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Scinai (NASDAQ: SCNI) posts Q1 2026 profit on Recipharm Israel gain

Filing Impact
(Neutral)
Filing Sentiment
(Neutral)
Form Type
6-K

Rhea-AI Filing Summary

Scinai Immunotherapeutics reported first quarter 2026 results and detailed a major expansion of its contract development and manufacturing (CDMO) platform. Revenue for the three months ended March 31, 2026 was $489 thousand, including about $200 thousand from the newly acquired Yavne facility.

Operating loss widened to $2.5 million as CDMO costs and reclassified expenses increased, but net income reached $3.6 million due mainly to a $6.2 million non-cash bargain purchase gain from acquiring Recipharm Israel. Total assets rose to $17.6 million, shareholders’ equity to $11.8 million, and cash, cash equivalents and restricted cash to $3.1 million as of March 31, 2026.

The Recipharm Israel deal added a second manufacturing site in Yavne, broadened capabilities across biologics, sterile injectables and small-molecule APIs, and consolidated CDMO activities under Scinai Biopharma Services. Management is pursuing non-dilutive grants to fund PC111 and NanoAb programs, while prioritizing a systemic IL-17 bispecific antibody as the lead NanoAb development path.

Positive

  • Balance sheet strengthened by acquisition: Recipharm Israel added approximately $6.2 million of net identifiable assets, increasing total assets to $17.6 million and shareholders’ equity to $11.8 million as of March 31, 2026.
  • Expanded CDMO footprint and capabilities: The acquisition created a two-site CDMO platform in Jerusalem and Yavne, covering biologics, sterile injectables and small-molecule API services under Scinai Biopharma Services.

Negative

  • None.

Insights

One-time bargain gain masks operating loss while CDMO platform scales.

Scinai transformed its balance sheet in Q1 2026 by acquiring Recipharm Israel. The transaction added net identifiable assets of about $6.2M, including $2.8M in cash and $3.6M of manufacturing infrastructure, and produced a non-cash bargain purchase gain.

Core operations remain loss-making, with revenue of $489k and an operating loss of $2.5M for the quarter. Cost of revenues jumped as CDMO activities expanded and certain employee and facility costs moved from R&D into cost of revenues, so period comparisons need caution.

Strategically, the combined Jerusalem and Yavne CDMO footprint and multiple FENG and Israel Innovation Authority grant applications could support growth with less dilution if approved. Actual impact will depend on execution of the Recipharm collaboration and future grant decisions expected in the second half of 2026.

Q1 2026 revenue $489 thousand For the three months ended March 31, 2026
Operating loss $2.5 million Operating loss for the three months ended March 31, 2026
Net income $3.6 million Net profit for the three months ended March 31, 2026
Bargain purchase gain $6.2 million Non-cash gain from Recipharm Israel acquisition in Q1 2026
Cash, cash equivalents and restricted cash $3.1 million As of March 31, 2026
Total assets $17.6 million As of March 31, 2026 after Recipharm Israel acquisition
Shareholders’ equity $11.8 million As of March 31, 2026
Net identifiable assets acquired $6.2 million Preliminary purchase price allocation for Recipharm Israel
CDMO financial
"a revenue-generating CDMO subsidiary, today reported financial results"
A contract development and manufacturing organization (CDMO) is a company that provides specialized services to help develop and produce pharmaceutical products for other businesses. Think of it as a contract factory that takes a company's recipe and makes the product on their behalf. For investors, CDMOs are important because they support the growth of pharmaceutical companies and can be key partners in bringing new medicines to market.
bargain purchase gain financial
"primarily reflecting a non-cash bargain purchase gain of $6.2 million"
A bargain purchase gain happens when a buyer acquires another company's assets for less than those assets' estimated fair value, producing an immediate accounting profit for the buyer. For investors, it matters because that one-time gain boosts the acquirer's reported earnings and can signal a very favorable deal — like finding a valuable item at a steep discount — but it may also prompt scrutiny about whether asset values or the deal terms were estimated correctly.
non-dilutive funding financial
"advanced multiple non-dilutive funding initiatives supporting the Company’s PC111"
Non-dilutive funding is money a company raises that does not require issuing new shares or reducing existing owners’ percentage ownership, such as grants, certain loans, contract revenue, or licensing deals. It matters to investors because it lets a company finance growth or research without shrinking shareholder stakes or changing control, much like topping up a car’s gas tank instead of selling part of the car to pay for the trip.
systemic IL-17 bispecific antibody medical
"Prioritized development of a systemic IL-17 bispecific antibody as the lead validation program"
FENG grant financial
"advanced through the initial stages of evaluation under separate Polish FENG grant applications"
SEPA financing agreement financial
"Shares issued for SEPA financing agreement"
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FAQ

How did Scinai Immunotherapeutics (SCNI) perform financially in Q1 2026?

Scinai reported Q1 2026 revenue of $489 thousand and an operating loss of $2.5 million. A non-cash bargain purchase gain of $6.2 million from acquiring Recipharm Israel turned results into net income of $3.6 million for the quarter.

What impact did the Recipharm Israel acquisition have on Scinai (SCNI)?

The Recipharm Israel acquisition added about $6.2 million of net identifiable assets, including $2.8 million in cash and $3.6 million in manufacturing infrastructure. It also provided a second CDMO site in Yavne and drove a $6.2 million bargain purchase gain.

How did Scinai’s balance sheet change as of March 31, 2026?

Total assets increased to $17.6 million and shareholders’ equity to $11.8 million as of March 31, 2026. Cash, cash equivalents and restricted cash rose to $3.1 million, up from $1.8 million at December 31, 2025, reflecting the Recipharm Israel transaction.

What are Scinai’s key non-dilutive funding initiatives in 2026?

Scinai advanced multiple FENG and Israel Innovation Authority grant applications supporting PC111, a systemic IL-17 bispecific NanoAb program, and CDMO expansion. Management noted that several grant decisions are expected in the second half of 2026, aiming to minimize shareholder dilution.

How is Scinai’s CDMO business evolving after the Recipharm deal?

Following the Recipharm Israel acquisition, Scinai consolidated CDMO activities under Scinai Biopharma Services with sites in Jerusalem and Yavne. The combined platform now offers biologics, sterile injectables and small-molecule API services, targeting broader revenue diversification and a more resilient operating model.

What are the main R&D priorities for Scinai Immunotherapeutics?

Scinai is advancing PC111, a monoclonal antibody for severe dermatological diseases, and prioritizing a systemic IL-17 bispecific antibody as the lead NanoAb program. The company also maintains collaborations with the Max Planck Society and University Medical Center Göttingen.

 

 

UNITED STATES

SECURITIES AND EXCHANGE COMMISSION

Washington, D.C. 20549

 

FORM 6-K

 

Report of Foreign Private Issuer Pursuant to Rule 13a-16 or 15d-16

Under the Securities Exchange Act of 1934

 

For the Month of June 2026

 

Commission File Number: 001-37353

 

SCINAI IMMUNOTHERAPEUTICS LTD.

(Translation of registrant’s name into English)

 

Jerusalem BioPark, 2nd Floor

Hadassah Ein Kerem Campus

Jerusalem, Israel

(Address of principal executive office)

 

Indicate by check mark whether the registrant files or will file annual reports under cover Form 20-F or Form 40-F.

 

Form 20-F ☒       Form 40-F ☐

 

 

 

 

 

 

Explanatory Note 

 

On June 10, 2026, Scinai Immunotherapeutics Ltd. issued a press release reporting first quarter 2026 financial results and providing corporate update highlighting expansion of CDMO platform and advancement of strategic growth initiatives.

 

A copy of the press release is furnished herewith as Exhibit 99.1.

 

This Report on Form 6-K is hereby incorporated by reference into the registrant’s Registration Statements on Form S-8 (File Nos. 333-291460, 333-271293 and 333-239344) and Form F-3 (File Nos. 333-295698, 333-274078 and 333-276767), to be a part thereof from the date on which this report is submitted, to the extent not superseded by documents or reports subsequently filed or furnished..

 

1

 

 

Exhibit Index

 

Exhibit No.   Description
99.1   Press release dated June 10, 2026.

 

2

 

 

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, thereunto duly authorized.

 

  Scinai Immunotherapeutics Ltd.
     
Date: June 15, 2026 By: /s/ Amir Reichman
    Amir Reichman
    Chief Executive Officer

 

3

 

Exhibit 99.1

 

Scinai Reports First Quarter 2026 Financial Results and Provides Corporate Update Highlighting Expansion of CDMO Platform and Advancement of Strategic Growth Initiatives

 

JERUSALEM, June 10, 2026 /PRNewswire/ – Scinai Immunotherapeutics Ltd. (Nasdaq: SCNI), (“Scinai” or the “Company”), a biopharmaceutical company combining innovative therapeutic development with a revenue-generating CDMO subsidiary, today reported financial results for the three months ended March 31, 2026 and provided a corporate update.

 

Corporate Highlights

 

Completed the acquisition of Recipharm Israel, expanding the Company’s CDMO platform through the addition of a second manufacturing site in Yavne, Israel, and establishing a strategic commercial collaboration with global CDMO leader Recipharm AB.
   
 Advanced multiple non-dilutive funding initiatives supporting the Company’s PC111 and NanoAb development programs.
   
 Prioritized development of a systemic IL-17 bispecific antibody as the lead validation program for the Company’s NanoAb platform.
   
 Continued strategic collaboration activities with the Max Planck Society and University Medical Center Göttingen.

 

Amir Reichman, Chief Executive Officer of Scinai, commented:

 

“The first quarter of 2026 marked an important milestone in Scinai’s evolution. Through the acquisition of Recipharm Israel and the subsequent consolidation of our CDMO activities under Scinai Biopharma Services, we have expanded our operational footprint, manufacturing capabilities and commercial reach.

 

Scinai today consists of two complementary businesses: a focused immunology R&D organization advancing innovative therapeutic programs and Scinai Biopharma Services, our wholly owned CDMO subsidiary. We believe this structure provides multiple avenues for value creation, including CDMO growth, strategic partnerships, non-dilutive grant funding and advancement of innovative therapeutic programs.

 

During the quarter, we strengthened our balance sheet through the Recipharm transaction, advanced multiple grant applications and refined our R&D strategy around programs that we believe offer the strongest scientific, commercial and partnering potential.

 

As we move forward, our priorities remain clear: grow our CDMO business, secure non-dilutive funding, advance PC111 and our NanoAb platform, and continue building a capital-efficient biotechnology company capable of creating sustainable long-term shareholder value.”

 

Financial Results for the First Quarter of 2026

 

Revenues for the three months ended March 31, 2026 were $489 thousand, compared to $586 thousand for the three months ended March 31, 2025. Revenue for the quarter included approximately $200 thousand generated by the Yavne facility following completion of the Recipharm Israel acquisition.
   
Cost of revenues increased to $1.6 million from $0.4 million in the comparable prior-year period. The increase primarily reflected growth of the Company’s CDMO operations and implementation of a revised cost allocation methodology under which certain employee and facility costs previously classified as research and development expenses are now allocated to cost of revenues. Accordingly, cost of revenues and R&D expenses are not directly comparable between periods.

 

 

 

 

Research and development expenses were $0.6 million, compared to $1.3 million in the prior-year period. The decrease primarily reflects the revised cost allocation methodology referred to above and does not represent a corresponding reduction in R&D activities.
   
Marketing, general and administrative expenses were $0.7 million, compared to $0.5 million in the prior-year period primarily reflecting the expansion of the Company’s operations following the Recipharm Israel acquisition.
   
Operating loss was $2.5 million, compared to $1.6 million in the prior-year period. The increase primarily reflects increased expenses resulting from the expansion of the Company’s CDMO activities, including the acquisition of the Yavne facility, as well as changes in cost allocation methodology that affect period-to-period comparability.
   
Net income was $3.6 million, compared to a net loss of $1.6 million in the prior-year period, primarily reflecting a non-cash bargain purchase gain of $6.2 million associated with the acquisition of Recipharm Israel.
   
Cash, cash equivalents and restricted cash totaled $3.1 million as of March 31, 2026, compared to $1.8 million as of December 31, 2025. Total assets increased to $17.6 million and shareholders’ equity increased to $11.8 million.

 

Operational Update

 

Expansion of CDMO Platform

 

During the quarter, Scinai completed the acquisition of Recipharm Israel and entered into a strategic commercial collaboration agreement with Recipharm AB. The Company subsequently consolidated its CDMO activities, assets and employees under Scinai Biopharma Services Ltd.

 

Through the commercial collaboration, Scinai seeks to leverage Recipharm’s global network and commercial reach while providing customers with development and manufacturing solutions spanning early-stage development through commercial-scale manufacturing. The acquisition added a second manufacturing and development site in Yavne, Israel, complementing the Company’s existing biologics-focused facility in Jerusalem. The combined platform now offers customers broader capabilities spanning biologics, sterile injectable products and small-molecule API development and manufacturing services. Based on the preliminary purchase price allocation, the acquisition added approximately $6.2 million of net identifiable assets to the Company’s balance sheet, including approximately $2.8 million of cash and $3.6 million of manufacturing infrastructure and equipment.

 

The acquisition also expanded the Company’s commercial opportunity pipeline by broadening the range of development and manufacturing services available to customers and adding an established portfolio of active projects and customer relationships. Management believes the combined Jerusalem and Yavne platform provides greater revenue diversification and a more resilient operating model, while enabling more efficient utilization of shared corporate resources and infrastructure across both sites.

 

2

 

 

Non-Dilutive Funding Strategy

 

Scinai continues to pursue a capital-efficient development strategy centered on non-dilutive funding opportunities. During the quarter and subsequent period, the Company advanced multiple grant applications supporting both its therapeutic pipeline and its CDMO expansion initiatives.

 

The Company’s PC111 program and systemic IL-17 bispecific NanoAb program successfully advanced through the initial stages of evaluation under separate Polish FENG grant applications. In addition, the Company’s local intradermal IL-17 NanoAb program advanced to the final interview stage of the FENG review process, with a professional examiner evaluation meeting scheduled for June 16, 2026.

 

Scinai has also entered the formal review process for an Israel Innovation Authority grant application supporting development of the systemic IL-17 bispecific NanoAb program and is preparing an additional Israel Innovation Authority application supporting expansion of its CDMO platform through installation of GMP lyophilization capabilities.

 

Management expects several grant decisions during the second half of 2026. These initiatives reflect the Company’s strategy of pursuing multiple non-dilutive funding opportunities across its R&D and CDMO businesses in order to support future growth while minimizing shareholder dilution.

 

R&D Update

 

PC111

 

Scinai continues to advance PC111, a fully human monoclonal antibody targeting soluble Fas Ligand for the treatment of severe dermatological conditions including pemphigus and Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis (SJS/TEN). The Company submitted a revised FENG grant application supporting development of the program and extended its option agreement with PinCell through August 2026.

 

NanoAb Platform

 

Following scientific, commercial and regulatory evaluation of multiple development paths, Scinai has prioritized development of a systemic IL-17 bispecific antibody program as the primary validation program for its NanoAb platform. Management believes this program offers an attractive combination of commercial opportunity, differentiated scientific profile, partner interest and a more conventional development pathway than certain alternative NanoAb delivery strategies. The Company also continues its collaboration with the Max Planck Society and University Medical Center Göttingen and is engaged in discussions regarding expansion and amendment of existing license arrangements.

 

Outlook

 

Management remains focused on expanding CDMO revenues and customer relationships, integrating and optimizing the expanded CDMO platform, securing non-dilutive grant funding, advancing PC111 and the IL-17 bispecific NanoAb program, pursuing strategic partnering opportunities and maintaining disciplined capital allocation

 

3

 

 

About Scinai Immunotherapeutics

 

Scinai Immunotherapeutics Ltd. (NASDAQ: SCNI) is a biopharmaceutical company focused on the development of innovative immunology therapies. The Company is advancing a pipeline of therapeutic candidates licensed from the Max Planck Society and from PinCell S.r.l.

 

Scinai also owns Scinai Biopharma Services Ltd., a contract development and manufacturing organization (CDMO), providing development and manufacturing services to biotechnology and pharmaceutical companies through facilities in Jerusalem and Yavne, Israel.

 

For more information, please visit: www.scinai.com

 

Company Contacts

 

Business Development | +972 8 930 2529 | bd@scinai.com

Investor Relations – Allele Capital Partners | +1 978 857 5075 | aeriksen@allelecapital.com

 

Forward-Looking Statements

 

This press release contains forward-looking statements within the meaning of the U.S. Private Securities Litigation Reform Act of 1995 and other applicable securities laws. Forward-looking statements include, among other things, statements regarding the Company’s CDMO growth strategy; expansion of operational capabilities; integration of the Yavne facility into Scinai Biopharma Services’ CDMO platform; execution of commercial collaboration activities with Recipharm AB; purchase price allocation resulting from the acquisition of Recipharm Israel; advancement of the Company’s PC111 and NanoAb development programs; development of the systemic IL-17 bispecific antibody program; grant applications and potential non-dilutive funding opportunities; strategic collaborations with the Max Planck Society and University Medical Center Göttingen; future business development and partnering opportunities; and the Company’s ability to create long-term shareholder value.

 

These statements are based on current expectations and assumptions and are subject to risks and uncertainties that could cause actual results to differ materially from those expressed or implied by such statements. These risks and uncertainties include, without limitation, risks related to the Company’s ability to execute its operational and strategic plans; successfully integrate acquired operations; expand its CDMO activities and benefit from the commercial collaboration agreement with Recipharm AB; changes in the purchase price allocation resulting from the acquisition of Recipharm Israel; attract and retain customers, collaborators and partners; advance its product candidates through development; obtain regulatory approvals; ability secure sufficient financing or non-dilutive funding, including through grant applications; successfully execute commercial collaboration activities; realize anticipated benefits from strategic transactions and collaborations; and general market, industry, regulatory, geopolitical and economic conditions. More detailed information regarding these and other risks and uncertainties is included in the Company’s filings with the U.S. Securities and Exchange Commission.

 

Forward-looking statements speak only as of the date of this press release. Except as required by applicable law, the Company undertakes no obligation to update or revise any forward-looking statements, whether as a result of new information, future events or otherwise.

 

4

 

 

SCINAI IMMUNOTHERAPEUTICS LTD.

 

CONDENSED CONSOLIDATED FINANCIAL STATEMENTS

 

March 31, 2026

Unaudited

 

CONDENSED CONSOLIDATED BALANCE SHEETS

U.S. dollars in thousands

 

   March 31,   December 31, 
   2026   2025 
   Unaudited   Audited 
ASSETS        
         
CURRENT ASSETS:        
Cash and cash equivalents  $2,963   $1,661 
Restricted cash   151    150 
Prepaid expenses and other receivables   350    170 
Trade receivables   150    73 
           
Total current assets   3,614    2,054 
           
NON-CURRENT ASSETS:          
Property, plant and equipment, net   10,988    7,793 
Operating lease right-of-use assets   2,986    1,779 
           
Total non-current assets   13,974    9,572 
           
Total assets  $17,588   $11,626 

 

The accompanying notes are an integral part of the condensed consolidated financial statements. 

 

5

 

 

SCINAI IMMUNOTHERAPEUTICS LTD

 

CONDENSED CONSOLIDATED BALANCE SHEETS

U.S. dollars in thousands (except share data)

 

   March 31,   December 31, 
   2026   2025 
   Unaudited   Audited 
LIABILITIES NET OF CAPITAL DEFICIENCY        
         
CURRENT LIABILITIES:        
Trade payables  $779   $407 
Operating lease liabilities   354    329 
Other payables   1,552    849 
           
Total current liabilities   2,685    1,585 
           
NON-CURRENT LIABILITIES:          
Loan from others   287    294 
Non-current operating lease liabilities   2,855    1,644 
           
Total non-current liabilities   3,142    1,938 
           
CONTINGENT LIABILITIES AND COMMITMENTS          
           
SHAREHOLDERS’ EQUITY:          
Ordinary shares of no par value: Authorized: 100,000,000,000 shares at March 31, 2026 and at December 31, 2025; Issued and outstanding 14,141,955,584, shares at March 31, 20261 and 13,872,899,584 shares at December 31, 2025   -    - 
Preferred shares, no par value; Authorized: 1,000 shares at March 31, 2026 and 1,000 shares at December 31, 2025 (redemption amount of $34,000); Issued and outstanding: 1,000 shares at March 31, 2026 and 1,000 shares at December 31, 2025.   5,627    5,627 
Additional paid-in capital   130,143    130,062 
Accumulated deficit   (122,269)   (125,846)
Accumulated other comprehensive loss   1,740)   (1,740)
           
Total shareholders’ equity   11,761    8,103 
           
Total liabilities and shareholders’ equity  $17,588   $11,626 

 

 
1As of June 10, 2026, the number of ordinary shares outstanding was 20,677,532,000 (representing 5,169,383 American Depositary Shares). [Note: This footnote did not appear in the financial tables attached to the press release issued on June 10, 2026.]

 

6

 

 

SCINAI IMMUNOTHERAPEUTICS LTD

 

CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS

U.S. dollars in thousands (except share data)

 

   For the three months ended
March 31,
 
   2026   2025 
   Unaudited   Unaudited 
         
Revenues   489    586 
Cost of revenues  $(1,607)  $(358)
Gross profit (loss)   (1,118)   228 
           
Research and development expenses, net   (628)   (1,295)
Marketing, general, and administrative expenses   (721)   (501)
Total operating expenses   (1,349)   (1,796)
           
Total operating profit (loss)   (2,467)   (1,568)
           
Gain from bargain purchase   6,156      
           
Total Financial Income ( Expenses)  net,   (112)   11 
           
Net profit (loss)  $3,577   $(1,557)
           
Weighted average number of shares used in computing net loss per share attributable to ordinary shareholders, basic and diluted   15,146,206,517    7,718,499,584 

 

7

 

 

SCINAI IMMUNOTHERAPEUTICS LTD

 

CONDENSED CONSOLIDATED STATEMENTS OF CHANGES IN SHAREHOLDERS’ EQUITY

U.S. dollars in thousands (except share data)

 

   Ordinary shares   Preferred shares   Additional
paid-in
   Accumulated
comprehensive
   Accumulated
equity
   Total
shareholders’
equity
 
   Number   Amount   Number   Amount   capital   loss   (deficit)   (deficit) 
Balance as of January 1, 2026   13,872,899,584    -    1,000   $5,627    130,062    (1,740)   (125,846)   8,103 
Vested RSU’s   219,128,000    -    -    -    -    -         - 
Share-based compensation   -    -    -    -    70    -         70 
Issuance of ordinary shares   49,928,000    -    -    -    11    -         11 
Net profit (loss)   -    -    -    -    -    -    3,577    3,577 
Balance as of March 31, 2026   14,141,955,584    -    1,000    5,627    130,143    (1,740)   (122,269)   11,761 

 

*Ordinary shares have no par value

 

   Ordinary shares   Preferred shares   Additional
paid-in
   Accumulated
comprehensive
   Accumulated
equity
   Total
shareholders’
equity
 
   Number   Amount   Number   Amount   capital   loss   (deficit)   (deficit) 
Balance as of January 1, 2025   3,411,983,584         *    1,000   $5,627   $123,629   $      (1, 740)   $(117,539)  $9,977 
Vested RSU’s   22,628,000    -    -    -    -    -    -    - 
Exercise of warrants, net   322,944,000    -    -    -    -    -    -    - 
Issuance of ordinary shares, net of issuance costs of $100   242,120,000    -    -    -   $104    -    -   $104 
Net loss   -    -    -    -    -    -    (1,557)   (1,557)
Balance as of March 31, 2025   3,999,675,584    -    1,000   $5,627   $123,733   $(1,740)  $(119,096)  $8,524 

 

8

 

 

SCINAI IMMUNOTHERAPEUTICS LTD

 

CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS

U.S. dollars in thousands

 

   For the three months ended
March 31,
 
   2026   2025 
         
Cash flows from operating activities:        
         
Net gain (loss)  $3,577   $(1,557)
           
Adjustments to reconcile net loss to net cash used in operating activities:          
           
Depreciation of property, plant and equipment   453    351 
Financial expense (income) related to loan from others   (6)   10 
Share-based compensation   70    - 
Decrease (increase)  in trade receivables   53    (104)
Gain from bargain purchase   (6,156)   - 
Decrease (increase) in other receivables   (22)   47 
Changes in operating lease right-of-use assets   106    70 
Increase in trade payables   199    169 
Changes in operating lease liabilities   (78)   (84)
Increase (decrease) in other payables   348    57 
           
Net cash used in operating activities   (1,456)   (1,041)
           
Cash flows from investing activities:          
           
Purchase of property, plant and equipment   (3)   (9)
Cash acquired in business combination   2,751    - 
           
Net cash used in investing activities  $2,748   $(9)

 

9

 

 

SCINAI IMMUNOTHERAPEUTICS LTD

 

CONDENSED CONSOLIDATED STATEMENTS OF CASH FLOWS

U.S. dollars in thousands

 

   For the three months ended
March 31,
 
   2026   2025 
Cash flows from financing activities:          
           
Proceeds from issuance of ordinary shares for SEPA holders, net   11    104 
Proceed from exercise of warrants, net  $        
           
Net cash provided by financing activities   11    104 
           
Effect of exchange rate changes on cash, cash equivalents and restricted cash   -    - 
           
Increase (decrease) in cash, cash equivalents and restricted cash   1,303    (946)
Cash, cash equivalents and restricted cash at beginning of period   1,811    2,095 
           
Cash, cash equivalents and restricted cash at end of period  $3,114    1,149 
           
Supplementary disclosure of cash flows activities:          
(1) Cash paid during the period for:          
Interest  $-    - 
           
(2) Non-cash transactions:          
Shares issued for SEPA financing agreement  $6    - 
Loan convert into preferred shares          
Exercise of warrants liability into shares  $6    - 
           
Reconciliation of cash, cash equivalents and restricted cash:          
           
Cash and cash equivalents  $2,963    1,018 
Restricted cash   151    131 
           
Cash, cash equivalents and restricted cash  $3,114    1,149 

 

10

 

 

The preliminary allocation of the purchase price is summarized below (in thousands of U.S. dollars):

 

Cash and cash equivalents   2,751 
Trade receivables   130 
Other receivables   158 
Property and equipment   3,645 
Operating lease right-of-use assets   1,314 
Trade payables   (173)
Other payables   (355)
Operating lease liabilities   (1,314)
Net identifiable assets acquired   6,156 

 

As the consideration transferred was nominal (€1), substantially all of the fair value of the net identifiable assets acquired resulted in a gain from bargain purchase of approximately $6.1 million.

 

11

 

Filing Exhibits & Attachments

1 document