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Cara Therapeutic Stock Price, News & Analysis

CARA NASDAQ

Company Description

Cara Therapeutics, Inc. (CARA) is a biopharmaceutical company whose activities have been focused on pruritus, or chronic itch. According to multiple company disclosures, Cara Therapeutics describes itself as a development-stage or commercial-stage biopharmaceutical company leading a new treatment paradigm to improve the lives of patients suffering from pruritus.

The company has developed difelikefalin, a selective, peripherally acting, non-scheduled kappa opioid receptor agonist. Cara Therapeutics developed an intravenous (IV) formulation of difelikefalin, which is approved in the United States, the European Union, and multiple other countries for the treatment of moderate-to-severe pruritus associated with advanced chronic kidney disease in adults undergoing hemodialysis. The company states that this IV formulation is out-licensed worldwide.

In addition to the IV product, Cara Therapeutics has been developing an oral formulation of difelikefalin for chronic pruritus associated with notalgia paresthetica (NP), which the company describes as a common, underdiagnosed neuropathy affecting the upper back for which there are no FDA-approved therapies. Company communications describe a Phase 2/3 clinical program in NP, referred to as the KOURAGE program, including the KOURAGE 1 and KOURAGE 2 studies evaluating oral difelikefalin for moderate-to-severe pruritus in patients with NP.

Cara Therapeutics has also reported that it has prioritized its late-stage NP clinical program, including a dose-finding portion (KOURAGE 1 Part A) and planned pivotal portions, and that it has taken steps such as a streamlined operating plan focused on cost-containment and cash conservation. The company has discussed exploring strategic alternatives and engaging a financial advisor in connection with that process.

In later disclosures, Cara Therapeutics describes itself as a biopharmaceutical company that has been focused on leading a new treatment paradigm to improve the lives of patients suffering from chronic pruritus. It notes that it developed the IV formulation of difelikefalin, which is approved for the treatment of moderate-to-severe pruritus associated with advanced kidney disease in adults undergoing hemodialysis in the United States, European Union, and multiple other countries, and that this IV formulation is out-licensed worldwide.

In addition to its development activities, Cara Therapeutics has reported collaborative revenue, commercial supply revenue, and other revenue related to KORSUVA (the brand name used for difelikefalin injection in certain markets) and Kapruvia under agreements with partners. The company has disclosed that KORSUVA injection generated net sales and that it records collaborative revenue representing its share of profit from sales of KORSUVA injection. It has also noted royalty and milestone payments related to ex-U.S. sales of KORSUVA/Kapruvia under agreements with partners.

From a capital markets perspective, Cara Therapeutics’ common stock has traded on the Nasdaq Capital Market under the symbol "CARA". The company has implemented reverse stock splits of its outstanding common stock, including a 1-for-12 reverse stock split that became effective on December 30, 2024, after which the stock continued to trade on a reverse stock split-adjusted basis on Nasdaq under the symbol CARA. The company has stated that this reverse stock split was part of its plan to regain compliance with the minimum bid price requirement for continued listing on the Nasdaq Capital Market.

Subsequently, Cara Therapeutics announced that its Board of Directors approved a 1-for-3 reverse stock split of its outstanding shares of common stock in connection with a proposed merger with Tvardi Therapeutics, Inc. The company stated that Cara’s common stock is expected to begin trading on a reverse stock split-adjusted basis under the new name “Tvardi Therapeutics, Inc.” and under the new symbol “TVRD” following the anticipated closing of the merger with Tvardi Therapeutics, Inc. The announcement explains that, at the effective time of this reverse stock split, every three issued and outstanding shares of the company’s common stock will automatically be combined into one issued and outstanding share, with no change in par value per share, and that fractional shares will not be issued.

These disclosures indicate that the ticker symbol CARA historically represents Cara Therapeutics, Inc., a biopharmaceutical company focused on pruritus, the development and commercialization (through partners) of difelikefalin injection for pruritus associated with advanced chronic kidney disease in adults undergoing hemodialysis, and the clinical development of an oral formulation of difelikefalin for notalgia paresthetica. The company has also described plans and actions related to strategic alternatives and a proposed merger with Tvardi Therapeutics, Inc., with an anticipated transition to a new company name and ticker symbol in connection with that merger.

Business focus and therapeutic areas

Cara Therapeutics’ disclosures emphasize its focus on chronic pruritus. The company describes its work in:

  • Developing and commercializing, through partners, an IV formulation of difelikefalin for moderate-to-severe pruritus associated with advanced chronic kidney disease in adults undergoing hemodialysis.
  • Developing an oral formulation of difelikefalin for chronic pruritus associated with notalgia paresthetica, a neuropathic disorder characterized by chronic pruritus of the upper back for which there are no FDA-approved therapies.

The company characterizes difelikefalin as a selective, peripherally acting, non-scheduled kappa opioid receptor agonist, and positions its clinical programs as part of a new treatment paradigm for patients suffering from pruritus.

Clinical development programs

Cara Therapeutics has described a Phase 2/3 clinical program in notalgia paresthetica under the name KOURAGE, consisting of two studies, KOURAGE 1 and KOURAGE 2. Company communications explain that KOURAGE 1 includes a dose-finding Part A and a pivotal portion, and that KOURAGE 2 is also designed as a double-blind, placebo-controlled study. The company has reported enrollment in KOURAGE 1 Part A and has discussed expectations for topline efficacy and safety results from that portion of the program.

In later updates, Cara Therapeutics announced that oral difelikefalin did not demonstrate a meaningful clinical benefit compared to placebo in the dose-finding Part A of the KOURAGE-1 study in notalgia paresthetica, and that, as a result, the company decided to discontinue the clinical program in NP and explore strategic alternatives.

Commercial and partnered activities

Cara Therapeutics has reported that KORSUVA (difelikefalin) injection generated net sales in the United States, and that the company recorded collaborative revenue representing its share of profit from sales of KORSUVA injection to third parties under agreements with a partner. It has also reported commercial supply revenue related to sales of KORSUVA injection to a partner, as well as royalty and milestone payments related to ex-U.S. sales of KORSUVA/Kapruvia under agreements with partners.

The company has discussed reimbursement aspects for KORSUVA injection in the U.S., including the end of a Transitional Drug Add-On Payment Adjustment (TDAPA) period and subsequent reimbursement through a bundled payment system for end stage renal disease.

Corporate and capital structure developments

Cara Therapeutics has disclosed several corporate and capital structure developments, including:

  • A 1-for-12 reverse stock split of its outstanding shares of common stock, effective as of December 30, 2024, with trading on a reverse stock split-adjusted basis on the Nasdaq Capital Market under the symbol CARA beginning December 31, 2024. The company stated that this reverse stock split was part of its plan to regain compliance with the minimum bid price requirement for continued listing on the Nasdaq Capital Market.
  • A subsequent 1-for-3 reverse stock split of its outstanding shares of common stock approved by the Board of Directors in connection with a proposed merger with Tvardi Therapeutics, Inc., with the expectation that, following the anticipated closing of the merger, the combined company would trade under the new name “Tvardi Therapeutics, Inc.” and the new symbol “TVRD”.

The company has also discussed a process of exploring strategic alternatives, including engaging a financial advisor, and has described a streamlined operating plan focused on cost-containment and cash conservation.

Historical context for the CARA ticker

Based on the company’s own announcements, the ticker symbol CARA has historically been associated with Cara Therapeutics, Inc., a biopharmaceutical company focused on pruritus and the development and commercialization (through partners) of difelikefalin-based therapies. Company communications indicate a planned transition in connection with a proposed merger, under which the stock is expected to trade under a new company name and symbol after the anticipated closing of that merger.

FAQs about Cara Therapeutics (CARA)

  • What does Cara Therapeutics do?

    Cara Therapeutics is described in its public communications as a biopharmaceutical company focused on improving the lives of patients suffering from pruritus. It developed an IV formulation of difelikefalin for moderate-to-severe pruritus associated with advanced chronic kidney disease in adults undergoing hemodialysis, and it has pursued clinical development of an oral formulation of difelikefalin for chronic pruritus associated with notalgia paresthetica.

  • What is difelikefalin?

    The company describes difelikefalin as a selective, peripherally acting, non-scheduled kappa opioid receptor agonist. Cara Therapeutics developed an IV formulation of difelikefalin that is approved in the United States, European Union, and multiple other countries for the treatment of moderate-to-severe pruritus associated with advanced chronic kidney disease in adults undergoing hemodialysis, and it has also worked on an oral formulation for notalgia paresthetica.

  • What conditions has Cara Therapeutics targeted?

    Cara Therapeutics has focused on pruritus-related conditions. It developed an IV formulation of difelikefalin for moderate-to-severe pruritus associated with advanced chronic kidney disease in adults undergoing hemodialysis, and it has conducted a Phase 2/3 clinical program of oral difelikefalin in notalgia paresthetica, a neuropathic disorder characterized by chronic pruritus of the upper back for which there are no FDA-approved therapies.

  • What is KORSUVA injection?

    Company disclosures refer to KORSUVA (difelikefalin) injection as a product that generated net sales in the United States. Cara Therapeutics reports collaborative revenue representing its share of profit from sales of KORSUVA injection and commercial supply revenue from sales of KORSUVA injection to a partner. KORSUVA injection is associated with the treatment of moderate-to-severe pruritus in adults undergoing hemodialysis.

  • What is the KOURAGE clinical program?

    The KOURAGE program is described by the company as a Phase 2/3 clinical program evaluating oral difelikefalin for the treatment of moderate-to-severe pruritus in patients with notalgia paresthetica. It includes two studies, KOURAGE 1 and KOURAGE 2, with KOURAGE 1 composed of a dose-finding Part A and a pivotal portion.

  • What did Cara Therapeutics report about oral difelikefalin in notalgia paresthetica?

    Cara Therapeutics announced that in the dose-finding Part A of the KOURAGE-1 study, oral difelikefalin did not demonstrate a meaningful clinical benefit compared to placebo. As a result, the company stated that it would discontinue the clinical program in notalgia paresthetica and explore strategic alternatives.

  • How has Cara Therapeutics described its commercial arrangements?

    The company has reported collaborative revenue related to its share of profit from sales of KORSUVA injection by a partner, commercial supply revenue from sales of KORSUVA injection to that partner, and royalty and milestone payments related to ex-U.S. sales of KORSUVA/Kapruvia under agreements with partners. It has also described a purchase and sale agreement under which another party receives future royalty and milestone payments for certain ex-U.S. sales up to capped amounts.

  • What stock exchange has Cara Therapeutics traded on?

    Cara Therapeutics has stated that its common stock trades on the Nasdaq Capital Market under the symbol “CARA”. In connection with a proposed merger and a 1-for-3 reverse stock split, the company has indicated that, following the anticipated closing of the merger, the combined company’s stock is expected to trade under a new name and symbol.

  • What reverse stock splits has Cara Therapeutics announced?

    The company announced a 1-for-12 reverse stock split of its outstanding shares of common stock, effective as of December 30, 2024, after which its common stock began trading on a reverse stock split-adjusted basis on the Nasdaq Capital Market under the symbol CARA. It later announced that its Board of Directors approved a 1-for-3 reverse stock split in connection with a proposed merger with Tvardi Therapeutics, Inc., with the expectation that the stock would trade under a new company name and ticker symbol following the anticipated closing of the merger.

  • What corporate actions has Cara Therapeutics discussed regarding strategic alternatives?

    Cara Therapeutics has publicly stated that it engaged a financial advisor to assist in exploring and reviewing strategic alternatives. It has also described a streamlined operating plan focused on cost-containment and cash conservation, and later communications link a reverse stock split to a proposed merger with Tvardi Therapeutics, Inc.

  • What happens to the CARA ticker in light of the proposed merger?

    In its announcement of the 1-for-3 reverse stock split, Cara Therapeutics stated that its common stock is expected to begin trading under the new name “Tvardi Therapeutics, Inc.” and under the new symbol “TVRD” following the anticipated closing of the merger with Tvardi Therapeutics, Inc. This indicates that the CARA ticker represents the historical listing for Cara Therapeutics prior to that anticipated transition.

Stock Performance

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Last updated:
-37.56%
Performance 1 year
$22.1M

SEC Filings

No SEC filings available for Cara Therapeutic.

Financial Highlights

Revenue (TTM)
Net Income (TTM)
Operating Cash Flow

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Short Interest History

Last 12 Months
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Short interest in Cara Therapeutic (CARA) currently stands at 71.0 thousand shares, up 6.8% from the previous reporting period, representing 1.8% of the float. This relatively low short interest suggests limited bearish sentiment.

Days to Cover History

Last 12 Months
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Days to cover for Cara Therapeutic (CARA) currently stands at 1.5 days, down 74.9% from the previous period. This low days-to-cover ratio indicates high liquidity, allowing short sellers to quickly exit positions if needed. The days to cover has decreased 65.6% over the past year, suggesting improved liquidity for short covering. The ratio has shown significant volatility over the period, ranging from 1.5 to 6.1 days.

Frequently Asked Questions

What is the current stock price of Cara Therapeutic (CARA)?

The current stock price of Cara Therapeutic (CARA) is $5.32 as of April 29, 2025.

What is the market cap of Cara Therapeutic (CARA)?

The market cap of Cara Therapeutic (CARA) is approximately 22.1M. Learn more about what market capitalization means .

What is Cara Therapeutics’ main area of focus?

Cara Therapeutics describes its focus as improving the lives of patients suffering from pruritus. The company developed an IV formulation of difelikefalin for moderate-to-severe pruritus associated with advanced chronic kidney disease in adults undergoing hemodialysis and has pursued an oral formulation of difelikefalin for chronic pruritus associated with notalgia paresthetica.

What is difelikefalin and how does Cara Therapeutics describe it?

Cara Therapeutics describes difelikefalin as a selective, peripherally acting, non-scheduled kappa opioid receptor agonist. The company developed an IV formulation of difelikefalin that is approved in the United States, European Union, and multiple other countries for moderate-to-severe pruritus associated with advanced chronic kidney disease in adults undergoing hemodialysis.

What approved therapy is associated with Cara Therapeutics’ work?

The company states that it 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. This IV formulation is out-licensed worldwide.

What is notalgia paresthetica and how is Cara Therapeutics involved?

Cara Therapeutics describes notalgia paresthetica as a common, underdiagnosed neuropathy affecting the upper back for which there are no FDA-approved therapies. The company has been developing an oral formulation of difelikefalin for chronic pruritus associated with notalgia paresthetica and has conducted a Phase 2/3 clinical program referred to as the KOURAGE program.

What is the KOURAGE clinical program?

The KOURAGE program is a Phase 2/3 clinical program described by Cara Therapeutics that evaluates oral difelikefalin for moderate-to-severe pruritus in patients with notalgia paresthetica. It includes the KOURAGE 1 and KOURAGE 2 studies, with KOURAGE 1 composed of a dose-finding Part A and a pivotal portion.

What did Cara Therapeutics report about oral difelikefalin in the KOURAGE-1 Part A study?

Cara Therapeutics announced that in the dose-finding Part A of the KOURAGE-1 study evaluating oral difelikefalin in notalgia paresthetica, oral difelikefalin did not demonstrate a meaningful clinical benefit at any dose compared to placebo. The company stated that it would discontinue the clinical program in notalgia paresthetica and explore strategic alternatives.

How does Cara Therapeutics describe its commercial activities around KORSUVA injection?

The company reports that KORSUVA (difelikefalin) injection generated net sales in the United States and that it records collaborative revenue representing its share of profit from sales of KORSUVA injection to third parties. It also reports commercial supply revenue related to sales of KORSUVA injection to a partner and royalty and milestone payments related to ex-U.S. sales of KORSUVA/Kapruvia under agreements with partners.

On which exchange has Cara Therapeutics’ stock traded and under what symbol?

Cara Therapeutics has stated that its common stock trades on the Nasdaq Capital Market under the symbol “CARA”. In connection with a proposed merger, the company has indicated that, following the anticipated closing of the merger, the combined company is expected to trade under a new name and symbol.

What reverse stock splits has Cara Therapeutics implemented?

Cara Therapeutics announced a 1-for-12 reverse stock split of its outstanding shares of common stock, effective as of December 30, 2024, after which its common stock began trading on a reverse stock split-adjusted basis on the Nasdaq Capital Market under the symbol CARA. The company later announced that its Board of Directors approved a 1-for-3 reverse stock split in connection with a proposed merger with Tvardi Therapeutics, Inc.

What strategic alternatives has Cara Therapeutics discussed?

Cara Therapeutics has stated that it engaged a financial advisor to assist in exploring and reviewing strategic alternatives. It has also described a streamlined operating plan focused on cost-containment and cash conservation and has linked a later reverse stock split to a proposed merger with Tvardi Therapeutics, Inc., with an expectation of trading under a new company name and ticker symbol after the anticipated closing of that merger.