United States securities and exchange commission logo





                                July 7, 2020

       Joseph Moscato
       Chief Executive Officer
       NuGenerex Immuno-Oncology, Inc.
       10102 USA Today Way
       Miramar, FL 33025

                                                        Re: NuGenerex
Immuno-Oncology, Inc.
                                                            Amendment No. 1 to
Registration Statement on Form 10-12G
                                                            Filed June 12, 2020
                                                            File No. 000-56153

       Dear Mr. Moscato:

              We have reviewed your filing 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 these comments within ten business days by
providing the requested
       information or advise us as soon as possible when you will respond. If
you do not believe our
       comments apply to your facts and circumstances, please tell us why in
your response.

            After reviewing your response and any amendment you may file in
response to these
       comments, we may have additional comments.

       Amendment No. 1 to Registration Statement on Form 10-12G

       Introductory Comment, page 3

   1.                                                   Please revise to
clarify that the registration statement is effective and clarify your
                                                        reporting status.
       Item 1. Business
       AE37     Ii-Key/HER2/neu Hybrid Immunotherapeutic Vaccine, page 4

   2.                                                   We note your disclosure
in this section that you are currently developing AE37 for the
                                                        treatment of cancer,
including breast, bladder, prostate, and potentially other
                                                        indications yet you
state on page 13 that your Phase II clinical study using AE37 in
                                                        combination with
Keytruda for treatment of metastatic triple negative breast cancer is
                                                        your only ongoing
research and development project. Please revise or advise. In that
                                                        regard, we note your
response to our prior comment 4 that you are waiting to see
 Joseph Moscato
FirstName
NuGenerexLastNameJoseph   Moscato
             Immuno-Oncology, Inc.
Comapany
July 7, 2020NameNuGenerex Immuno-Oncology, Inc.
July 7,2 2020 Page 2
Page
FirstName LastName
         whether Shenzhen is successful in achieving positive results in the
prostate cancer
         development program before determining how to proceed. Accordingly,
please revise to
         disclose, if true, that you are not in the process of developing AE37
for prostate cancer as
         stated on page 4.
3.       We note your response to our prior comments 2 and 3. Please revise to
disclose the term
         and the termination provisions for each of the Merck, NSABP and
Shenzhen agreements.
         Please also indicate whether the royalty term under the Shenzhen
agreement is the same as
         the term of the agreement.
4.       We note your response to our prior comment 8, but we do not see any
disclosure
         concerning the failure to achieve the primary endpoint which prevented
moving to a Phase
         III trial of AE37 in breast cancer. Please revise or advise.
5.       We note your disclosure that the primary and secondary endpoints were
met in the 2006
         and 2007 trials for AE37. Please provide the data from the trials that
support these
         statements and disclose how many subjects were in the 2006 trial.
6.       We note your response to our prior comment 5 and reissue in part.
Please revise to clarify
         the next steps for each of your product candidates, including how much
funding you will
         need, what steps remain to achieve regulatory approval and the planned
timeline.
7.       Please revise the disclosure on page 5 to explain your basis for the
statement that "funding
         for the development of a vaccine of SARS-CoV-2 virus is in advanced
discussions and
         currently expected that the development costs will be borne by the
U.S. and foreign
         government agencies."
Clinical Development Plans for Ii-Key Immunotherapeutic Peptides, page 6

8.       We note your response to our prior comment 9. Please revise to provide
the detail from
         your response that the discussions with the major oncology research
centers are currently
         confidential, and the clinical trials are in the planning stages.
Competition, page 7

9.       We note your response to our prior comment 11. Please revise to
disclose, if true, that
         NGIO has never received regulatory approval for a product candidate or
had commercial
         sales.
Note 2- Summary of Significant Accounting Policies
Research and Development Costs, page F-8

10.      We note from your response and revised disclosures to comment 21 that
you completed a
         Phase IIb trial of AE37 in combination with GM-CSF in November of
2019. Please
         address the following:

                Clarify in the filing if the trial which was completed, as
discussed on page 4, is the
 Joseph Moscato
NuGenerex Immuno-Oncology, Inc.
July 7, 2020
Page 3
              same trial in which costs were incurred for AE37 in combination
with Keytruda as
              disclosed on page 13 in which you incurred $251,459 of costs. If
not, please tell us
              where the costs for AE37 in combination with GM-CSF were recorded
in your
              financial statements and revise your MD&A as necessary to discuss
the costs
              incurred.

                You state on page 5 that "based on the results from the Phase
II trial described above,
              NGIO entered into a Clinical Trial Collaboration and Supply
Agreement" on June 28,
              2017 with Merck. Since the Phase IIb trial was not completed
until November of
              2019. Please clarify in the filing what results you are referring
to which resulted in
              the collaboration agreement with Merck in 2017.
11.      We acknowledge your response and revised disclosures to comment 20. We
believe the
         significant terms of each material agreement are required to be
presented in the filing such
         as the rights and obligations of each party, including any significant
milestone payments
         paid/received to date and aggregate potential milestones and the
triggering factors thereof,
         the royalty percentages or a range, profit sharing, and termination
clauses. For instance, it
         does not appear sufficient to omit disclosure of the termination
provision in the agreement
         with Merck because you do not believe an accrual for a liability is
warranted. Please
         revise your disclosure accordingly.
Note 3 - Commitments and Contingencies
Payable to Foundation, page F-10

12.      We note from your response and revised disclosures to comment 22 that
effective August
         1, 2015, you capitalized all outstanding unpaid interest on the
outstanding balance. Please
         explain to us your basis for capitalizing the unpaid interest on this
payable.
Exhibits
FirstName LastNameJoseph Moscato
Comapany
13.         NameNuGenerex
        Please file an executedImmuno-Oncology,    Inc.In this regard, we note
that it is unclear
                                copy of Exhibit 10.3.
July 7, whether
        2020 Pagethe3counterparty signed the agreement.
FirstName LastName
 Joseph Moscato
FirstName
NuGenerexLastNameJoseph   Moscato
             Immuno-Oncology, Inc.
Comapany
July 7, 2020NameNuGenerex Immuno-Oncology, Inc.
July 7,4 2020 Page 4
Page
FirstName LastName
        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.

        You may contact Eric Atallah at 202-551-3663 or Mary Mast at
202-551-3613 if you
have questions regarding comments on the financial statements and related
matters. Please
contact Ada D. Sarmento at 202-551-3798 or Joe McCann at 202-551-6262 with any
other
questions.




                                                          Sincerely,

                                                          Division of
Corporation Finance
                                                          Office of Life
Sciences
cc:      Jeffrey Wofford, Esq.