
      proceeds of this offering. Please remove the reference to
"commercialization" if you do
      not believe that you will be able to fund any product candidates through
      commercialization using the proceeds and specify what stage of clinical
development you
      expect to reach with the proceeds. For example, will you be advancing
your product
      candidates that have completed Phase 1 clinical trials into Phase 2
trials using the
      proceeds of this offering and, if so, will you be able to complete those
Phase 2 trials with
      the proceeds or will you be able to complete human proof of concept
trials for a certain
      number of product candidates?
Business
Bayer, page 239

7.    We note your revisions in response to prior comment 17. Please revise to
clarify whether
      the royalty term is the same as the term of the license agreement.
General

8.    We note your response to prior comment 19. Please revise the statement
that you are
      among the leaders in the space to briefly disclose the basis for the
statement as described
      in your response or revise your leadership statement as appropriate.
       You may contact Eric Atallah at 202-551-3663 or Kevin Vaughn at
202-551-3494 if you
have questions regarding comments on the financial statements and related
matters. Please
contact Ada D. Sarmento at 202-551-3798 or Tim Buchmiller at 202-551-3635 with
any other
questions.



                                                            Sincerely,
FirstName LastNameChristopher Gibson, Ph.D.
                                                            Division of
Corporation Finance
Comapany NameRecursion Pharmaceuticals, Inc.
                                                            Office of Life
Sciences
March 19, 2021 Page 3
cc:       Philip H. Oettinger, Esq.
FirstName LastName