SEC Company Response from Sorrento Therapeutics, Inc. (SRNE) (CIK 0000850261) — Aug 15, 2022
Sorrento Therapeutics, Inc. (SRNE) (CIK 0000850261)
Date: Aug. 15, 2022 · CIK: 0000850261 · Accession: 0001104659-22-091442
AI Filing Summary & Sentiment
File numbers found in text: 001-36150
Referenced dates: July 25, 2022
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Sorrento Therapeutics,
Inc.
4955 Directors Place
San Diego, California 92121
August 15, 2022
VIA EDGAR
U.S. Securities and Exchange Commission
Division of Corporation Finance
100 F Street, N.E.
Mail Stop 3561
Washington, DC 20549
Attention: Sasha Parikh
Daniel Gordon
Re: Sorrento Therapeutics, Inc.
Form 10-K for Fiscal Year Ended December 31, 2021
Filed March 11, 2022
Form 10-Q for Fiscal Quarter Ended March 31, 2022
Filed May 5, 2022
File No. 001-36150
Ladies and Gentlemen:
This letter responds
to the comments of the Staff (the “Staff”) of the Securities and Exchange Commission (the “Commission”)
to Henry Ji, Chairman of the Board, CEO and President of Sorrento Therapeutics, Inc., a Delaware corporation (the “Company”),
in the comment letter dated July 25, 2022 (the “Comment Letter”) relating to the Company’s Annual Report
on Form 10-K (File No. 001-36150) for the fiscal year ended December 31, 2021 filed with the Commission on March 11, 2022 and the Company’s
Quarterly Report on Form 10-Q (File No. 001-36150) for the fiscal quarter ended March 31, 2022 filed with the Commission on May 5, 2022.
Set forth below
are the Staff’s comments (in bold italics) and the Company’s responses for each comment, organized as set forth in the Comment
Letter.
Form 10-K for Fiscal Year Ended December
31, 2021
Item 7. Management's Discussion and
Analysis of Financial Condition and Results of Operations
Results of Operations
Comparison of the Years Ended December
31, 2021 and 2020, page 77
1. Please
quantify each of the factors you noted for the selling, general and administrative expenses
line item that explains the increase and/or decrease from the current period to the respective
prior period, as applicable. For example, you disclosed that selling, general and administrative
expenses for your Sorrento Therapeutics segment increased as compared to the prior fiscal
year and were primarily attributed to higher headcount, professional fees and stock-based
compensation expense as compared to the same period of the prior year.
Please
quantify each of the factors noted.
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U.S. Securities and Exchange Commission
August 15, 2022
Page 2
Sorrento’s response:
The Company respectfully
acknowledges the Staff’s comment, advises the Staff that the Company will enhance its disclosure in future filings to quantify
the noted factors and notes that it has included the following disclosures in the Management’s Discussion and Analysis section
of the Company’s Form 10-Q for the quarter ended June 30, 2022 filed with the SEC on August 15, 2022 (the “Q2 2022
Form 10-Q”).
Selling, General and Administrative
(“SG&A”) Expenses
The decrease in
SG&A expenses in our Sorrento segment during the three months ended June 30, 2022 was attributed to lower professional fees, including
a decrease in legal and consulting costs by approximately $6.4 million, and lower stock-based compensation expenses of $2.9 million.
Personnel costs and infrastructure-related expenses increased by $2.1 million and $1.6 million, respectively, compared to the same period
of the prior year.
The decrease in
SG&A expenses in our Sorrento segment during the six months ended June 30, 2022 was attributed to lower professional fees, including
a decrease in legal and consulting costs, by approximately $4.8 million, and lower stock-based compensation expenses of $5.7 million.
Personnel costs and infrastructure-related expenses increased by $6.9 million and $1.1 million, respectively, compared to the same period
of the prior year.
For the three and
six months ended June 30, 2022, the increases in SG&A expenses in our Scilex segment were attributed to increases in personnel costs
and professional fees compared to the same periods of the prior year.
2. You
disclosed that research and development expenses for your Sorrento Therapeutics segment increased
by $96.3 million as compared to the prior fiscal year and were primarily driven by higher
headcount and increased clinical development costs spent on advancing your various research
and development programs. As research and development expenses constitute your most significant
expense in the periods presented, please provide us proposed disclosure to be provided in
future filings the costs incurred during each period presented for each of your key research
and development projects. If you do not track your research and development costs by project,
please disclose that fact and explain why you do not maintain and evaluate research and development
costs by project. Provide other quantitative or qualitative disclosure that provides more
transparency as to the type of research and development expenses incurred (i.e. by nature
or type of expense) which should reconcile to total research and development expense on the
Statements of Operations.
Sorrento’s
response:
The Company respectfully
acknowledges the Staff’s comment, advises the Staff that the Company will enhance the disclosure in its future filings to discuss
in more detail the research and development expenses for each period presented and notes that it has included the following disclosures
in the Management’s Discussion and Analysis section of the Q2 2022 Form 10-Q:
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U.S. Securities and Exchange Commission
August 15, 2022
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Results of Operations
Comparison of the three and six months
ended June 30, 2022 and 2021
Research and
Development (“R&D”) Expenses.
Three Months Ended June 30,
Increase (decrease)
Dollars in thousands
2022
2021
$
%
Sorrento segment
$ 45,876
$ 52,088
$ (6,212 )
(12 %)
Scilex segment
2,591
2,418
173
7 %
Total research and development expenses
$ 48,467
$ 54,506
$ (6,039 )
(11 %)
Six Months Ended June 30,
Increase (decrease)
Dollars in thousands
2022
2021
$
%
Sorrento segment
$ 106,971
$ 93,203
$ 13,768
15 %
Scilex segment
5,222
5,136
86
2 %
Total research and development expenses
$ 112,193
$ 98,339
$ 13,854
14 %
R&D expenses
include expenses associated with isolating and advancing human antibody drug candidates derived from our libraries, as well as advancing
our COVID-19, SP-102, SP-103, RTX, oncolytic virus, ADC and oncology programs. Such expenses consist primarily of salaries and personnel-related
expenses, stock-based compensation expense, clinical development expenses, preclinical testing, lab supplies, consulting costs, depreciation
and other expenses. We track external development costs by program; however, we do not allocate laboratory supplies, R&D materials,
personnel costs, share-based payments, facilities costs or other internal costs to specific development programs.
The following table
summarizes our research and development expenses for the three months ended June 30, 2022 and 2021:
Three months ended June 30,
Increase (decrease)
Type of expense
2022
2021
$
%
Third party clinical and pre-clinical R&D expenses by program
Abivertinib
$ 2,169
$ 432
$ 1,737
402 %
Resiniferatoxin (“RTX”)
612
2,006
(1,394 )
-69 %
COVID-19 therapies and diagnostics, excluding Abivertinib
4,715
10,170
(5,455 )
-54 %
Immuno-oncology and other programs
5,183
6,944
(1,761 )
-25 %
Total third party clinical and pre-clinical R&D expenses by program
12,679
19,552
(6,873 )
-35 %
Laboratory supplies and R&D materials expenses
2,751
6,964
(4,213 )
-60 %
Salary, consulting and other personnel costs
16,140
12,572
3,568
28 %
Non-cash share-based compensation expenses
2,947
5,052
(2,105 )
-42 %
Facility, depreciation and other expenses
11,359
7,948
3,411
43 %
Total research and development expenses - Sorrento segment
45,876
52,088
(6,212 )
-12 %
Total research and development expenses - Scilex segment
2,591
2,418
173
7 %
Total research and development expenses
$ 48,467
$ 54,506
$ (6,039 )
-11 %
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U.S. Securities and Exchange Commission
August 15, 2022
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The following table
summarizes our research and development expenses for the six months ended June 30, 2022 and 2021:
Six months ended June 30,
Increase (decrease)
Type of expense
2022
2021
$
%
Third party clinical and pre-clinical R&D expenses by program
Abivertinib
$ 4,382
$ 432
$ 3,950
914 %
Resiniferatoxin (“RTX”)
2,132
4,339
(2,207 )
-51 %
COVID-19 therapies and diagnostics, excluding Abivertinib
14,041
24,120
(10,079 )
-42 %
Immuno-oncology and other programs
14,575
12,096
2,479
20 %
Total third party clinical and pre-clinical R&D expenses by program
35,130
40,987
(5,857 )
-14 %
Laboratory supplies and R&D materials expenses
12,280
10,001
2,279
23 %
Salary, consulting and other personnel costs
30,821
18,892
11,929
63 %
Non-cash share-based compensation expenses
6,136
7,886
(1,750 )
-22 %
Facility, depreciation and other expenses
22,604
15,437
7,167
46 %
Total research and development expenses - Sorrento segment
106,971
93,203
13,768
15 %
Total research and development expenses - Scilex segment
5,222
5,136
86
2 %
Total research and development expenses
$ 112,193
$ 98,339
$ 13,854
14 %
Third party clinical
and pre-clinical R&D expenses for our Sorrento segment largely fluctuated as a result of the timing of clinical trial spend and the
timing of our acquisition of ACEA Therapeutics, Inc. (“ACEA”) (Abivertinib), which occurred in June 2021. Salaries,
personnel costs and facilities expenses increased as compared to the same periods in the prior year as we continue expanding our R&D
personnel headcount and infrastructure to support our R&D programs.
Form 10-Q
for the period ended March 31, 2022
Item 4. Controls and Procedures
Evaluation of Disclosure Controls
and Procedures, page 25
3. We
noted that you did not state management's conclusion with regards to the effectiveness of
your disclosure controls and procedures as of the end of March 31, 2022. As required by Item
307 of Regulation S-K, please disclose management's conclusion with regards to the effectiveness
of your disclosure controls and procedures in future filings.
Sorrento’s
response:
The Company respectfully
advises the Staff that, as required by Item 307 of Regulation S-K, it will disclose management’s conclusion with regards to the
effectiveness of the Company’s disclosure controls and procedures in future filings. The Company further advises the Staff that
it has disclosed management’s conclusion with regards to the effectiveness of the Company’s disclosure controls and procedures
as of March 31, 2022 and as of June 30, 2022 in Part I, Item 4 of the Q2 2022 Form 10-Q.
******
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U.S. Securities and Exchange Commission
August 15, 2022
Page 5
We appreciate the
time that you have taken to review our public filings. Please contact me if you have any further comments or need additional information
with respect to the filing. The Company’s future filings will reflect the responses set forth in this letter, as applicable.
Thank you for your assistance.
SORRENTO THERAPEUTICS, INC.
By:
/s/ Elizabeth Czerepak
Name:
Elizabeth Czerepak
Title:
Executive Vice President and Chief Financial Officer
cc: Andy
Kimball, Ernst & Young LLP
Jeffrey T. Hartlin, Paul Hastings LLP
Samantha H, Eldredge, Paul
Hastings LLP
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