Scinai Reports Q1 2025 Financial Results Highlighting Strong CDMO Revenue Momentum and Reduced Cash Burn
- CDMO revenue growth with Q1 2025 revenue of $586k compared to full-year 2024 revenue of $658k
- Net loss reduced by 27.9% to $1,557k from $2,159k year-over-year
- R&D expenses decreased by 17.3% to $1,296k from $1,568k
- Financial position improved with net financial income of $11k versus expenses of $231k in Q1 2024
- Cash position declined 48.2% to $1,018k from $1,964k year-over-year
- Marketing and administrative expenses increased to $500k from $484k
- Company continues to operate at a significant net loss
Insights
Scinai shows promising CDMO revenue growth while reducing losses, but concerning cash position requires immediate attention.
Scinai's Q1 2025 results demonstrate encouraging momentum in their Contract Development and Manufacturing Organization (CDMO) business. The company generated
The company has made meaningful progress in reducing their net loss, which decreased from
- R&D expenses declined from
$1.57 million to$1.30 million - Financial expenses improved dramatically, shifting from a
$231,000 expense to$11,000 in income - Gross income recognition from their growing CDMO operations
The financial expense improvement resulted from converting their European Investment Bank loan to preferred shares in Q3 2024, eliminating interest expenses.
However, the cash position is concerning. Cash and short-term deposits stand at just
The company's dual business model—developing novel biological drug candidates while providing CDMO services—appears to be transitioning toward greater emphasis on the revenue-generating CDMO operations, which could eventually provide sustainable funding for their R&D pipeline.

Three (3) Months of 2025 Financial Summary
- Revenues for the three months ended March 31, 2025, totaled
. The Company's CDMO unit began generating revenues in the second quarter ended June 30, 2024. As disclosed in the Company's Annual Report on Form 20-F for the year ended December 31, 2024, filed with the SEC on May 7, 2025, CDMO revenues for the full year 2024 were$586 thousand . The year-over-year increase in revenues for the first quarter of 2025 reflects a higher number of contracts executed during the period, driven by continued growth in the CDMO business.$658 thousand - R&D expenses for the three months ended March 31, 2025, amounted to
, compared to$1,296 thousand for the same period in 2024. The decrease was primarily due to lower wages and reduced direct R&D expenses.$1,568 thousand - Marketing, general and administrative expenses for the three months ended March 31, 2025, amounted to
compared to$500 thousand for the three months ended March 31, 2024.$484 thousand - Financial income, net, for the three months ended March 31, 2025, amounted to
, compared to financial expenses of$11 thousand for the same period in 2024. The improvement was primarily due to the conversion of the EIB loan into preferred shares of the Company stock in the third quarter of 2024.$231 thousand - Net loss for the three months ended March 31, 2025, was
, compared to a net loss of$1,557 thousand for the three months ended March 31, 2024. The decrease was primarily due to lower R&D expenses, reduced financial expenses, and the recognition of gross income.$2,159 thousand
As of March 31, 2025, Scinai had cash and cash equivalents and short-term deposits of
About Scinai Immunotherapeutics
Scinai Immunotherapeutics Ltd. (NASDAQ: SCNI) is a biopharmaceutical company with two complementary business units, one focused on in-house development of inflammation and immunology (I&I) biological therapeutic products beginning with an innovative, de-risked pipeline of nanosized VHH antibodies (nanoAbs) targeting diseases with large unmet medical needs, and the other a boutique CDMO providing biological drug development, analytical methods development, clinical cGMP manufacturing, and pre-clinical and clinical trial design and execution services for early stage biotech drug development projects.
Company website: www.scinai.com.
Company Contacts
Investor Relations - Allele Capital Partners | +1 978 857 5075 | aeriksen@allelecapital.com
Business Development | +972 8 930 2529 | bd@scinai.com
Forward-Looking Statements
This press release contains forward-looking statements within the meaning of the Private Litigation Reform Act of 1995. Words such as "expect," "believe," "intend," "plan," "continue," "may," "will," "anticipate," and similar expressions are intended to identify forward-looking statements. All statements, other than statements of historical facts, are forward-looking statements. These forward-looking statements reflect management's current views with respect to certain current and future events and are subject to various risks, uncertainties and assumptions that could cause the results to differ materially from those expected by the management of Scinai Immunotherapeutics Ltd. Risks and uncertainties include, but are not limited to; the risk that the Company will otherwise be unable to remain compliant with the continued listing requirements of Nasdaq; lower than anticipated revenues of Scinai's CDMO business in 2025 and thereafter; failure to sign agreements with other potential clients of the CDMO business; a delay in the commencement and results of pre-clinical and clinical studies, including the Phase 1/2a study for psoriasis, the risk of delay in, Scinai's inability to conduct, or the unsuccessful results of, its research and development activities, including the contemplated in-vivo studies and a clinical trial; the risk that Scinai will not be successful in expanding its CDMO business or in-license other nanoAbs; the risk that Scinai may not be able to secure additional capital on attractive terms, if at all; the risk that the therapeutic and commercial potential of nanoAbs will not be met or that Scinai will not be successful in bringing the nanoAbs towards commercialization; the risk of a delay in the preclinical and clinical trials data for nanoAbs, if any; the risk that our business strategy may not be successful; Scinai's ability to acquire rights to additional product opportunities; Scinai's ability to enter into collaborations on terms acceptable to Scinai or at all; timing of receipt of regulatory approval of Scinai's manufacturing facility in
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