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Cara Therapeutics, Inc.NasdaqCM:CARA 株式レポート

時価総額 US$24.3m
株価
n/a
私の公正価値
n/a
1Y-39.4%
7D8.6%
1D
ポートフォリオ価値
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Cara Therapeutics, Inc.

NasdaqCM:CARA 株式レポート

時価総額:US$24.3m

This company is no longer active

The company may no longer be operating, as it may be out of business. Find out why through their latest events.

Cara Therapeutics(CARA)株式概要

カラ・セラピューティクス社は、米国で慢性そう痒症治療薬の開発・商品化に注力するバイオ医薬品企業である。 詳細

CARA ファンダメンタル分析
スノーフレーク・スコア
評価2/6
将来の成長2/6
過去の実績0/6
財務の健全性0/6
配当金0/6

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Cara Therapeutics, Inc. 競合他社

価格と性能

株価の高値、安値、推移の概要Cara Therapeutics
過去の株価
現在の株価US$15.96
52週高値US$31.32
52週安値US$8.13
ベータ0.41
1ヶ月の変化3.90%
3ヶ月変化15.65%
1年変化-39.43%
3年間の変化-96.61%
5年間の変化-97.18%
IPOからの変化-96.57%

最新ニュース

Recent updates

分析記事 Nov 01

Cara Therapeutics, Inc.'s (NASDAQ:CARA) Share Price Is Matching Sentiment Around Its Revenues

Cara Therapeutics, Inc.'s ( NASDAQ:CARA ) price-to-sales (or "P/S") ratio of 1.5x might make it look like a buy right...
分析記事 Jul 18

Cara Therapeutics, Inc.'s (NASDAQ:CARA) Price Is Right But Growth Is Lacking After Shares Rocket 34%

Cara Therapeutics, Inc. ( NASDAQ:CARA ) shareholders are no doubt pleased to see that the share price has bounced 34...
分析記事 May 29

We Think Cara Therapeutics, Inc.'s (NASDAQ:CARA) CEO Compensation Package Needs To Be Put Under A Microscope

Key Insights Cara Therapeutics to hold its Annual General Meeting on 4th of June CEO Chris Posner's total compensation...
分析記事 May 25

Why Investors Shouldn't Be Surprised By Cara Therapeutics, Inc.'s (NASDAQ:CARA) Low P/S

You may think that with a price-to-sales (or "P/S") ratio of 2.2x Cara Therapeutics, Inc. ( NASDAQ:CARA ) is a stock...
分析記事 Feb 16

We're A Little Worried About Cara Therapeutics' (NASDAQ:CARA) Cash Burn Rate

There's no doubt that money can be made by owning shares of unprofitable businesses. For example, although...
分析記事 Dec 19

The Market Doesn't Like What It Sees From Cara Therapeutics, Inc.'s (NASDAQ:CARA) Revenues Yet As Shares Tumble 43%

To the annoyance of some shareholders, Cara Therapeutics, Inc. ( NASDAQ:CARA ) shares are down a considerable 43% in...
分析記事 Nov 04

News Flash: Analysts Just Made A Notable Upgrade To Their Cara Therapeutics, Inc. (NASDAQ:CARA) Forecasts

Celebrations may be in order for Cara Therapeutics, Inc. ( NASDAQ:CARA ) shareholders, with the analysts delivering a...
分析記事 Oct 25

Can Cara Therapeutics (NASDAQ:CARA) Afford To Invest In Growth?

Just because a business does not make any money, does not mean that the stock will go down. For example, although...
分析記事 Jul 20

Is Cara Therapeutics (NASDAQ:CARA) In A Good Position To Deliver On Growth Plans?

Just because a business does not make any money, does not mean that the stock will go down. For example, biotech and...
分析記事 Jun 04

Take Care Before Jumping Onto Cara Therapeutics, Inc. (NASDAQ:CARA) Even Though It's 30% Cheaper

Unfortunately for some shareholders, the Cara Therapeutics, Inc. ( NASDAQ:CARA ) share price has dived 30% in the last...
分析記事 Mar 11

News Flash: 8 Analysts Think Cara Therapeutics, Inc. (NASDAQ:CARA) Earnings Are Under Threat

The latest analyst coverage could presage a bad day for Cara Therapeutics, Inc. ( NASDAQ:CARA ), with the analysts...
分析記事 Feb 15

Cara Therapeutics, Inc. (NASDAQ:CARA) Analysts Just Slashed Next Year's Estimates

The analysts covering Cara Therapeutics, Inc. ( NASDAQ:CARA ) delivered a dose of negativity to shareholders today, by...
分析記事 Feb 06

We Think Cara Therapeutics (NASDAQ:CARA) Can Afford To Drive Business Growth

Just because a business does not make any money, does not mean that the stock will go down. For example, biotech and...
分析記事 Oct 18

We're Interested To See How Cara Therapeutics (NASDAQ:CARA) Uses Its Cash Hoard To Grow

We can readily understand why investors are attracted to unprofitable companies. For example, biotech and mining...
Seeking Alpha Sep 28

Cara's partner files for Japanese approval of Korsuva to treat itch in hemodialysis patients

Cara Therapeutics (NASDAQ:CARA) said its licensing partner Maruishi Pharmaceutical submitted a new drug application (NDA) in Japan for approval of Korsuva (difelikefalin) to treat (itching) pruritus in hemodialysis patients. The NDA is backed by data from a phase 3 trial in Japan, the company said in a Sept. 28 press release. Cara's markets Korsuva in the U.S. with CSL Vifor. The drug is also approved in the U.K., EU and Switzerland, under the name Kapruvia, where Cara's partner is Vifor Fresenius Medical Care Renal Pharma. Vifor Fresenius is a joint company of CSL (OTCPK:CSLLY) (OTCPK:CMXHF) and Fresenius Medical Care (FMS).
Seeking Alpha Sep 12

Cara Therapeutics hires new finance chief

Cara Therapeutics (NASDAQ:CARA) has appointed Ryan Maynard as its new CFO, effective Sep 12, 2022, the biopharmaceutical company announced in a regulatory filing on Monday. Maynard holds over 20 years of experience in leading finance organizations at both public and private biopharmaceutical companies. He previously served as CFO at global healthcare solutions company, LetsGetChecked. At Cara (CARA), Maynard will serve as the company's principal financial officer and principal accounting officer.
Seeking Alpha Sep 01

Cara Therapeutics: All Eyes On Korsuva Launch Metrics

Summary Korsuva has been approved in an indication for which, it faces little in the way of competition. A number of expansion opportunities await oral difelikefalin, with positive phase 2 data for NP opening the door to additional indications. Language surrounding launch metrics and sales for Q3 sounds cautious, and a near-term disappointment could weigh on share price. Steady history of insider sales and lack of specialist biotech funds holding positions here are possible negative indicators. CARA is a Buy, but only suitable for long-term investors. Key risks include disappointing data for ongoing studies (especially placebo effect) and competition in certain indications (atopic dermatitis). Shares of Cara Therapeutics (CARA) are down 20% over the past 5 years. So far in 2022, they are 15% in the red. I'm always on the lookout for commercial-stage ideas, especially new product launches as that potent combination of accelerating sales momentum and pipeline progress can be hard to resist. Cara caught my eye given the Korsuva launch is underway for an indication (CKD-aP in HD) in which it is the first and only product approved, in addition to bullish remarks from management in the Q2 report where they state "we anticipate demand to accelerate in the coming months, driven by large dialysis organizations that started purchasing early in the third quarter." From what I understand, the positive KOMFORT phase 2 readout in notalgia paresthetica could serve as POC and open the door to multiple other disease categories in both the neurological and dermatology space. Let's take a closer look to determine if Cara fits our criteria for the Core Biotech portfolio and whether there's sufficient commercial and clinical momentum to merit gaining exposure here. Chart FinViz Figure 1: CARA weekly chart When looking at charts, clarity often comes from taking a look at distinct time frames in order to determine important technical levels and get a feel for what's going on. In the weekly chart above, we can see a share price spike to the $30 level in Q2 2021 when the FDA and EMA accepted regulatory applications for difelikefalin injection (Korsuva) for the treatment of pruritus associated with chronic kidney disease in hemodialysis patients. From there, the market certainly "taketh away" as the stock plunged on a setback in a mid-stage study in atopic dermatitis. In summer 2022, the share price bottomed around in the $8 level and has slightly rebounded to $10. Overall, I think we are looking at a depressed chart and valuation, so long term investors who believe better days are coming would do well to accumulate a position in the current range. Overview Founded in 2004 with headquarters in Connecticut (84 employees), Cara Therapeutics currently sports an enterprise value of ~$350M and Q2 cash position of $204M providing them operational runway for roughly 2 years (I imagine they will access funds via financing by mid 2023 or so). Management's presentation at Canaccord Genuity Growth Conference provides an excellent overview: CEO Christopher Posner and CMO Joana Goncalvez are present, with Posner noting that the company is focused on pruritus (itching) and has an approved therapy Korsuva injection (approved last August). They launched in April this year with partner Vifor Pharma (recently acquired by CSL) with favorable economics in terms of launch. They also have a pipeline-in-a-drug approach with oral difelikefalin and two phase 3 programs initiated this quarter or Q1 (atopic dermatitis and chronic kidney disease in patients pre-dialysis). Third priority is around expanding utilization of oral difelikefalin via two phase 2 programs (recent positive topline data for notalgia paresthetica or NP, and a small phase 2 POC study in primary biliary cholangitis with data readout 2H 22). They have a very strong balance sheet, $204M and guidance to 1H 24 (does not include revenue received from launch). Corporate Slides Figure 2: Combined patient opportunity across lead indications Q2 was the first quarter of launch, total net sales were $17M of which Cara's profit share was $8M. That was comprised mainly of channel stocking (launch inventory in anticipation of future demand). Initial demand is driven by smaller dialysis organizations and recently they got formulary coverage of two largest dialysis organizations (comprise 80% of the market). Recently they announced that the Fresenius Medical Care salesforce is joining the promotional mix as well. They expect demand to steadily increase over the next couple quarters and Q3 will draw down some of that inventory they put in the channel (sounds conservative). Total addressable patient population is 200,000 and most of those preside with Fresenius and DaVita for whom they have formulary coverage. They are fully reimbursed by Medicare for minimum of 2 years (granted in April) via TDAPA designation (only other analogue is Amgen's parsabiv launched in 2018 and they had TDAPA designation for 3 years). Once they get out of the TDAPA payment, the product goes into the bundle and they would expect it to increase to cover an innovative drug like Korsuva. One distinction though is that parsabiv went into the bundle with two other drugs including generic oral version that shifted incentive to generic, whereas Korsuva would go into the bundle with additional funding without any additional competition as there are no competitors in that functional category). CMS recently came out with proposed rule for 2023 for end stage renal disease patients in the bundle/payment system, and they specifically call out concerns for drugs designated with TDAPA (proposed four options that all are positive in terms of adding additional money outside the bundle for an innovative drug like Korsuva). We probably won't hear back from them on this issue until 2024. Early days of launched, shipped 1800 vials to dialysis clinics and anecdotally feedback is quite positive (very high levels of awareness among nephrologists and very high intent to treat). Week over week they are seeing increases in number of clinics ordering and majority of them reordering (gives hope that they are having positive first experiences with the product). Moving on to oral Korsuva, NP indication is an interesting opportunity and affects 650,000 patients. It's treated by medical dermatologists and there are no FDA-approved therapies for this neuropathic itch. The strategy is to look at their drug in systemic, dermatologic and neuropathic conditions to demonstrate broad utility. Data showed that the drug works broadly across disease areas regardless of the underlying pathogenesis (what's causing that itch). It also confirmed the mechanism of action, works with strong neuro-modulatory manner to inhibit the itch. Corporate Slides Figure 3: Positive POC data in NP shows path forward to broader utility NP is a more homogenous type of itch and patient (itch is just neuropathic and strong data is a result of strong neuro-modulatory effect). Atopic dermatitis itch is a combination of inflammatory component as well as neuro-modulatory, so oral difelikefalin should work there. The company's phase 3 program is using it as an adjunct to topical corticosteroids (address inflammatory itch) while difelikefalin addresses the neuro-modulatory. In systemic itch, pathogenesis is multi-factorial and drug should work there given prior data. Placebo response does vary by condition. NP is the first study (nothing else is in trials) and going forward data has been submitted to dermatological conference (placebo response could go higher in the future). 4 point response was the primary endpoint and was around 20%. In Atopic dermatitis they saw 20% placebo effect in mild-to-moderate patient population as well. Stage 3 patients (higher placebo response) have not been included in the ongoing phase 3 study. On the con side, pain and itch are very subjective endpoints. Corporate Slides Figure 4: Phase 2 data in AD focusing on mild-to-moderate subgroup For atopic dermatitis, management acknowledges the evolving competitive landscape and flurry of development in the moderate to severe space and it's all focused on inflammatory component coupled with disease modification. Topicals are still utilized in mild to moderate cases and they are not always effective. Placebo effect to my eyes is the big risk for phase 3 study especially considering the prior phase 2 trial failed to meet the primary endpoint in the moderate to severe population and the company chose to instead focus on the key secondary endpoint (percentage of patients who achieved an improvement from a baseline of ≥4 points in the weekly mean of the daily 24-hour Itch NRS score at week 12, which is now the registration endpoint). They are confident about design being optimal, but reading between the lines I think the CEO sounded less confident on actually achieving the primary endpoint. Majority of these patients they are enrolling are mild to moderate. Safety profile repeatedly shows consistency and predictability. Across different disease areas they see predominantly GI effects, headache and dizziness. With long term use they do not expect it to look any different (events did not increase over time, some decrease over time as they typically occur in first few weeks on treatment). As for phase 2 in PBC, this is a small proof of concept study (just want to see numerical separation and positive signal). They want to see consistent pattern of effect, early onset of action and sustained effect. For the IV product, they are fully-partnered with Vifor in the US and EU (who owns nearly 14% of the company, not a stretch to think they decide to simply buy Cara out at some point). For wholly-owned oral difelikefalin, they will look for ex US partnerships and in the US retain the option to 'go it solo' in commercializing (especially for concentrated markets). Other Information For the second quarter of 2022, the company reported cash and equivalents of $204M as compared to $30M cash used in operating activities. Net loss was $4.2M, while total revenues amounted to $23M ($15M milestone payment for Kapruvia approval and $8M in collaboration revenue related to profit-sharing). Research and development expenses fell to $19.9M, while G&A rose to $7.6M. Again, management is guiding for operational runway into 1H 2024 (this is conservative, as they are not including any product revenue received or milestone payments that could come). Accumulated deficit is $480M and again I would expect another financing at some point in 2023, perhaps the back half of the year. On the conference call, regarding launch metrics and what to expect in the future, management reminds us that for them to record revenue Vifor must ship to wholesalers and then demand is generated (sounds again like Q3 could be soft or below expectations before the ensuing uptick). The CEO expects demand to accelerate into the back half of the year as Fresenius and Davita are online, formulary protocols are in place and they are starting to see ordering done by clinics. Again, keep in mind that the $8M in revenue received on net sales of just under $17M amounts to 47% of net sales (assumes 60% profit split at non-Fresenius accounts). As for prior financings, the July 2019 secondary offering took place at price point of $23/share (representing a double from current levels). Moving on to nuggets from other presentations, the KOMFORT readout call was certainly worth listening to: The big idea here with oral difelikefalin (DFK) is to provide clinical benefit regardless of underlying cause of pruritus, to treat it across a broad variety of disease categories. NP data affirms core strategy is on target and on track. As for market opportunity in NP, they estimate 2.7M adults have neuropathic itch including NP (disease significantly underdiagnosed with only a quarter of NP patients under care of a provider). There are no FDA approved therapies and off label treatments currently used have little or no efficacy or safety & tolerability concerns. In addition to data mentioned in Figure 3, significantly greater proportion of patients on DFK achieved 4 point improvement in WI-NRS compared to placebo (endpoint regulators will be looking at in pivotal studies). 41% of patients on DFK versus 18% on placebo with statistical separation versus placebo seen as early as week 2 and sustained through week 8. Corporate presentation Figure 5: Promising efficacy in NP on registrational endpoint As for safety data, there were similar proportion of patients reporting 1 treatment related adverse event on DFK and placebo. Most events were mild to moderate in severity, with one severe event occurring on placebo. 12 patients on DFK (19.4%) and 4 on placebo (6.3%) discontinued due to adverse event (concerningly high number on DFK arm). Dizziness and nausea were most common events. In Q&A, as for rates of discontinuation, management states that discontinuation rate in NP was consistent with what they saw in atopic dermatitis. They will need to do some "dose finding" going forward, but are not considering titration. As for institutional investors of note, I mentioned prior that Vifor owns nearly 14% of the company. Otherwise, a possible red flag or at least neutral point is that I see mainly generalist funds in this one (BlackRock with 13.5% stake and Vanguard with 5.6% stake). As for insiders, CEO Chris Posner owns over 200,00 shares. Steady history of sales by multiple members of leadership over the past year(s) is not encouraging.
Seeking Alpha Aug 19

Cara, Vifor's Kapruvia gets approval in Switzerland to treat itch in hemodialysis patients

The Swiss Agency for Therapeutic Products (Swissmedic) approved Cara Therapeutics (NASDAQ:CARA) and Vifor Fresenius Medical Care Renal Pharma's Kapruvia (difelikefalin) to treat moderate-to-severe pruritus (itching) associated with chronic kidney disease in adult hemodialysis patients. The companies said Kapruvia is the first and only therapy approved through consortium filing for treating this particular condition in these patients. The approval was backed by data from two pivotal phase 3 trials – KALM-1, conducted in the U.S., and the global study, dubbed KALM-2 — plus supportive data from an additional 32 clinical studies. Kapruvia is approved in Canada under the name Korsuva. The companies expect regulatory decisions in Australia and Singapore by the end of 2022. Vifor Fresenius is a joint company of CSL (OTCPK:CSLLY) (OTCPK:CMXHF) and Fresenius Medical Care (FMS). CSL had acquired Vifor Pharma (OTCPK:GNHAY) in a ~$11.7B deal.
Seeking Alpha Aug 08

Cara Therapeutics GAAP EPS of -$0.08 beats by $0.18, revenue of $23M beats by $1.97M

Cara Therapeutics press release (NASDAQ:CARA): Q2 GAAP EPS of -$0.08 beats by $0.18. Revenue of $23M beats by $1.97M. Cash, cash equivalents and marketable securities at June 30, 2022 totaled $204.7 million compared to $236.8 million at December 31, 2021. The decrease in the balance primarily resulted from $30.0 million of cash used in operating activities. Shares -6.43%.
Seeking Alpha Jun 24

Calls A Much Safer Way To Buy Cara Therapeutics

Since I wrote my bullish call on Cara Therapeutics, the shares have absolutely collapsed. I thought I'd revisit the name again to see if I should add, hold, or sell. The company reported earnings, and the same trend persists: the company sells more, and loses more, and this trend needs to be reversed. I think call options are the best way to play this. They give most of the upside, at a fraction of the cost.
分析記事 Jun 15

We're Not Very Worried About Cara Therapeutics' (NASDAQ:CARA) Cash Burn Rate

Even when a business is losing money, it's possible for shareholders to make money if they buy a good business at the...
分析記事 May 12

Brokers Are Upgrading Their Views On Cara Therapeutics, Inc. (NASDAQ:CARA) With These New Forecasts

Cara Therapeutics, Inc. ( NASDAQ:CARA ) shareholders will have a reason to smile today, with the analysts making...
Seeking Alpha Mar 21

Taking A (Speculative) Position In Cara Therapeutics

I think the financial history here has been pretty bad. The company has only turned a profit in one of the past nine years. That said, investors in companies like this care far less about the past than the future, and the shares are reasonably priced in my view. Since this is a bit of a lottery ticket, most of my bullishness will be expressed via call options. These offer most of the taste at far less calories.
分析記事 Mar 09

Companies Like Cara Therapeutics (NASDAQ:CARA) Are In A Position To Invest In Growth

We can readily understand why investors are attracted to unprofitable companies. For example, biotech and mining...

株主還元

CARAUS PharmaceuticalsUS 市場
7D8.6%1.9%-0.8%
1Y-39.4%41.8%27.1%

業界別リターン: CARA過去 1 年間で41.8 % の収益を上げたUS Pharmaceuticals業界を下回りました。

リターン対市場: CARAは、過去 1 年間で27.1 % のリターンを上げたUS市場を下回りました。

価格変動

Is CARA's price volatile compared to industry and market?
CARA volatility
CARA Average Weekly Movement10.3%
Pharmaceuticals Industry Average Movement10.0%
Market Average Movement7.2%
10% most volatile stocks in US Market16.3%
10% least volatile stocks in US Market3.2%

安定した株価: CARA 、 US市場と比較して、過去 3 か月間で大きな価格変動はありませんでした。

時間の経過による変動: CARAの 週次ボラティリティ は、過去 1 年間で17%から10%に減少しました。

会社概要

設立従業員CEO(最高経営責任者ウェブサイト
200410Chris Posnerwww.caratherapeutics.com

Cara Therapeutics, Inc.は、米国で慢性そう痒症治療薬の開発・商業化に注力するバイオ医薬品企業です。同社の主力製品は、血液透析を受けている成人の慢性腎臓病(CKD)に伴う中等度から重度のそう痒症を治療するコルスバ(ジフェリケファリン)注射剤である。また、ジフェリケファリン経口剤の開発も行っており、感覚鈍麻を伴う慢性そう痒症の治療薬として第II/III相臨床試験中である。日本では丸石製薬株式会社と急性疼痛および尿毒症性そう痒症を適応症とするジフェリケファリン含有製剤の開発・製造・販売に関するライセンス契約を、Vifor Fresenius Medical Care Renal Pharma Ltd.と血液透析を受けている成人患者における中等度から重度のそう痒症を適応症とするコルスバ注射剤の開発・販売に関するライセンス契約を、Chong Kun Dang Pharmaceutical Corporationと韓国におけるジフェリケファリン含有製剤の開発・製造・販売に関するライセンス契約を締結しています。カラ・セラピューティクス社は2004年に設立され、コネチカット州スタンフォードに本社を置いている。

Cara Therapeutics, Inc. 基礎のまとめ

Cara Therapeutics の収益と売上を時価総額と比較するとどうか。
CARA 基礎統計学
時価総額US$24.33m
収益(TTM)-US$70.87m
売上高(TTM)US$7.14m
3.4x
P/Sレシオ
-0.3x
PER(株価収益率

収益と収入

最新の決算報告書(TTM)に基づく主な収益性統計
CARA 損益計算書(TTM)
収益US$7.14m
売上原価US$36.39m
売上総利益-US$29.25m
その他の費用US$41.62m
収益-US$70.87m

直近の収益報告

Dec 31, 2024

次回決算日

該当なし

一株当たり利益(EPS)-46.48
グロス・マージン-409.85%
純利益率-992.95%
有利子負債/自己資本比率-967.7%

CARA の長期的なパフォーマンスは?

過去の実績と比較を見る

企業分析と財務データの現状

データ最終更新日(UTC時間)
企業分析2025/04/16 17:24
終値2025/04/15 00:00
収益2024/12/31
年間収益2024/12/31

データソース

企業分析に使用したデータはS&P Global Market Intelligence LLC のものです。本レポートを作成するための分析モデルでは、以下のデータを使用しています。データは正規化されているため、ソースが利用可能になるまでに時間がかかる場合があります。

パッケージデータタイムフレーム米国ソース例
会社財務10年
  • 損益計算書
  • キャッシュ・フロー計算書
  • 貸借対照表
アナリストのコンセンサス予想+プラス3年
  • 予想財務
  • アナリストの目標株価
市場価格30年
  • 株価
  • 配当、分割、措置
所有権10年
  • トップ株主
  • インサイダー取引
マネジメント10年
  • リーダーシップ・チーム
  • 取締役会
主な進展10年
  • 会社からのお知らせ

* 米国証券を対象とした例であり、非米国証券については、同等の規制書式および情報源を使用

特に断りのない限り、すべての財務データは1年ごとの期間に基づいていますが、四半期ごとに更新されます。これは、TTM(Trailing Twelve Month)またはLTM(Last Twelve Month)データとして知られています。詳細はこちら

分析モデルとスノーフレーク

本レポートを生成するために使用した分析モデルの詳細は当社のGithubページでご覧いただけます。また、レポートの使用方法に関するガイドYoutubeのチュートリアルも掲載しています。

シンプリー・ウォールストリート分析モデルを設計・構築した世界トップクラスのチームについてご紹介します。

業界およびセクターの指標

私たちの業界とセクションの指標は、Simply Wall Stによって6時間ごとに計算されます。

アナリスト筋

Cara Therapeutics, Inc. 1 これらのアナリストのうち、弊社レポートのインプットとして使用した売上高または利益の予想を提出したのは、 。アナリストの投稿は一日中更新されます。12

アナリスト機関
Jason Matthew GerberryBofA Global Research
Kenneth TrbovichBrean Capital Historical (Janney Montgomery)
Corey DavisCanaccord Genuity