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UNITED
STATES
SECURITIES
AND EXCHANGE COMMISSION
Washington,
D.C. 20549
FORM
8-K
CURRENT
REPORT
PURSUANT
TO SECTION 13 OR 15(D) OF THE SECURITIES EXCHANGE ACT OF 1934
Date
of Report (Date of earliest event reported): December 17, 2024
SONNET
BIOTHERAPEUTICS HOLDINGS, INC.
(Exact
name of registrant as specified in its charter)
Delaware |
|
001-35570 |
|
20-2932652 |
(State or other jurisdiction
of incorporation) |
|
(Commission
File Number) |
|
(IRS Employer
Identification No.) |
100
Overlook Center, Suite 102
Princeton, New Jersey |
|
08540 |
(Address of principal executive
offices) |
|
(Zip Code) |
Registrant’s
telephone number, including area code: (609) 375-2227
N/A
(Former
name or former address, if changed since last report.)
Check
the appropriate box below if the Form 8-K filing is intended to simultaneously satisfy the filing obligation of the registrant under
any of the following provisions:
☐ |
Written communications
pursuant to Rule 425 under the Securities Act (17 CFR 230.425) |
|
|
☐ |
Soliciting material pursuant
to Rule 14a-12 under the Exchange Act (17 CFR 240.14a-12) |
|
|
☐ |
Pre-commencement communications
pursuant to Rule 14d-2(b) under the Exchange Act (17 CFR 240.14d-2(b)) |
|
|
☐ |
Pre-commencement communications
pursuant to Rule 13e-4(c) under the Exchange Act (17 CFR 240.13e-4(c)) |
Securities
registered pursuant to Section 12(b) of the Act:
Title
of each class |
|
Trading
Symbol(s) |
|
Name
of each exchange on which registered |
Common Stock, $0.0001 Par
Value |
|
SONN |
|
The Nasdaq Capital Market
LLC |
Indicate
by check mark whether the registrant is an emerging growth company as defined in Rule 405 of the Securities Act of 1933 (§230.405
of this chapter) or Rule 12b-2 of the Securities Exchange Act of 1934 (§240.12b-2 of this chapter).
Emerging
growth company ☐
If
an emerging growth company, indicate by check mark if the registrant has elected not to use the extended transition period for complying
with any new or revised financial accounting standards provided pursuant to Section 13(a) of the Exchange Act. ☐
Item
2.02. Results of Operations and Financial Condition.
On
December 17, 2024, Sonnet BioTherapeutics Holdings, Inc. (the “Registrant”) issued a press release regarding its financial
results for the fiscal year ended September 30, 2024. A copy of the press release is furnished as Exhibit 99.1 hereto and is incorporated
by reference herein.
Item
7.01. Regulation FD.
See
“Item 2.02 Results of Operation and Financial Condition” above.
The
information in this Current Report on Form 8-K under Items 2.02 and 7.01, including the information contained in Exhibit 99.1, is being
furnished to the Securities and Exchange Commission (the “SEC”), and shall not be deemed to be “filed”
for the purposes of Section 18 of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise
subject to the liabilities of that section, and shall not be deemed to be incorporated by reference into any filing under the Securities
Act of 1933, as amended, or the Exchange Act, except as shall be expressly set forth by a specific reference in such filing.
Forward-Looking
Statements
This
Current Report on Form 8-K, including Exhibit 99.1 furnished herewith, contains certain forward-looking statements within the meaning
of Section 27A of the Securities Act of 1933 and Section 21E of the Exchange Act and Private Securities Litigation Reform Act, as amended,
including those relating to the outcome of the Company’s clinical trials, the Company’s cash runway, the Company’s
product development, clinical and regulatory timelines, market opportunity, competitive position, possible or assumed future results
of operations, business strategies, potential growth opportunities and other statements that are predictive in nature. These forward-looking
statements are based on current expectations, estimates, forecasts and projections about the industry and markets in which we operate
and management’s current beliefs and assumptions.
These
statements may be identified by the use of forward-looking expressions, including, but not limited to, “expect,” “anticipate,”
“intend,” “plan,” “believe,” “estimate,” “potential,” “predict,”
“project,” “should,” “would” and similar expressions and the negatives of those terms. These statements
relate to future events or the Company’s financial performance and involve known and unknown risks, uncertainties, and other factors
which may cause actual results, performance or achievements to be materially different from any future results, performance or achievements
expressed or implied by the forward-looking statements. Such factors include those set forth in the Company’s filings with the
SEC. Prospective investors are cautioned not to place
undue reliance on such forward-looking statements, which speak only as of the date of this Current Report. The Company undertakes no
obligation to publicly update any forward-looking statement, whether as a result of new information, future events or otherwise.
Item
9.01. Financial Statements and Exhibits.
(d)
Exhibits.
SIGNATURES
Pursuant
to the requirements of the Securities Exchange Act of 1934, the registrant has duly caused this report to be signed on its behalf by
the undersigned hereunto duly authorized.
|
Sonnet BioTherapeutics Holdings, Inc. |
|
a Delaware corporation |
|
(Registrant) |
|
|
Date: December 17, 2024 |
By: |
/s/ Pankaj
Mohan, Ph.D. |
|
Name: |
Pankaj Mohan, Ph.D. |
|
Title: |
Chief Executive Officer |
Exhibit
99.1
Sonnet
BioTherapeutics Reports Fiscal Year 2024 Financial Results and Provides Corporate Update
Continued
progress with both clinical trials of lead program, SON-1010, for solid tumors and Platinum-Resistant Ovarian Cancer (PROC)
Executed
licensing agreement to support initiation of a Phase 2 clinical trial of SON-080 in Diabetic Peripheral Neuropathy (DPN)
Multiple
value-driving milestones expected throughout calendar year 2025 as well as pipeline expansion opportunities across the solid tumor market
Total
annual operating expenses reduced by an approximate 37% as compared to fiscal year 2023
Approximately
43% of total annual operating expenses during fiscal year 2024 were covered by non-dilutive funding received during fiscal year 2024
from the New Jersey Tax Certificate Transfer and Australia R&D Tax Incentive Programs
PRINCETON,
NJ / ACCESSWIRE / December 17, 2024 / Sonnet BioTherapeutics Holdings, Inc. (the “Company” or “Sonnet”) (NASDAQ:
SONN), a clinical-stage company developing targeted immunotherapeutic drugs, reported today financial results for the fiscal year ended
September 30, 2024 and provided a corporate update.
“We
are very pleased with the progress we have made across all facets of the company’s operations. On the financial front, we have
delivered on our stated objective of cutting costs through an approximate 37% reduction in total operating expenses versus last year,
which will help to extend our cash runway, combined with being able to leverage non-dilutive funding and capital markets financings.
Additionally, we have executed on our partnership plans to advance both our SON-080 program and SON-1210 program to their respective
next stages of development and continue to believe in their potential to address indications of significant unmet need,” commented
Pankaj Mohan, Ph.D., Founder and Chief Executive Officer of Sonnet. “Looking ahead, our focus is on advancing our lead program,
SON-1010, and we are pleased to be on track for key data readouts from our ongoing SB101 trial for solid tumors and our SB221 trial for
PROC. We look forward to the upcoming data readouts to help further unlock the intrinsic value of our FHAB technology platform.”
Recent
Highlights
|
● |
Announced
topline safety data following successful completion of SON-1010 monotherapy dose escalation in the Phase 1 SB101 trial; |
|
|
|
|
● |
Announced
the publication of extensive discovery, development, and preclinical data regarding SON-1010, demonstrating its mechanism
of action in a paper entitled, “SON-1010: an albumin-binding IL-12 fusion protein that improves cytokine half-life, targets
tumors, and enhances therapeutic efficacy,” in Frontiers in Immunology; |
|
● |
Granted
U.S. Patent No. 12,134,635 covering two of its novel drug candidates, SON-1411 (IL-18BPR-FHAB-IL12) and
SON-1400 (IL-18BPR-FHAB), each containing a modified version of recombinant human interleukin-18 (BPR = Binding
Protein Resistant); |
|
|
|
|
● |
Entered
into a licensing agreement with Alkem Laboratories Limited for the research, development, manufacturing, marketing, and commercialization
of the SON-080 molecule for the treatment of DPN in India; |
|
|
|
|
● |
Received
preliminary approval for the sale of tax credits from the New Jersey Technology Business Tax Certificate Transfer Program
administered by the New Jersey Economic Development Authority (NJEDA); and |
|
|
|
|
● |
Entered
into a Master Clinical Collaboration Agreement with the Sarcoma Oncology Center to advance the development of SON-1210 in
combination with chemotherapy for the treatment of metastatic pancreatic cancer. |
Lead
Clinical Programs Update
SON-1010:
Targeted Immune Activation Cancer Therapy, Turning ‘Cold’ Tumors ‘Hot’, Initially Targeting Solid Tumors and
Platinum-Resistant Ovarian Cancer (PROC)
Phase
1 Trial (SB101 Trial): Advanced Solid Tumors (Monotherapy)
This
first-in-human study is primarily designed to evaluate the safety, tolerability, PK, and PD of multiple ascending doses of SON-1010 in
cancer patients and is being conducted at several sites across the United States. The Company recently completed enrollment and dose
escalation in the Phase 1 SB101 clinical trial of SON-1010 (IL12-FHAB) in adult patients with advanced solid tumors. Additionally,
the Company reported that results of SON-1010 at the highest dose have been formally evaluated by the Safety Review Committee. The study
has enrolled 24 subjects to date. Primary outcome measures for the study were to evaluate the safety and tolerability of SON-1010 and
establish the MTD.
For
more information about the SB101 clinical trial, visit clinicaltrials.gov and reference identifier NCT05352750.
Phase
1b/2a Trial (SB221 Trial): Advanced Solid Tumors and PROC (Combo with Atezolizumab)
The
second trial is a global Phase 1b/2a multicenter, dose-escalation and randomized proof-of-concept study to assess the safety, tolerability,
PK, PD, and efficacy of SON-1010 administered subcutaneously (SC) in combination with atezolizumab given intravenously (IV) (in collaboration
with Genentech, a member of the Roche Group). This study was recently expanded to include the MTD of SON-1010 from SB101. Enrollment
remains ongoing and an update on safety at the MTD in that trial is expected in Q1 2025.
For
more information about the SB221 clinical trial, visit clinicaltrials.gov and reference identifier NCT05756907.
SON-1010
Upcoming Milestones
|
● |
Phase
1: Solid Tumors (Monotherapy) |
|
○ |
H1
calendar year 2025: Topline Efficacy Data |
|
● |
Phase
1b/2a: PROC (Combo with Atezolizumab) |
|
○ |
Q1
calendar year 2025: Additional Safety Data |
|
○ |
H2
calendar year 2025: RP2D & Topline Efficacy
Data |
SON-1210:
Proprietary, Bifunctional Version of Human Interleukins 12 (IL-12) and 15 (IL-15), Configured Using Sonnet’s Fully Human
Albumin Binding (FHAB®) platform, in Combination with Chemotherapy for the Treatment of Advanced Solid Tumors
and Metastatic Pancreatic Cancer
As
previously announced, the Company successfully completed two IND-enabling toxicology studies of SON-1210 in non-human primates (NHPs),
which demonstrated no overt toxicity in the GLP study apart from the expected and mild, on-target changes in hematology and clinical
chemistry parameters that resolved completely within 14 to 21 days post-dosing. A significant increase in interferon gamma (IFNγ),
which was controlled and prolonged, was noted as early as one day following administration, with no apparent increase in other proinflammatory
cytokines. IFNγ is a well-known pharmacodynamic biomarker that is required for anti-tumor efficacy in preclinical models. Other
signs of cytokine imbalance, or uncontrolled increase of pro-inflammatory cytokines (including TNF-α, IL-1β, and IL-6) were
notably absent from all dose levels tested in the study.
In
August 2024, the Company entered into a Master Clinical Collaboration Agreement with the Sarcoma Oncology Center, to conduct an investigator-initiated
Phase 1/2a clinical study to evaluate SON-1210 in combination with several chemotherapeutic agents including but not limited to NALIRIFOX
(the combination of liposomal irinotecan, 5-fluorouracil/leucovorin, and oxaliplatin) for the specific treatment of metastatic pancreatic
cancer. The NALIRIFOX regimen is U.S. FDA-approved for the treatment of metastatic pancreatic cancer in the front-line and refractory
settings.
SON-1210
Upcoming Milestones
|
● |
Q1
calendar year 2025: IND Submission |
|
● |
H1
calendar year 2025: 1st Patient Dosed
in Investigator-Initiated Phase 1/2a Study |
SON-080:
Low dose of rhIL-6 for Chemotherapy-Induced Peripheral Neuropathy (CIPN) and Diabetic Peripheral Neuropathy (DPN)
In
October 2024, the Company entered into a licensing agreement (the “Licensing Agreement”) with Alkem Laboratories Limited
(“Alkem”) for the research, development, manufacturing, marketing, and commercialization of its SON-080 molecule for the
treatment of DPN in India and the manufacturing, marketing, and commercialization of SON-080 for chemotherapy induced neuropathy (CIPN)
and autonomic neuropathy in India. Alkem will conduct all clinical trials it believes appropriate to obtain regulatory approval in India
of SON-080 for the treatment of DPN.
Summary
of Financial Results for the Fiscal Year 2024
As
of September 30, 2024, Sonnet had $0.1 million cash on hand. The Company believes that based on cash on hand at September 30, 2024, together
with the approximate $7.7 million recently received through the sale of common stock and warrants in November and December 2024, $0.7
million received from the R&D Tax Incentive Program in Australia in November 2024 to satisfy the Company’s incentive tax receivable,
and $0.5 million received in October 2024 as an upfront payment related to the License Agreement, which after tax withholdings resulted
in a net payment of $0.4 million, it has sufficient funds for projected operations into July
2025.
Research
and development expenses were $5.7 million for the year ended September 30, 2024, compared to $11.8 million for the year ended September
30, 2023.
General
and administrative expenses were $6.1 million for the year ended September 30, 2024, compared to $7.1 million for the year ended September
30, 2023.
About
Sonnet BioTherapeutics Holdings, Inc.
Sonnet
BioTherapeutics is an oncology-focused biotechnology company with a proprietary platform for innovating biologic drugs of single or bifunctional
action. Known as FHAB (Fully Human Albumin Binding), the technology utilizes a fully human single chain antibody fragment
(scFv) that binds to and “hitch-hikes” on human serum albumin (HSA) for transport to target tissues. Sonnet’s FHAB
was designed to specifically target tumor and lymphatic tissue, with an improved therapeutic window for optimizing the safety and efficacy
of immune modulating biologic drugs. FHAB is the foundation of a modular, plug-and-play construct for potentiating a range
of large molecule therapeutic classes, including cytokines, peptides, antibodies, and vaccines.
Forward-Looking
Statements
This
press release contains certain forward-looking statements within the meaning of Section 27A of the Securities Act of 1933 and Section
21E of the Securities Exchange Act of 1934 and Private Securities Litigation Reform Act, as amended, including those relating to the
outcome of the Company’s clinical trials, the Company’s cash runway, the Company’s product development, clinical and
regulatory timelines, market opportunity, competitive position, possible or assumed future results of operations, business strategies,
potential growth opportunities and other statements that are predictive in nature. These forward-looking statements are based on current
expectations, estimates, forecasts and projections about the industry and markets in which we operate and management’s current
beliefs and assumptions.
These
statements may be identified by the use of forward-looking expressions, including, but not limited to, “expect,” “anticipate,”
“intend,” “plan,” “believe,” “estimate,” “potential,” “predict,”
“project,” “should,” “would” and similar expressions and the negatives of those terms. These statements
relate to future events or our financial performance and involve known and unknown risks, uncertainties, and other factors which may
cause actual results, performance or achievements to be materially different from any future results, performance or achievements expressed
or implied by the forward-looking statements. Such factors include those set forth in the Company’s filings with the Securities
and Exchange Commission. Prospective investors are cautioned not to place undue reliance on such forward-looking statements, which speak
only as of the date of this press release. The Company undertakes no obligation to publicly update any forward-looking statement, whether
as a result of new information, future events or otherwise.
Investor
Relations Contact:
JTC
Team, LLC
Jenene
Thomas
908-824-0775
SONN@jtcir.com
Sonnet
BioTherapeutics Holdings, Inc.
Consolidated
Balance Sheets
| |
September 30, | |
| |
2024 | | |
2023 | |
Assets | |
| | | |
| | |
Current assets: | |
| | | |
| | |
Cash and cash equivalents | |
$ | 149,456 | | |
$ | 2,274,259 | |
Prepaid expenses and other current assets | |
| 1,206,409 | | |
| 1,677,396 | |
Incentive tax receivable | |
| 762,078 | | |
| 786,574 | |
Total current assets | |
| 2,117,943 | | |
| 4,738,229 | |
Property and equipment, net | |
| 20,523 | | |
| 33,366 | |
Operating lease right-of-use asset | |
| 123,417 | | |
| 193,689 | |
Deferred offering costs | |
| 15,000 | | |
| 49,988 | |
Other assets | |
| 494,147 | | |
| 414,206 | |
Total assets | |
$ | 2,771,030 | | |
$ | 5,429,478 | |
Liabilities and stockholders’ deficit | |
| | | |
| | |
Current liabilities: | |
| | | |
| | |
Accounts payable | |
$ | 2,183,416 | | |
$ | 2,201,999 | |
Accrued expenses and other current liabilities | |
| 942,489 | | |
| 3,230,922 | |
Current portion of operating lease liability | |
| 84,291 | | |
| 73,048 | |
Deferred income | |
| — | | |
| 18,626 | |
Total current liabilities | |
| 3,210,196 | | |
| 5,524,595 | |
Operating lease liability, net of current portion | |
| 46,573 | | |
| 130,863 | |
Total liabilities | |
| 3,256,769 | | |
| 5,655,458 | |
Commitments and contingencies (Note 5) | |
| | | |
| | |
Stockholders’ deficit: | |
| | | |
| | |
Preferred stock, $0.0001 par value: 5,000,000 shares authorized; no shares issued or outstanding | |
| — | | |
| — | |
Common stock, $0.0001 par value: 125,000,000 shares authorized; 650,284 and 218,786 issued and outstanding at September 30, 2024 and 2023, respectively | |
| 65 | | |
| 22 | |
Additional paid-in capital | |
| 117,195,181 | | |
| 110,017,751 | |
Accumulated deficit | |
| (117,680,985 | ) | |
| (110,243,753 | ) |
Total stockholders’ deficit | |
| (485,739 | ) | |
| (225,980 | ) |
Total liabilities and stockholders’ deficit | |
$ | 2,771,030 | | |
$ | 5,429,478 | |
Sonnet
BioTherapeutics Holdings, Inc.
Consolidated
Statements of Operations
| |
Years ended September 30, | |
| |
2024 | | |
2023 | |
Collaboration revenue | |
$ | 18,626 | | |
$ | 147,805 | |
Operating expenses: | |
| | | |
| | |
Research and development | |
| 5,737,252 | | |
| 11,814,690 | |
General and administrative | |
| 6,130,845 | | |
| 7,125,732 | |
Total operating expense | |
| 11,868,097 | | |
| 18,940,422 | |
Loss from operations | |
| (11,849,471 | ) | |
| (18,792,617 | ) |
Foreign exchange gain (loss) | |
| 84,293 | | |
| (40,077 | ) |
Other income | |
| 4,327,946 | | |
| — | |
Net loss | |
$ | (7,437,232 | ) | |
$ | (18,832,694 | ) |
| |
| | | |
| | |
Per share information: | |
| | | |
| | |
Net loss per share, basic and diluted | |
$ | (11.35 | ) | |
$ | (145.13 | ) |
Weighted average shares outstanding, basic and diluted | |
| 655,240 | | |
| 129,760 | |
v3.24.4
Cover
|
Dec. 17, 2024 |
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