NasdaqCM:MTVA - アナリストの将来予測と過去の財務データ ( )USD Millions
日付	収益	収益	フリー・キャッシュフロー	営業活動によるキャッシュ	平均アナリスト数
12/31/2028	N/A	-33	N/A	N/A	3
12/31/2027	N/A	-28	N/A	N/A	3
12/31/2026	N/A	-18	N/A	N/A	3
12/31/2025	N/A	-13	-16	-16	N/A
9/30/2025	N/A	-16	-16	-16	N/A
6/30/2025	N/A	-18	-19	-19	N/A
3/31/2025	N/A	-25	-23	-23	N/A
12/31/2024	N/A	-28	-25	-25	N/A
9/30/2024	N/A	-28	-23	-23	N/A
6/30/2024	N/A	-26	-20	-20	N/A
3/31/2024	N/A	-17	-15	-15	N/A
12/31/2023	N/A	-12	-11	-11	N/A
9/30/2023	N/A	-12	-9	-9	N/A
6/30/2023	N/A	-11	-9	-9	N/A
3/31/2023	N/A	-14	-9	-9	N/A
12/31/2022	N/A	-14	-12	-12	N/A
9/30/2022	N/A	-14	-13	-13	N/A
6/30/2022	N/A	-14	-13	-13	N/A
3/31/2022	N/A	-15	-14	-14	N/A
12/31/2021	N/A	-15	-15	-15	N/A
9/30/2021	N/A	-30	-15	-15	N/A
6/30/2021	N/A	-30	-14	-14	N/A
3/31/2021	N/A	-28	-13	-13	N/A
12/31/2020	N/A	-30	-11	-11	N/A
9/30/2020	N/A	-23	-10	-10	N/A
6/30/2020	N/A	-24	-11	-11	N/A
3/31/2020	N/A	-24	-10	-10	N/A
12/31/2019	N/A	-21	-7	-7	N/A
9/30/2019	N/A	-12	N/A	-10	N/A
6/30/2019	N/A	-11	N/A	-9	N/A
3/31/2019	N/A	-13	N/A	-12	N/A
12/31/2018	N/A	-16	N/A	-14	N/A

アナリストによる今後の成長予測

収入対貯蓄率: MTVA今後 3 年間、利益が出ない状態が続くと予測されています。

収益対市場: MTVA今後 3 年間、利益が出ない状態が続くと予測されています。

高成長収益: MTVA今後 3 年間、利益が出ない状態が続くと予測されています。

収益対市場: MTVAの収益がUS市場よりも速く成長すると予測されるかどうかを判断するにはデータが不十分です。

高い収益成長: MTVA来年は収益がないと予測されています。

一株当たり利益成長率予想

将来の株主資本利益率

将来のROE: MTVAの自己資本利益率が 3 年後に高くなると予測されるかどうかを判断するにはデータが不十分です

成長企業の発掘

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	2026/05/14 09:34
終値	2026/05/14 00:00
収益	2025/12/31
年間収益	2025/12/31

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	SECフォーム10-K SECフォーム10-Q
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	アナリストリサーチレポート Blue Matrix
市場価格	30年	株価配当、分割、措置	ICEマーケットデータ SECフォームS-1
所有権	10年	トップ株主インサイダー取引	SECフォーム4 SECフォーム13D
マネジメント	10年	リーダーシップ・チーム取締役会	SECフォーム10-K SECフォームDEF 14A
主な進展	10年	会社からのお知らせ	SECフォーム8-K

* 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

MetaVia Inc. 3 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。3

アナリスト	機関
Andrew Fein	H.C. Wainwright & Co.
Jason McCarthy	Maxim Group
David Bautz	Zacks Small-Cap Research

MetaVia 将来の成長

Future 基準チェック /06

主要情報

今後の成長に関する最新情報

Price target decreased by 16% to US$132

Price target increased by 40% to US$20.00

Price target decreased by 7.5% to US$14.33

Price target decreased by 35% to US$17.33

No longer forecast to breakeven

No longer forecast to breakeven

Recent updates

MetaVia Inc., Annual General Meeting, Jun 08, 2026

Metavia Inc Doses First Patient in Higher-Dose Phase 1 Study of Da-1726

Metavia Inc. Advances GLP-1-Based Obesity Program with IRB Approval for Higher-Dose Phase 1 Studies of DA-1726

MetaVia Inc Expands Global Patent Protection For Vanoglipel Supporting Metabolic And Liver Disease Therapy Through 2035

MetaVia Inc. Announces Positive AI-Modeling Results from its Ongoing Syntekabio Collaboration, Confirming Key Therapeutic Targets for Vanoglipel

MetaVia Inc. has completed a Composite Units Offering in the amount of $8.099988 million.

Metavia Inc. Reports Positive Statistically Significant Results from Its Phase 1B Clinical Trial of DA-1726 in Metabolic Disease - Demonstrating Strong Glycemic Response, Significant Direct Hepatic Effects, Robust Weight Loss and Favorable Safety Profile

Price target decreased by 16% to US$132

Nasdaq Grants Extension to MetaVia Inc. to Regain Minimum Bid Price Compliance

MetaVia Inc. Presents Positive New Phase 2A Data on Vanoglipel (Da-1241) in Patients with Presumed Mash At the Aasld the Liver Meeting®? 2025

We're Keeping An Eye On MetaVia's (NASDAQ:MTVA) Cash Burn Rate

Price target increased by 40% to US$20.00

New major risk - Financial position

MetaVia Inc. Extends 48 Mg Mad Portion of Its Phase 1 Clinical Trial of Da-1726 for the Treatment of Obesity to 8 Weeks and Announces Fifth Weekly Dose in First Patient

MetaVia Inc. Doses First Patient in the 48 mg MAD Cohort of Its Phase 1 Clinical Trial Evaluating DA-1726 for the Treatment of Obesity to Further Explore Maximum Tolerated Dose

MetaVia Inc. Presents Pre-Clinical Data on DA-1241 Demonstrating Additive Hepatoprotective Effects in Combination with Efruxifermin at the ADA's 85th Scientific Session

MetaVia Receives Non-Compliance Letter from Nasdaq Regarding Minimum Bid Price Requirement

MetaVia Inc., Annual General Meeting, Jun 30, 2025

Price target decreased by 7.5% to US$14.33

MetaVia Inc. announced that it has received $9.995395 million in funding

MetaVia Inc. announced that it expects to receive $9.995395 million in funding

Metavia Inc. Presents Data on DA-1241, GPR119 Agonist, Demonstrating Both Hepatoprotective and Glucose-Regulating Effects in Patients with Presumed Mash, at the EASL Congress 2025

MetaVia Inc. Reports Additional Positive Top-Line Results from the MAD Part 2 of Its Phase 1 Study of DA-1726

New major risk - Market cap size

MetaVia Inc. Announces Clinical Trials

Price target decreased by 35% to US$17.33

MetaVia Inc. Announces Positive Top-Line Results From Its Phase 2a Clinical Trial of DA-1241 in Patients with Presumed MASH

New major risk - Financial position

NeuroBo Pharmaceuticals, Inc. Completes Last Patient Last Visit in Its Phase 2a Clinical Trial Evaluating DA-1241 for the Treatment of MASH

Here's Why We're A Bit Worried About NeuroBo Pharmaceuticals' (NASDAQ:NRBO) Cash Burn Situation

Neurobo Pharmaceuticals Announces Positive Top-Line Data from the Sad Part 1 of Its Phase 1 Clinical Trial Evaluating Da-1726 for the Treatment of Obesity

NeuroBo Pharmaceuticals, Inc. Completes Enrollment of the SAD Part 1 of Its Phase 1 Clinical Trial Evaluating DA-1726 for the Treatment of Obesity

NeuroBo Pharmaceuticals, Inc. announced that it has received $17.000005 million in funding from Dong-A ST Co., Ltd.

NeuroBo Pharmaceuticals, Inc. Doses First Patient in the MAD Part 2 of its Phase 1 Clinical Trial Evaluating DA-1726 for the Treatment of Obesity

NeuroBo Pharmaceuticals, Inc. has filed a Follow-on Equity Offering in the amount of $3.000001 million.

NeuroBo Pharmaceuticals, Inc., Annual General Meeting, Jun 07, 2024

NeuroBo Pharmaceuticals, Inc. Doses First Patient in Its Phase 1 Clinical Trial Evaluating Da-1726 for the Treatment of Obesity

NeuroBo Pharmaceuticals, Inc. Completes Enrollment of Part 1 of Its Phase 2A Clinical Trial Evaluating DA-1241 for the Treatment of Mash

NeuroBo Pharmaceuticals, Inc. Receives Safety Review Committee Approval to Continue with Its Phase 2A Clinical Trial Evaluating DA-1241 for the Treatment of Mash

NeuroBo Pharmaceuticals Announces FDA Clearance of IND for a Phase 1 Clinical Trial of DA-1726 for the Treatment

Neurobo Pharmaceuticals Reports Positive Pre-Clinical Safety Data of Da-1241 in Combination with Sitagliptin and Opens Enrollment for Part 2 of Its Phase 2A Clinical Trial Evaluating Da-1241 for the Treatment of Mash

NeuroBo Pharmaceuticals Submits IND Application to the FDA for a Phase 1 Clinical Trial of DA-1726 for the Treatment of Obesity

NeuroBo Pharmaceuticals, Inc. Appoints James P. Tursi to its Board of Directors and as Member of Nominating and Corporate Governance Committee

NeuroBo Pharmaceuticals, Inc. Appoints Marshall H. Woodworth as Acting Chief Financial Officer

NeuroBo Pharmaceuticals, Inc. Announces Resignation of Na Yeon (Irene) Kim from the Board of Directors

NeuroBo Pharmaceuticals, Inc. Doses First Patient in Its Phase 2a Clinical Trial Evaluating DA-1241 for the Treatment of Nash

NeuroBo Pharmaceuticals, Inc. Announces Executive Changes

NeuroBo Pharmaceuticals Receives 180-Day Extension to February 5, 2024 from Nasdaq to Regain Compliance with the Minimum Bid Price Requirement

Neurobo Pharmaceuticals, Inc. Receives First Site IRB Approval for Its Phase 2A Clinical Trial Evaluating DA-1241 for the Treatment of NASH

NeuroBo Pharmaceuticals, Inc., Annual General Meeting, Jun 28, 2023

Neurobo Pharmaceuticals, Inc. Appoints Pharmaceutical Industry Executive, Mark A. Glickman, to Its Board of Directors

NeuroBo Pharmaceuticals Receives Non-Compliance Notice from Nasdaq

NeuroBo Pharmaceuticals, Inc. Appoints Joseph Hooker as President

NeuroBo Pharmaceuticals, Inc. announced that it has received $15 million in funding from Dong-A ST Co., Ltd.

NeuroBo Pharmaceuticals Compliant with All Applicable Nasdaq Listing Criteria

NeuroBo Pharmaceuticals regains compliance with Nasdaq minimum bid price requirement

NeuroBo Pharmaceuticals, Inc. announced that it expects to receive $37 million in funding from Dong-A ST Co., Ltd.

Here's Why NeuroBo Pharmaceuticals (NASDAQ:NRBO) Must Use Its Cash Wisely

NeuroBo Pharmaceuticals climbs higher on announcing reverse stock split

NeuroBo Pharmaceuticals, Inc., Annual General Meeting, Jun 09, 2022

Neurobo Pharmaceuticals, Inc. Appoints Matthew Bardin as Senior Vice President Operations

High number of new and inexperienced directors

NeuroBo Pharmaceuticals, Inc. Appoints D. Gordon Strickland to its Board of Directors

NeuroBo Pharmaceuticals: Advancing Therapies For Viral, Neuropathic And Neurodegenerative Diseases

No longer forecast to breakeven

Independent Director Jeong Gyun Oh has left the company

No longer forecast to breakeven

Price target decreased to US$16.00

NeuroBo Pharmaceuticals, Inc.(NasdaqCM:NRBO) dropped from Russell 3000E Index