Zevra Therapeutics Temettüler ve Geri Alımlar

Temettü kriter kontrolleri 0/6

Zevra Therapeutics şirketinin temettü ödeme geçmişi bulunmamaktadır.

Anahtar bilgiler

n/a

Temettü verimi

-14.9%

Geri Alım Getirisi

Toplam Hissedar Getirisi	-14.9%
Gelecekteki Temettü Verimi	n/a
Temettü Büyümesi	n/a
Bir sonraki temettü ödeme tarihi	n/a
Eski temettü tarihi	n/a
Hisse başına temettü	n/a
Ödeme oranı	n/a

Son temettü ve geri alım güncellemeleri

Recent updates

Ödemelerde İstikrar ve Büyüme

Temettü verilerini getirme

İstikrarlı Temettü: 1GDA şirketinin hisse başına düşen temettülerinin geçmişte istikrarlı olup olmadığını belirlemek için yeterli veri yok.

Büyüyen Temettü: 1GDA şirketinin temettü ödemelerinin artıp artmadığını belirlemek için yeterli veri yok.

Piyasaya Karşı Temettü Getirisi

Zevra Therapeutics Piyasaya Karşı Temettü Getirisi

1GDA temettü verimi piyasa ile karşılaştırıldığında nasıldır?
Segment	Temettü Verimi
Şirket (1GDA)	n/a
Pazarın Alt %25'i (DE)	1.7%
Pazarın En İyi %25'i (DE)	4.8%
Sektör Ortalaması (Pharmaceuticals)	1.4%
Analist tahmini (1GDA) (3 yıla kadar)	n/a

Önemli Temettü: 1GDA şirketinin temettü getirisi, şirketin yakın zamanda herhangi bir ödeme bildirmemesi nedeniyle, temettü ödeyenlerin en alttaki %25'lik dilimine göre değerlendirilemiyor.

Yüksek Temettü: Şirketin yakın zamanda herhangi bir ödeme bildirmemesi nedeniyle, 1GDA şirketinin temettü getirisi, temettü ödeyenlerin en üst %25'ine göre değerlendirilemiyor.

Hissedarlara Ödenen Kazanç

Kazanç Kapsamı: 1GDA şirketinin temettü ödemelerinin kazançlarla karşılanıp karşılanmadığını belirlemek için ödeme oranını hesaplamak üzere yeterli veri yok.

Hissedarlara Nakit Ödeme

Nakit Akışı Kapsamı: 1GDA herhangi bir ödeme bildirmediğinden temettülerin sürdürülebilirliği hesaplanamıyor.

Zevra Therapeutics Temettüler ve Geri Alımlar

Temettü kriter kontrolleri 0/6

Anahtar bilgiler

Son temettü ve geri alım güncellemeleri

KemPharm, Inc. (NasdaqGS:KMPH) announces an Equity Buyback for $50 million worth of its shares.

Recent updates

Zevra Therapeutics, Inc. Announces U.S. Commercial Availability of MIPLYFFA for Treatment of Niemann-Pick Disease Type C

Third quarter 2024 earnings released: US$0.69 loss per share (vs US$0.40 loss in 3Q 2023)

Zevra Therapeutics, Inc. to Report Q3, 2024 Results on Nov 12, 2024

High number of new directors

Second quarter 2024 earnings released: US$0.48 loss per share (vs US$0.15 loss in 2Q 2023)

Zevra Therapeutics, Inc. has completed a Follow-on Equity Offering in the amount of $60.000005 million.

New major risk - Shareholder dilution

Zevra Therapeutics, Inc. Announces FDA Advisory Committee Votes Favorably that the Data Support Arimoclomol as Effective Treatment for Patients with Niemann-Pick Disease Type C

Zevra Therapeutics, Inc. to Report Q2, 2024 Results on Aug 13, 2024

Independent Director recently bought €54k worth of stock

Zevra Therapeutics, Inc. has filed a Follow-on Equity Offering in the amount of $75 million.

Zevra Therapeutics, Inc. Expands Executive Leadership Team

Zevra Therapeutics Announces Positive Final Results from Phase 2 Clinical Trial of Kp1077 for Idiopathic Hypersomnia At Sleep 2024 Annual Meeting

First quarter 2024 earnings released: US$0.40 loss per share (vs US$0.34 loss in 1Q 2023)

Zevra Therapeutics, Inc. to Report Q1, 2024 Results on May 08, 2024

Zevra Therapeutics, Inc., Annual General Meeting, May 13, 2024

Full year 2023 earnings released: US$1.30 loss per share (vs US$1.21 loss in FY 2022)

Zevra Therapeutics, Inc. Announces Top-Line Data from the Phase 2 Clinical Trial of Kp1077 for Idiopathic Hypersomnia

Zevra Therapeutics, Inc. to Report Fiscal Year 2023 Results on Mar 28, 2024

Forecast breakeven date pushed back to 2026

Zevra Therapeutics, Inc. Appoints Alvin Shih to the Board of Directors

Zevra Therapeutics, Inc. Receives FDA Acceptance of Resubmission of NDA for Arimoclomol as a Treatment for Niemann-Pick Disease Type C

Zevra Therapeutics, Inc. Announces Resubmission of Arimoclomol New Drug Application to the U.S. Food and Drug Administration

New minor risk - Shareholder dilution

No longer forecast to breakeven

Zevra Therapeutics, Inc. to Report Q3, 2023 Results on Nov 07, 2023

Zevra Therapeutics, Inc. Announces Executive Changes

Zevra Therapeutics, Inc. Presents Full Data Set on the Cardiovascular Safety and Pharmacokinetics of Sdx, the Sole Active Pharmaceutical Ingredient in Kp1077, in Healthy Volunteers At Psych Congress 2023

New minor risk - Profitability

Zevra Therapeutics, Inc. (NasdaqGS:ZVRA) entered into definitive Agreement to acquire Acer Therapeutics Inc. (NasdaqCM:ACER) for $91 million.

Second quarter 2023 earnings released: US$0.15 loss per share (vs US$0.70 loss in 2Q 2022)

No longer forecast to breakeven

Zevra Therapeutics, Inc. Announces Board Changes

High number of new directors

First quarter 2023 earnings released: US$0.34 loss per share (vs US$0.054 loss in 1Q 2022)

Zevra Therapeutics, Inc. Announces Change of CEO, Effective June 1, 2023

Full year 2022 earnings released: US$1.21 loss per share (vs US$2.11 loss in FY 2021)

KemPharm, Inc. Appoints Daniel Gallo as Senior Vice President of Medical Affairs and Advocacy

KemPharm, Inc., Annual General Meeting, Apr 25, 2023

KemPharm, Inc. Announces Promotion of Sven Guenther to Chief Scientific Officer and Christal Mickle to Chief Product Development Officer

KemPharm, Inc. Appoints Richard W. Pascoe, as Chief Executive Officer

KemPharm Announces Initiation of Phase 2 Clinical Trial Investigating KP1077 for the Treatment of Idiopathic Hypersomnia (IH)

KemPharm, Inc. Appoints Christopher Posner as New Independent Director

KemPharm, Inc. Announces That the U.S. Food and Drug Administration (The FDA) Grants the Orphan Drug Designation to Serdexmethylphenidate

Third quarter 2022 earnings released: US$0.19 loss per share (vs US$0.05 loss in 3Q 2021)

No longer forecast to breakeven

No longer forecast to breakeven

Third quarter 2022 earnings released: US$0.19 loss per share (vs US$0.05 loss in 3Q 2021)

Kempharm Announces Positive Topline Data from Phase 1 Clinical Trial Evaluating Cardiovascular Safety of Serdexmethylphenidate (Sdx)

Second quarter 2022 earnings released: US$0.70 loss per share (vs US$0.40 loss in 2Q 2021)

Forecast breakeven date pushed back to 2024

KemPharm, Inc.(NasdaqGS:KMPH) dropped from Russell Microcap Value Index

First quarter 2022 earnings released: US$0.054 loss per share (vs US$2.49 loss in 1Q 2021)

KemPharm, Inc., Annual General Meeting, Jun 28, 2022

KemPharm, Inc. Announces Submission of Investigational New Drug Application for Phase 2 Trial of KP1077 in Idiopathic Hypersomnia (IH)

Forecast breakeven date pushed back to 2023

Kempharm, Inc. Doses First Subject in Phase 1 Clinical Trial Evaluating Cardiovascular Safety of Serdexmethylphenidate

Forecast breakeven date pushed back to 2023

Full year 2021 earnings released: US$2.11 loss per share (vs US$3.21 loss in FY 2020)

KemPharm, Inc. Completes KP1077 Pre-IND Meeting Process with FDA

KemPharm, Inc. (NasdaqGS:KMPH) announces an Equity Buyback for $50 million worth of its shares.

Kempharm, Inc. Announces Top-Line Results from Clinical Trial Evaluating the Safety and Pharmacokinetics of “Higher-Dose Sdx”

Forecast to breakeven in 2022

Third quarter 2021 earnings released: US$0.05 loss per share (vs US$0.68 loss in 3Q 2020)

Forecast breakeven pushed back to 2023

Second quarter 2021 earnings released: US$0.37 loss per share (vs US$0.21 profit in 2Q 2020)

KemPharm Announces U.S. Launch of Innovative ADHD Treatment AZSTARYS™ (serdexmethylphenidate and dexmethylphenidate capsules) by Corium, Inc

Forecast breakeven pushed back to 2022

Forecast breakeven pushed back to 2022

Insider recently bought €71k worth of stock

Forecast breakeven moved forward to 2021

Full year 2020 earnings released: US$3.21 loss per share (vs US$13.23 loss in FY 2019)

Revenue beats expectations

KemPharm, Inc. to Report Q4, 2020 Results on Mar 11, 2021