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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): August 11, 2023
JASPER
THERAPEUTICS, INC.
(Exact
name of registrant as specified in its charter)
Delaware |
|
001-39138 |
|
84-2984849 |
(State or other jurisdiction
of incorporation) |
|
(Commission File Number) |
|
(I.R.S. Employer
Identification No.) |
2200 Bridge Pkwy Suite #102 |
|
|
Redwood City, CA |
|
94065 |
(Address of principal executive offices) |
|
(Zip Code) |
(650) 549-1400
Registrant’s telephone number, including
area code
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 |
Voting Common Stock, par value $0.0001 per share |
|
JSPR |
|
The Nasdaq Stock Market LLC |
Redeemable Warrants, each whole warrant exercisable for one share of Voting Common Stock at an exercise price of $11.50 |
|
JSPRW |
|
The Nasdaq Stock 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 or Rule 12b-2 of the Securities Exchange Act of 1934.
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 August 11, 2023, Jasper Therapeutics,
Inc. issued a press release reporting its financial results for the quarter ended June 30, 2023 and providing a business update. A copy
of the press release is furnished as Exhibit 99.1 to this Current Report on Form 8-K.
In accordance with General Instructions
B.2 of Form 8-K, the information in this Item 2.02, including the press release attached hereto as Exhibit 99.1, is being furnished
under Item 2.02 and Item 9.01 of Current Report on Form 8-K and shall not be deemed “filed” for purposes of Section 18
of the Securities Exchange Act of 1934, as amended (the “Exchange Act”), or otherwise subject to the liability of that section,
and shall not be deemed incorporated by reference in any filing under the Securities Act of 1933, as amended, or the Exchange Act, except
as shall be expressly set forth by specific reference in such a filing.
Item 9.01. Financial Statements and Exhibits.
(d) Exhibits.
SIGNATURE
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 thereunto duly authorized.
|
JASPER THERAPEUTICS, INC. |
|
|
Date: August 11, 2023 |
By: |
/s/ Jeet Mahal |
|
|
Name: |
Jeet Mahal |
|
|
Title: |
Chief
Operating Officer and Chief Financial
Officer |
Exhibit 99.1
Jasper Therapeutics Reports Second Quarter 2023
Financial Results and Provides a Business Update
| ● | First
Patient Dosed in Phase 1 trial of Briquilimab in Lower-Risk Myelodysplastic Syndrome |
| | |
| ● | Strengthened
the Board of Directors and Management Team with Multiple Appointments |
REDWOOD
CITY, Calif., August 11, 2023 – Jasper Therapeutics, Inc. (Nasdaq: JSPR) (Jasper), a biotechnology company focused on development
of briquilimab, a novel antibody therapy targeting c-Kit (CD117) to address diseases such as chronic spontaneous urticaria, lower to
intermediate risk myelodysplastic syndromes (LR-MDS) as well as novel stem cell transplant conditioning regimes, today announced results
for the fiscal quarter ended June 30, 2023, and provided a business update.
“During
our second quarter, we continued our preparations to begin a study in chronic spontaneous urticaria, which we anticipate initiating in
the coming months,” said Ronald Martell, President and Chief Executive Officer of Jasper. “We also dosed the first patient
in our Phase 1 trial evaluating briquilimab as second-line therapy in subjects with LR-MDS, and took significant additional steps taken
to strengthen our Board and leadership teams. With a strong balance sheet, enhanced organization and a sound development plan, we believe
we are well-positioned to advance our priority briquilimab development programs in rare and chronic diseases driven by mast and stem
cells.”
Highlights
for Q2 2023 and Recent Weeks
| ● | Dosed
first patients in a Phase 1 trial of briquilimab in LR-MDS |
| o | The
open-label, single-arm Phase 1 trial will evaluate the safety and tolerability of briquilimab
as a second-line therapy in subjects with LR-MDS. The trial will employ a 3+3 dose escalation
design to identify the maximum tolerated dose or optimal biologic dose and recommended Phase
2 dose of briquilimab monotherapy as a chronic therapeutic for LR-MDS patients with documented
cytopenia, such as red blood cell transfusion dependence, thrombocytopenia or neutropenia. |
| | |
| o | The
trial is being conducted at Moffitt Cancer Center in Tampa, FL, and is expected to enroll
up to 30 patients that will receive briquilimab every 56 days for 4 consecutive cycles. |
| | |
| o | Scott
Brun, M.D. appointed to the Board of Directors |
| | |
| o | Stephen
J. Galli, M.D. appointed to Scientific Advisory Board |
| | |
| o | Daniel
Adelman, M.D. appointed to Scientific Advisory Board |
| | |
| o | Edwin
J. Tucker, M.D. appointed as Chief Medical Officer |
| | |
| o | Patricia
Carlos appointed as Senior Vice President of Regulatory and Quality Affairs |
| | |
| o | Annette
Marcantonio appointed as Vice President of Clinical Operations |
Q2
2023 Financial Results
| ● | Cash
and Cash Equivalents: Cash and cash equivalents as of June 30, 2023, were $115.8 million,
compared to $38.3 million as of December 31, 2022. The increase in cash and cash equivalents
was due to net proceeds from the Company’s public offering in January 2023 and sales
through its at-the-market facility in January 2023. Cash and cash equivalents are expected
to be sufficient to fund the Company’s planned operating and capital expenditures through
2024. |
| ● | Research
and Development (R&D) Expenses: R&D expenses for the quarter ended June 30, 2023,
were $13.3 million compared to $8.1 million for the quarter ended June 30, 2022. The increase
was primarily due to additional costs associated with advancing Jasper’s clinical trials
and clinical manufacturing expenses. The increase also relates to higher research spending
and employee-related costs following hiring in 2022 and 2023 to support the ongoing development
of its product candidates. |
| ● | General
and Administrative (G&A) Expenses: G&A expenses for the quarter ended June 30,
2023, were $4.5 million compared to $3.8 million for the quarter ended June 30, 2022. The
increase was primarily related to higher employee compensation related costs, including stock-based
compensation expenses, to support the growth in Jasper’s operations. |
| ● | Total
Other Income, Net: Total other income, net was $1.7 million for the quarter ended June
30, 2023, compared to total other income, net of $1.6 million for the quarter ended June
30, 2022. Total other income, net, consists of interest income and changes in fair values
of common stock warrant liability and earnout liability at the end of the respective quarters.
|
| ● | Net
Loss: For the quarter ended June 30, 2023, net loss was $16.1 million compared to net
loss of $10.4 million for the quarter ended June 30, 2022. |
About
Briquilimab (formerly known as JSP191)
Briquilimab
is a targeted, monoclonal antibody that blocks stem cell factor from binding to the cell-surface receptor c-Kit, also known as CD117,
thereby inhibiting signaling through the receptor. Jasper intends to start clinical studies of briquilimab as a primary treatment in
Chronic Spontaneous Urticaria and Lower to Intermediate Risk myelodysplastic syndromes (MDS). It is also being studied as a conditioning
agent for cell and gene therapies for rare diseases. To date, briquilimab has a demonstrated efficacy and safety profile in 130 dosed
subjects and healthy volunteers, with clinical outcomes as a conditioning agent in severe combined immunodeficiency (SCID), acute myeloid
leukemia (AML), MDS, Fanconi anemia (FA), and sickle cell disease (SCD).
About
Jasper
Jasper
is a clinical-stage biotechnology company developing briquilimab, a monoclonal antibody targeting c-Kit (CD117) as a therapeutic for
chronic mast and stem cell diseases such as chronic urticaria and lower to intermediate risk myelodysplastic syndromes (MDS) and as a
conditioning agent for stem cell transplants for rare diseases such as sickle cell disease (SCD), Fanconi anemia (FA) and severe combined
immunodeficiency (SCID). To date, briquilimab has a demonstrated efficacy and safety profile in over 130 dosed subjects and healthy volunteers,
with clinical outcomes as a conditioning agent in SCID, acute myeloid leukemia (AML), MDS, FA, and SCD. In addition, briquilimab is being
advanced as a transformational non-genotoxic conditioning agent for gene therapy. For more information, please visit us at www.jaspertherapeutics.com.
Forward-Looking
Statements
Certain
statements included in this press release that are not historical facts are forward-looking statements for purposes of the safe harbor
provisions under the United States Private Securities Litigation Reform Act of 1995. Forward-looking statements are sometimes accompanied
by words such as “believe,” “may,” “will,” “estimate,” “continue,” “anticipate,”
“intend,” “expect,” “should,” “would,” “plan,” “predict,” “potential,”
“seem,” “seek,” “future,” “outlook” and similar expressions that predict or indicate
future events or trends or that are not statements of historical matters. These forward-looking statements include, but are not limited
to, statements regarding briquilimab’s potential, including with respect to its potential to address diseases such as chronic spontaneous
urticaria, lower to intermediate risk myelodysplastic syndromes as well as novel stem cell transplant conditioning regimes, Jasper’s
expectations regarding the initiation and timing of studies and clinical trials and recruitment for clinical trials, Jasper’s expectations
regarding the advancement of its briquilimab development programs and Jasper’s expectations regarding its cash and cash equivalents
and planned operating and capital expenditures. These statements are based on various assumptions, whether or not identified in this
press release, and on the current expectations of Jasper and are not predictions of actual performance. These forward-looking statements
are provided for illustrative purposes only and are not intended to serve as, and must not be relied on by an investor as, a guarantee,
an assurance, a prediction or a definitive statement of fact or probability. Many actual events and circumstances are beyond the control
of Jasper. These forward-looking statements are subject to a number of risks and uncertainties, including general economic, political
and business conditions; the risk that the potential product candidates that Jasper develops may not progress through clinical development
or receive required regulatory approvals within expected timelines or at all; the risk that clinical trials may not confirm any safety,
potency or other product characteristics described or assumed in this press release; the risk that Jasper will be unable to successfully
market or gain market acceptance of its product candidates; the risk that prior study results may not be replicated; the risk that Jasper’s
product candidates may not be beneficial to patients or successfully commercialized; patients’ willingness to try new therapies
and the willingness of physicians to prescribe these therapies; the effects of competition on Jasper’s business; the risk that
third parties on which Jasper depends for laboratory, clinical development, manufacturing and other critical services will fail to perform
satisfactorily; the risk that Jasper’s business, operations, clinical development plans and timelines, and supply chain could be
adversely affected by the effects of health epidemics, including the ongoing COVID-19 pandemic; the risk that Jasper will be unable to
obtain and maintain sufficient intellectual property protection for its investigational products or will infringe the intellectual property
protection of others; and other risks and uncertainties indicated from time to time in Jasper’s filings with the SEC, including
its Annual Report on Form 10-K for the year ended December 31, 2022. If any of these risks materialize or Jasper’s assumptions
prove incorrect, actual results could differ materially from the results implied by these forward-looking statements. While Jasper may
elect to update these forward-looking statements at some point in the future, Jasper specifically disclaims any obligation to do so.
These forward-looking statements should not be relied upon as representing Jasper’s assessments of any date subsequent to the date
of this press release. Accordingly, undue reliance should not be placed upon the forward-looking statements.
Contacts:
John Mullaly (investors)
LifeSci
Advisors
617-429-3548
jmullaly@lifesciadvisors.com
Jeet
Mahal (investors)
Jasper
Therapeutics
650-549-1403
jmahal@jaspertherapeutics.com
Lauren
Barbiero (media)
Real
Chemistry
646-564-2156
lbarbiero@realchemistry.com
--- tables
to follow---
JASPER THERAPEUTICS, INC.
CONDENSED CONSOLIDATED STATEMENTS
OF OPERATIONS AND COMPREHENSIVE LOSS
(in thousands, except share and
per share data)
(unaudited)
| |
Three Months Ended
June 30, | | |
Six Months Ended
June 30, | |
| |
2023 | | |
2022 | | |
2023 | | |
2022 | |
Operating expenses | |
| | |
| | |
| | |
| |
Research and development(1) | |
$ | 13,297 | | |
$ | 8,135 | | |
$ | 23,102 | | |
$ | 16,323 | |
General and administrative(1) | |
| 4,530 | | |
| 3,828 | | |
| 8,672 | | |
| 8,418 | |
Total operating expenses | |
| 17,827 | | |
| 11,963 | | |
| 31,774 | | |
| 24,741 | |
Loss from operations | |
| (17,827 | ) | |
| (11,963 | ) | |
| (31,774 | ) | |
| (24,741 | ) |
Interest income | |
| 1,436 | | |
| 92 | | |
| 2,532 | | |
| 94 | |
Change in fair value of earnout liability | |
| 420 | | |
| 625 | | |
| (344 | ) | |
| 5,218 | |
Change in fair value of common stock warrant liability | |
| — | | |
| 845 | | |
| (575 | ) | |
| 6,895 | |
Other expense, net | |
| (109 | ) | |
| (3 | ) | |
| (179 | ) | |
| (77 | ) |
Total other income, net | |
| 1,747 | | |
| 1,559 | | |
| 1,434 | | |
| 12,130 | |
Net loss and comprehensive loss | |
$ | (16,080 | ) | |
$ | (10,404 | ) | |
$ | (30,340 | ) | |
$ | (12,611 | ) |
Net loss per share attributable to common stockholders, basic
and diluted | |
$ | (0.15 | ) | |
$ | (0.29 | ) | |
$ | (0.31 | ) | |
$ | (0.35 | ) |
Weighted-average shares used in computing net loss per share attributable to common stockholders, basic and diluted | |
| 109,213,669 | | |
| 36,397,822 | | |
| 98,605,265 | | |
| 36,353,509 | |
| (1) | Amounts include non-cash stock based compensation expense as
follows (in thousands): |
| |
Three Months Ended
June 30, | | |
| Six Months Ended
June 30, | |
| |
| 2023 | | |
| 2022 | | |
| 2023 | | |
| 2022 | |
| |
| | | |
| | | |
| | | |
| | |
Research and development | |
$ | 491 | | |
$ | 585 | | |
$ | 959 | | |
$ | 807 | |
General and administrative | |
| 900 | | |
| 480 | | |
| 1,699 | | |
| 1,036 | |
Total | |
$ | 1,391 | | |
$ | 1,065 | | |
$ | 2,658 | | |
$ | 1,843 | |
JASPER THERAPEUTICS, INC.
CONDENSED CONSOLIDATED BALANCE SHEETS
(in thousands)
(unaudited)
| |
June 30, | | |
December 31, | |
Assets | |
2023 | | |
2022 | |
Current assets: | |
| | |
| |
Cash and cash equivalents | |
$ | 115,812 | | |
$ | 38,250 | |
Other receivables | |
| - | | |
| 663 | |
Prepaid expenses and other current assets | |
| 2,755 | | |
| 2,818 | |
Total current assets | |
| 118,567 | | |
| 41,731 | |
Property and equipment, net | |
| 3,056 | | |
| 3,568 | |
Operating lease right-of-use assets | |
| 1,685 | | |
| 1,886 | |
Restricted cash | |
| 417 | | |
| 417 | |
Other non-current assets | |
| 445 | | |
| 759 | |
Total assets | |
$ | 124,170 | | |
$ | 48,361 | |
| |
| | | |
| | |
Liabilities and Stockholders’ Equity | |
| | | |
| | |
Current liabilities: | |
| | | |
| | |
Accounts payable | |
$ | 1,581 | | |
$ | 1,768 | |
Current portion of operating lease liabilities | |
| 917 | | |
| 865 | |
Accrued expenses and other current liabilities | |
| 6,474 | | |
| 4,432 | |
Total current liabilities | |
| 8,972 | | |
| 7,065 | |
Non-current portion of operating lease liabilities | |
| 2,317 | | |
| 2,786 | |
Common stock warrant liability | |
| — | | |
| 150 | |
Earnout liability | |
| 362 | | |
| 18 | |
Other non-current liabilities | |
| 2,314 | | |
| 2,353 | |
Total liabilities | |
| 13,965 | | |
| 12,372 | |
| |
| | | |
| | |
Commitments and contingencies | |
| | | |
| | |
Stockholders’ equity: | |
| | | |
| | |
Preferred stock | |
| — | | |
| — | |
Common stock | |
| 11 | | |
| 4 | |
Additional paid-in capital | |
| 245,669 | | |
| 141,120 | |
Accumulated deficit | |
| (135,475 | ) | |
| (105,135 | ) |
Total stockholders’ equity | |
| 110,205 | | |
| 35,989 | |
Total liabilities and stockholders’ equity | |
$ | 124,170 | | |
$ | 48,361 | |
5
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|
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|
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|
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|
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|
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|
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