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89bio 過去の業績
過去 基準チェック /06
89bioの収益は年平均-42.8%で減少しているが、Biotechs業界はgrowingで33.8%年平均の収益となった。
主要情報
-42.77%
収益成長率
12.63%
EPS成長率
| Biotechs 業界の成長 | 17.04% |
| 収益成長率 | n/a |
| 株主資本利益率 | -86.29% |
| ネット・マージン | n/a |
| 前回の決算情報 | 30 Jun 2025 |
最近の業績更新
更新なし
Recent updates
Seeking Alpha • Sep 18
89bio: Pegozafermin MASH Drug Advancement Nets Roche Acquisition
Summary Roche has agreed to acquire 89bio for up to $3.5 billion, driven by pegozafermin's promise in MASH and SHTG. ETNB shareholders will receive $14.50 per share in cash upfront, with an additional $6.00 per share via non-tradeable CVRs tied to milestones. Pegozafermin's best-in-disease profile and accelerated approval pathways for MASH were key to Roche's interest, despite competition from GSK and Akero. The acquisition relieves ETNB's cash runway concerns, but risks remain regarding deal closure, milestone achievement, and competitive landscape. Read the full article on Seeking Alpha分析記事 • May 22
Is 89bio (NASDAQ:ETNB) A Risky Investment?
David Iben put it well when he said, 'Volatility is not a risk we care about. What we care about is avoiding the...Seeking Alpha • Apr 17
89bio: Primary Asset Targeting 2 Potential Indications And Is In Late-Stage Development
Summary 89bio, Inc. is a clinical-stage biotech focused on liver and cardio-metabolic diseases, with its lead drug candidate pegozafermin in late-stage development. Analysts are mostly optimistic on the company, and 89bio has recently addressed its near-term funding needs. ETNB stock is trading much lower than the first time I looked at it just over a year and a half ago. An updated analysis around 89bio, Inc. follows in the paragraphs below. Read the full article on Seeking AlphaSeeking Alpha • Jan 30
89bio's Pegozafermin Is Now Gaining Momentum
Summary 89bio's main value driver is Pegozafermin. It has two Phase 3 trials: one for MASH and the other for SHTG. Management mentioned we should get its SHTG topline data by 2H2025. This could be a pivotal milestone for ETNB's long-term prospects. After AKRO’s recent Phase 2b data, I think ETNB’s prospects have improved because it indirectly validated its FGF21 approach as well. I still have some cash burn concerns, even after the recent $250 million raise. However, ETNB has ample upside potential if it’s successful. Read the full article on Seeking AlphaSeeking Alpha • Jan 13
89bio: Advancement Of Pegozafermin For SHTG Is Another Path Forward
Summary 89bio, Inc. results from the phase 3 ENTRUST study using pegozafermin for the treatment of patients with Severe Hypertriglyceridemia are expected in the 2nd half of 2025. Prior data from the phase 2 ENTRIGUE study indicated that patients treated with all doses of pegozafermin were able to achieve the primary endpoint with statistical significance. The global severe hypertriglyceridemia treatment market is expected to reach $2.67 billion by 2033. Pegozafermin is also being explored in the two phase 3 studies ENLIGHTEN-fibrosis and ENLIGHTEN-cirrhosis, which target patients with non-cirrhotic F2-F3 MASH and compensated cirrhotic F4 MASH. Read the full article on Seeking AlphaSeeking Alpha • Oct 29
89bio: Surviving A Competitive Space - For Now
Summary Madrigal's resmetirom approval impacted THR-β stocks positively, while non-THR-β stocks like 89bio's pegozafermin fell, highlighting a market preference for THR-β mechanisms. Pegozafermin, an FGF21 analog, showed promising Phase 2b results, but faces competition from other FGF21 molecules and GLP-1 drugs with strong efficacy. The MASH market is expected to diversify across multiple mechanisms, suggesting a strategy of spreading investments rather than focusing on a single approach. ETNB has a solid financial runway but faces risks from GLP-1 data and competition within the FGF21 space, making it a Hold for now. Read the full article on Seeking Alpha分析記事 • Sep 26
Health Check: How Prudently Does 89bio (NASDAQ:ETNB) Use Debt?
Legendary fund manager Li Lu (who Charlie Munger backed) once said, 'The biggest investment risk is not the volatility...Seeking Alpha • Aug 07
89bio: Bullish In Light Of Further MOA Being Established By Peer
Summary 89bio, Inc. has two phase 3 studies underway, known as ENLIGHTEN-Fibrosis and ENLIGHTEN-Cirrhosis, which are using pegozafermin to target F2 — F3 and F4 compensated cirrhosis MASH patients respectively. The promise of the two ongoing phase 3 ENLIGHTEN studies is that there was alignment gained with the FDA that each could use an interim analysis endpoint for potential Accelerated Approval. The global non-alcoholic steatohepatitis market is projected to reach $24.26 billion by 2028. Results from the ongoing phase 3 ENTRUST study, using pegozafermin for the treatment of patients with severe hypertriglyceridemia, expected in 2025. Read the full article on Seeking AlphaSeeking Alpha • May 23
89bio: Pegozafermin Could Be A Game-Changer For Liver Disease - Strong Buy
Summary 89bio is a clinical-stage biopharmaceutical company that develops therapies for liver and cardiometabolic conditions. Their drug candidate, pegozafermin, has shown positive results in reducing liver fat and insulin resistance and is in phase 3 trials for metabolic dysfunction-associated steatohepatitis (MASH) and severe hypertriglyceridemia (SHTG). Pegozafermin has the potential to tap into a large market and has been granted FDA Breakthrough Therapy designation for treating MASH with fibrosis. Due to its metabolic regulation properties, pegozafermin's broader potential includes applications in Type 2 Diabetes, obesity, and other inflammatory diseases. I rate ETNB stock a “strong buy” due to Pegozafermin’s promising clinical data, substantial market potential, and robust financials. Read the full article on Seeking AlphaSeeking Alpha • Oct 06
89bio Still Has A Chance As NASH Race Heats Up
Summary 89bio's share price is up >100% over the past three months. The company is developing Pegozafermin, a potential therapy for NASH and SHTG. Data released by Akero for its drug Efruxifermin - which has the same mechanism of action as Pego - suggested it would meet the FDA's approval criteria in NASH. 89bio will release Phase 2b NASH data in Q123 - there's a chance its data could be as strong as Akero's. 89Bio is a gamble - this is a small biotech taking on industry giants in a field where no drug has ever been approved. Risk-on investors may sense opportunity, however. Overview - Akero's Data for FGF21 Mimic EFX Is Best In Class For NASH - 89bio's Pegozafermin Has Same MoA At the beginning of September, the share price of Akero Therapeutics (AKRO) - a small biotech ~7% owned by Pharma giant Pfizer (PFE) - rose from $12, to $27, and a few days later, from $27, to $40 - an overall gain of 233%. The reason for the gains was the company's publication of data from a Phase 2b trial - HARMONY - of its lead asset, Efruxifermin ("EFX') in patients with pre-cirrhotic nonalcoholic steatohepatitis ("NASH"), fibrosis stage 2 or 3 ("F2-F3"). In the study, at the 50mg and 28mg dose levels, 41% and 39% of EFX-treated patients respectively experienced at least a one-stage improvement in liver fibrosis with no worsening of NASH by Week 24, compared to 20% within the placebo group. The secondary goal of the study - achieving NASH resolution without worsening of fibrosis - also was achieved, with 76% of the 50mg arm and 47% of the 28mg arm meeting this criteria, vs. 15% of patients in the placebo arm. Given that the FDA's approval criteria for a NASH drug is improvement of ≥1 stage in fibrosis with no worsening of NASH, or improvement in NASH resolution with no worsening of fibrosis, hopes are high that Akero could wind up winning the "NASH Dash," the race to be the first drug approved to treat the disease, which has a prevalence of ~16.5m cases, expected to rise to 27m cases by 2030, and is the "fastest growing reason for a liver transplant in the United States," according to the subject of this article - 89bio (ETNB). Akero's drug EFX is engineered to mimic the biological activity profile of native FGF21. As I explained in my last note on 89bio: FGF21 is an "endogenous metabolic hormone that regulates energy homeostasis, glucose-lipid-protein metabolism and insulin sensitivity", which is secreted primarily by the liver, and has been clinically proven to reduce liver steatosis by increasing fatty acid oxidation, reducing free fatty acid deposits migrating from peripheral tissue to the liver, and reducing de-novo lipogenesis ("DNL"). 89bio has developed its own NASH candidate, now called Pegozafermin, which is a "a specifically engineered glycoPEGylated analog of fibroblast growth factor 21 (“FGF21”)." In other words, it had the same mechanism of action ("MoA") as Akero's EFX. A third company, pharma giant Novo Nordisk (NVO), also has a NASH candidate targeting FGF21. 89bio's share price has also been rising in recent months - by >140% since early July, no doubt due to the progress being made by Akero, but while Akero's market cap valuation currently stands at $1.83bn, 89bio's is just $266m 89bio - Progress to Date In an expansion cohort of a Phase 1b/2a study, in which 19 of 20 patients received end-of-treatment biopsies, Pegozafermin demonstrated clinically meaningful changes on endpoints including 26% of patients achieving a one-point or more improvement in fibrosis, and 47% achieving NASH resolution or improvement in fibrosis. The data does not seem quite as strong as Akero's, although there was only one patient withdrawal, out of 81 total patients, vs. five in the EFX study, out of 72 patients, suggesting Pegozafermin may have the superior safety profile. Pegozafermin also performed well across a host of other endpoints, including NAFLD Activity Score (NAFLD stands for Non-alcoholic Fatty Liver Disease which can lead to NASH) - 63% of patients had a 2-point or more improvement in NASH and no worsening of fibrosis - liver fat reduction - 50% of patients in Cohort 6 achieved a 50% of higher reduction in liver fat, and >70% in Cohort 4 and 7 - and reduction in alanine transaminase ("ALT") levels, with the same cohorts all achieving >40% reduction, versus 4% of the placebo arm. Based on the positive data, 89bio now has a fully enrolled Phase 2b study - ENLIVEN - ongoing, as shown in the diagram below: 89Bio Phase 2b study design (89Bio) The study will read out data in Q123, management promises in its Q222 10Q submission, whilst also noting that it has: completed a pharmacokinetic study of pegozafermin in NASH patients with compensated cirrhosis (fibrosis stage F4) demonstrating that pegozafermin 30 mg has similar single-dose pharmacokinetics and pharmacodynamics in F4 as it does in non-cirrhotic NASH. In other words, if the drug works in F2 and F3 patients, it could potentially work in F4 stage patients also, who have a more debilitating form of the disease, as shown below. NASH explained (89Bio) In short, 89bio's drug Pegozafermin appears to tick a lot of the boxes required to position itself as a genuine contender in the "NASH Dash," an admittedly crowded field, encompassing many different approaches and drug classes. It's interesting to note a comparison made by 89bio between leading contenders in the race to approval. NASH contenders compared (89Bio) Once again, EFX appears to have the slight edge over its competitors at this stage - and bear in mind this table was created by 89bio - but it doesn't seem impossible that Pegozafermin could make up the small differences in a larger trial. Akero is planning a second Phase B study in NASH patients whose condition is worse than in its HARMONY study, with results expected to be available next year, as well as a Phase 3 study. Meanwhile, Madrigal Pharmaceuticals has reported positive data from a Phase trial in NAFLD, and has a second Phase 3 ongoing that includes some patients with non-cirrhotic NASH. Sizing Up The Market NASH is a potentially massive (~$30bn+) market - as mentioned above, close to 30m people in the US may be diagnosed with the disease by 2030 - although it's not necessarily a clearly defined market. For example, many patients with NASH also have Type 2 diabetes, and two major drugs have recently hit the Type 2 diabetes market - Eli Lilly's (LLY) Mounjaro, and Novo Nordisk's Ozempic, that are also indicated to treat obesity under different brand names - Lilly's Tirzepatide is not yet approved in obesity (it will be approved under a different name to Mounjaro), while Novo Nordisk's once-weekly semaglutide subcutaneous injection is approved in obesity under the brand name Wegovy. These two drugs are forecast to potentially generate peak sales of >$20bn, and may be prescribed off-label to treat NASH, meaning that drugs approved specifically for NASH, such as Pegozafermin and EFX, could struggle to find a market. Additionally, many physicians have expressed unwillingness to prescribe drugs to treat NASH, preferring to encourage patients to embrace healthier lifestyle choices. Nevertheless, the response to Akero's data suggests that the market believes a drug approved for NASH could thrive, and in 89bio's case, with its small market cap valuation, it's not hard to see the share price rocketing if data from the Phase 2b is genuinely competitive. The path to commercial success would be tricky - 89bio reported a cash position of just $139m as of Q222, and management does not have the necessary experience - although the company could raise huge sums if the share price spikes without upsetting its existing shareholders, and make some key hires - who wouldn't want to work on the commercialization of one of the first ever approved NASH drugs?Seeking Alpha • Aug 18
89bio completes enrollment in phase 2 trial for NASH treatment
89bio (NASDAQ:ETNB) said it had completed enrollment of 219 patients in the Phase 2b trial of its drug, pegozafermin, to treat NASH. The company expects to report topline data from the trial, Enliven, in the first quarter of 2023. ENLIVEN is a placebo-controlled Phase 2b trial in biopsy-confirmed NASH patients with fibrosis stage 2 or 3. Patients will receive either one of two weekly doses (15mg or 30mg) or an every two-week dose (44mg) of pegozafermin in a liquid formulation or placebo for 24 weeks.Seeking Alpha • Jul 07
89Bio rallies on Deep Track Capital disclosing 10% stake
89Bio (NASDAQ:ETNB) announced that Deep Track Capital disclosed a 9.99% stake in the company which equals to 4.3M shares ownership. Shares trading 12% higher premarket. Quick look at ownership structure:収支内訳
収支内訳
89bio の稼ぎ方とお金の使い方。LTMベースの直近の報告された収益に基づく。
収益と収入の歴史
| 日付 | 収益 | 収益 | G+A経費 | 研究開発費 |
|---|---|---|---|---|
| 30 Jun 25 | 0 | -450 | 45 | 421 |
| 31 Mar 25 | 0 | -387 | 41 | 362 |
| 31 Dec 24 | 0 | -367 | 40 | 345 |
| 30 Sep 24 | 0 | -289 | 37 | 267 |
| 30 Jun 24 | 0 | -175 | 34 | 157 |
| 31 Mar 24 | 0 | -165 | 33 | 147 |
| 31 Dec 23 | 0 | -142 | 29 | 122 |
| 30 Sep 23 | 0 | -127 | 28 | 108 |
| 30 Jun 23 | 0 | -119 | 25 | 98 |
| 31 Mar 23 | 0 | -105 | 22 | 83 |
| 31 Dec 22 | 0 | -102 | 21 | 81 |
| 30 Sep 22 | 0 | -104 | 20 | 83 |
| 30 Jun 22 | 0 | -105 | 20 | 84 |
| 31 Mar 22 | 0 | -101 | 20 | 80 |
| 31 Dec 21 | 0 | -90 | 19 | 70 |
| 30 Sep 21 | 0 | -76 | 18 | 58 |
| 30 Jun 21 | 0 | -63 | 17 | 46 |
| 31 Mar 21 | 0 | -54 | 15 | 39 |
| 31 Dec 20 | 0 | -49 | 13 | 36 |
| 30 Sep 20 | 0 | -56 | 12 | 35 |
| 30 Jun 20 | 0 | -60 | 10 | 30 |
| 31 Mar 20 | 0 | -64 | 8 | 25 |
| 31 Dec 19 | 0 | -57 | 5 | 21 |
| 30 Sep 19 | 0 | -44 | 4 | 19 |
| 30 Jun 19 | 0 | -30 | 3 | 16 |
質の高い収益: ETNBは現在利益が出ていません。
利益率の向上: ETNBは現在利益が出ていません。
フリー・キャッシュフローと収益の比較
過去の収益成長分析
収益動向: ETNBは利益が出ておらず、過去 5 年間で損失は年間42.8%の割合で増加しています。
成長の加速: ETNBの過去 1 年間の収益成長を 5 年間の平均と比較することはできません。現在は利益が出ていないためです。
収益対業界: ETNBは利益が出ていないため、過去 1 年間の収益成長をBiotechs業界 ( 43% ) と比較することは困難です。
株主資本利益率
高いROE: ETNBは現在利益が出ていないため、自己資本利益率 ( -86.29% ) はマイナスです。
総資産利益率
使用総資本利益率
過去の好業績企業の発掘
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 | 2025/10/29 20:10 |
| 終値 | 2025/10/29 00:00 |
| 収益 | 2025/06/30 |
| 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 |
| |
| アナリストのコンセンサス予想 | +プラス3年 |
|
|
| 市場価格 | 30年 |
| |
| 所有権 | 10年 |
| |
| マネジメント | 10年 |
| |
| 主な進展 | 10年 |
|
* 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や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
89bio, Inc. 7 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。4
| アナリスト | 機関 |
|---|---|
| Geoffrey Meacham | Citigroup Inc |
| Andrea Newkirk | Goldman Sachs |
| Andrea Newkirk | Goldman Sachs |