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Jasper Therapeutics Reports Second Quarter 2026 Financial Results and Provides Corporate Update

(Very High)
(Positive)
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Jasper Therapeutics (Nasdaq:JSPR) reported second quarter 2026 results and detailed its post‑merger strategy following completion of the all‑stock acquisition of Kira Pharmaceuticals on July 16, 2026. Concurrently, Jasper closed a PIPE financing of non‑voting convertible preferred stock, generating approximately $132 million in gross proceeds, which the company believes will fund planned operations into the second half of 2028.

The combined company is advancing three key clinical assets: KP‑104, a Phase 2 basket trial in rare renal indications with interim data expected in Q4 2026; briquilimab, moving toward a pre‑BLA meeting with the FDA with next‑step guidance expected in Q1 2027; and KP‑701, for which a Phase 1 CTA/IND filing is targeted for Q1 2027. As of June 30, 2026, cash and cash equivalents were $7.3 million. Q2 2026 research and development expense was $5.1 million and general and administrative expense was $4.1 million, resulting in a net loss of $2.8 million, or $0.10 per basic and diluted share, compared with a net loss of $26.7 million, or $1.74 per share, in Q2 2025.

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Positive

  • $132 million PIPE financing completed, extending runway per company into H2 2028
  • Acquisition of Kira Pharmaceuticals closed July 16, 2026 in all‑stock deal
  • Q2 2026 net loss fell to $2.8 million from $26.7 million year over year
  • Warrant liability decreased to $2.5 million from $16.2 million at December 31, 2025
  • Total operating expenses in Q2 2026 dropped to $9.2 million from $27.1 million in Q2 2025

Negative

  • Cash and cash equivalents were only $7.3 million as of June 30, 2026, pre‑PIPE
  • Total assets declined to $11.8 million from $35.8 million at year‑end 2025
  • Stockholders’ equity decreased to $1.4 million from $4.2 million at December 31, 2025
  • The company remains loss‑making, with $3.9 million net loss for the first half of 2026

News Explained

The financing adds approximately $132 million gross but leaves its ownership impact unquantified because preferred-stock conversion terms are undisclosed.

On July 16, 2026, Jasper Therapeutics completed the Kira acquisition and sold non-voting convertible preferred stock in a concurrent private placement for approximately $132 million gross, creating a potential ownership change for existing common holders if the preferred stock converts.

A private placement is a sale of securities to selected investors outside a public offering; here, the security sold was non-voting convertible preferred stock.

Before those July transactions, cash and equivalents were $14.144 million as of March 31, 2026, against first-quarter operating cash use of $14.548 million; that cash balance equals 87.5 days of the reported quarterly operating cash use.

The release does not state the preferred stock's conversion price, conversion ratio, or resulting common-share count, so the specific preferred-stock line items in a subsequent filing would establish the financing's dilution effect.

Sources and calculations
  • Cash and equivalents vs quarterly operating cash outflow, in days of cash use $14,144,000 / ($14,548,000 / 90) = [object Object]

Market reaction after 2Q26 earnings report: JSPR -4.36%

-4.36% $0.83
15m delay
-4.36% Vs previous close
$0.83 Last Price
$0.83 $0.87 Day Range
$26.22M Market Cap
0.5x Rel. Volume

Following this news, JSPR has declined 4.36%, reflecting a moderate negative market reaction. Our momentum scanner has triggered 5 alerts so far, indicating moderate trading interest and price volatility. The stock is currently trading at $0.83.

Data tracked by StockTitan Argus (15 min delayed). Upgrade to Gold for real-time data.

Market Context

Recent insider activity showed Net Buying, totaling 1,769 shares purchased and none sold. That platf...
Analysis

Recent insider activity showed Net Buying, totaling 1,769 shares purchased and none sold. That platform signal adds governance context to the financing and pipeline update, while the reported quarterly loss remains a risk factor.

Key Figures

PIPE financing: $132 million gross proceeds Cash and equivalents: $7.3 million R&D expense: $5.1 million +5 more
8 metrics
PIPE financing $132 million gross proceeds Concurrent private placement
Cash and equivalents $7.3 million As of June 30, 2026
R&D expense $5.1 million Three months ended June 30, 2026
G&A expense $4.1 million Three months ended June 30, 2026
Net loss $2.8 million Three months ended June 30, 2026
Net loss per share $0.10 Basic and diluted, three months ended June 30, 2026
Interim data timing Fourth quarter of 2026 Stage 1 of the KP-104 Phase 2 basket trial
CTA/IND filing timing First quarter of 2027 KP-701 Phase 1 evaluation

Previous Earnings Reports

5 past events · Latest: May 14 (Positive)
Same Type Pattern 5 events
Date Event Sentiment 24h Move Catalyst
May 14 First-quarter earnings Positive -11.4% Positive briquilimab update and reported cash position preceded a negative price reaction.
Mar 30 Year-end earnings Negative -2.6% Large annual loss and capital-dependent trial timing accompanied a negative price reaction.
Nov 10 Third-quarter earnings Negative +0.0% Liquidity pressure and clinical uncertainty were followed by a flat price reaction.
Aug 13 Second-quarter earnings Negative +2.0% Trial anomalies and program delays accompanied a positive price reaction.
May 12 First-quarter earnings Positive +1.7% Clinical program progress and upcoming data catalysts accompanied a positive price reaction.

24h Move is the share-price change in the day after each event; other market factors may also have contributed.

Pattern Detected

Earnings-tagged events produced mixed reactions, with an average move of -2.06% and divergence between several operating or clinical updates and subsequent price reactions.

Key Terms

pipe financing, convertible preferred stock, complement cascade, investigational new drug, +1 more
5 terms
pipe financing financial
"Completed a concurrent PIPE financing raising $132 million in gross proceeds"
Pipe financing is a way for companies to raise money quickly by selling new shares or bonds directly to investors, often before their stock is publicly traded or in the early stages of a project. It’s similar to a company securing a loan from investors, providing quick capital needed for growth or operations. For investors, it can offer opportunities for early involvement and potentially higher returns, but it may also carry increased risk due to the immediate nature of the deal.
convertible preferred stock financial
"sale of non-voting convertible preferred stock"
Convertible preferred stock is a special class of company shares that pays priority, usually fixed, payments to holders and can be exchanged later for a set number of common shares. It matters to investors because it combines steady income and added protection with the chance to share in a company’s upside; think of it as a hybrid between a bond that pays regularly and an option to convert into growth-oriented stock, where the conversion rules influence both potential gains and how much common shareholders’ ownership may be reduced.
complement cascade medical
"a novel dual inhibitor of the complement cascade"
A chain-reaction of blood proteins that acts like a built-in emergency sprinkler system: when triggered, proteins cascade in sequence to tag and help remove microbes or damaged cells and to call immune cells to the scene. It matters to investors because drugs that block or boost parts of this cascade can treat or cause serious disease, affect clinical trial outcomes, regulatory risk, market size, and safety profiles for therapies.
investigational new drug regulatory
"an investigational new drug (IND) for Phase 1 evaluation"
An investigational new drug is a medication that is still being tested in clinical trials to determine if it is safe and effective for treating a specific condition. For investors, it represents a potential breakthrough that could lead to a new treatment and significant financial gains if successful, but also carries risks since it has not yet been approved for widespread use.
clinical trial application regulatory
"file a clinical trial application (CTA) and/or an investigational new drug"
An application submitted to a regulatory authority requesting formal permission to begin testing a new drug, medical device, or treatment in humans. Like asking for a building permit before construction, it summarizes safety data, plans for how the study will be run, and monitoring procedures; investors watch these filings closely because approval lets a program move from lab research to clinical testing, reducing uncertainty and creating value-driving milestones.

AI-generated analysis. How Rhea-AI works. Not financial advice.

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Acquisition of Kira Pharmaceuticals closed in July creating a combined company with a robust portfolio of clinical stage assets focused on immunologically-driven disorders 

Completed a concurrent PIPE financing raising $132 million in gross proceeds

REDWOOD CITY, Calif., Aug. 14, 2026 (GLOBE NEWSWIRE) -- Jasper Therapeutics, Inc. (Nasdaq: JSPR) (“Jasper”), a clinical stage biotechnology company focused on the design and development of innovative therapies to treat immune-mediated diseases, today reported results for the fiscal quarter ended June 30, 2026, and provided a corporate update.

“We are excited to unite Jasper Therapeutics and Kira Pharmaceuticals to advance our shared mission of developing a differentiated portfolio of innovative therapies for patients with significant immune-mediated diseases. Supported by our recent $132 million financing led by leading life sciences investors, we believe that we have sufficient capital to fund planned operations through the second half of 2028.  We plan to advance development of our lead asset KP-104, a novel dual inhibitor of the complement cascade, in multiple indications, progress briquilimab towards a potential BLA, and to commence first in human studies for KP-701,” said Jeet Mahal, President and Chief Executive Officer of Jasper. “The combined company now has access to significant resources in the United States and China, which we believe will allow us to rapidly advance our portfolio across multiple diseases of unmet need.”

Corporate Updates for Second Quarter 2026 and Recent Weeks

  • On July 16, 2026, Jasper completed the acquisition of Kira Pharmaceuticals (“Kira”), a former Cayman limited company that was engaged in the design of complement therapies to treat immune-mediated diseases, in an all-stock transaction.
  • Concurrently with the acquisition, Jasper entered into a securities purchase agreement for the sale of non-voting convertible preferred stock (the “Preferred Stock”) in a private placement co-led by Affinity Asset Advisors, LLC and Ikarian Capital LLC with participation from other leading life science investors. The private placement resulted in total gross proceeds of approximately $132 million.
  • The combined company is focused on advancing its consolidated pipeline of potential best-in-class innovative therapies for immunologically-driven disorders, including:
    • KP-104 (Vensobafusp alfa), a Phase 2/3 ready, potentially best-in-disease, bifunctional biologic targeting both the alternative and terminal pathways within the complement cascade  for the treatment of paroxysmal nocturnal hemoglobinuria (PNH) and high unmet need nephrology disorders. KP-104 is currently being evaluated in a Phase 2 basket trial in rare renal indications and interim data from Stage 1 of the trial is expected in the fourth quarter of 2026. Based on previous, positive results in treatment-naïve PNH, the combined company is also planning for an end-of-Phase 2 meeting with the U.S. Food and Drug Administration (FDA) and plans to announce next steps for development in PNH in the first half of 2027;
    • Briquilimab, a late-stage, potentially best-in-class anti-KIT antibody with broad therapeutic utility across multiple transplant and immunologic indications. Based on positive, long-term data generated in SCID, the combined company is progressing its efforts towards a pre-BLA meeting with the FDA and expects to announce next steps in the first quarter of 2027; and
    • KP-701, a novel, dual-acting anti-CD79BxCD32B monoclonal antibody (mAb) for autoantibody-mediated disorders. The combined company expects to file a clinical trial application (CTA) and/or an investigational new drug (IND) for Phase 1 evaluation in the first quarter of 2027.

Second Quarter Fiscal 2026 Financial Results

  • Cash and cash equivalents as of June 30, 2026, totaled $7.3 million.
  • Research and development expense for the three months ended June 30, 2026, was $5.1 million.
  • General and administrative expense for the three months ended June 30, 2026, was $4.1 million.
  • Jasper reported a net loss of $2.8 million, or basic and diluted net loss per share attributable to common stockholders of $0.10 for the three months ended June 30, 2026.

About Jasper

The combined company is a clinical stage biotechnology company focused on the design and development of innovative therapies to treat immune-mediated diseases. The combined company is advancing a pipeline of medicines including KP-104, briquilimab, and KP-701. KP-104 is a potential best-in-class dual-complement inhibitor that has demonstrated positive outcomes in paroxysmal nocturnal hemoglobinuria (PNH) and is under evaluation in other high unmet need nephrology disorders. Briquilimab is an anti-KIT antibody which has demonstrated positive clinical results both as a conditioning agent for stem cell transplant and mast cell mediated diseases such as chronic urticarias and allergic asthma. KP-701, a novel, dual-acting anti-CD79BxCD32B monoclonal antibody (mAb) for autoantibody-mediated disorders currently advancing to the clinic.

Forward-Looking Statements
Certain statements contained in this press release are or may be considered “forward-looking statements” as defined in the Private Securities Litigation Reform Act of 1995. These statements can be identified by the fact that they do not relate strictly to historic or current facts. They use words such as “estimate,” “expect,” “intend,” “believe,” “plan,” “anticipate,” “potential,” “projected” and other words and terms of similar meaning in connection with any discussion of future operating or financial performance or condition. Jasper cautions that these statements are based upon the current beliefs and expectations of Jasper’s management and are subject to significant risks, uncertainties and assumptions, including, without limitation, risks related to the market price of Jasper’s common stock relative to the value suggested by the exchange ratio in connection with the merger; unexpected costs, charges or expenses resulting from the merger; potential adverse reactions or changes to business relationships resulting from the announcement or completion of the merger; the uncertainties associated with the Combined Company’s product candidates, as well as risks associated with the clinical development and regulatory approval of product candidates, including potential delays in the commencement, enrollment and completion of clinical trials; risks related to the inability of the Combined Company to obtain sufficient additional capital to continue to advance product candidates and its preclinical programs; uncertainties in obtaining successful clinical results for product candidates and unexpected costs that may result therefrom; risks related to the failure to realize any value from product candidates and preclinical programs being developed and anticipated to be developed in light of inherent risks and difficulties involved in successfully bringing product candidates to market; risks associated with the possible failure to realize certain anticipated benefits of the merger, including with respect to future financial and operating results; risks related to the integration of Kira and realization of anticipated benefits from the combination; the possibility that holders of CVRs may never receive any proceeds; risks related to the possibility that Jasper’s shareholders may not approve the conversion of the Preferred Stock and the consequences if such approval is not obtained, and such additional risks and uncertainties contained in the “Risk Factors” section of Jasper’s Annual Reports on Form 10-K for the year ended December 31, 2025, Quarterly Reports on Form 10-Q and Current Reports on Form 8-K that Jasper has subsequently filed or may subsequently file with the SEC. Statements regarding future actions, future performance and/or future results including, without limitation, those relating to the timing for completion, and results of, scheduled or additional clinical trials and the FDA’s or other regulatory review and/or approval and commercial launch and sales results (if any) of the Combined Company’s formulations and product candidates and regulatory filings related to the same, financial projections and targets, including, without limitation, cash runway, operating plans, future capital requirements and the sufficiency of existing cash resources, business strategy, plans and objectives for future operations, statements regarding the Combined Company and its operations and prospects, may not occur, and actual results could differ materially and adversely from those anticipated or implied in the forward-looking statements. In light of these risks, uncertainties and assumptions, the forward-looking events and circumstances discussed in this press release are inherently uncertain and may not occur, and actual results could differ materially and adversely from those anticipated or implied in the forward-looking statements. Accordingly, you should not rely upon forward-looking statements as predictions of future events. There is no obligation to update publicly or revise any forward-looking statements for any reason after the date of this press release or to conform these statements to actual results or to changes in the Combined Company’s expectations, whether as a result of new information, future events, inaccuracies that become apparent after the date hereof or otherwise, except as may be required under applicable securities laws.

Contacts:
Alex Gray (investors)
Jasper Therapeutics
650-549-1454 
agray@jaspertx.com

Argot Partners (investors and media)
kira@argotpartners.com 

 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, 2026 Six Months Ended June 30,
  2026
 2025
 2026
 2025
 Operating expenses       
 Research and development(1)$5,135  $21,196  $10,949  $37,353 
 General and administrative(1) 4,072   5,880   9,210   11,525 
 Total operating expenses 9,207   27,076   20,159   48,878 
 Loss from operations (9,207)  (27,076)  (20,159)  (48,878)
 Interest income 82   437   246   1,061 
 Change in fair value of warrant liability 3,980      13,620    
 Other income (expense), net 2,385   (84)  2,359   (147)
 Total other income, net 6,447   353   16,225   914 
 Net loss and comprehensive loss$(2,760) $(26,723) $(3,934) $(47,964)
 Net loss per share attributable to common stockholders, basic and diluted$(0.10) $(1.74) $(0.14) $(3.16)
 Weighted-average shares used in computing net loss per share attributable to common stockholders, basic and diluted 28,696,937   15,333,962   28,684,447   15,178,904 
         
         
 (1) Amounts include non-cash stock based compensation expense as follows (in thousands):    
         
  Three Months Ended June 30, 2026 Six Months Ended June 30,
  2026
 2025
 2026
 2025
         
 Research and development$185  $543  $406  $1,114 
 General and administrative 579   1,274   781   2,514 
 Total$764  $1,817  $1,187  $3,628 
         


 JASPER THERAPEUTICS, INC.
 CONDENSED CONSOLIDATED BALANCE SHEETS
 (in thousands)
 (unaudited)
     
  June 30, December 31,
 Assets2026
 2025
 Current assets:   
 Cash and cash equivalents$                      7,314  $                    28,692 
 Restricted cash, current                            417    -  
 Prepaid expenses and other current assets 3,840   5,953 
 Total current assets 11,571   34,645 
 Property and equipment, net 60   102 
 Operating lease right-of-use assets 128   502 
 Restricted cash, non-current -   417 
 Other non-current assets                              43                              113 
 Total assets$                    11,802  $                    35,779 
     
 Liabilities and Stockholders’ Equity    
 Current liabilities:   
 Accounts payable$                      2,778  $                      6,220 
 Current portion of operating lease liabilities   270     1,235 
 Accrued expenses and other current liabilities 4,797   5,745 
 Total current liabilities 7,845   13,200 
 Warrant liability   2,544     16,164 
 Other non-current liabilities -     2,264 
 Total liabilities 10,389   31,628 
     
 Stockholders’ equity:   
 Preferred stock   —     — 
 Common stock   3     3 
 Additional paid-in capital   322,014     320,818 
 Accumulated deficit   (320,604)    (316,670)
 Total stockholders’ equity   1,413     4,151 
 Total liabilities and stockholders’ equity$                    11,802  $                    35,779 

FAQ

What did Jasper Therapeutics (JSPR) report for its Q2 2026 net loss?

Jasper Therapeutics reported a Q2 2026 net loss of $2.8 million, or $0.10 per basic and diluted share. According to Jasper, this compares with a net loss of $26.7 million, or $1.74 per share, in the same quarter of 2025.

How much cash did Jasper Therapeutics (JSPR) have at June 30, 2026?

Jasper Therapeutics held $7.3 million in cash and cash equivalents as of June 30, 2026. According to Jasper, total current assets were $11.6 million, compared with $34.6 million at December 31, 2025, before the July 2026 PIPE financing closed.

What are the key clinical programs for Jasper Therapeutics (JSPR) after acquiring Kira Pharmaceuticals?

The combined company’s main programs are KP‑104, briquilimab, and KP‑701. According to Jasper, KP‑104 is Phase 2/3 ready, briquilimab is being advanced toward a pre‑BLA meeting, and KP‑701 is expected to enter Phase 1 evaluation in 2027.

When will Jasper Therapeutics (JSPR) release data from the KP-104 renal basket trial?

Interim data from Stage 1 of the KP‑104 Phase 2 basket trial in rare renal indications are expected in the fourth quarter of 2026. According to Jasper, the trial targets high unmet need nephrology disorders, complementing earlier positive data in treatment‑naïve PNH.

What are Jasper Therapeutics’ (JSPR) regulatory timelines for briquilimab and KP-701?

For briquilimab, Jasper is progressing toward a pre‑BLA meeting with the FDA and expects to announce next steps in Q1 2027. According to Jasper, KP‑701’s CTA/IND filing for Phase 1 evaluation is also targeted for Q1 2027.

How did Jasper Therapeutics’ (JSPR) operating expenses change in Q2 2026 versus Q2 2025?

Total operating expenses decreased to $9.2 million in Q2 2026 from $27.1 million in Q2 2025. According to Jasper, research and development expense was $5.1 million and general and administrative expense was $4.1 million in the 2026 quarter.

What does the $132 million PIPE financing mean for Jasper Therapeutics (JSPR) shareholders?

The PIPE raised approximately $132 million in gross proceeds through non‑voting convertible preferred stock. According to Jasper, this financing, alongside the Kira acquisition, is expected to fund planned operations into the second half of 2028, supporting advancement of its clinical pipeline.