STOCK TITAN

Jasper Therapeutics Announces Merger with Kira Pharmaceuticals

(Very High)
(Very Positive)

Jasper Therapeutics (Nasdaq: JSPR) has completed an all-stock acquisition of Kira Pharmaceuticals, creating a combined company focused on biologic therapies for immunologically-driven disorders. Concurrently, Jasper entered a private placement of non-voting convertible preferred stock expected to raise approximately $132 million, led by specialist life sciences investors, to fund the consolidated pipeline.

The portfolio centers on KP-104 for paroxysmal nocturnal hemoglobinuria and rare renal disorders, briquilimab for transplant and immunologic indications including SCID, and preclinical KP-701 for autoantibody-mediated diseases. Kira also out-licensed KP-301 and KP-402 to Mirador Therapeutics for a $12 million upfront payment plus potential milestones. According to Jasper Therapeutics, pro-forma cash, including the placement and out-licensing proceeds, is expected to fund operations and multiple clinical milestones through the second half of 2028, while the combined company continues to trade under the ticker JSPR.

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

Positive

  • $132 million gross proceeds from private placement to fund development
  • $12 million upfront from KP-301/KP-402 out-licensing to Mirador Therapeutics
  • Cash runway expected to extend through second half of 2028
  • Multiple defined KP-104 Phase 2 readouts planned between Q4 2026–Q2 2027
  • Briquilimab progressing toward FDA pre-BLA meeting with next steps by Q1 2027
  • KP-701 CTA/IND filing targeted for Q1 2027 and first-in-human data in Q3 2027

Negative

  • All-stock acquisition of Kira implies equity dilution for existing JSPR shareholders
  • Private placement of non-voting convertible preferred stock may create future share dilution

Market Context

Set against JSPR’s tendency to trade lower on past announcements, a balanced reaction to this acquis...
Analysis

Set against JSPR’s tendency to trade lower on past announcements, a balanced reaction to this acquisition and financing would suggest investors are weighing the extended runway into the second half of 2028 against execution and integration risks, with low short interest limiting squeeze-driven volatility.

Key Figures

Private placement proceeds: $132 million Out-licensing upfront payment: $12 million Cash runway: through second half of 2028 +5 more
8 metrics
Private placement proceeds $132 million Gross proceeds from non-voting convertible preferred stock private placement
Out-licensing upfront payment $12 million Upfront payment from Mirador Therapeutics for KP-301 and KP-402
Cash runway through second half of 2028 Pro-forma funding horizon including private placement and out-licensing proceeds
KP-104 interim data Q4 2026 Stage 1 interim data from Phase 2 basket trial in rare renal indications
KP-104 data update Q2 2027 Updated data from Stage 1 of Phase 2 basket trial
KP-104 Stage 2 interim Q2 2027 Interim data from Stage 2 of Phase 2 basket study
KP-701 first-in-human data Q3 2027 Planned initial clinical data from Phase 1 testing
KP-701 CTA/IND filing Q1 2027 Expected submission for Phase 1 clinical testing

Historical Context

4 past events · Latest: Jun 01 (Negative)
Pattern 4 events
Date Event Sentiment 24h Move Catalyst
Jun 01 Strategic alternatives review Negative -35.6% Board initiated review of strategic alternatives including potential sale or wind-down.
May 14 Q1 2026 earnings Negative -11.4% Reported low cash balance and quarterly net loss alongside briquilimab update.
Mar 30 Q4 2025 earnings Negative -2.6% Year-end losses and commentary that further trial progress depends on capital.
Feb 24 Conference participation Neutral +1.4% Announcement of management presentation at TD Cowen healthcare conference.

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

Pattern Detected

Recent JSPR headlines, especially around strategic reviews and earnings, have generally been followed by share price declines.

Key Terms

all-stock transaction, private placement, monoclonal antibody, biologics license application, +2 more
6 terms
all-stock transaction financial
"completed the acquisition of Kira Pharmaceuticals ... in an all-stock transaction"
An all-stock transaction is a deal where one company acquires another using only its own shares instead of cash or other assets. For investors, this means exchanging ownership stakes rather than cash, which can affect the value and control of the companies involved. It often signals a focus on growth and can influence the stock prices of both companies.
private placement financial
"Preferred Stock in a private placement transaction co-led by Affinity Asset Advisors"
A private placement is a sale of securities directly to a selected group of investors, typically institutions or accredited investors, instead of through a public offering. It lets a company raise money faster and with fewer regulatory steps; for existing shareholders it matters because the newly issued shares, often sold at a discount, increase the share count and can dilute their ownership.
monoclonal antibody medical
"KP-301, a long-acting anti-C5a monoclonal antibody, and KP-402"
A monoclonal antibody is a laboratory-made protein designed to recognize and attach to a specific target in the body, such as a disease-causing substance or cell. It functions like a highly precise lock-and-key tool, helping to treat or detect illnesses. For investors, companies developing monoclonal antibodies can represent promising opportunities in the healthcare sector, especially as these treatments often address unmet medical needs.
biologics license application regulatory
"towards a pre-Biologics License Application (BLA) meeting with the FDA"
A biologics license application is a formal request submitted to regulatory authorities seeking approval to market a new biological medicine, such as vaccines or treatments made from living organisms. It is a comprehensive review process that evaluates the safety, effectiveness, and manufacturing quality of the product. For investors, receiving approval signals that a biological therapy can be sold to the public, potentially leading to revenue growth and market success.
investigational new drug regulatory
"expects to file a clinical trial application (CTA) or an investigational new drug (IND)"
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
"expects to file a clinical trial application (CTA) 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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Combined company positioned to advance portfolio of biologic agents designed to improve outcomes in patients with numerous immunologically-driven disorders 

Concurrent $132 million private investment with participation from leading life sciences investors and Mirador Therapeutics

Kira out-licenses KP-301, a long-acting anti-C5a monoclonal antibody, and KP-402, a small molecule C5a receptor antagonist, to Mirador Therapeutics, for $12 million upon signing and potential development and sales milestone payments

Combined financing and transactions expected to fund combined company operations through the second half of 2028, including multiple clinical milestones

REDWOOD CITY, Calif. and CAMBRIDGE, Mass., July 16, 2026 (GLOBE NEWSWIRE) -- Jasper Therapeutics, Inc. (Nasdaq: JSPR) (“Jasper” or the “Company”), today announced that Jasper has 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 (together, the “Combined Company”). Concurrent 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 transaction co-led by Affinity Asset Advisors, LLC and Ikarian Capital LLC with participation from Columbia Threadneedle Investments, Sirenia Capital Management LP, Brahma Capital, Balyasny Asset Management, SilverArc Capital, Squadron Capital Management, Nazare Partners LP, and Mirador Therapeutics as well as other leading life sciences investors and certain members of Kira management. The private placement is expected to result in total gross proceeds of approximately $132 million. The proceeds from the private placement will be used to fund development of the Combined Company’s pipeline through the second half of 2028. The Combined Company will focus on advancing a consolidated pipeline of potential best-in-class innovative therapies for immunologically-driven disorders, including KP-104, a potential best-in-class dual-complement inhibitor for the treatment of paroxysmal nocturnal hemoglobinuria (PNH) and high unmet need nephrology disorders, briquilimab, an anti-KIT antibody with broad therapeutic utility across multiple transplant and immunologic indications, and KP-701, a novel, dual-acting anti-CD79BxCD32B monoclonal antibody (mAb) for autoantibody-mediated disorders. The Combined Company will continue to trade on Nasdaq under the ticker symbol “JSPR.”

The Combined Company’s cash and cash equivalents balance at closing, including the proceeds from the private placement and out-licensing transaction, but excluding any milestone payments, is anticipated to fund the Combined Company’s operations through the second half of 2028 and provide runway through key clinical milestones, including KP-104 Phase 2 results in potential renal disorders, an end-of-Phase 2 meeting with the U.S. Food and Drug Administration (FDA) to support the potential initiation of a Phase 3 study evaluating KP-104 for PNH, the advancement of briquilimab in Severe Combined Immunodeficiency (SCID) to a pre-Biologics License Application (BLA) meeting, and first-in-human data for KP-701.

“We are pleased to announce this transaction with Kira following a thorough evaluation of strategic alternatives. Kira has built a truly differentiated complement portfolio that includes dual MOA beyond single-pathway agents and long-acting complement inhibitors, reflecting the quality of their science and the deep expertise of their team. We are excited by the robust pipeline that this transaction creates, and are looking forward to advancing these important medicines for patients,” said Jeet Mahal, President and Chief Executive Officer of Jasper.

“Today’s announcement marks a transformative step for the product candidates that Kira has developed. As we advance as part of Jasper, our mission is to develop biologic agents designed to improve outcomes in patients suffering from numerous immunologically-driven disorders. We will leverage the Combined Company’s management team with deep expertise in antibody drug development and support from leading life science investors,” said Patrick Crutcher, MSc, formerly the Chairman of the Board of Kira. “In conjunction, the out-licensing of KP-301 and KP-402 to Mirador and their highly experienced team allows for the Combined Company to rapidly accelerate its potentially best-in-class portfolio toward significant value creating milestones, while also allowing for the development of these potentially best-in-class assets. With this strengthened foundation, and the synergies between our team and the Jasper team, we believe the Combined Company is exceptionally well-positioned to progress our portfolio of biologic agents targeting high-value immunology targets. We are now focused on executing on multiple upcoming clinical milestones that have the potential to impact patients in need of better therapeutic options.”

Transaction Highlights:

  • Consolidated innovative pipeline of high-value immunology targets: The Combined Company plans to advance a consolidated pipeline across 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
      • The Combined Company expects to report interim data from Stage 1 of the ongoing Phase 2 basket trial in rare renal indications in the fourth quarter of 2026, and updated data in the second quarter of 2027. Additionally, the Combined Company plans to report interim data from Stage 2 of the study in the second quarter of 2027.
      • Based on previous, positive data in treatment-naïve PNH, the Combined Company is planning for an end-of-Phase 2 meeting with the FDA and plans to announce next steps in the first half of 2027.
      • By the end of the year, the Combined Company anticipates that it will announce a new indication for KP-104.
    • Briquilimab: a late-stage, potentially best-in-class anti-KIT antibody
      • Following positive, long-term data 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.
      • The Combined Company also continues to assess the mast-cell mediated disease landscape and will provide an update on its anticipated clinical development in the second half of this year.
    • KP-701: a preclinical, B-cell receptor targeted therapy
      • In the first quarter of 2027, the Combined Company expects to file a clinical trial application (CTA) or an investigational new drug (IND) for Phase 1 testing and plans to report first in human data in the third quarter of 2027.
  • KP-301 and KP-402 out-licensing deal: Kira has out-licensed KP-301, a long-acting anti-C5a monoclonal antibody, and KP-402, a small molecule C5a receptor antagonist to Mirador Therapeutics. This transaction will provide a $12 million upfront payment and potential development and sales milestone payments. Mirador brings deep experience across drug development and translational immunology that supports the advancement of these potential best-in-class molecules. Out-licensing these assets allows the Combined Company to focus its resources on its current portfolio of high-value immunology targets.
  • Management and Organization: The Combined Company will be comprised of a highly experienced team, including:
    • Jeet Mahal, President and Chief Executive Officer;
    • Herb Cross, Chief Financial Officer;
    • Greg Keenan, M.D., Chief Medical Officer;
    • Matthew E. Ros, Chief Operating Officer;
    • Wenru Song, M.D., Ph.D., Executive Vice President and Head of R&D;
    • In conjunction with the transaction, the Board of Directors of the Combined Company will be comprised of Patrick Crutcher, MSc, Jeet Mahal, Thomas Wiggans, Judith Shizuru, M.D., Ph.D., Svetlana Lucas, Ph.D., and Kurt von Emster.
  • Cash Runway: Pro-forma cash for the Combined Company is expected to fund operations of the Combined Company, as currently intended to be carried out, through multiple anticipated clinical milestones through the second half of 2028.

About the Transaction

The acquisition of Kira was structured as a stock-for-stock transaction whereby all of Kira’s outstanding equity interests were exchanged for a combination of shares of Jasper common stock and Preferred Stock. Subject to approval by Jasper’s stockholders in accordance with Nasdaq listing rules, each share of Preferred Stock will automatically convert into 61 shares of Jasper common stock, subject to certain beneficial ownership limitations. Concurrently with the acquisition of Kira, Jasper entered into a securities purchase agreement pursuant to which Jasper agreed to sell approximately 4.7 million shares of Preferred Stock for an aggregate purchase price of approximately $132 million. The private placement is expected to close on July 20, 2026.

In connection with the acquisition of Kira, each holder of Jasper common stock as of immediately before the closing of the transaction will be entitled to a non-transferrable contingent value right (“CVR”). Holders of the CVR will be entitled to receive an aggregate of $30 million in payments related to Jasper obtaining a priority review voucher (“PRV”) by December 31, 2028 for briquilimab, provided that such payments shall only be due upon the monetization of the CVR or in the event of an acquisition of the Combined Company subsequent to the receipt of the PRV.

The acquisition was approved by the Board of Directors of Jasper and the Board of Directors and shareholders of Kira. The approval of Jasper’s stockholders is required, among other things, under the terms of the Preferred Stock in order for the Preferred Stock to be converted into shares of Jasper common stock, and Jasper is required to hold a stockholder meeting for such vote. As a result of the transactions, equityholders of Jasper immediately prior to the acquisition will own approximately 6.68% of Jasper’s common stock, equityholders of Kira immediately prior to the acquisition will own approximately 49.86% of Jasper’s common stock and investors in the private placement financing will own approximately 43.46% of Jasper’s common stock, in each case, calculated on a fully-diluted, as-converted-to-common-basis (and without giving effect to any beneficial ownership limitations), and based on the implied equity values of Jasper and Kira. On an as-converted basis and after accounting for these transactions, the total number of shares of Jasper common stock outstanding would be approximately 653.6 million immediately after the closing of the transactions.

This press release shall not constitute an offer to sell or a solicitation of an offer to buy any securities, nor shall there be any sale of these securities in any state or other jurisdiction in which such offer, solicitation or sale would be unlawful prior to the registration or qualification under the securities laws of any such state or other jurisdiction.

Advisors

Piper Sandler & Co. served as the exclusive financial advisor and DLA Piper LLP (US) served as legal counsel to Kira. H.C. Wainwright & Co. served as financial advisor and Paul Hastings LLP served as legal counsel to Jasper. Piper Sandler & Co. served as lead placement agent and LifeSci Capital LLC served as co-placement agent for the concurrent financing.

About Jasper

Jasper is a clinical-stage biotechnology company focused on the development of briquilimab, a targeted anti-KIT monoclonal antibody with a demonstrated safety and efficacy profile in patients and healthy volunteers in multiple chronic immunological and inflammatory diseases. Briquilimab is a targeted aglycosylated monoclonal antibody that blocks stem cell factor from binding to the KIT receptor, inhibiting an essential survival signal for mast cells and a maintenance signal for hematopoietic stem cells. KIT inhibition with briquilimab has demonstrated positive clinical outcomes both as a conditioning agent for stem cell transplant in SCID and Fanconi anemia, and via mast cell depletion in diseases such as chronic urticarias and allergic asthma. For more information, please visit us at www.jaspertx.com.

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 these 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; the risk that the private placement is not consummated; 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 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, 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.

For Investor Inquiries

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

Jasper Therapeutics

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

Media:
media@jaspertx.com  


FAQ

What did Jasper Therapeutics (JSPR) announce about its merger with Kira Pharmaceuticals on July 16, 2026?

Jasper Therapeutics announced completion of an all-stock acquisition of Kira Pharmaceuticals, forming a combined immunology-focused company. According to Jasper Therapeutics, the merged entity will advance KP-104, briquilimab and KP-701 across multiple immunologically-driven disorders while continuing to trade on Nasdaq under the ticker JSPR.

How much new capital will Jasper Therapeutics (JSPR) raise in the July 2026 private placement?

Jasper Therapeutics expects approximately $132 million in gross proceeds from a private placement of non-voting convertible preferred stock. According to Jasper Therapeutics, the financing is co-led by Affinity Asset Advisors and Ikarian Capital, with participation from several specialist life sciences investors.

What are the key terms of the KP-301 and KP-402 out-licensing deal mentioned by Jasper Therapeutics (JSPR)?

Kira, now part of Jasper, out-licensed KP-301 and KP-402 to Mirador Therapeutics for a $12 million upfront payment plus potential development and sales milestones. According to Jasper Therapeutics, this allows the combined company to focus resources on its core high-value immunology pipeline assets.

How long is Jasper Therapeutics’ (JSPR) cash runway expected to last after the Kira merger and financing?

Pro-forma cash is expected to fund operations through the second half of 2028. According to Jasper Therapeutics, this runway includes proceeds from the private placement and out-licensing transaction and is intended to cover multiple key clinical milestones across KP-104, briquilimab and KP-701.

What are the upcoming clinical milestones for KP-104 after the Jasper Therapeutics (JSPR) and Kira merger?

KP-104 has interim Phase 2 renal basket data expected in Q4 2026 and updated data in Q2 2027. According to Jasper Therapeutics, further Stage 2 data, an end-of-Phase 2 FDA meeting for PNH, and a new indication announcement are planned by 2027.

How will the Jasper Therapeutics (JSPR) and Kira merger affect briquilimab’s development timeline?

Following positive long-term SCID data, briquilimab is being advanced toward a pre-BLA FDA meeting. According to Jasper Therapeutics, the company expects to announce next steps in the first quarter of 2027 and provide a separate update on mast-cell disease plans in the second half of 2026.

What is KP-701 and when will Jasper Therapeutics (JSPR) start clinical trials?

KP-701 is a preclinical dual-acting anti-CD79BxCD32B monoclonal antibody for autoantibody-mediated disorders. According to Jasper Therapeutics, the combined company expects to file a CTA or IND in the first quarter of 2027 and report first-in-human Phase 1 data in the third quarter of 2027.