<SEC-DOCUMENT>0000000000-20-005999.txt : 20210111
<SEC-HEADER>0000000000-20-005999.hdr.sgml : 20210111
<ACCEPTANCE-DATETIME>20200706140018
<PRIVATE-TO-PUBLIC>
ACCESSION NUMBER:		0000000000-20-005999
CONFORMED SUBMISSION TYPE:	UPLOAD
PUBLIC DOCUMENT COUNT:		2
FILED AS OF DATE:		20200706

FILED FOR:		

	COMPANY DATA:	
		COMPANY CONFORMED NAME:			Nanobiotix S.A.
		CENTRAL INDEX KEY:			0001760854
		STANDARD INDUSTRIAL CLASSIFICATION:	PHARMACEUTICAL PREPARATIONS [2834]
		IRS NUMBER:				000000000
		STATE OF INCORPORATION:			I0
		FISCAL YEAR END:			1231

	FILING VALUES:
		FORM TYPE:		UPLOAD

	BUSINESS ADDRESS:	
		STREET 1:		60 RUE DE WATTIGNIES
		CITY:			PARIS
		STATE:			I0
		ZIP:			75012
		BUSINESS PHONE:		33140260470

	MAIL ADDRESS:	
		STREET 1:		60 RUE DE WATTIGNIES
		CITY:			PARIS
		STATE:			I0
		ZIP:			75012
</SEC-HEADER>
<DOCUMENT>
<TYPE>LETTER
<SEQUENCE>1
<FILENAME>filename1.pdf
<TEXT>
<PDF>
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<TEXT>
United States securities and exchange commission logo





                             July 2, 2020

       Philippe Mauberna
       Chief Financial Officer
       Nanobiotix S.A.
       60, rue de Wattignies
       75012 Paris, France

                                                        Re: Nanobiotix S.A.
                                                            Draft Registration
Statement on Form F-1/A
                                                            Filed June 5, 2020
                                                            CIK No. 0001760854

       Dear Mr. Mauberna:

             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.

       Draft Registration Statement on Form F-1/A, filed on June 5, 2020

       Summary
       NBTXR3 Development Pipeline, page 4

   1.                                                   We note your response
to prior comment 1 that there are no immediate plans to pursue
                                                        application for market
approval for NBTRX3 in soft tissue sarcoma in Asia. Please clarify
                                                        this fact in your
pipeline table here and in the Business section. Please also clarify your
                                                        disclosure regarding
whether Hensify has been commercialized or if commercialization is
                                                        pending.
   2.                                                   Please ensure that your
pipeline table accurately reflects the stages of your trials. For
                                                        example, you state on
page 3 that you "intend to initiate" the Phase III Study 312 once the
 Philippe Mauberna
FirstName
NanobiotixLastNamePhilippe  Mauberna
             S.A.
Comapany
July 2, 2020NameNanobiotix S.A.
July 2,2 2020 Page 2
Page
FirstName LastName
         FDA determines that your trial may proceed, and accordingly, please
revise the line in
         your pipeline table for Study 312 here and in the Business section so
that it extends no
         further than Phase II. Similarly, revise the lines in the table here
and in the Business
         section for lung cancer and esophageal cancer to the beginning of the
IND phase as you
         state on page 6 that MD Anderson is preparing to submit IND
applications to the FDA for
         these trials, and revise the line for the pancreatic trial to reflect
that the Phase I trial has
         not yet begun. Additionally, we note your statement that the FDA has
accepted available
         data from your Study 102 Escalation for its evaluation of Study 312,
but please explain
         whether you expect to need to provide any additional data before
proceeding to Phase III,
         including any data from your ongoing Phase 1 Study 102 Expansion
trial, which you state
         will produce final data in mid-2021.
Our Competitive Strengths, page 5

3.       We refer to your revised disclosure that none of the patents covering
your NBTXR3
         technology is expected to expire until at least 2036. However, the
table on page 107
         relating to your owned patents appears to indicate earlier expiration
dates for your
         NanoXray technology. Please revise your disclosure to address this
discrepancy, and also
         revise your intellectual property disclosure in the Business section
to clarify which patents
         are relevant to the NBTXR3 technology, the type of patent protection
provided by the
         various patents (e.g., composition of matter), and their applicable
expiration dates.
Business
Our Clinical Programs
Locally Advanced Head and Neck Cancers, page 90

4.       We refer to the newly included table on page 91 referencing published
results from other
         head and neck trials and your statement on page 92 comparing
preliminary data to these
         results. Please revise your disclosures to remove this comparison as
your results are
         preliminary, your comparisons are not based on a head-to-head study,
and you
         acknowledge on page 96 that the data "cannot be compared."
Dose Escalation Results, page 93

5.       Please revise the second chart on page 94 so that all information is
legible.
6.       We refer to your revised disclosure on page 96 regarding serious
adverse events, and your
         examples of certain of these events. Please revise to identify the
other serious adverse
         events. In addition, to the extent there are any, please also identify
any serious adverse
         events for the other trials you describe elsewhere, such as the trials
for liver cancer and
         prostate cancer.
Liver Cancers
Phase I/II Trial Design (   Study 103   ), page 97

7.       We refer to your revised disclosure on page 97 that your preliminary
results showed a
 Philippe Mauberna
FirstName
NanobiotixLastNamePhilippe  Mauberna
             S.A.
Comapany
July 2, 2020NameNanobiotix S.A.
July 2,3 2020 Page 3
Page
FirstName LastName
         "favorable safety and tolerability profile," and that there were
"positive signs of
         efficacy." As we have previously noted, safety and efficacy
determinations are within the
         authority of the FDA or comparable regulatory authorities, and such
statements are not
         appropriate. Please remove all such statements in your registration
statement.
Significant Collaborations and Research Agreements
NBTXR3 Clinical Collaboration with MD Anderson, page 104

8.       We note your revised disclosure in response to prior comment 6. Please
further revise to
         disclose the aggregate amount of milestone payments that may be
payable.
Other Collaborations, page 105

9.       In your revised disclosure, you refer to partnerships with various
research institutions to
         conduct preclinical research that contributed to the rationale for the
I-O program you are
         developing. Please disclose the ownership and rights to the research
conducted in
         collaboration with these partners.
Intellectual Property, page 106

10.      You state that there are material patents and patent applications in
co-ownership. Please
         revise to disclose the co-owner(s) and any material terms of such
co-ownership.
Note 4. Significant Transactions
4.2 Financing Agreement with the European Investment Bank, page F-15

11.      You disclose that you agreed to pay EIB an additional fee based on the
consolidated
            forecasted    sales generated by the company. Please clarify
whether the contractual
         royalties are based on actual sales or forecasted sales.
Note 12. Financial Liabilities, page F-31

12.      Please disclose how the company accounts for subsequent changes in the
estimated
         amount of royalties owed on the EIB loan. Refer to IFRS 7.21. Tell us
whether you apply
         paragraph B5.4.6 of IFRS 9.
Note 14. Financial Instruments Included in the Statement of Financial Position
and Impact on
Income
Fair Value, page F-38

13.      Consistent with IFRS 13.97, please disclose how you determined the
fair value of your
         non-current financial liabilities as shown on page F-36.
Exhibits

14.      On page 130, you refer to employment agreements with Mr. Philippe
Mauberna
         and Ms. Anne-Juliette Hermant. Please file such agreements as exhibits
to your
 Philippe Mauberna
Nanobiotix S.A.
July 2, 2020
Page 4
      registration statement. Additionally, we note you filed summaries of
various equity plans
      with your latest amendment. Please revise to file the plans or explain
why it is not
      necessary. See Item 601(b)(10) of Regulation S-K and Item 8.a of Form
F-1.
       You may contact David Burton at 202-551-3626 or Kate Tillan at
202-551-3604 if you
have questions regarding comments on the financial statements and related
matters. Please
contact Paul Fischer at 202-551-3415 or Dorrie Yale at 202-551-8776 with any
other questions.



                                                           Sincerely,
FirstName LastNamePhilippe Mauberna
                                                           Division of
Corporation Finance
Comapany NameNanobiotix S.A.
                                                           Office of Life
Sciences
July 2, 2020 Page 4
cc:       Peter Devlin, Esq.
FirstName LastName
</TEXT>
</DOCUMENT>
</SEC-DOCUMENT>
