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CalciMedica Reports Second Quarter 2024 Financial Results and Provides Clinical & Corporate Updates Positive topline data announced from CARPO, Phase 2b trial of Auxora in acute pancreatitis (AP); additional data to be p

Key Takeaway: CalciMedica has reported positive topline data from its Phase 2b CARPO trial of Auxora in acute pancreatitis, meeting its primary objectives and setting the stage for future FDA discussions and a potential Phase 3 trial. The first patient has been enrolled in the KOURAGE trial for severe acute kidney injury, with topline data expected in 2025. Despite these advancements, the company reported financial losses of approximately $6.5 million for the quarter, and its future success relies on continued favorable outcomes from its clinical trials.

Market Sentiment Analysis

POSITIVE FACTORS

  • Positive topline data from Phase 2b CARPO trial of Auxora in acute pancreatitis, meeting primary objectives.
  • Enrollment of the first patient in the KOURAGE trial for severe acute kidney injury.
  • Expected to share additional data from the CARPO trial later this year.
  • Inclusion in the Russell Microcap Index, indicating positive recognition.

CONCERNS & RISKS

  • Financial losses reported for the second quarter of 2024.
  • Dependent on successful future trials for Auxora's market entry.

Full Press Release Details

CalciMedica Reports Second Quarter 2024 Financial Results and Provides Clinical & Corporate Updates
Positive topline data announced from CARPO, Phase 2b trial of Auxora in acute pancreatitis (AP); additional data to be presented at a medical meeting later this year
First patient enrolled in KOURAGE, Phase 2 trial of Auxora in severe acute kidney injury (AKI), with data expected in 2025
LA JOLLA, Calif., August 12, 2024 CalciMedica Inc. ( CalciMedica or the Company ) (Nasdaq: CALC), a clinical-stage biopharmaceutical company focused on developing novel calcium release-activated calcium (CRAC) channel inhibition therapies for acute and chronic inflammatory and immunologic illnesses, today reported financial results for the second quarter ended June 30, 2024.
CalciMedica continues to progress steadily with the successful execution of multiple milestones across our pipeline. In the second quarter, we completed enrollment in our Phase 2b CARPO trial in patients with AP and subsequently announced positive topline data, which met our primary objective and further support Auxora's potential as an effective treatment for critically ill patients with acute inflammatory disease. We look forward to sharing additional data from this trial later in the year and are also planning to meet with the FDA to discuss the design of a Phase 3 trial, said Rachel Leheny, Ph.D., Chief Executive Officer of CalciMedica. In addition, we are excited about KOURAGE, our Phase 2 trial in patients with severe AKI. We are enrolling patients and opening new sites and expect to share topline data from this study in 2025.
Recent Clinical Updates and Anticipated Milestones:
-Positive topline data announced from Phase 2b CARPO trial: In June 2024, CalciMedica hosted a conference call to review positive topline data from CARPO, the Company's randomized, double-blind, placebo-controlled Phase 2b trial of Auxora in patients with acute pancreatitis (AP) and accompanying systemic inflammatory response syndrome (SIRS). The trial met its primary objective with a statistically significant dose response in median time to solid food tolerance in a pre-specified subgroup of hyper-inflamed patients with AP as well as in reduction of severe organ failure across the full patient population. Full data from the trial are expected in the second half of 2024 and the Company plans to present them at future medical meetings. Further, the Company plans to discuss the full results with the U.S. Food and Drug Administration (FDA) in an end-of-phase 2 meeting and to be in a position to initiate a pivotal trial in AP in 2025.
-First patient enrolled in Phase 2 KOURAGE trial: In July 2024, CalciMedica announced that the first patient has been dosed in KOURAGE, the Company's randomized, double-blind, placebo-controlled Phase 2 trial of Auxora in patients with severe AKI with associated acute hypoxemic respiratory failure (AHRF). CalciMedica expects to enroll 150 patients with stage 2 and stage 3 AKI who have AHRF and are receiving oxygen either by non-invasive mechanical ventilation, high flow nasal cannula or intermittent mandatory ventilation. Topline data are expected in 2025.
-CalciMedica added to Russell Microcap Index: In July 2024, CalciMedica announced that the Company would be joining the Russell Microcap Index at the conclusion of the 2024 Russell U.S. Indexes annual reconstitution, which became effective at the open of U.S. equity markets on July 1, 2024.
-CRSPA study expanded and continuing to enroll in Phase 2 portion of trial: The CRSPA study in asparaginase-induced pancreatic toxicity (AIPT) has been expanded to additional sites as the dose used in the initial cohort has been established as the recommended Phase 2 dose. CalciMedica expects this trial to enroll approximately 24 patients and data are expected in 2025.
Financial Results for the Three and Six Months Ended June 30, 2024:
-As of June 30, 2024, CalciMedica had approximately $19.1 million in cash, cash equivalents and short-term investments, which, based on its current operating plan, CalciMedica expects to be sufficient to fund its operations into the second half of 2025.
-Total loss from operations for the three months ended June 30, 2024, was approximately $6.5 million. Total loss from operations for the six months ended June 30, 2024, was approximately $12.3 million.
-Including the impact of a $2.3 million non-cash gain from the fair value adjustment of the warrant liability and $0.3 million of interest income, the net loss for the three months ended June 30, 2024, was approximately $4.0 million, or $0.36 per share (basic and diluted). Including the impact of a $7.9 million non-cash gain from the fair value adjustment of the warrant liability and $0.6 million of interest income, net loss for the six months ended June 30, 2024, was $3.8 million, or $0.37 per share (basic and diluted).
CalciMedica is a clinical-stage biopharmaceutical company focused on developing novel CRAC channel inhibition therapies for inflammatory and immunologic diseases. CalciMedica's proprietary technology targets the inhibition of CRAC channels to modulate the immune response and protect against tissue cell injury, with the potential to provide therapeutic benefits in life-threatening inflammatory and immunologic diseases for which there are currently no approved therapies. CalciMedica's lead product candidate Auxora has demonstrated positive and consistent clinical results in multiple completed efficacy clinical trials. CalciMedica has announced topline data for a Phase 2b trial (called CARPO NCT04681066) in patients with AP with SIRS and completed a Phase 2 trial (called CARDEA NCT04345614) in patients with COVID pneumonia. The Company is currently conducting a Phase 2 trial (called KOURAGE NCT06374797) in patients with AKI with associated AHRF with data expected in 2025 and continuing to support the ongoing Phase 1/2 trial (called CRSPA NCT04195347) in patients with AIPT with data expected in 2025. CalciMedica was founded by scientists from Torrey Pines Therapeutics and
the Harvard CBR Institute for Biomedical Research, and is headquartered in La Jolla, CA. For more information, please visit www.calcimedica.com.
Forward-Looking Statements
This communication contains forward-looking statements which include, but are not limited to, CalciMedica's expected cash runway; CalciMedica's planned and ongoing clinical trials and the timing, design, expected patient enrollment thereof and the expected timing for the release of data from those trials, including its Phase 2b CARPO trial of Auxora for AP with accompanying SIRS, its Phase 2 KOURAGE trial of Auxora in AKI with associated AHRF, and its ongoing Phase 1/2 CRSPA trial of Auxora in pediatric patients with AIPT; plans for an end of phase 2 meeting with the FDA for CARPO and to be in a position to initiate a pivotal trial in AP in 2025; the potential benefits of Auxora for the treatment of AP, AKI and AIPT; and the potential of CalciMedica's proprietary technology to provide therapeutic benefits in life-threatening inflammatory and immunologic diseases. These forward-looking statements are subject to the safe harbor provisions under the Private Securities Litigation Reform Act of 1995. CalciMedica's expectations and beliefs regarding these matters may not materialize. Actual outcomes and results may differ materially from those contemplated by these forward-looking statements as a result of uncertainties, risks, and changes in circumstances, including but not limited to risks and uncertainties related to: the impact of fluctuations in global financial markets on CalciMedica's business and the actions it may take in response thereto; CalciMedica's ability to execute its plans and strategies; the ability to obtain and maintain regulatory approval for Auxora; results from clinical trials or preclinical studies may not be indicative of results that may be observed in the future; potential safety and other complications from Auxora; the scope, progress and expansion of developing and commercializing Auxora; the size and growth of the market therefor and the rate and degree of market acceptance thereof; economic, business, competitive, and/or regulatory factors affecting the business of CalciMedica generally; CalciMedica's ability to protect its intellectual property position; the impact of government laws and regulations; and CalciMedica's financial position and need for additional capital. Additional risks and uncertainties that could cause actual outcomes and results to differ materially from those contemplated by the forward-looking statements are included under the caption Risk Factors in CalciMedica's Quarterly Report on Form 10-Q for the quarter ended June 30, 2024, being filed with the Securities and Exchange Commission (SEC) later today, and elsewhere in CalciMedica's subsequent reports on Form 10-K, Form 10-Q or Form 8-K filed with the SEC from time to time and available at www.sec.gov. These documents can be accessed on CalciMedica's web page at ir.calcimedica.com/financials-filings/sec-filings. The forward-looking statements contained herein are made as of the date hereof, and CalciMedica undertakes no obligation to update them after this date, except as required by law.
CalciMedica Contact:
Sarah Sutton/Kevin Murphy
Condensed Consolidated Balance Sheets
(in thousands, except par value and share amounts)
June 30, 2024 December 31, 2023
Assets
Current assets
Cash and cash equivalents $ 5,056 $ 5,530
Short-term investments 14,081 5,708
Prepaid expenses and other current assets 1,305 367
Total current assets 20,442 11,605
Property and equipment, net 138 167
Other assets 472 413
Total assets $ 21,052 $ 12,185
Liabilities and Stockholders' Equity
Current liabilities
Accounts payable $ 2,144 $ 1,419
Accrued clinical trial costs 829 1,141
Accrued expenses 941 1,468
Total current liabilities 3,914 4,028
Long-term liabilities
Warrant liability 3,300
Total liabilities 7,214 4,028
Commitments and contingencies (Note 9)
Stockholders' equity
Preferred stock, $0.0001 par value; 10,000,000 shares and no shares authorized at June 30, 2024 and December 31, 2023, respectively; no shares issued and outstanding at June 30, 2024 and December 31, 2023, respectively
Common stock, $0.0001 par value; 500,000,000 shares authorized at June 30, 2024 and December 31, 2023; 10,750,156 and 5,754,505 issued and outstanding at June 30, 2024 and December 31, 2023, respectively 3 1
Additional paid-in capital 163,732 154,218
Accumulated deficit (149,888 ) (146,064 )
Accumulated other comprehensive income (loss) (9 ) 2
Total stockholders' equity 13,838 8,157
Total liabilities and stockholders' equity $ 21,052 $ 12,185
Condensed Consolidated Statements of Operations
(in thousands, except share and per share amounts)
Three Months Ended June 30, Six Months Ended June 30,
2024 2023 2024 2023
Operating expenses:
Research and development $ 4,157 $ 3,814 $ 7,101 $ 10,305
General and administrative 2,372 2,769 5,195 18,618
Total operating expenses 6,529 6,583 12,296 28,923
Loss from operations (6,529 ) (6,583 ) (12,296 ) (28,923 )
Other income
Change in fair value of financial instruments 2,300 7,890 3,168
Other income 275 279 582 163
Total other income 2,575 279 8,472 3,331
Net loss $ (3,954 ) $ (6,304 ) $ (3,824 ) $ (25,592 )
Net loss per share - basic and diluted $ (0.36 ) $ (1.11 ) $ (0.37 ) $ (7.86 )
Weighted-average number of shares outstanding used in computing net loss per share basic and diluted 11,129,053 5,661,933 10,441,785 3,255,868

Frequently Asked Questions

What are the recent results from the CARPO trial?

The CARPO trial announced positive topline data, showing significant dose response and reducing severe organ failure in acute pancreatitis patients.

When will data from the KOURAGE trial be available?

Topline data from the KOURAGE trial is expected to be released in 2025.

How much cash does CalciMedica have as of June 30, 2024?

CalciMedica reported approximately $19.1 million in cash and investments as of June 30, 2024.

What is Auxora's role in these trials?

Auxora is being tested for its efficacy in treating acute pancreatitis, severe acute kidney injury, and asparaginase-induced pancreatic toxicity.

When is CalciMedica planning to meet with the FDA?

CalciMedica plans to meet with the FDA to discuss the Phase 3 trial design following CARPO results.

Last updated: Aug 12, 2024