Cara Therapeutics Reports First Quarter 2024 Financial Results
Cara Therapeutics (Nasdaq: CARA) reported its Q1 2024 results. Net sales from KORSUVA injections totaled $1.8 million, with collaborative revenue contributing $800,000. However, total revenue decreased to $2.1 million from $6.2 million YoY. The company’s net loss widened to $30.7 million from $26.7 million in Q1 2023. Cash balance dropped to $69.8 million from $100.8 million in December 2023, largely due to $30.5 million used in operations. R&D expenses decreased to $22 million, but restructuring expenses added $2.4 million. The KOURAGE 1 Part A study for NP is progressing ahead of schedule, with results expected by the end of Q2 2024. Cara’s financial guidance indicates sufficient cash to fund operations into 2026.
- KOURAGE 1 Part A study for NP is progressing ahead of schedule, with results expected by the end of Q2 2024.
- Generated $1.8 million in net sales from KORSUVA injections in Q1 2024.
- Collaborative revenue stood at $800,000 in Q1 2024.
- R&D expenses decreased to $22 million, indicating cost control measures.
- Cara expects current cash reserves to fund operations into 2026.
- Total revenue decreased to $2.1 million from $6.2 million YoY.
- Net loss widened to $30.7 million from $26.7 million in Q1 2023.
- Cash, cash equivalents, and marketable securities dropped to $69.8 million from $100.8 million in December 2023.
- Restructuring expenses added $2.4 million in Q1 2024.
- Cost of goods sold decreased to $0.6 million from $2.6 million, indicating lower sales activity.
Insights
The financial results for Cara Therapeutics reveal some key trends that investors should be aware of. The company's cash reserves have seen a significant decrease from
Revenue for the quarter was significantly lower at
On the positive side, the company has controlled R&D expenses, which fell from
The transition of KORSUVA injection to the ESRD PPS bundle post-TDAPA period might impact future revenue streams. However, the company maintains that its cash reserves are sufficient to fund operations into 2026, provided that planned pivotal trials proceed as expected.
The clinical progression of Cara Therapeutics is noteworthy, especially the advancement of the KOURAGE 1 Part A portion of the notalgia paresthetica (NP) pivotal program. This program is ahead of schedule, with topline efficacy and safety results expected by the end of Q2 2024.
The KOURAGE 1 Part A study focuses on dose-finding for oral difelikefalin, an anti-pruritic treatment aimed at moderate-to-severe pruritus in NP patients. With 214 patients enrolled, the results from this phase will be important in determining the dosage and sample size for the subsequent Phase 3 pivotal trials (KOURAGE 1 Part B and KOURAGE 2). However, this part is not powered for statistical significance, which means the outcomes will primarily inform future trial designs rather than provide conclusive efficacy data.
Successful advancement in this study can open doors for treating a common but under-explored sensory neuropathy, addressing significant unmet needs in the medical dermatology field. Nevertheless, the long-term impacts and potential market adoption will depend on the final outcomes expected by 2025 and 2026. Thus, while the progress is promising, investors should closely monitor subsequent phases.
Topline efficacy and safety results from KOURAGE 1 Part A portion of notalgia paresthetica (NP) pivotal program now expected by the end of 2Q24
STAMFORD, Conn., May 13, 2024 (GLOBE NEWSWIRE) -- Cara Therapeutics, Inc. (Nasdaq: CARA), a development-stage biopharmaceutical company leading a new treatment paradigm to improve the lives of patients suffering from pruritus, today announced financial results and operational highlights for the first quarter ended March 31, 2024.
“Our notalgia paresthetica (NP) pivotal clinical program is progressing ahead of schedule and we now expect to report topline efficacy and safety results from KOURAGE 1 Part A by the end of the second quarter of 2024,” said Christopher Posner, President and Chief Executive Officer of Cara Therapeutics. “We believe the medical dermatology community’s interest in our clinical program underscores the significant unmet need for an effective and safe anti-pruritic treatment for the sizeable NP patient population. We look forward to rapidly advancing the ongoing Phase 2/3 program of our differentiated asset, oral difelikefalin, in this common but under-explored sensory neuropathy.”
KOURAGE Update
KOURAGE 1 Part A is the dose-finding portion of the Phase 2/3 clinical program evaluating oral difelikefalin for the treatment of moderate-to-severe pruritus in patients with NP. The Company enrolled 214 patients and expects topline efficacy and safety results from KOURAGE 1 Part A by the end of the second quarter of 2024. Part A is not powered for statistical significance. This readout will provide key information, specifically the dose and sample size to initiate the Phase 3 pivotal portion of the program – Part B of KOURAGE 1 and the second study KOURAGE 2. Final topline results from the first pivotal study are expected by the end of 2025 with the second pivotal study results in early 2026.
In March 2024, the Company hosted a virtual event, Meet the NP Experts, featuring a panel of leading dermatologists and key opinion leaders to discuss the unmet need in NP and the potential of oral difelikefalin. A replay of the webcast is available under “Events & Presentations” in the Investors section of the Company’s website, www.CaraTherapeutics.com.
1Q24 KORSUVA Injection U.S. Update
In the first quarter of 2024, KORSUVA® (difelikefalin) injection generated net sales of approximately
Wholesalers shipped 111,720 vials to dialysis centers during the first quarter of 2024.
On March 31, 2024, the Transitional Drug Add-On Payment Adjustment (TDAPA) period for KORSUVA injection expired. After the TDAPA period, KORSUVA injection is reimbursed through the ESRD PPS bundle.
First Quarter 2024 Financial Results
Cash, cash equivalents and marketable securities at March 31, 2024 totaled
For the first quarter of 2024, net loss was
Revenues: Total revenue was
$0.8 million and$2.8 million of collaborative revenue related to our share of the profit from CSL Vifor’s sales of KORSUVA injection to third parties during the three months ended March 31, 2024 and 2023, respectively.$0.6 million and$3.2 million of commercial supply revenue related to sales of KORSUVA injection to CSL Vifor during the three months ended March 31, 2024 and 2023, respectively.$0.6 million of other revenue related to royalty payments earned in conjunction with ex U.S. sales of KORSUVA/Kapruvia under agreements with CSL Vifor and Maruishi Pharmaceuticals Co. Ltd., or Maruishi, during the three months ended March 31, 2024, which were sold under the Purchase and Sale agreement with HCRX Investments Holdco, L.P. and Healthcare Royalty Partners IV, L.P., or the HCR Agreement, and considered non-cash. There was no other revenue during the three months ended March 31, 2023.
Cost of Goods Sold: Cost of goods sold was
Research and Development (R&D) Expenses: R&D expenses were
General and Administrative (G&A) Expenses: G&A expenses were essentially flat at
Restructuring Expenses: Restructuring expenses were
Other Income, net: Other income, net was approximately
Non-cash interest expense on liability related to sales of future royalties and milestones: Non-cash interest expense was
Financial Guidance
Cara expects that our current unrestricted cash and cash equivalents and available-for-sale marketable securities will be sufficient to fund our currently anticipated operating plan into 2026. Our current operating plan assumes certain costs related to our planned pivotal trials in NP.
About the KOURAGE Phase 2/3 Clinical Program in Notalgia Paresthetica
KOURAGE is a Phase 2/3 clinical program evaluating oral difelikefalin for the treatment of moderate-to-severe pruritus in patients with notalgia paresthetica (NP). The program is comprised of two studies – KOURAGE 1 and KOURAGE 2 – which will likely be double-blind, placebo-controlled, 8-week studies with patients allowed to roll-over into open-label 52-week extensions.
KOURAGE 1 is composed of two parts. The dose-finding portion of KOURAGE 1 (Part A) includes 214 patients who are randomized equally to four arms (0.25 mg BID, 1.0 mg BID, 2.0 mg BID, placebo BID). Part A is not powered for statistical significance.
Part B and KOURAGE 2 will likely be double-blind, placebo-controlled, 8-week studies with patients randomized 1:1 to either difelikefalin or matching placebo. The primary endpoint for both the dose-finding portion of KOURAGE 1 (Part A) and the two pivotal studies Part B and KOURAGE 2 will likely be the proportion of patients with a ≥4-point improvement at Week 8 from baseline in the worst itch numeric rating scale.
About Cara Therapeutics
Cara Therapeutics is a development-stage biopharmaceutical company leading a new treatment paradigm to improve the lives of patients suffering from pruritus. The Company is developing an oral formulation of difelikefalin, a selective, peripherally acting, non-scheduled kappa opioid receptor agonist, for the treatment of chronic pruritus associated with notalgia paresthetica (NP), a common, underdiagnosed neuropathy affecting the upper back for which there are no FDA-approved therapies. The Company is conducting a Phase 2/3 clinical program in NP with topline results of the dose-finding portion expected by the end of the second quarter of 2024. Cara Therapeutics also developed an IV formulation of difelikefalin, which is approved in the United States, EU, and multiple other countries for the treatment of moderate-to-severe pruritus associated with advanced chronic kidney disease in adults undergoing hemodialysis. The IV formulation is out-licensed worldwide. For more information, visit www.CaraTherapeutics.com and follow the company on X (Twitter), LinkedIn and Instagram.
Forward-looking Statements
Statements contained in this press release regarding matters that are not historical facts are "forward-looking statements" within the meaning of the Private Securities Litigation Reform Act of 1995. Examples of these forward-looking statements include statements concerning the Company’s planned future regulatory submissions and potential future regulatory approvals, future product launches, expected timing of the initiation, enrollment and data readouts from the Company’s planned and ongoing clinical trials, the potential results of ongoing clinical trials, timing of future regulatory and development milestones for the Company’s product candidate, the potential for the Company’s product candidate to be an alternative in the therapeutic areas investigated, including notalgia paresthetica, the size and growth of the potential markets for pruritus management such as notalgia paresthetica, the commercial potential of the Company’s product candidate, and the Company’s cash runway. Because such statements are subject to risks and uncertainties, actual results may differ materially from those expressed or implied by such forward-looking statements. The risks are described more fully in Cara Therapeutics’ filings with the Securities and Exchange Commission, including the “Risk Factors” section of the Company’s Annual Report on Form 10-K for the year ending December 31, 2023 and its other documents subsequently filed with or furnished to the Securities and Exchange Commission, including its Form 10-Q for the quarter ended March 31, 2024. All forward-looking statements contained in this press release speak only as of the date on which they were made. Cara Therapeutics undertakes no obligation to update such statements to reflect events that occur or circumstances that exist after the date on which they were made, except as required by law.
| CARA THERAPEUTICS, INC. | |||||||
| CONDENSED CONSOLIDATED BALANCE SHEETS | |||||||
| (in thousands) | |||||||
| (unaudited) | |||||||
| March 31, | December 31, | ||||||
| 2024 | 2023 | ||||||
| Assets | |||||||
| Current assets: | |||||||
| Cash and cash equivalents | $ | 46,996 | $ | 51,775 | |||
| Marketable securities | 22,777 | 48,983 | |||||
| Accounts receivable, net - related party | 1,718 | 2,765 | |||||
| Inventory, net | 2,741 | 2,821 | |||||
| Income tax receivable | 697 | 697 | |||||
| Other receivables | 506 | 555 | |||||
| Prepaid expenses | 5,790 | 8,154 | |||||
| Restricted cash | - | 408 | |||||
| Total current assets | 81,225 | 116,158 | |||||
| Operating lease right-of-use assets | 3,826 | 4,864 | |||||
| Property and equipment, net | 3,548 | 3,322 | |||||
| Restricted cash, non-current | 1,500 | 1,500 | |||||
| Total assets | $ | 90,099 | $ | 125,844 | |||
| Liabilities and stockholders’ equity | |||||||
| Current liabilities: | |||||||
| Accounts payable and accrued expenses | $ | 14,875 | $ | 25,592 | |||
| Operating lease liability, current | 220 | - | |||||
| Total current liabilities | 15,095 | 25,592 | |||||
| Liability related to sales of future royalties and milestones, net | 38,376 | 37,079 | |||||
| Operating lease liability, non-current | 6,825 | 6,088 | |||||
| Total liabilities | 60,296 | 68,759 | |||||
| Commitments and contingencies | - | - | |||||
| Stockholders' equity: | |||||||
| Preferred stock | - | - | |||||
| Common stock | 54 | 54 | |||||
| Additional paid-in capital | 745,381 | 742,036 | |||||
| Accumulated deficit | (715,441 | ) | (684,745 | ) | |||
| Accumulated other comprehensive loss | (191 | ) | (260 | ) | |||
| Total stockholders’ equity | 29,803 | 57,085 | |||||
| Total liabilities and stockholders’ equity | $ | 90,099 | $ | 125,844 | |||
| CARA THERAPEUTICS, INC. | |||||||||
| CONDENSED CONSOLIDATED STATEMENTS OF OPERATIONS | |||||||||
| (amounts in thousands, except share and per share data) | |||||||||
| (unaudited) | |||||||||
| Three Months Ended March 31, | |||||||||
| 2024 | 2023 | ||||||||
| Revenue: | |||||||||
| Collaborative revenue | $ | 788 | $ | 2,750 | |||||
| Commercial supply revenue | 640 | 3,191 | |||||||
| Royalty revenue | - | 125 | |||||||
| Clinical compound revenue | 84 | 99 | |||||||
| Other revenue | 623 | - | |||||||
| Total revenue | 2,135 | 6,165 | |||||||
| Operating expenses: | |||||||||
| Cost of goods sold | 620 | 2,590 | |||||||
| Research and development | 21,964 | 24,334 | |||||||
| General and administrative | 6,816 | 6,891 | |||||||
| Restructuring | 2,401 | - | |||||||
| Total operating expenses | 31,801 | 33,815 | |||||||
| Operating loss | (29,666 | ) | (27,650 | ) | |||||
| Other income, net | 952 | 985 | |||||||
| Non-cash interest expense on liability related to sales of future royalties and milestones | (1,982 | ) | - | ||||||
| Net loss | $ | (30,696 | ) | $ | (26,665 | ) | |||
| Net loss per share: | |||||||||
| Basic and Diluted | $ | (0.56 | ) | $ | (0.49 | ) | |||
| Weighted average shares: | |||||||||
| Basic and Diluted | 54,588,090 | 53,872,038 | |||||||
MEDIA CONTACT:
Annie Spinetta
6 Degrees
973-768-2170
aspinetta@6degreespr.com
INVESTOR CONTACT:
Iris Francesconi, Ph.D.
Cara Therapeutics
203-406-3700
investor@caratherapeutics.com
FAQ
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