CalciMedica Reports Second Quarter 2025 Financial Results and Provides Clinical & Corporate Updates
Enrollment ongoing in Phase 2 KOURAGE trial of Auxora™ in acute kidney injury (AKI) with respiratory failure; data expected in early 2026
Productive initial meeting with the FDA on Auxora in acute pancreatitis (AP); conversations continue, with alignment on a pivotal trial anticipated around the end of 2025
Cash position expected to fund operations into mid-2026
"We have continued to spotlight the growing body of evidence supporting the development of Auxora for the treatment of AKI with respiratory failure, including publications in two peer-reviewed journals, multiple presentations at medical meetings, and a symposium at the 43rd Vicenza Course AKI-CRRT-EBPT and Critical Care Nephrology meeting. We look forward to the readout of our Phase 2 KOURAGE trial expected in early 2026," said Rachel Leheny, Ph.D., Chief Executive Officer of CalciMedica. "Additionally, we are encouraged by our initial meeting with the FDA regarding our program in AP. The meeting was constructive, and we are eager to continue our discussions with the agency, with the objective of reaching alignment on a pivotal trial around the end of 2025."
Recent Clinical & Corporate Highlights:
Clinical Updates & Anticipated Milestones
Acute Kidney Injury (AKI) with Respiratory Failure Program Update
- Enrollment ongoing in Phase 2 KOURAGE trial: Enrollment is ongoing in KOURAGE, the Company's randomized, double-blind, placebo-controlled Phase 2 trial of Auxora™ in patients with Stage 2 or Stage 3 AKI with associated respiratory failure.
CalciMedica plans to enroll 150 patients in KOURAGE, with data expected in early 2026. - Publication in the
American Journal of Nephrology (AJN): InJune 2025 ,CalciMedica announced a publication in AJN, titled, "Inhibition of Calcium Release-Activated Calcium (CRAC) Channels to Treat Acute Kidney Injury: Design and Rationale of the KOURAGE Study." The manuscript describes the preclinical and clinical evidence supporting Auxora as a potential treatment for AKI with respiratory failure, as well as the rationale for the patient selection and endpoint selection for the Company's Phase 2 KOURAGE trial. - "Auxora for the Treatment of AKI" Symposium: In
June 2025 , the Company presented a symposium titled "Auxora for the Treatment of AKI" at the 43rd Vicenza Course AKI-CRRT-EBPT and Critical Care Nephrology meeting. The symposium featured oral presentations delivered bySudarshan Hebbar , M.D., CMO ofCalciMedica ;Javier Neyra , M.D., Associate Professor of Medicine and Associate Director of theNephrology Research & Training Center atUniversity of Alabama at Birmingham ; andLakhmir Chawla , M.D., Clinical Professor of Medicine atUniversity of California San Diego , CMO atExThera Medical , and Chair of theKOURAGE Steering Committee . Webcasts of the presentations are available on the "Medical Events and Presentations" section ofCalciMedica's IR website. - Publication in the Thrombosis Update: In
July 2025 , a manuscript authored byCalciMedica and collaborators, titled, "Reduction in D-dimer Levels After Treatment with Auxora in Patients with Severe Covid-19 Pneumonia," was published in the Thrombosis Update. The manuscript highlights a biomarker analysis from patients treated with Auxora in the Company's previously completed Phase 2 CARDEA trial in severe COVID-19 pneumonia. In the analysis, Auxora was found to significantly decrease D-dimer levels and other biomarkers of systemic inflammation, with these decreases correlating with positive outcomes in patients. These findings showing Auxora's anti-inflammatory effects and endothelial stabilization support its continued development for the treatment of acute illnesses with a strong inflammatory component, such as AKI and AP. - Oral presentation and panel discussion at the
American Society of Nephrology (ASN) 3rd Acute Kidney Injury: From Bench toBedside Conference : InMay 2025 ,Dr. Hebbar delivered an oral presentation titled "Experiences with AKI Clinical Trial Design" and participated in a panel discussion at the ASN 3rd Acute Kidney Injury: From Bench toBedside Conference .
Acute Pancreatitis (AP) Program Update
- Conducted initial meeting with the
U.S. Food and Drug Administration (FDA) on next steps in AP program: The Company conducted a productive initial meeting with the FDA to present the findings from the Phase 2b CARPO trial and discuss the design of a pivotal trial in AP. Additional meetings with the FDA are anticipated in the second half of 2025, with alignment on trial design anticipated around the end of the year. This will be the first pivotal trial in theU.S. for a therapeutic in AP. - Poster presentation at Digestive Disease Week (DDW) 2025: In
May 2025 ,Kenneth A. Stauderman , Ph.D., co-Founder and CSO ofCalciMedica , presented a poster titled "Patients with Acute Pancreatitis (AP) and Accompanying Systemic Inflammatory Response Syndrome (SIRS) Have a Larger Volume of Distribution Compared toHealthy Volunteers " at DDW 2025.
Financial Results for the Second Quarter Ended
Cash Position: Cash, cash equivalents, and short-term investments were
R&D Expenses: Research and development expenses were
G&A Expenses: General and administrative expenses were
Other Income: Other income was
Net Loss: Net loss was
About
Forward-Looking Statements
This communication contains forward-looking statements which include, but are not limited to
Contact Information
calcimedica@argotpartners.com
(212) 600-1902
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Condensed Consolidated Balance Sheets (in thousands, except par value and share amounts) (Unaudited) |
||||
|
|
|
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Assets |
||||
|
Current assets |
||||
|
Cash and cash equivalents |
$ 5,918 |
$ 7,935 |
||
|
Short-term investments |
12,039 |
10,734 |
||
|
Prepaid clinical trial expenses |
352 |
748 |
||
|
Other prepaid expenses and current assets |
655 |
248 |
||
|
Total current assets |
18,964 |
19,665 |
||
|
Property and equipment, net |
105 |
119 |
||
|
Other assets |
11 |
10 |
||
|
Total assets |
$ 19,080 |
$ 19,794 |
||
|
Liabilities and Stockholders' Equity |
||||
|
Current liabilities |
||||
|
Accounts payable |
$ 1,912 |
$ 1,998 |
||
|
Accrued clinical trial costs |
670 |
820 |
||
|
Accrued expenses |
895 |
866 |
||
|
Total current liabilities |
3,477 |
3,684 |
||
|
Long-term liabilities |
||||
|
Promissory note |
8,500 |
— |
||
|
Warrant liability |
1,000 |
1,700 |
||
|
Total liabilities |
12,977 |
5,384 |
||
|
Commitments and contingencies (Note 8) |
||||
|
Stockholders' equity |
||||
|
Preferred stock, respectively; no shares issued and outstanding at |
— |
— |
||
|
Common stock, respectively; 13,971,990 and 13,481,917, issued and outstanding at |
4 |
4 |
||
|
Additional paid-in capital |
176,865 |
174,166 |
||
|
Accumulated deficit |
(170,762) |
(159,764) |
||
|
Accumulated other comprehensive (loss) income |
(4) |
4 |
||
|
Total stockholders' equity |
6,103 |
14,410 |
||
|
Total liabilities and stockholders' equity |
$ 19,080 |
$ 19,794 |
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|
Condensed Consolidated Statements of Operations (in thousands, except share and per share amounts) (Unaudited) |
||||||||
|
Three Months Ended |
Six Months Ended |
|||||||
|
2025 |
2024 |
2025 |
2024 |
|||||
|
Operating expenses: |
||||||||
|
Research and development |
$ 4,052 |
$ 4,157 |
$ 8,276 |
$ 7,101 |
||||
|
General and administrative |
2,569 |
2,372 |
4,842 |
5,195 |
||||
|
Total operating expenses |
6,621 |
6,529 |
13,118 |
12,296 |
||||
|
Loss from operations |
(6,621) |
(6,529) |
(13,118) |
(12,296) |
||||
|
Other income (expense): |
||||||||
|
Change in fair value of financial instruments |
500 |
2,300 |
2,200 |
7,890 |
||||
|
Interest expense |
(324) |
— |
(771) |
— |
||||
|
Interest income |
220 |
275 |
422 |
582 |
||||
|
Other income |
269 |
— |
269 |
— |
||||
|
Total other income |
665 |
2,575 |
2,120 |
8,472 |
||||
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Net loss |
$ (5,956) |
$ (3,954) |
$ (10,998) |
$ (3,824) |
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Net loss per share - basic and diluted |
$ (0.40) |
$ (0.36) |
$ (0.76) |
$ (0.37) |
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Weighted-average number of shares outstanding used in |
14,995,404 |
11,129,053 |
14,560,900 |
10,441,785 |
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